TECHNICAL FIELD

The present invention relates to a therapeutic drug for ischemic stroke.

BACKGROUND ART

S-Adenosyl-L-homocysteine hydrolase (hereinafter to be referred to as â€œSAHHâ€ as appropriate) is the sole enzyme that synthesizes homocysteine in the body. This enzyme controls a reaction to hydrolyze S-adenosyl-L-homocysteine (hereinafter to be referred to as â€œSAHâ€ as appropriate) into adenosine and homocysteine, and a reversible reaction to conversely synthesize SHA from adenosine and homocysteine.

Homocysteine is a sulfur amino acid, and is an important intermediate for the metabolism of an essential amino acid, methionine. Homocysteine is maintained at an extremely low concentration in the cell, and redundant homocysteine is extracellularly released, i.e., into the blood. Dr. McCully reported that homocysteine causes vascular pathology such as arteriosclerosis and myocardial infarction (non-patent document 1). Thereafter, clinical tests verified that patients having arteriosclerosis in the peripheral vessel or cerebral vessel show high homocysteine values (non-patent document 2). In almost any clinical tests thereafter, a correlation between increased homocysteine value and ischemic stroke has been reported (non-patent documents 3-8). In a large scale test, it was reported that when the blood homocysteine value increases by 25% (3 Î¼M in absolute value), the risk of coronary artery disease increases by 10%, and the risk of ischemic stroke increases by 20% (non-patent document 9), and it is now suggested that homocysteine is an independent risk factor.

As a compound showing an SAHH inhibitory action, an adenine derivative and the like (patent document 1) have been reported. However, there is no report that specifically suggests effectiveness of these compounds for the treatment of ischemic stroke.

PRIOR ART DOCUMENTSPatent Document

patent document 1: WO2005/009334

Non-Patent Documents

non-patent document 1: Am. J. Pathol. 1969; 56: 111-128
non-patent document 2: N. Eng. J. Med. 1985; 313: 709-715
non-patent document 3: Stroke. 1984; 15: 1012-1016
non-patent document 4: Eur. J. Cli. Invest. 1992; 22: 214-221
non-patent document 5: Stroke. 1990; 21: 572-576
non-patent document 6: Lancet. 1995; 346: 1395-1398
non-patent document 7: Stroke. 1994; 25: 1924-1930
non-patent document 8: Stroke. 1998; 29: 2478-2483
non-patent document 9: J. A. M. A. 2002; 288: 2015-2022

SUMMARY OF THE INVENTIONProblems to be Solved by the Invention

The present invention aims to provide a therapeutic drug for ischemic stroke, which contains a compound having an SAHH inhibitory action as an active ingredient.

Means of Solving the Problems

The present inventors have conducted intensive studies in an attempt to solve the above-mentioned problems and found that a compound having an SAHH inhibitory action can achieve a desired object, which resulted in the completion of the present invention.

Effect of the Invention

A compound having an SAHH inhibitory action can be a medicament effective for the treatment of ischemic stroke.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows the results of walking time on Rota-Rod when 3-deazaadenosine was used as a test drug in Experimental Example 3.

FIG. 2 shows the results of infarct volume suppression ratio when 3-deazaadenosine was used as a test drug in Experimental Example 3.

EMBODIMENT OF THE INVENTION

The present invention relates to a drug for the prophylaxis or treatment of diseases relating to SAHH, a therapeutic drug for ischemic stroke or a homocysteine synthase inhibitor, which contains the following compound having an SAHH inhibitory action as an active ingredient.

(1) A therapeutic drug for ischemic stroke comprising, as an active ingredient, an amide derivative represented by the following formula (I)

[Image Omitted]

wherein
R¹is a hydrogen atom or a C₁-C₃alkyl group,
R²is an optionally substituted heterocyclic group (said heterocyclic group contains at least one nitrogen atom in the ring), or â€”N(R^2a) (R^2b),
R^2aand R^2bare independently selected and each is a hydrogen atom, a C₁-C₆alkyl group, a haloalkyl group or an optionally substituted aryl group,
R⁹is a hydrogen atom,
R⁴, R⁵, R⁶, R⁷are independently selected and each is a hydrogen atom or a C₁-C₄alkyl group,
L is a linker represented by the following formula

[Image Omitted]

wherein s is an integer of 0-2,
t is an integer of 0-2,
R^8a, R^8b, R^8cand R^8dare independently selected and each is a hydrogen atom or a C₁-C₃alkyl group,
Ar is a substituent represented by any of the following formulas (II)-(IV),

[Image Omitted]

wherein
l is an integer of 0-4,
k is an integer of 0-4,
Cy¹and Cy²are independently selected and each is a carbocyclic group, a heterocyclic group or a heteroaryl group,
X is a bond, an oxygen atom or a sulfur atom,
R⁹is a halogen atom or R¹²,
wherein

R¹²is

a hydrogen atom,
an optionally substituted C₁-C₈alkyl group,
an optionally substituted C₂-C₆alkenyl group,
an optionally substituted C₂-C₆alkynyl group,
an optionally substituted C₃-C₈cycloalkyl group,
an optionally substituted heterocyclic group,
an optionally substituted aryl group,
an optionally substituted heteroaryl group, or
an optionally substituted arylalkyl group,

R¹⁰is

a halogen atom,
a cyano group,
an optionally substituted C₁-C₆alkyl group,

â€”CF₃,

â€”Oâ€”R¹³(wherein R¹³is a hydrogen atom, a C₁-C₄alkyl group or â€”CF₃),
â€”COâ€”R¹⁴(wherein R¹⁴is a hydroxy group, a C₁-C₆alkyl group, a C₁-C₆alkoxy group, or an optionally substituted amino group),
an optionally substituted amino group,
an optionally substituted aryl group,
an optionally substituted heteroaryl group,
an optionally substituted heterocyclic group, or
an â€”S(O)_mâ€”C₁-C₆alkyl group wherein m is an integer of 0-2,
R¹¹is a halogen atom, an optionally substituted C₁-C₄alkyl group or CF₃,

A is

an optionally substituted aryl group,
an optionally substituted aryl-C₁-C₄alkyl group,
an optionally substituted heteroaryl-C₁-C₄alkyl group,
a C₃-C₆alkynyl group,
an optionally substituted C₃-C₈cycloalkyl group, or
a group represented by any of the following formulas (V)-(VIII)

[Image Omitted]

wherein
[Image Omitted]
is a single bond or a double bond,
n is an integer of 0-2,
g is an integer of 0-2,
h is an integer of 0-1,
i is an integer of 1-2,
R¹⁵is a C₁-C₄alkyl group, a C₁-C₄alkoxy group, a cyano group or a halogen atom,
R¹⁶is a C₁-C₄alkyl group,

W is â• CHâ€” or â• Nâ€”, and

D is an oxygen atom, a sulfur atom, â• N-(E)u-R¹⁷wherein u is an integer of 0-1, E is â€”SO₂â€” or â€”COâ€”, R¹⁷is a hydrogen atom, a C₁-C₄alkyl group, an aryl group, a C₁-C₄alkylamino group, a C₁-C₆alkoxy group, an arylamino group or an aryloxy group, or â• CHâ€”R¹⁷wherein R¹⁷is as defined above,
or a pharmacologically acceptable salt thereof, or a solvate thereof.
(2) The therapeutic drug for ischemic stroke of the aforementioned (1), wherein the amide derivative represented by the formula (I) is represented by the following formula (IX)

[Image Omitted]

the formula (IX) is the formula (I) wherein
R¹is a C₁-C₃alkyl group, R³is a hydrogen atom, R⁴, R⁵, R⁶and R⁷are each a hydrogen atom, and other symbols are as defined above.
(3) The therapeutic drug for ischemic stroke of the aforementioned (1) or (2), wherein R¹is a C₁-C₃alkyl group.
(4) The therapeutic drug for ischemic stroke of any of the aforementioned (1) to (3), wherein A is selected from the groups represented by the following formulas (V)-(VIII)

[Image Omitted]

wherein
[Image Omitted]
is a single bond or a double bond,
n is an integer of 0-2,
g is an integer of 0-2,
h is an integer of 0-1,
i is an integer of 1-2,
R¹⁵is a C₁-C₄alkyl group, a C₁-C₄alkoxy group, a cyano group or a halogen atom,
R¹⁶is a C₁-C₄alkyl group,

W is â• CHâ€” or â• Nâ€”, and

D is an oxygen atom, a sulfur atom, â• N-(E)u-R¹⁷wherein u is an integer of 0-1, E is â€”SO₂â€” or â€”COâ€”, R¹⁷is a hydrogen atom, a C₁-C₄alkyl group, an aryl group, a C₁-C₄alkylamino group, a C₁-C₆alkoxy group, an arylamino group or an aryloxy group, or â• CHâ€”R¹⁷wherein R¹⁷is as defined above.
(5) The therapeutic drug for ischemic stroke of any of the aforementioned (1)-(4), wherein A is a group represented by the following formula (V)

[Image Omitted]

wherein
[Image Omitted]
is a single bond or a double bond,
n is an integer of 0-2,
h is an integer of 0-1,
i is an integer of 1-2,
R¹⁵is a C₁-C₄alkyl group, a C₁-C₄alkoxy group, a cyano group or a halogen atom,

W is â• CHâ€” or â• Nâ€”.

(6) The therapeutic drug for ischemic stroke of any of the aforementioned (1)-(5), wherein L is a linker represented by the following formula

[Image Omitted]

wherein R^8a, R^8b, R^8cand R^8dare each a hydrogen atom, and other symbols are as defined above.
(7) The therapeutic drug for ischemic stroke of any of the aforementioned (1)-(6), wherein R¹⁰is
a halogen atom,
a cyano group,
â€”COâ€”R¹⁴wherein R¹⁴is as defined above,
an optionally substituted aryl group,
an optionally substituted heteroaryl group, or
an optionally substituted heterocyclic group.
(8) The therapeutic drug for ischemic stroke of any of the aforementioned (1)-(7), wherein R¹⁰is a heteroaryl group having a substituent, or a heterocyclic group having a substituent.
(9) The therapeutic drug for ischemic stroke of any of the aforementioned (1)-(8), wherein the heteroaryl group for R¹⁰is selected from a furyl group, a thienyl group, a pyrazolyl group, a 1,2,4-triazolyl group, a tetrazolyl group, an oxazolyl group, a thiazolyl group, an isoxazolyl group, a 1,2,4-oxadiazolyl group, a 1,3,4-oxadiazolyl group, a 1,3,4-thiadiazolyl group, a pyridyl group, a pyrazinyl group and a pyrimidyl group.
(10) The therapeutic drug for ischemic stroke of any of the aforementioned (1)-(9), wherein R¹⁰is a heteroaryl group having a substituent, and the substituent is a group selected from a halogen atom, a cyano group, a C₁-C₄alkyl group, a C₁-C₄alkoxy group, a â€”CH₂OH group, a â€”CF₃group, a â€”CHF₂group, a â€”CH₂F group, a â€”OCF₃group, a â€”OCHF₂group, a â€”OCH₂F group, a â€”CONH₂group, a â€”CONHCH₃group and a â€”CON(CH₃)₂group.
(11) The therapeutic drug for ischemic stroke of any of the aforementioned (1)-(10), wherein R¹²is
an optionally substituted C₁-C₆alkyl group,
an optionally substituted C₂-C₆alkenyl group,
an optionally substituted C₂-C₆alkynyl group,
an optionally substituted C₃-C₈cycloalkyl group,
an optionally substituted aryl group, or
an optionally substituted heteroaryl group.
(12) The therapeutic drug for ischemic stroke of any of the aforementioned (1)-(11), wherein A is an isoindolinyl group optionally substituted at R¹⁵.
(13) The therapeutic drug for ischemic stroke of any of the aforementioned (1)-(12), wherein R²is â€”N(R^2a) (R^2b) wherein R^2aand R^2bare as defined above.
(14) The therapeutic drug for ischemic stroke of any of the aforementioned (1)-(13), wherein Ar is a group represented by the aforementioned formula (II)f.
(15) The therapeutic drug for ischemic stroke of any of the aforementioned (1)-(13), wherein Ar is a group represented by the aforementioned formula (III).
(16) The therapeutic drug for ischemic stroke of any of the aforementioned (1)-(13), wherein Ar is a group represented by the aforementioned formula (IV).
(17) The therapeutic drug for ischemic stroke of any of the aforementioned (1)-(15), wherein R⁹is a C₁-C₆alkyl group.
(18) The therapeutic drug for ischemic stroke of any of the aforementioned (1)-(13), (15) and (17), wherein X is a bond.
(19) The therapeutic drug for ischemic stroke of any of the aforementioned (1)-(13), (15), (17) and (18), wherein Cy¹is a 8- to 12-membered fused ring heterocyclic group, or 5-membered ring heteroaryl.
(20) The therapeutic drug for ischemic stroke of the aforementioned (1), comprising an amide derivative selected from the following compounds, or a pharmacologically acceptable salt thereof, or a solvate thereof as an active ingredient:

N²-(5-acetyl-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide (compound of Example 56),
N²-(5-acetyl-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide (compound of Example 57),
N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide (compound of Example 64),
N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide (compound of Example 65),
N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide (compound of Example 204),
N²-(5-cyano-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide (compound of Example 1),
N²-(5-cyano-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide (compound of Example 2),
N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide (compound of Example 15),
N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide (compound of Example 16),
N²-{2-[(4-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide (compound of Example 19),
N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide (compound of Example 20),
N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide (compound of Example 21),
N²-{2-[(5-methoxy-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide (compound of Example 24),
N²-{2-[2,3-dihydro-1H-inden-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide (compound of Example 26),
N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(3-methyl-1,2,4-oxadiazol-5-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide (compound of Example 84),
N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(3-methyl-1,2,4-oxadiazol-5-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide (compound of Example 85),
N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(3-methyl-1,2,4-oxadiazol-5-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide (compound of Example 87),
N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide (compound of Example 88),
N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide (compound of Example 89),
N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[5-(4-ethyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-2-methylphenyl]-N¹-[2-(ethylamino)ethyl]glycinamide (compound of Example 92),
N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2-methyl-5-pyrimidin-2-ylphenyl)-N¹-[2-(ethylamino)ethyl]glycinamide (compound of Example 129),
N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(1-ethyl-7-methyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-yl)-N¹-[2-(isopropylamino)ethyl]glycinamide (compound of Example 176),
N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(1-ethyl-7-methyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-yl)-N¹-[2-(ethylamino)ethyl]glycinamide (compound of Example 177),
N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3,6-dimethyl-1,2-benzisoxazol-5-yl)-N¹-[2-(isopropylamino)ethyl]glycinamide (compound of Example 180),
N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3,6-dimethyl-1,2-benzisoxazol-5-yl)-N¹-[2-(ethylamino)ethyl]glycinamide (compound of Example 181),
N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3,5-dimethyl-1,2-benzisoxazol-6-yl)-N¹-[2-(isopropylamino)ethyl]glycinamide (compound of Example 184),
N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3,5-dimethyl-1,2-benzisoxazol-6-yl)-N¹-[2-(ethylamino)ethyl]glycinamide (compound of Example 185),
N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3,6-dimethyl-1,3-benzoxazol-2(3H)-on-5-yl)-N¹-[2-(isopropylamino)ethyl]glycinamide (compound of Example 190),
N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3,6-dimethyl-1,3-benzoxazol-2(3H)-on-5-yl)-N¹-[2-(ethylamino)ethyl]glycinamide (compound of Example 191),
N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3,5-dimethyl-1,3-benzoxazol-2(3H)-on-6-yl)-N¹-[2-(isopropylamino)ethyl]glycinamide (compound of Example 192),
N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3,5-dimethyl-1,3-benzoxazol-2(3H)-on-6-yl)-N¹-[2-(ethylamino)ethyl]glycinamide (compound of Example 193),
N²-{2-[(4-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide (compound of Example 205),
N²-(4-acetyl-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide (compound of Example 210),
N²-(4-acetyl-2-methylphenyl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide (compound of Example 211),
N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(6-methyl-3-oxo-2,3-dihydro-1H-inden-5-yl)-N¹-[2-(ethylamino)ethyl]glycinamide (compound of Example 214),
N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-(6-methyl-3-oxo-2,3-dihydro-1H-inden-5-yl)-N¹-[2-(ethylamino)ethyl]glycinamide (compound of Example 215),
N²-{2-[(4-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-(6-methyl-3-oxo-2,3-dihydro-1H-inden-5-yl)-N¹-[2-(ethylamino)ethyl]glycinamide (compound of Example 216),
N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(3-methyl-1,2,4-oxadiazol-5-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide (compound of Example 229), and
N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(3-methyl-1,2,4-oxadiazol-5-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide (compound of Example 231).
(21) A therapeutic drug for ischemic stroke, comprising a compound having an S-adenosyl-L-homocysteine hydrolase inhibitory action as an active ingredient.
(22) The therapeutic drug for ischemic stroke of the aforementioned (21), wherein the compound having an S-adenosyl-L-homocysteine hydrolase inhibitory action is the amide derivative, or a pharmacologically acceptable salt thereof, or a solvate thereof, which is the active ingredient of the drugs of the aforementioned (1) to (20).
(23) The therapeutic drug for ischemic stroke of the aforementioned (21), wherein the compound having an S-adenosyl-L-homocysteine hydrolase inhibitory action is 3-deazaadenosine or a pharmacologically acceptable salt thereof, or a solvate thereof.
(24) A method of treating ischemic stroke, comprising administering an effective amount of a compound having an S-adenosyl-L-homocysteine hydrolase inhibitory action.
(25) A method of treating ischemic stroke, comprising administering an effective amount of the amide derivative, or a pharmacologically acceptable salt thereof, or a solvate thereof, which is the active ingredient of the drugs of the aforementioned (1) to (20).
(26) The method of treating ischemic stroke of the aforementioned (24), wherein the compound having an S-adenosyl-L-homocysteine hydrolase inhibitory action is 3-deazaadenosine or a pharmacologically acceptable salt thereof, or a solvate thereof.
(27) An S-adenosyl-L-homocysteine hydrolase inhibitor comprising the amide derivative, or a pharmacologically acceptable salt thereof, or a solvate thereof, which is the active ingredient of the drugs of the aforementioned (1) to (20).
(28) A drug for the prophylaxis or treatment of hyperhomocysteinemia, comprising the amide derivative, or a pharmacologically acceptable salt thereof, or a solvate thereof, which is the active ingredient of the drugs of the aforementioned (1) to (20).
(29) Use of a compound having an S-adenosyl-L-homocysteine hydrolase inhibitory action for the production of a therapeutic drug for ischemic stroke.
(30) The use of the aforementioned (29), wherein the compound having an S-adenosyl-L-homocysteine hydrolase inhibitory action is 3-deazaadenosine or a pharmacologically acceptable salt thereof, or a solvate thereof.
(31) Use of the amide derivative, or a pharmacologically acceptable salt thereof, or a solvate thereof, which is the active ingredient of the drugs of the aforementioned (1) to (20), for the production of a therapeutic drug for ischemic stroke.

In the following, the above-mentioned amide derivative represented by the formula (I) is sometimes indicated as â€œcompound (1)â€ .

In addition, the above-mentioned amide derivative represented by the formula (I), or a pharmacologically acceptable salt thereof, or a solvate thereof is sometimes indicated as â€œthe compound of the present inventionâ€ .

Furthermore, the above-mentioned â€œtherapeutic drug for ischemic stroke, comprising an amide derivative represented by the formula (I) or a pharmacologically acceptable salt thereof, or a solvate thereof as an active ingredientâ€ , â€œtherapeutic drug for ischemic stroke, comprising a compound having an S-adenosyl-L-homocysteine hydrolase inhibitory action as an active ingredientâ€ , â€œS-adenosyl-L-homocysteine hydrolase inhibitor, comprising the amide derivative, or a pharmacologically acceptable salt thereof, or a solvate thereof, which is the active ingredient of the drugs of the aforementioned (1) to (20)â€ , and/or â€œdrug for the prophylaxis or treatment of hyperhomocysteinemia, comprising the amide derivative, or a pharmacologically acceptable salt thereof, or a solvate thereof, which is the active ingredient of the drugs of the aforementioned (1) to (20)â€ are/is sometimes indicated as â€œthe medicament of the present inventionâ€ .

The symbols and definitions of the terms used in the present invention are explained in detail in the following.

In the formula (III),

Cy¹is a carbocyclic group, a heterocyclic group or a heteroaryl group, preferably a C₅-C₇cycloalkyl ring, a 5- to 7-membered heterocyclic ring, a benzene ring or a 5- to 7-membered heteroaryl ring, more preferably a cyclopentane ring, a cyclohexane ring, a dioxolane ring, a dioxane ring, a pyrrolidine ring, an imidazolidine ring, a piperidine ring, a piperazine ring, an oxazolidine ring, a thiazolidine ring, a pyrrole ring, an oxazole ring, a thiazole ring, an isoxazole ring, a pyrazole ring, a morpholine ring, an azepane ring, a benzene ring, a pyridine ring, a pyrazine ring, a pyrimidine ring, a pyridazine ring or a dihydropyridine ring, and particularly preferably an oxazole ring, a thiazole ring, an isoxazole ring or a pyrazole ring.

Examples of the formula (III) include a benzoisoxazole ring, a tetrahydroquinoline ring, a benzoxazolidine ring, a benzothiazolidine ring, an indazole ring, a naphthalene ring, an indane ring, a tetrahydronaphthalene ring, a 6,7,8,9-tetrahydro-5H-benzo[7]annulene ring, a 1,3-benzodioxole ring, a 1-indanone ring, a 1-tetralone ring and a 1-benzosuberone ring.

In the formula (IV), Cy²is a carbocyclic group, a heterocyclic group or a heteroaryl group, preferably a C₅-C₇cycloalkyl ring, a 5- to 7-membered heterocyclic ring, a benzene ring or a 5- to 7-membered heteroaryl ring, and more preferably a cyclopentane ring, a cyclohexane ring, a tetrahydrofuran ring or a benzene ring.

Examples of the formula (IV) include a dihydrobenzofuran ring, a naphthalene ring, an indane ring and a tetrahydronaphthalene ring.

In the formula (I), A is an optionally substituted aryl group, an optionally substituted aryl-C₁-C₄alkyl group, an optionally substituted heteroaryl-C₁-C₄alkyl group, a C₃-C₆alkynyl group, an optionally substituted C₃-C₈cycloalkyl group, or any group selected from the formulas (V)-(VIII).

Examples of the following formula (V)

[Image Omitted]

which is A include an indane ring, an isoindoline ring, an octahydro-1H-isoindole ring and an octahydrocyclopenta[c]pyrrole ring.

Examples of the following formula (VI)

[Image Omitted]

which is A include a cyclopentene ring and a 2,5-dihydro-1H-pyrrole ring.

Examples of the following formula (VII)

[Image Omitted]

which is A include a morpholine ring, a 1-piperidine ring, a 4-piperidine ring, a piperazine ring, a thiomorpholine ring, an azepane ring, a cyclopentane ring, a cyclohexane ring and a cycloheptane ring.

Examples of the following formula (VIII)

[Image Omitted]

which is A include a 5,6-dihydro-4H-thieno[2,3-c]pyrrole ring.

In the present specification, the â€œalkyl groupâ€ preferably has a carbon number of 1 to 6, and may be a linear or branched chain. Examples of the group include methyl, ethyl, normal (hereinafter to be indicated as n-) propyl, isopropyl, n-butyl, isobutyl, tertiary (hereinafter to be indicated as t-) butyl, n-pentyl, n-hexyl and the like.

As the â€œC₁-C₃alkyl groupâ€ for R¹, preferred is methyl or ethyl, and more preferred is methyl.

As the â€œC₁-C₆alkyl groupâ€ for R^2aor R^2b, preferred is methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl or t-butyl, and more preferred is methyl, ethyl or isopropyl.

As the â€œC₁-C₄alkyl groupâ€ for R⁴, R⁵, R⁶or R⁷, preferred is methyl.

As the â€œC₁-C₃alkyl groupâ€ for R^8a, R^8b, R^8cor R^8d, preferred is methyl.

As the â€œC₁-C₆alkyl groupâ€ for R¹⁰, preferred is methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl or t-butyl, and more preferred is methyl.

As the â€œC₁-C₄alkyl groupâ€ for R¹¹, preferred is methyl, ethyl, n-propyl or isopropyl, and more preferred is methyl or ethyl.

As the â€œC₁-C₆alkyl groupâ€ for R¹², preferred is methyl, ethyl, n-propyl or isopropyl, and more preferred is methyl or ethyl.

As the â€œC₁-C₄alkyl groupâ€ for R¹³, preferred is methyl, ethyl, n-propyl or isopropyl, and more preferred is methyl.

As the â€œC₁-C₆alkyl groupâ€ for R¹⁴, preferred is methyl, ethyl, n-propyl or isopropyl, and more preferred is methyl or ethyl.

As the â€œC₁-C₄alkyl groupâ€ for R¹⁵, preferred is methyl or ethyl, and more preferred is methyl.

As the â€œC₁-C₄alkyl groupâ€ for R¹⁶, preferred is methyl, ethyl, n-propyl or isopropyl, and more preferred is methyl.

As the â€œC₁-C₆alkyl groupâ€ for R¹⁷, preferred is a methyl group, an ethyl group, an isopropyl or t-butyl, and more preferred is methyl or ethyl.

The substituent of the â€œoptionally substituted C₁-C₆alkyl groupâ€ for R¹⁰includes a halogen atom, a hydroxy group, a cyano group, a C₃-C₇cycloalkyl group, a 5- to 7-membered heterocyclic group, an aryl group and a C₁-C₄alkoxy group, with preference given to a halogen atom, a hydroxy group, a C₃-C₆cycloalkyl group and a C₁-C₄alkoxy group.

The substituent of the â€œoptionally substituted C₁-C₄alkyl groupâ€ for R¹¹includes a halogen atom, a hydroxy group and a cyano group, with preference given to fluorine.

The substituent of the â€œoptionally substituted C₁-C₆alkyl groupâ€ for R¹²includes a halogen atom, a cyano group, a C₃-C₇cycloalkyl group, a 5- to 7-membered heterocyclic group, a hydroxy group and a C₁-C₄alkoxy group, with preference given to a halogen atom, a C₃-C₆cycloalkyl group and a C₁-C₄alkoxy group.

In the present specification, the â€œhaloalkyl groupâ€ is a linear or branched chain alkyl group having one or more, preferably 1 to 3, halogen atoms, and a carbon number of 1 to 6, preferably 1 to 4. Examples thereof include trifluoromethyl, fluoroethyl, difluoroethyl, trifluoroethyl, trifluoro-n-propyl, trifluoroisopropyl, trifluoro-n-butyl, trifluoroisobutyl, trifluoro-t-butyl, trifluoro-n-pentyl, trifluoro-n-hexyl and the like.

As the â€œhaloalkyl groupâ€ for R^2aor R^2b, preferred is fluoroethyl, difluoroethyl or trifluoroethyl, and more preferred is 2-fluoroethyl, 2,2-difluoroethyl or trifluoroethyl.

In the present specification, the â€œalkenyl groupâ€ preferably has a carbon number of 2 to 6, may be linear or branched chain, and has at least one carbon double bond. Examples thereof include an ethenyl group, a propenyl group, butenyl group and the like.

As the â€œC₂-C₆alkenyl groupâ€ for R¹², an ethenyl group, a 1-propenyl group, a 2-propenyl group, a 1-butenyl group, a 2-butenyl group, a 3-butenyl group and the like are preferable, and an ethenyl group, a 1-propenyl group and a 2-propenyl group are more preferable.

The substituent of the â€œoptionally substituted C₂-C₆alkenyl groupâ€ for R¹²includes a halogen atom, a cyano group, a C₃-C₇cycloalkyl group, a 5- to 7-membered heterocyclic group, an aryl group, a hydroxy group and a C₁-C₄alkoxy group, with preference given to a halogen atom, a C₃-C₆cycloalkyl group and a C₁-C₄alkoxy group.

In the present specification, the â€œalkynyl groupâ€ preferably has a carbon number of 2 to 6, may be linear or branched chain, and has at least one carbon triple bond. Examples thereof include an ethynyl group, a propynyl group, a butynyl group and the like.

As the â€œC₂-C₆alkynyl groupâ€ for R¹², preferred is an ethynyl group, a 1-propynyl group, a 2-propynyl group, a 1-butynyl group, a 2-butynyl group or a 3-butynyl group, and more preferred is an ethynyl group, a 1-propynyl group, a 2-propynyl group or a 2-butynyl group.

As the â€œC₃-C₆alkynyl groupâ€ for A, preferred is a 2-propynyl group, a 1-methyl-2-propynyl group, a 2-butynyl group, a 3-butynyl group or a 1-methyl-2-butynyl group, and more preferred is a 2-propynyl group or a 2-butynyl group.

The substituent of the â€œoptionally substituted C₂-C₆alkynyl groupâ€ for R¹²includes a halogen atom, a cyano group, a C₃-C₇cycloalkyl group, a 5- to 7-membered heterocyclic group, an aryl group, a hydroxy group and a C₁-C₄alkoxy group, with preference given to a halogen atom, a C₃-C₆cycloalkyl group and a C₁-C₄alkoxy group.

In the present specification, the â€œcycloalkyl groupâ€ is alicyclic hydrocarbon containing only a saturated structure, and includes monocyclic hydrocarbon, fused polycyclic hydrocarbon, and crosslinked hydrocarbon. The carbon number is preferably 3 to 8, and examples of the cycloalkyl group include a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cyclooctyl group and the like.

As the â€œC₃-C₈cycloalkyl groupâ€ for R¹², preferred is cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl or cyclooctyl, and more preferred is cyclopentyl or cyclohexyl.

As the â€œC₃-C₈cycloalkyl groupâ€ for A, preferred is cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl or cycloheptyl, and more preferred is cyclohexyl.

The substituent of the â€œoptionally substituted C₃-C₈cycloalkyl groupâ€ for R¹²include an aryl group, a heteroaryl group, a halogen atom, a cyano group, a C₁-C₄alkyl group, a C₃-C₇cycloalkyl group, a C₁-C₄alkoxy group, a â€”CF₃group and a â€”OCF₃group, with preference given to a halogen atom, a C₁-C₄alkyl group and a C₁-C₄alkoxy group.

The substituent of the â€œoptionally substituted C₃-C₈cycloalkyl groupâ€ for A include an aryl group, a heteroaryl group, a halogen atom, a cyano group, a C₁-C₄alkyl group, a hydroxyl group, a C₃-C₇cycloalkyl group, a C₁-C₄alkoxy group, a â€”CF₃group and a â€”OCF₃group, with preference given to an aryl group, a halogen atom, a C₁-C₄alkyl group and a C₁-C₄alkoxy group.

The â€œaryl groupâ€ in the present specification is a cyclic hydrocarbon having aromatic property, which is monocyclic hydrocarbon or polycyclic hydrocarbon having a carbon number of 6 to 10, and may be condensed or fused with a cycloalkyl group, a heterocyclic group and a heteroaryl group. For example, a phenyl group, a 1-naphthyl group, a 2-naphthyl group, a 5-indanyl group, a 5-benzofuranyl group, a 6-benzofuranyl group, a 5-benzothienyl group, a 6-benzothienyl group, a 5-benzimidazolyl group, a 5-benzoxazolyl group, a 6-benzoxazolyl group, a 5-benzothiazolyl group, a 6-benzothiazolyl group, a 5-benzoisoxazolyl group, a 6-benzoisoxazolyl group, a 5-indolyl group, a 6-indolyl group, a 1H-indazol-5-yl group, a 1H-indazol-6-yl group, a 6-quinolinyl group, a 7-quinolinyl group, a 6-isoquinolinyl group, a 7-isoquinolinyl group, a 6-phthalazinyl group, a 7-phthalazinyl group, a 6-quinoxalinyl group, a 7-quinoxalinyl group, a 6-quinazolinyl group, a 7-quinazolinyl group, a 6-cinnolinyl group, a 7-cinnolinyl group and the like can be mentioned.

As the â€œaryl groupâ€ for R^2aor R^2b, preferred is a phenyl group.

As the â€œaryl groupâ€ for Rⁿ, preferred is a phenyl group.

As the â€œaryl groupâ€ for R¹², preferred is a phenyl group.

As the â€œaryl groupâ€ for R¹⁷, preferred is a phenyl group, a 1-naphthyl group or a 2-naphthyl group.

As the â€œaryl groupâ€ for A, preferred is a phenyl group, a 1-naphthyl group, a 2-naphthyl group or a 5-indanyl group, and particularly preferred is a phenyl group.

Examples of the substituent of the â€œoptionally substituted aryl groupâ€ for R^2aor R^2binclude a halogen atom, a cyano group, a hydroxy group, a C₁-C₄alkyl group, a C₁-C₄alkoxy group, a â€”CF₃group and a â€”OCF₃group.

Examples of the substituent of the â€œoptionally substituted aryl groupâ€ for R¹⁰include a halogen atom, a cyano group, a C₁-C₄alkyl group, a C₁-C₄alkoxy group, a â€”CH₂OH group, a â€”CF₃group, a â€”CHF₂group, a â€”CH₂F group, a â€”OCF₃group, a â€”OCHF₂group, a â€”OCH₂F group, a â€”CONH₂group, a â€”CONHCH₃group and a â€”CON(CH₃)₂group, and preferable examples include a halogen atom and a cyano group.

Examples of the substituent of the â€œoptionally substituted aryl groupâ€ for R¹²include a halogen atom, a cyano group, a hydroxy group, a C₁-C₄alkyl group, a C₁-C₄alkoxy group, a â€”CF₃group, a â€”OCF₃group and a benzyloxy group.

Examples of the substituent of the â€œoptionally substituted aryl groupâ€ for A include a halogen atom, a cyano group, a C₁-C₄alkyl group, a C₁-C₄alkoxy group, a â€”CF₃group and a â€”OCF₃group, with preference given to a halogen atom.

In the present specification, the â€œcarbocyclic groupâ€ is alicyclic hydrocarbon containing only a saturated structure, alicyclic hydrocarbon containing a partially unsaturated structure, or cyclic hydrocarbon having aromatic property, and includes monocyclic hydrocarbon, fused polycyclic hydrocarbon and crosslinked hydrocarbon. The carbon number is preferably 3 to 10, and they may be condensed or fused with a cycloalkyl group, a heterocyclic group or a heteroaryl group. Furthermore, the carbon atom on the aforementioned cycloalkyl group may be partially substituted by an oxo group or a thioxo group, and the carbon atom or hetero atom on the aforementioned heterocyclic group may be partially substituted by an oxo group or a thioxo group. Examples of the carbocyclic group include the substituents recited for the aforementioned cycloalkyl group and aryl group, as well as a cycloalkenyl group.

As the â€œcarbocyclic groupâ€ for Cy¹, preferred is a C₅-C₇cycloalkyl ring or a benzene ring, and more preferred is a cyclopentane ring, a cyclohexane ring or a benzene ring.

As the â€œcarbocyclic groupâ€ for Cy², preferred is a C₅-C₇cycloalkyl ring or a benzene ring, and more preferred is a cyclopentane ring, a cyclohexane ring or a benzene ring.

The â€œheterocyclic groupâ€ in the present specification is a cyclic compound having at least one hetero atom (nitrogen, oxygen or sulfur) and a carbon atom, and a completely saturated or partially unsaturated structure. The heterocyclic group of present specification includes a 3- to 8-membered monocyclic compound, a 8- to 12-membered fused ring compound or heterocyclic spiro compound condensed, fused or bonded with other heterocyclic group, a heteroaryl group, a cycloalkyl group or an aryl group. The carbon atom or hetero atom on the heterocyclic group may be partially substituted by an oxo group or a thioxo group. The monocyclic hetero ring is preferably a 4- to 7-membered ring, and the fused heterocycle is preferably a 8- to 10-membered ring.

Examples of the heterocyclic group include a tetrahydrofuranyl group, a tetrahydropyranyl group, a dioxolanyl group, a dioxanyl group, a pyrrolidinyl group, a piperidinyl group, a dihydropyridinyl group, a tetrahydropyridinyl group, a piperazinyl group, an azepanyl group, an azocanyl group, a morpholinyl group, a thiomorpholinyl group, an oxazolidinyl group, a thiazolidinyl group, a tetrahydrothienyl group, a tetrahydrothiopyranyl group, a dihydrooxadiazolyl group, a dihydrotriazolyl group, a dihydrobenzofuranyl group, a chromanyl group, an indolinyl group, an isoindolinyl group, a tetrahydroquinolinyl group, a tetrahydroisoquinolinyl group and the like.

Examples of the â€œheterocyclic groupâ€ for Cy¹include a 3- to 8-membered monocyclic compound having a completely saturated or partially unsaturated structure, or a 8- to 12-membered fused ring compound condensed with other heterocyclic group, heteroaryl group, cycloalkyl group or aryl group.

Specific examples of the 3- to 8-membered monocyclic compound include a dioxolanyl group (particularly preferably 1,3-dioxolanyl), a pyrrolidinyl group, a piperidinyl group, an oxazolidinyl group and the like.

Specific examples of the 8- to 12-membered fused ring compound include 5,6,7,8-tetrahydro-4H-pyrazolo[1,5-a]azepine, 4,5,6,7-tetrahydro-pyrazolo[1,5-a]pyridine, 5,6-dihydro-4H-pyrazolo[1,2-b]pyrazole, 5,6-dihydro-4H-pyrrolo[1,2-b]pyrazole, 6,7,8,9-tetrahydro-5H-imidazolo[1,2-a]azepine, 5,6,7,8-tetrahydro-imidazolo[1,2-a]pyridine, 6,7-dihydro-5H-pyrrolo[1,2-a]imidazole and the like. Of these, preferably 5,6,7,8-tetrahydro-4H-pyrazolo[1,5-a]azepine, 4,5,6,7-tetrahydro-pyrazolo[1,5-a]pyridine, and 5,6-dihydro-4H-pyrrolo[1,2-b]pyrazole.

Examples of the â€œheterocyclic groupâ€ for Cy²include a 3- to 8-membered monocyclic compound having a completely saturated or partially unsaturated structure, and a 8- to 12-membered fused ring compound condensed with other heterocyclic group, heteroaryl group, cycloalkyl group or aryl group.

Specific examples of the 3- to 8-membered monocyclic compound include tetrahydrofuran.

Specific examples of the 8- to 12-membered fused ring compound include 5,6,7,8-tetrahydro-4H-pyrazolo[1,5-a]azepine, 4,5,6,7-tetrahydro-pyrazolo[1,5-a]pyridine, 5,6-dihydro-4H-pyrazolo[1,2-b]pyrazole, 6,7,8,9-tetrahydro-5H-imidazolo[1,2-a]azepine, 5,6,7,8-tetrahydro-imidazolo[1,2-a]pyridine, 6,7-dihydro-5H-pyrrolo[1,2-a]imidazole and the like.

The â€œheterocyclic groupâ€ for R²contains at least one nitrogen atom as a hetero atom, preferably a pyrrolidinyl group, a piperidinyl group, a piperazinyl group, a morpholinyl group, a thiomorpholinyl group or a thiazolidinyl group, and more preferably a 1-pyrrolidinyl group, a 2-pyrrolidinyl group, a 3-pyrrolidinyl group, a 1-piperidinyl group, a 2-piperidinyl group or a 4-morpholinyl group.

As the â€œheterocyclic groupâ€ for R¹⁰, preferred is a dihydrooxadiazolyl group, a dihydrotriazolyl group or a pyrrolidinyl group, and more preferred is a 1,2,4-dihydrooxadiazolyl group, a 1,3,4-dihydrooxadiazolyl group or a pyrrolidinyl group.

As the â€œheterocyclic groupâ€ for R¹², preferred is a tetrahydrofuranyl group, a tetrahydropyranyl group, a pyrrolidinyl group, a piperidinyl group, a tetrahydrothienyl group or a tetrahydrothiopyranyl group, and more preferred is a 3-tetrahydrofuranyl group or a 4-tetrahydropyranyl group.

The substituent of the â€œoptionally substituted heterocyclic groupâ€ for R²include a halogen atom, a cyano group, a hydroxy group, a C₁-C₄alkyl group, a hydroxy C₁-C₄alkyl group, a C₃-C₇cycloalkyl group, a C₁-C₄alkoxy group, a â€”CF₃group and a â€”OCF₃group, with preference given to a hydroxy group.

The substituent of the â€œoptionally substituted heterocyclic groupâ€ for R¹⁰include an aryl group, a heteroaryl group, a halogen atom, a cyano group, a C₁-C₄alkyl group, a C₃-C₇cycloalkyl group, a C₁-C₄alkoxy group, a â€”CF₃group, a â€”OCF₃group, a â€”CONH₂group, a â€”CONHCH₃group and a â€”CON(CH₃)₂group, with preference given to a C₁-C₄alkyl group and a â€”CONH₂group.

The â€œheteroaryl groupâ€ in the present specification is an aromatic ring compound having at least one hetero atom (nitrogen, oxygen or sulfur) and a carbon atom, and includes a 5- or 6-membered monocyclic compound, and a 8- to 12-membered fused ring compound condensed or fused with other heterocyclic group, heteroaryl group, cycloalkyl group or aryl group. Examples of the heteroaryl group include a furyl group, a thienyl group, a pyrrolyl group, an imidazolyl group, a pyrazolyl group, a triazolyl group, a tetrazolyl group, an oxazolyl group, a thiazolyl group, an isoxazolyl group, an isothiazolyl group, an oxadiazolyl group, a thiadiazolyl group, a furazanyl group, a pyridyl group, a pyrazinyl group, a pyrimidyl group, a pyridazinyl group, a triazinyl group, an indolizinyl group, an isoindolyl group, an indolyl group, an indazolyl group, a benzimidazolyl group, a purinyl group, a quinolyl group, an isoquinolyl group, a phthalazinyl group, a quinoxalinyl group, a quinazolinyl group, a cinnolinyl group, a benzofuranyl group, a benzothienyl group, a benzoxazolyl group, a benzothiazolyl group, a benzoisoxazolyl group, a benzoisothiazolyl group and the like.

Preferable examples of the â€œheteroaryl groupâ€ for Cy¹or Cy²include a pyrrolyl group, an oxazolyl group, a thiazolyl group, an isoxazolyl group, a pyrazolyl group, a pyridyl group, a pyrazinyl group, a pyrimidyl group, a pyridazinyl group and the like, and more preferable examples include an oxazolyl group, a thiazolyl group, an isoxazolyl group, a pyrazolyl group and the like.

As the â€œheteroaryl groupâ€ for Rⁿ, preferred is a furyl group, a thienyl group, a pyrazolyl group, a triazolyl group, a tetrazolyl group, an oxazolyl group, an isoxazolyl group, a thiazolyl group, an oxadiazolyl group, a thiadiazolyl group, a pyridyl group, a pyrazinyl group, a pyrimidyl group or a pyridazinyl group, and more preferred is a furyl group, a thienyl group, a pyrazolyl group, a 1,2,4-triazolyl group, a tetrazolyl group, an oxazolyl group, a thiazolyl group, an isoxazolyl group, a 1,2,4-oxadiazolyl group, a 1,3,4-oxadiazolyl group, a 1,3,4-thiadiazolyl group, a pyridyl group, a pyrazinyl group or a pyrimidyl group, particularly preferably a 1,2,4-oxadiazolyl group, a 1,3,4-oxadiazolyl group or a 1,3,4-thiadiazolyl group.

As the â€œheteroaryl groupâ€ for R¹², preferred is a thienyl group or a pyrimidyl group, and more preferred is a 2-thienyl group.

Examples of the substituent of the â€œoptionally substituted heteroaryl groupâ€ for R¹⁰include a halogen atom, a cyano group, a C₁-C₄alkyl group (e.g., methyl group, ethyl group, t-butyl group), a C₁-C₄alkoxy group, a â€”CHF₂group, a â€”CF₃group, an â€”OCF₃group, a â€”CONH₂group, a â€”CONHCH₃group, a â€”CON(CH₃)₂group, an amino group and a hydroxy-C₁-C₄alkyl group (e.g., hydroxymethyl group).

Preferable examples of the substituent of the â€œoptionally substituted heteroaryl groupâ€ for R¹⁰include a halogen atom, a cyano group, a C₁-C₄alkyl group, a C₁-C₄alkoxy group, a â€”CF₃group, an â€”OCF₃group, a â€”CONH₂group, a â€”CONHCH₃group and a â€”CON(CH₃)₂group, more preferably a C₁-C₄alkyl group, a C₁-C₄alkoxy group, a â€”CF₃group, an â€”OCF₃group can be mentioned, with further preference given to a C₁-C₄alkyl group (preferably, methyl group, ethyl group).

Examples of the substituent of the â€œoptionally substituted heteroaryl groupâ€ for R¹²include a halogen atom, a cyano group, a C₁-C₄alkyl group, a C₁-C₄alkoxy group, a â€”CF₃group and an â€”OCF₃group.

The â€œarylalkyl groupâ€ in the present specification has an aryl moiety which is as defined above. The alkyl moiety preferably has a carbon number of 1 to 4 and may be linear or branched chain. Examples thereof include benzyl, phenethyl, 3-phenylpropyl, 1-naphthylmethyl, 2-(1-naphthyl)ethyl, 2-(2-naphthyl)ethyl, 3-(2-naphthyl)propyl and the like.

As the â€œarylalkyl groupâ€ for R¹², preferred is a benzyl group or a phenethyl group, and more preferred is a benzyl group.

As the â€œaryl-C₁-C₄alkyl groupâ€ for A, preferred is a benzyl group, a phenethyl group or a 3-phenylpropyl group, and more preferred is a benzyl group or a phenethyl group.

Examples of the substituent of the â€œoptionally substituted arylalkyl groupâ€ for R¹²include a halogen atom, a cyano group, a C₁-C₄alkyl group, a C₁-C₄alkoxy group, a â€”CF₃group and an â€”OCF₃group, and the aryl moiety of the arylalkyl group may be substituted.

Examples of the substituent of the â€œoptionally substituted aryl-C₁-C₄alkyl groupâ€ for A include a halogen atom, a cyano group, a C₁-C₄alkyl group, a C₁-C₄alkoxy group, a â€”CF₃group and an â€”OCF₃group, and the aryl moiety of the arylalkyl group may be substituted.

The â€œheteroarylalkyl groupâ€ in the present specification has a heteroaryl moiety which is as defined above. The alkyl moiety preferably has a carbon number of 1 to 4 and may be linear or branched chain. Examples thereof include pyridylmethyl, pyridylethyl, furylmethyl, thienylmethyl, furylethyl, thienylethyl and the like.

As the â€œheteroaryl-C₁-C₄alkyl groupâ€ for A, preferred is pyridylethyl, furylethyl or thienylethyl, and more preferred is 2-(2-furyl)ethyl or 2-(2-thienyl)ethyl.

Examples of the substituent of the â€œoptionally substituted heteroaryl-C₁-C₄alkyl groupâ€ for A include a halogen atom, a cyano group, a C₁-C₄alkyl group, a C₁-C₄alkoxy group, a CF₃group and an OCF₃group. The heteroaryl moiety of the heteroarylalkyl group may be substituted.

The â€œalkoxy groupâ€ in the present specification is a Monovalent group resulting from removal of a hydrogen atom from the hydroxyl group of alcohols, which has a carbon number of 1 to 6 and may be linear or branched chain. Examples thereof include methoxy, ethoxy, propoxy, butoxy, pentyloxy, hexyloxy and the like.

As the â€œC₁-C₆alkoxy groupâ€ for R¹⁴, preferred is a methoxy group, an ethoxy group, a propoxy group, an isopropoxy group or a t-butoxy group, and more preferred is a methoxy group or an ethoxy group.

As the â€œC₁-C₄alkoxy groupâ€ for R¹⁵, preferred is a methoxy group or an ethoxy group, and more preferred is a methoxy group.

As the â€œC₁-C₆alkoxy groupâ€ for R¹⁷, preferred is a methoxy group, an ethoxy group or a t-butoxy group, and more preferred is a methoxy group.

Examples of the â€œhalogen atomâ€ in the present specification include fluorine, chlorine, bromine and iodine. Preferred is fluorine, chlorine or bromine, and particularly preferred is fluorine or chlorine.

As the halogen atom for R⁹, preferred is fluorine or chlorine.

As the halogen atom for R¹⁵, preferred is fluorine or chlorine.

As the halogen atom for R¹⁰, preferred is fluorine, chlorine or bromine.

As the halogen atom for R¹¹, preferred is fluorine or chlorine.

The â€œalkylamino groupâ€ in the present specification is one wherein 1 or 2 hydrogen atoms of the amino group are substituted by an alkyl group, and the alkyl moiety preferably has a carbon number of 1 to 4 and may be linear or branched chain. Examples of the alkylamino group include methylamino, ethylamino, isopropylamino, dimethylamino, diethylamino and the like.

As the â€œC₁-C₄alkylamino groupâ€ for R¹⁷, preferred is methylamino, dimethylamino, ethylamino or isopropylamino.

The â€œarylamino groupâ€ in the present specification is one wherein 1 or 2 hydrogen atoms of the amino group are substituted by an aryl group, and the aryl moiety is similar to that mentioned above. Examples thereof include a phenylamino group.

As the â€œarylamino groupâ€ for R¹⁷, preferred is a phenylamino group.

Examples of the â€œaryloxy groupâ€ in the present specification include a phenoxy group and a naphthyloxy group.

Preferable examples of the â€œaryloxy groupâ€ for R¹⁷include a phenoxy group.

In the present specification, examples of the substituent of the â€œoptionally substituted amino groupâ€ for R¹⁰include a C₁-C₄alkyl group, a C₁-C₄alkylsulfonyl group, a C₁-C₄acyl group, a C₁-C₄alkoxycarbonyl group, a C₁-C₄alkylaminocarbonyl group and the like.

Examples of the substituent of the â€œoptionally substituted amino groupâ€ for R¹⁴include a C₁-C₄alkyl group, a C₁-C₄alkylsulfonyl group, a C₁-C₄alkyl-amino group, a C₁-C₄alkylcarbonyl group, a C₁-C₄alkoxycarbonyl group and the like. Particularly preferred is a methyl group, a methylsulfonyl group, a methylamino group, a methylcarbonyl group, a methoxycarbonyl group and the like.

In the present specification, examples of the â€œringâ€ formed by R¹and A include a pyrrolidine ring, a piperidine ring, a piperazine ring and the like.

In the above-mentioned formulas (II) and (IV), 1 is preferably an integer of 0, 1 or 2, more preferably an integer of 1.

In the above-mentioned formula (III), k is preferably an integer of 0, 1 or 2, and X is preferably a bond or an oxygen atom.

In the above-mentioned formulas (V)-(VIII), n is preferably an integer of 0, 1 or 2, more preferably an integer of 0 or 1.

In the above-mentioned formula (VII), g is preferably an integer of 1.

In the above-mentioned formula (V), h is preferably an integer of 1.

In the above-mentioned formula (V), i is preferably an integer of 1 or 2.

In the above-mentioned formulas (V)-(VII), W is preferably â• CHâ€” or â• Nâ€”.

In the above-mentioned formula (VII), D is preferably â• N-(E)u-R¹⁷wherein E is preferably â€”SO₂â€” or â€”COâ€”, u is preferably an integer of 1, and R¹⁷is preferably a C₁-C₄alkyl group or a C₁-C₅alkoxy group.

Examples of the pharmacologically acceptable salt of compound (1) include salts with mineral acid such as hydrochloric acid, sulfuric acid, hydrobromic acid, phosphoric acid and the like; salts with organic acid such as methanesulfonic acid, p-toluenesulfonic acid, acetic acid, oxalic acid, citric acid, malic acid, fumaric acid and the like; salts with alkali metal such as sodium, potassium and the like; salts with alkaline earth metal such as magnesium and the like; salts with amine such as ammonia, ethanolamine, 2-amino-2-methyl-1-propanol and the like. Besides these, the kind of the salt is not particularly limited as long as it is pharmacologically acceptable.

Examples of the pharmacologically acceptable salt of 3-deazaadenosine include those similar to the pharmacologically acceptable salt of said compound (I).

Examples of the solvate of compound (I) include a solvate with water, ethanol, ethyl acetate and the like. Besides these, the kind of the solvate is not particularly limited as long as it is pharmacologically acceptable.

Examples of the solvate of 3-deazaadenosine or a pharmacologically acceptable salt thereof include those similar to the solvate of said compound (I).

The â€œS-adenosyl-L-homocysteine hydrolase (SAHH) inhibitionâ€ refers to reversible inhibition of the SAHH activity, which includes competitive inhibition, noncompetitive inhibition and uncompetitive inhibition.

The enzyme inhibition includes reversible inhibition that inhibits the reaction that should inherently proceed by reversible binding, and irreversible inhibition that prevents binding of a substrate by a strong binding such as covalent bond and the like with an amino acid residue near the deficient site.

The reversible inhibition includes 3 types.

The first is a competitive inhibition, wherein enzyme-inhibitor complex (EI) is formed between enzyme (E) and inhibitor (I) to antagonize the binding of the substrate to an enzyme. That is, a competitive inhibitor is bound to an enzyme substrate binding site instead of a substrate and reversibly inhibits enzyme activity. Therefore, even when a competitive inhibitor is present, the inhibitory activity disappears by sufficiently increasing the substrate concentration. The inhibitory constant Ki is defined to be [E][I]/[EI].

The second reversible inhibition is a noncompetitive inhibition, where an inhibitor does not influence free enzymes and the substrate-enzyme binding stage. It reversibly binds only to enzyme-substrate complex (ES) to show an inhibitory action. Therefore, an increased substrate concentration does not influence the inhibition intensity. In this case, the inhibitory constants Ki is [ES][I]/[ESI]. [ESI] is a concentration of enzyme-substrate-inhibitor complex.

The third reversible inhibition is an uncompetitive inhibition, wherein the inhibitor reversibly binds a free enzyme and enzyme-substrate complex to show an inhibitory action. An uncompetitive inhibitor binds an enzyme at a moiety different from the substrate binding site, and achieves inhibition by changing the molecular structure of the enzyme. In this case, two inhibitory constants Ki of Ki^EI=[E][I]/[EI] and Ki^ESI=[ES][I]/[ESI] are present.

These inhibitory modes can be determined by Lineweaver-Burk Plotplot.

Examples of the â€œcompound having an S-adenosyl-L-homocysteine hydrolase (SAHH) inhibitory action (hereinafter to be also referred to as an SAHH inhibitor)â€ include those that show, when measured in the same manner as in Experimental Example 1, IC₅₀of 100 Î¼m or less, preferably 10 Î¼m or less, particularly preferably 1 Î¼M or less.

Specific examples of the compound having an SAHH inhibitory action include the amide derivative which is the active ingredient of the drugs of the aforementioned (1) to (20), the compounds described in the Examples of the present application, 3-deazaadenosine described in Eur. J. Biochem., 2003, vol. 270, page 3507, adenine derivative described in WO2005/009334, Neplanocin A described in J. Med. Chem., 2003, vol. 46, No. 2, page 201, (âˆ’)-Aristeromycin described in Bioorg. Med. Chem., 2008, vol. 16, No. 7, page 3809, Aristeromycin derivative or adenosine derivative described in EP0304889, 4-substituted-5-hydroxymethyl-1,2-cyclopentanediol derivative or 1-cyclopentanol derivative obtained by substitution of the 3-position with a heterocycle group, which is described in U.S. Pat. No. 4,605,659, Noraristeromycin described in Tetrahedron, 2002, vol. 58, page 1271, and D-Eritadenine described in J. Biol. Chem., 2002, vol. 277., pages 7477-7482, pharmacologically acceptable salts of these compounds, solvates thereof and the like.

Preferable examples of the adenine derivative described in WO2005/009334 include 4-(9H-adenin-9-yl)-2-hydroxybutyric acid methyl ester (DZ-2002).

Preferable examples of the Aristeromycin derivative or adenosine derivative described in EP0304889 include (Z)-9-(5-deoxy-5-fluoro-beta-D-erythro-pent-4-enofuranosyl)adenine (MDL-28842).

Among those mentioned above, preferred are the amide derivative which is the active ingredient of the drugs of the aforementioned (1) to (20), the compounds described in the Examples of the present application and 3-deazaadenosine, pharmacologically acceptable salts of these compounds, and solvates thereof, and particularly preferred are the amide derivative which is the active ingredient of the drugs of the aforementioned (1) to (20), the compounds described in the Examples of the present application, pharmacologically acceptable salts of these compounds, and solvates thereof.

Now the production methods of the compound of the present invention are explained.

A compound represented by the formula (I), or a salt thereof can be synthesized by adopting various known synthesis methods, while utilizing the characteristics of basic skeleton or the kind of the substituent. Representative production methods are shown below as examples, which are not to be construed as limitative. Depending on the kind of the functional group, conversion of the functional group to a suitable protecting group, namely, a group easily convertible to the functional group, in the stage of a starting material or intermediate, may be effective for production techniques. In this case, the protecting group can be removed as necessary to give a desired compound. Examples of such functional group include a hydroxyl group, a carboxyl group, an amino group and the like. Examples of the protecting group include those described in Greene and Wutt, â€œProtective Groups in Organic Synthesis (third edition)â€ , and they may be used as appropriate according to the reaction conditions.

In the present specification, the â€œroom temperatureâ€ is generally 0-30Â° C.

[Image Omitted]

wherein Ar, R¹, R², R³, R⁴, R⁵, A, L are as defined above. G is a halogen atom, P is an amino-protecting group, and R²¹is a C₁-C₄alkyl group. When the nitrogen atom contained in R²is a primary or secondary amine, the reaction is preferably carried out using compound (8) wherein the nitrogen atom is protected, and after completion of the reaction, the resulting compound is subjected to a deprotection operation.

Step 1 (Alkylation Reaction)

This step is performed under warming in an inert solvent or without a solvent, in the presence of compound (1), 2 or more equivalents of compound (2) and 2 or more equivalents of a base. Examples of the base include alkali metal carbonates such as potassium carbonate, sodium carbonate, cesium carbonate and the like, alkali metal phosphates such as dipotassium hydrogenphosphate, disodium hydrogenphosphate, trisodium phosphate, tripotassium phosphate and the like, amines such as triethylamine, N,N-diisopropylethylamine, N-methylmorpholine, pyridine, 2,6-lutidine, N,N-dimethylaminopyridine, 1,8-diazabicyclo[5.4.0]undec-7-ene (hereinafter to be referred to as DBU) and the like, and the like. The amount of the base to be used is 2 or more equivalents, preferably 2 to 20 equivalents, relative to compound (1). The halogen atom of compound (2) is chlorine, bromine, iodine, fluorine or the like, and the amount thereof to be used is 2 or more equivalents, preferably 2 to 20 equivalents, relative to compound (1). The reaction can be carried out using the â€œinert solventâ€ include ethers such as tetrahydrofuran, 1,4-dioxane and the like, halogenated hydrocarbons such as chloroform, carbon tetrachloride, 1,2-dichloroethane and the like, hydrocarbons such as hexane, benzene, toluene, xylene and the like, nitriles such as acetonitrile and the like, amides such as N,N-dimethylformamide, N-methylpyrrolidone, N,N-dimethylacetamide and the like, sulfoxides such as dimethyl sulfoxide and the like, and the like. These solvents may be mixed at an appropriate ratio. Alternatively, the reaction can be carried out without a solvent. The reaction temperature is generally 40 to 200Â° C., preferably 50 to 150Â° C.

Step 2 (Hydrolysis of Ester)

This step is generally performed in the presence of an acid or base, in a water-containing solvent. Examples of the acid include formic acid, hydrochloric acid, acetic acid, sulfuric acid, hydrobromic acid, trifluoroacetic acid and the like. Examples of the base include alkali metal carbonates such as potassium carbonate, sodium carbonate and the like, alkali metal hydroxides such as potassium hydroxide, lithium hydroxide, sodium hydroxide and the like, and the like. The amount of the acid or base to be used is generally excess amount relative to compound (3). The preferable amount of the acid to be used is 2 to 100 equivalents relative to compound (3), and the preferable amount of the base to be used is 2 to 10 equivalents relative to compound (3). Examples of the water-containing solvent include a mixed solvent of water and one or more kinds of solvents selected from alcohols such as methanol, ethanol and the like, ethers such as tetrahydrofuran, 1,4-dioxane and the like, dimethyl sulfoxide and acetone and the like, and the like. When R²¹is a tert-butyl group, acid decomposition may be carried out besides the above-mentioned reaction in a water-containing solvent. Examples of the acid include formic acid, hydrochloric acid, acetic acid, sulfuric acid, hydrobromic acid, trifluoroacetic acid, methanesulfonic acid, p-toluenesulfonic acid and the like. In this case, the solvents may be mixed at an appropriate ratio. Examples of the solvent include halogenated hydrocarbons such as chloroform, dichloromethane, dichloroethane and the like, and the like. The amount of the acid to be used is generally excess amount relative to compound (3), preferably 2 to 200 equivalents relative to compound (3). The reaction temperature is generally âˆ’20 to 150Â° C., preferably âˆ’10 to 100Â° C.

Step 3 (Acid Anhydration Reaction)

This step is generally performed using a dehydrating-condensing agent in an inert solvent. Examples of the â€œinert solventâ€ include ethers such as tetrahydrofuran, 1,4-dioxane, diethyl ether and the like, halogenated hydrocarbons such as chloroform, dichloromethane and the like, nitriles such as acetonitrile and the like, amides such as N,N-dimethylformamide, N,N-dimethylacetamide, N-methylpyrrolidone and the like, sulfoxides such as dimethyl sulfoxide and the like, and the like. Of these, acetonitrile, dichloromethane, tetrahydrofuran, N,N-dimethylformamide and the like are preferable.

The reaction temperature is generally about âˆ’20Â° C. to 50Â° C., preferably at room temperature. The reaction time is generally about 30 min to about 24 hr. Examples of the dehydrating-condensing agent include dicyclohexylcarbodiimide (hereinafter to be referred to as DCC), N-(3-dimethylaminopropyl)-Nâ€²-ethylcarbodiimide hydrochloride (hereinafter to be referred to as WSC) and the like. Of these, WSC is preferable.

The amount of the condensing agent to be used is generally 1 to 3 equivalents relative to compound (4). In Step 3 and Step 4 (Amidation Reaction), a partitioning operation may be performed on the way. When the water-soluble condensing agent such as WSC and the like is used for the reaction, the condensing agent can be separated into an aqueous layer and the resultant product (5) can be separated into an organic layer by a partitioning operation. Therefore, a large excess amount of the condensing agent can be used. When the condensing agent cannot be separated by the partitioning operation, or when compound (6) is directly added to the reaction system without an extraction operation, 1 to 1.2 equivalents of the condensing agent is preferably added thereto.

Step 4 (Amidation Reaction)

This step is performed by removing the dehydrating-condensing agent by subjected the reaction mixture of Step 3 to a partitioning operation, concentrating the extraction solvent, dissolving again an â€œinert solventâ€ (described in Step 3). Alternatively this step is performed by directly using the reaction mixture without the extraction operation of the reaction mixture of Step 3. The amine of compound (6) is used in the form of a free form or a salt such as hydrochloride and the like. When the amine of compound (6) is used in the form of a salt, examples of the neutralizing agent include tertiary amines such as organic bases (e.g., DBU, N,N-diisopropylethylamine, triethylamine, 4-dimethylaminopyridine, N-methylmorpholine, pyridine, 2,6-lutidine and the like), inorganic bases such as alkali metal carbonates (e.g., sodium carbonate, sodium hydrogen carbonate, potassium carbonate, potassium hydrogen carbonate, cesium carbonate and the like), and the like, and the like. Of these, an organic base is preferable.

Step 5 (Amidation Reaction)

Examples of the method in this step include the following method i) a method using a dehydrating-condensing agent, ii) a method using a reactive derivative in carboxyl group, and the like.

i) Method Using a Dehydrating-Condensing Agent

Compound (7) is reacted with about 1 to 5 equivalents of compound (8) and about 1 to 2 equivalents of a dehydrating-condensing agent in an inert solvent. Examples of the â€œdehydrating-condensing agentâ€ include DCC, WSC and the like. Of these, WSC is preferable. Examples of the â€œinert solventâ€ include the solvents described in Step 3, and the like. These solvents may be used in a mixture of two or more kinds thereof mixed at an appropriate ratio. Of these, acetonitrile, dichloromethane, tetrahydrofuran, N,N-dimethylformamide and the like are preferable. The reaction temperature is generally âˆ’20Â° C. to 50Â° C., preferably âˆ’20Â° C. to room temperature. The reaction time is generally about 1 hr to about 72 hr, preferably about 1 hr to about 24 hr. Where necessary, this reaction may be carried out in the presence of about 1 to 2 equivalents of 1-hydroxybenzotriazole (hereinafter to be referred to as HOBt) or 1-hydroxy-7-azabenzotriazole (hereinafter to be referred to as HOAt). In addition, where necessary, this reaction may be carried out in the presence of a base. Examples of the â€œbaseâ€ include tertiary amines such as DBU, N,N-diisopropylethylamine, triethylamine, 4-dimethylaminopyridine, pyridine, 2,6-lutidine and the like, alkali metal or alkaline earth metal carbonates (e.g., sodium carbonate, potassium carbonate, cesium carbonate and the like), alkali metal or alkaline earth metal hydrogencarbonates (e.g., sodium hydrogen carbonate, potassium hydrogen carbonate and the like). Of these, triethylamine, N,N-diisopropylethylamine, 4-dimethylaminopyridine and the like are preferable.

ii) Method Using a Reactive Derivative in Carboxyl Group

The reactive derivative of compound (7) is reacted with about 1 to 5 equivalents (preferably 1 to 3 equivalents) of compound (8) in an inert solvent. Examples of the reactive derivative of the â€œreactive derivative of compound (7)â€ include acid halides (e.g., acid chloride, acid bromide), mixed anhydrides (e.g., anhydrides with a C_1-6alkyl-carboxylic acid or C_1-6alkyl carbonates, and the like), activated esters (e.g., esters with phenol optionally having substituent(s), HOBt, HOAt or N-hydroxysuccinimide, and the like). Examples of the â€œsubstituentâ€ of the â€œphenol optionally having substituent(s)â€ include a halogen atom, a nitro group and the like. The number of substituents is 1 to 5. Specific examples of the â€œphenol optionally having substituent(s)â€ include phenol, pentachlorophenol, pentafluorophenol, p-nitrophenol and the like. The reactive derivative is preferably acid halide. Examples of the â€œinert solventâ€ include the solvents described in Step 1. These solvents may be used in a mixture of two or more kinds thereof mixed at an appropriate ratio. Of these, tetrahydrofuran, dichloromethane, acetonitrile and the like are preferable. The reaction temperature is generally âˆ’20Â° C. to 50Â° C., preferably at room temperature. The reaction time is generally about 1 hr to 72 hr, preferably about 1 hr to 24 hr. Where necessary, this reaction may be carried out in the presence of about 1 to 10 equivalents, preferably about 1 to 3 equivalents, of a base. Examples of the â€œbaseâ€ include those exemplified for the aforementioned i) the â€œmethod using a dehydrating-condensing agentâ€ .

Step 6 (Deprotection Reaction of Amino Group)

This step and a protection reaction of an amino group are performed according to a known method, for example, the method described in Protective Groups in Organic Synthesis third edition, (1999) or the like. Examples of the amino-protecting group include formyl, C_1-6alkyl-carbonyl optionally substituted by halogen atom(s) (e.g., acetyl, propionyl, trifluoroacetyl and the like), C_1-6alkoxy-carbonyl optionally substituted by halogen atom(s) (e.g., methoxycarbonyl, ethoxycarbonyl, tert-butoxycarbonyl and the like), benzoyl, C_7-10aralkyl-carbonyl (e.g., benzylcarbonyl and the like), C_7-10aralkyloxy-carbonyl (e.g., benzyloxycarbonyl and the like), trityl, silyl (e.g., trimethylsilyl, tert-butyldimethylsilyl and the like), C_2-6alkenyl (e.g., 2-propenyl and the like), substituted benzenesulfonyl (e.g., 2-nitrobenzenesulfonyl) and the like. The amino-protecting group is preferably tert-butoxycarbonyl, trifluoroacetyl, benzyloxycarbonyl, 2-nitrobenzenesulfonyl or the like. The protecting group of compound (8) is preferably tert-butoxycarbonyl, trifluoroacetyl, benzyloxycarbonyl, 2-nitrobenzenesulfonyl or the like.

Step 7 (Amidation Reaction)

This step can be performed in the same manner as in Step 5. The object compound (10) can be obtained by reacting compound (7) with compound (11) under conditions explained in Step 5.

[Image Omitted]

wherein Ar, R¹, R², R³, R⁴, R⁵, A, L and P are as defined above.

When Step 4 and Step 5 (or 7) of Production Method 1 are performed, compounds (6) and (8) or (6) and (11) to be added may be exchanged. That is, compound (8) or (11) can be added in Step 4, and compound (6) can be added in Step 5.

[Image Omitted]

wherein Ar, R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R²¹, A, L and P are as defined above, and *Ar and A* mean substituent conversion.

Regarding Ar and A mentioned in Production Method 1, the conversion of the functional groups contained therein can be carried out by appropriately steps. The conversion method of the functional group is described in the below-mentioned â€œproduction method of starting material compoundsâ€ . Compound (3*) can be synthesized by subjecting the diester compound of compound (3) to conversion of the functional group in Ar. Compound (7) is led to Compound (7*) by protecting the carboxyl group of the monocarboxylic acid compound of compound (7), converting the functional group in Ar of the resulting compound (13), and subjecting the resulting compound (13*) to ester hydrolysis. Compound (9**) and (10**) can be synthesized by converting the functional group in Ar of compounds (9) and (10). Alternatively, Compounds (9**) and (10**) can be synthesized by converting the functional group in A of compounds (9*), (10*).

[Image Omitted]

wherein R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R²¹, Ar, A, L and G are as defined above.

Step 8 (Amidation Reaction)

In this step, compound (6) is subjected to an amidation reaction with compound (14) or (14â€²) to give compound (15). This step can be carried out in the same manner as in Step 5 or 7.

Step 9 (Alkylation Reaction)

In this step, compound (1) and compound (2) are subjected to an alkylation reaction to give compound (16). This reaction can be carried out in the same manner as in Step 1. When the reaction is carried out using 1 equivalent or more of compound (2), the amount of compound (2) to be used is preferably below 2 equivalents, more preferably 1 to 1.2 equivalents, since compound (3) may be produced as a by-product.

Step 10 (Alkylation Reaction)

In this step, compounds (16) and (15) are subjected to an alkylation reaction to give compound (17). This reaction can be carried out in the same manner as in Step 1. The amount of compound (15) to be used is 1 equivalent or more, preferably 1 to 10 equivalents, relative to compound (16).

Step 11 (Hydrolysis of Ester)

This reaction can be carried out in the same manner as in Step 2. The steps after compound (18) obtained in this step are the same as those in the method shown in [Production Method 1].

[Image Omitted]

wherein R¹, R⁴, R⁵, R⁶, R⁷, R²¹, Ar, A and G are as defined above.

Step 9 and Step 10 shown in Production Method 4 can be performed by changing the order. That is, compound (17) can be obtained by reacting compound (1) with compound (15), and then reacting the resulting compound (19) with compound (2).

[Image Omitted]

wherein R¹, R², R³, R⁴, R⁵, R⁶, R²¹, Ar, A, L and G are as defined above.

Step 12 (Amidation Reaction)

In this step, compound (8) is subjected to an amidation reaction with compound (20) or (20â€²) to give compound (21). This step can be carried out in the same manner as in Step 5 or 7.

Step 13 (Alkylation Reaction)

In this step, compound (1) and compound (22) are subjected to an alkylation reaction to give compound (23). This step can be carried out in the same manner as in Step 9. The amount of compound (22) to be used is preferably below 2 equivalents, more preferably 1 to 1.2 equivalents.

Step 14 (Alkylation Reaction)

In this step, compound (23) and (21) are subjected to an alkylation reaction to give compound (24). This step can be carried out in the same manner as in Step 10. The amount of compound (21) to be used is 1 equivalent or more, preferably 1 to 10 equivalents, relative to compound (23).

Step 15 (Hydrolysis of Ester)

This reaction can be carried out in the same manner as in Step 2.

Step 16 (Amidation Reaction)

In this step, compound (25) with and compound (6) are subjected to an amidation reaction to give compound (9). This step can be carried out in the same manner as in Step 5. The steps after compound (9) are the same as those in [Production Method 1].

[Image Omitted]

wherein R², R³, R⁴, R⁵, Ar, L and P are as defined above.

Step 13 and Step 24 shown in production method 6 can be performed by changing the order. That is, compound (24) can be obtained by reacting compound (1) with compound (21), and then reacting the resulting compound (26) with compound (22).

[Image Omitted]

wherein R¹, R², R³, R⁴, R⁵, R⁶, R⁷, Ar, A, L and P are as defined above.

Compound (1), compound (15) and compound (21) can be successively subjected to an alkylation reaction to give compound (9). In this case, the order of compounds (15) and (21) to be reacted may be exchanged. The alkylation reaction can be performed in the same manner as in the methods described in Steps 9, 10, 13 and 14.

The production methods of the starting material compounds used in the above-mentioned production are shown below.

[Production Method 1 of Compound'(1)]

A general production method of compound (1) wherein Ar is (II), (III) or (IV), from among the compounds of the formula (I), includes, for examples, nitrating compound (27a), (27b) or (27c) by a known method to give compound (28a), (28b) or (28c) (Step 17), and reducing the nitro group to give compound (29a), (29b) or (29c) (Step 18).

[Image Omitted]

wherein R⁹, R¹⁰, R¹¹, k, l, X, Cy¹and Cy²are as defined above.

Step 17 (Nitration Reaction)

In this step, compounds (27a), (27b) and (27c) are converted to compounds (28a), (28b) and (28c) by a nitration reaction, and they can be synthesized by a known method. For example, mixed acid method using conc. sulfuric acid-nitric acid, a method using nitric acid in an acetic acid solvent, a method using nitrite salt (e.g., sodium nitrite, nitrous acid tetrafluoroborate etc.) and nitrate salt (e.g., sodium nitrate etc.) in an acetic acid, trifluoroacetic acid or sulfuric acid solvent and the like can be mentioned.

Step 18 (Reduction of Nitro Group)

In this step, a nitro group is reduced and converted to an amino group, and it can be synthesized according to a known method, for example, the method described in Comprehensive Organic Transformations 3^rdedition page 821-828 VCH Publishers Inc. 1999, and the like, or a method analogous thereto. For example, it can be synthesized according to a hydrogenation reaction using palladium carbon, Raney-nickel and the like as a catalyst in an inert solvent, under a hydrogen atmosphere, or in the presence of a hydrogen source (e.g., ammonium formate, hydrazine etc.), a reaction using iron, tin chloride and the like under acidic conditions, a reaction using hydrazine and a catalytic amount of ferric chloride in the presence of activated carbon, and the like.

[Production Method 2 of Compound (1)]

A general production method of compound (1) wherein Ar is (II), (III) or (IV), from among the compounds of the formula (I), includes, for example, inducing carboxylic acid of compound (30a), (30b) or (30c) to compound (31a), (31b) or (31c) by a rearrangement reaction and performing deprotection to give compound (29a), (29b) or (29c).

[Image Omitted]

wherein R⁹, R¹⁰, R¹¹, R²¹, k, l, X, Cy¹and Cy²are as defined above.

Step 19 (Rearrangement Reaction)

In this step, carboxylic acid is converted to an amino group protected by a carbamate grotip by a rearrangement reaction, and the synthesis can be performed according to a known method, for example, the method described in Comprehensive Organic Transformations 3^rdedition page 867-869 VCH Publishers Inc. 1999, and the like, or a method analogous thereto. For example, a method including converting carboxylic acid to an aminocarbonyl group and leading same to an amino group by Hofmann rearrangement, Curtius rearrangement including converting carboxylic acid to acid azide, converting same to an amino group, or converting same to a carbamate group by using diphenylphosphoryl azide (hereinafter to be referred to as DPPA), and the like can be mentioned. In the Curtius rearrangement reaction using DPAA, by using tert-butanol as a solvent to be used, an amino group can be obtained with protection by a tert-butoxycarbonyl group which is a general protecting group for an amino group (R²¹=tert-butyl).

Step 20 (Deprotection Reaction)

In this step, deprotection of a carbamate group, which is an amino-protecting group, can be performed according to a known method, for example, the method described in â€œProtective Groups in Organic Synthesis (third edition) page 503-550â€ .

[Production Method 3 of Compound (1)]

A general production method of compound (1) wherein Ar is (III) and X is an oxygen atom or a sulfur atom, from among the compounds of the formula (I), includes, for example, reacting compound (32b) and compound (33) under basic conditions (Step 21) to give compound (34), and reducing the nitro group to convert same to an amino group to give compound (35) (Step 22).

[Image Omitted]

wherein R¹¹, R¹², k and Cy¹are as defined above, X is an oxygen atom or a sulfur atom, LG is a leaving group (e.g., a halogen atom or â€”OSO₂R²²), and R²²is a C_1-4alkyl group, a C_1-4haloalkyl group or an aryl group.

Step 21

This step is generally performed in an inert solvent in the presence of a base. The equivalent amount of compound (33) is 1 to 100 molar equivalents, preferably 1 to 10 molar equivalents, relative to compound (32b). As the base, alkali metal carbonates such as potassium carbonate, sodium carbonate, cesium carbonate and the like, alkali metal alkoxides such as sodium methoxide, sodium ethoxide, potassium tertiary butoxide and the like, alkali metal hydroxides such as potassium hydroxide, sodium hydroxide, lithium hydroxide and the like, metal hydrides such as potassium hydride, sodium hydride and the like, amines such as triethylamine, N,N-diisopropylethylamine, N-methylmorpholine, pyridine, 4-dimethylaminopyridine, DBU and the like, and the like can be used. The amount of the base to be used is preferably 1 to 10 molar equivalents relative to compound (33). The reaction can be generally performed at âˆ’50Â° C.-200Â° C., preferably âˆ’20Â° C. to 150Â° C. As the inert solvent, ethers such as diethyl ether, tetrahydrofuran, 1,4-dioxane and the like, halogenated hydrocarbons such as chloroform, dichloromethane, dichloroethane and the like, hydrocarbons such as hexane, benzene, toluene and the like, amides such as N,N-dimethylformamide, N-methylpyrrolidone and the like, sulfoxides such as dimethyl sulfoxide and the like, nitriles such as acetonitrile and the like, and the like can be used. These solvents may be mixed at an appropriate rate and used.

Step 22 (Reduction of Nitro Group)

In this step, the nitro group is reduced to an amino group, which can be performed in the same manner as in Step 18.

[Production Method 4 of Compound (1)]

A general production method of compound (1) wherein Ar is (III) and X is an oxygen atom or a sulfur atom, from among the compounds of the formula (I), includes, for example, reacting compound (36) with compound (37) under basic conditions to give compound (34) (Step 23), and thereafter obtaining compound (35) by the method of Step 22.

[Image Omitted]

wherein R¹¹, k, Cy¹and LG are as defined above, and X is an oxygen atom or a sulfur atom.

Step 23

In this step, compound (36) is reacted with compound (37) (alkylation reaction). The equivalent amount of compound (37) is 1 to 20 molar equivalents, preferably 1 to 10 molar equivalents, relative to compound (36). The amount of the base is preferably 1 to 10 molar equivalents relative to compound (36). The base and solvent to be used are similar to those described in Step 21.

[Production Method 5 of Compound (1)]

A general production method of compound (1) wherein Ar is (III) and X is an oxygen atom or a sulfur atom, from among the compounds of the formula (I), includes, for example, preferentially reacting compound (37) under basic conditions with a functional XH group contained in compound (38) (Step 24) to give compound (35).

[Image Omitted]

wherein R¹¹, k and Cy¹are as defined above, and X is an oxygen atom or a sulfur atom.

Step 24

In this step, compound (35) is synthesized by reacting a functional XH group wherein X is an oxygen or sulfur atom contained in compound (38) with compound (37). The equivalent amount of compound (37) is 1 to 2 equivalents, preferably 1-1.5 equivalents, relative to compound (38). The reaction solvent and base are similar to those described in Step 21.

[Production Method 6 of Compound (1)]

A general production method of compound (1) wherein Ar is (III) and X is an oxygen atom or sulfur atom, from among the compounds of the formula (I), includes, for example, reacting compound (39) with compound (37) under basic conditions to give compound (40) (Step 25), hydrolyzing ester (Step 26), and converting the carboxyl group to an amino group by a rearrangement reaction to give compound (35) (Steps 27 and 28).

[Image Omitted]

wherein R¹¹, R¹², R²¹, k and Cy¹are as defined above, and X is an oxygen atom or a sulfur atom.

Step 25

This step can be performed in the same manner as in Step 23.

Step 26

This step is ester hydrolysis which can be performed in the same manner as in Step 2.

Step 27, 28

In this step, carboxylic acid is converted to an amino group by a rearrangement reaction, which can be performed in the same manner as in Steps 19 and 20.

[Production Method 7 of Compound (1)]

A general production method of compound (1) wherein Ar is (II) or (III), R⁹is R¹², and X is a â€œbondâ€ , from among the compounds of the formula (I), includes, for example, cross-coupling reaction of compound (32a) or (32b) with compound (43) to give compound (44a) or (44b) (Step 29), and reducing the nitro group to give compound (45a) or (45b) (Step 30).

[Image Omitted]

wherein R¹⁰, R¹¹, R¹², k, l, Cy¹and LG are as defined above, and M¹is an atom group (e.g., groups of atoms bound by boron, tin etc. and the like) permitting a cross-coupling reaction.

Step 29

In this step, compound (44a) or (44b) is produced by subjecting compound (32a) or (32b) and compound (43) to a cross-coupling reaction (e.g., Suzuki coupling reaction, Stille coupling reaction, etc.) in the presence of a metal catalyst. This reaction can be generally performed in an inert solvent in the presence of a metal catalyst. In this case, a base may be added. Examples of the metal catalyst include zero-valent palladium, divalent palladium, zero-valent nickel and the like. Here, examples of the zero-valent palladium catalyst include tetrakis(triphenylphosphine)palladium, tris(dibenzylideneacetone)dipalladium and the like. Examples of the divalent palladium catalyst include palladium acetate, dichlorobis(triphenylphosphine)palladium, dichlorobis(tricyclohexylphosphine)palladium and the like. Examples of the zero-valent nickel catalyst include 1,1â€²-bis(diphenylphosphino)ferrocene nickel and the like. Monodentate ligand such as triphenylphosphine, tris(ortho-tolyl)phosphine and the like, didentate ligand such as diphenylphosphinopropane, diphenylphosphinobutane and the like and the like may be added. Examples of the base include alkali metal hydrogen carbonates such as sodium hydrogen carbonate and the like, alkali metal carbonates such as sodium carbonate, potassium carbonate, cesium carbonate and the like, alkali metal phosphates such as tripotassium phosphate and the like and the like. When M¹in compound (43) is an atom group bound by tin, a base is not necessarily used. The amount of the metal catalyst to be used is, for example, 0.001 to 1 equivalent, preferably 0.01 to 0.5 equivalent, relative to compound (32a) or (32b). The amount of the base to be used is 1 to 20 equivalents, preferably 1 to 10 equivalents, relative to compound (32a) or (32b). The reaction temperature can be generally from room temperature to the refluxing temperature of the solvent. As the inert solvent, alcohols such as methanol, ethanol, isopropanol, tert-butanol and the like, ethers such as tetrahydrofuran, 1,4-dioxane and the like, esters such as ethyl acetate and the like, halogenated hydrocarbons such as dichloromethane, chloroform, dichloroethane, carbon tetrachloride and the like, hydrocarbons such as hexane, benzene, toluene, xylene and the like, amides such as N,N-dimethylformamide, N-methylpyrrolidone, N,N-dimethylacetamide and the like, nitriles such as acetonitrile and the like, sulfoxides such as dimethyl sulfoxide and the like, water and the like can be used. These may be mixed at an appropriate rate and used. In addition, when M¹in compound (43) is an atom group containing tin, the reaction is preferably performed in a non-aqueous solvent. The amount of compound (43) to be used is, for example, 1 to 10 equivalents, preferably 1 to 3 equivalents, relative to compound (32a) or (32b).

Step 30

In this step, a reduction reaction of the nitro group can be performed in the same manner as in Step 18.

[Production Method 8 of Compound (1)]

A general production method of compound (1) wherein Ar is (II) or (III), R⁹is R¹², and X is â€œbondâ€ , from among the compounds of the formula (I), includes, for example, cross-coupling reaction of compound (46a) or (46b) with compound (43) to give compound (45a) or (45b) (Step 31).

[Image Omitted]

wherein R¹⁰, R¹¹, k, l, Cy¹and LG are as defined above.

Step 31

In this step, a cross-coupling reaction can be performed in the same manner as in Step 29.

In addition, the reaction can also be performed with protection of the amino group of compound (46a) or (46b), and deprotection after cross-coupling can afford compound (45a) or (45b). The amino-protecting group and deprotection method are as mentioned above.

[Production Method 9 of Compound (1)]

A general production method of compound (1) wherein Ar is (II) or (III), R⁹is R¹², and X is a â€œbondâ€ , from among the compounds of the formula (I), includes, for example, cross-coupling reaction of compound (47a) or (47b) with compound (43) to give compound (48a) or (48b) (Step 32), hydrolysis of ester (Step 33) and a rearrangement reaction of carboxylic acid to an amino group to give compound (45a) or (45b) (Steps 34 and 35).

[Image Omitted]

wherein R¹⁰, R¹¹, R¹², R²¹, k, l, Cy¹and LG are as defined above.

Step 32

In this step, a cross-coupling reaction can be performed in the same manner as in Step 29.

Step 33

In this step, an ester hydrolysis can be performed in the same manner as in Step 2.

Step 34, 35

In this step, the carboxylic acid is converted to an amino group by a rearrangement reaction, which can be performed in the same manner as in Steps 19 and 20.

[Production Method 10 of Compound (1)]

A general production method of compound (1) wherein Ar is (III), from among the compounds of the formula (I), is shown below. A production method when Ar is (III), particularly the formula (III-1) or (III-2) shown below, is described in the following.

[Image Omitted]

wherein R⁹and X are as defined above, and R²³is an optionally substituted C_1-4alkyl group.

The ortho-aminophenol derivative shown by compound (51a) or (51b) is cyclized by a known method to give a 1,3-benzoxazol-2-one derivative (Step 36). Substituent R²³is introduced by an alkylation reaction (Step 37), which is followed by nitration (Step 38), and reduction of the nitro group to give compound (56a) or (56b) (Step 39).

[Image Omitted]

wherein R⁹, R²³, X and LG are as defined above.

Step 36

This step can be performed according to a known method, for example, a method using 1,1â€²-carbonylbis-1H-imidazole (CDI) [Journal of Heterocyclic Chemistry, 19, 1545-1547 (1982) etc.], a method using urea [Journal of Heterocyclic Chemistry, 20, 1423-1425 (1983) etc.], a method using triphosgene [Bioorganic Medicinal Chemistry Letters, 8, 2467-2472 (1998) etc.], a method using dialkyl carbonate and potassium carbonate [Synthesis, 2003, vol. 18, 2872-2876 etc.] and the like. The method using dialkyl carbonate and potassium carbonate can be simultaneously performed with Step 37.

Step 37

In this step, an N-alkylation reaction is performed using compound (52a) or (52b) and compound (53) under basic conditions in an inert solvent. As the base, metal hydrides such as sodium hydride and the like, and the like are preferable. As the solvent, amides such as N,N-dimethylformamide, N-methylpyrrolidone and the like, sulfoxides such as dimethyl sulfoxide and the like, ethers such as tetrahydrofuran, 1,4-dioxane and the like are preferable. These solvents may be mixed at an appropriate rate and used. The reaction temperature is generally âˆ’20Â° C. to 150Â° C., preferably âˆ’10Â° C. to 100Â° C.

Step 38

In this step, nitration can be performed in the same manner as in Step 17.

Step 39

In this step, reduction of the nitro group to amine can be performed in the same manner as in Step 18.

[Production Method 11 of Compound (1)]

A general production method of compound (1) wherein Ar is (III), from among the compounds of the formula (I), is shown below. A production method when Ar is (III), particularly (III-3) or (III-4), is described in the following.

[Image Omitted]

wherein R⁹, R²³and X are as defined above, R²⁴and R²⁵are independently selected and each is hydrogen or an optionally substituted C_1-4alkyl group, and p is an integer of 1 to 3.

Compound (57a) or (57b) and compound (58) are subjected to an amidation reaction to give compound (59a) or (59b) (Step 41), and the resulting compound is cyclized by an intramolecular Friedel-Crafts reaction to give compound (60a) or (60b) (Step 42). The object compound (63a) or (63b) can be synthesized by the nitration reaction (Step 43), N-alkylation reaction (Step 44), and reduction reaction of the nitro group (Step 45).

[Image Omitted]

wherein R⁹, R²³, R²⁴, R²⁵, p, G, X and LG are as defined above.

Step 41, Step 42

These steps can be performed according to a known method, for example, the methods described in Berichte der Deutschen Chemischen Geselschaft, 60, 858-867 (1927), Journal of Medicinal Chemistry, 2000, 43, 3718-3735, Journal of Medicinal Chemistry, 2004, 47, 3546-3560 and the like. Step 41 can be performed by an amidation reaction of compound (57a) or (57b) with compound (58) and in the same manner as in Step 5. Step 42 is an intramolecular Friedel-Crafts reaction and the synthesis can be performed by, for example, mixing and reacting compound (59a) or (59b) with aluminum chloride under warming. The reaction temperature is generally 80Â° C.-250Â° C.

Step 43

In this step, nitration can be performed in the same manner as in Step 17.

Step 44

In this step, an N-alkylation reaction can be performed in the same manner as in Step 37.

Step 45

In this step, a reduction reaction of the nitro group can be performed in the same manner as in Step 18.

[Production Method 12 of Compound (1)]

A production method of compound (1) when Ar is (III), particularly (III-3a) or (III-4-a), from among the compounds of the formula (I), is described in the following.

[Image Omitted]

wherein R⁹, R²³and X are as defined above.

Compound (64a) or (64b) and malonic acid are subjected to a Knoevenagel reaction, or Horner-Emmons reaction with ethyl diethylphosphonoacetate and the like to give compound (65a) or (65b) (Step 46), and an intramolecular cyclization reaction by a simultaneous reduction reaction of the nitro group and the double bond is performed to give compound (66a) or (66b) (Step 47). Hereafter, the object compound (67a) or (67b) can be synthesized by the method described in Steps 43-45 of [Production Method 11 of compound (1)].

[Image Omitted]

wherein R⁹, R²³and X are as defined above, and R²⁶is hydrogen or a C_1-4alkyl group.

Steps 46, 47

These steps can be performed according to a known method, for example, the methods described in Berichte der Deutschen Chemischen Geselschaft, 13, 1680-1684 (1880), Journal of Medicinal Chemistry, 1987, 30, 295-303, Journal of Medicinal Chemistry, 2000, 43, 3718-3735, and the like.

Step 46 can be performed by i) Knoevenagel reaction, ii) Horner-Emmons reaction, and the like.

The synthesis method by i) includes reacting compound (64a) or (64b) with malonic acid in the presence of a catalytic amount of a base in an inert solvent. As the base, pyridine, piperidine and the like are preferable. As the inert solvent, ethanol, acetic acid and the like are preferable. The reaction is generally performed at 0Â° C.-120Â° C., preferably 60Â° C.-100Â° C.

The synthesis method by ii) includes reacting compound (64a) or (64b) with ethyl or methyl diethylphosphonoacetate or the like under basic conditions in an inert solvent. As the base, alkali metal carbonates such as sodium carbonate, potassium carbonate and the like, alkali metal alkoxides such as sodium methoxide, potassium tertiary butoxide and the like, alkali metal hydroxides such as potassium hydroxide, sodium hydroxide and the like, metal hydrides such as potassium hydride, sodium hydride and the like, alkali metal amides such as potassium hexamethyldisilasane, lithium hexamethyldisilasane, lithium diisopropylamide and the like, amines such as triethylamine, N,N-diisopropylethylamine, N-methylmorpholine, pyridine, 4-dimethylaminopyridine, DBU and the like, and the like can be used. The amount of the ethyl or methyl diethylphosphonoacetateto be used is 1 to 10 equivalents, preferably 1 to 1.5 equivalents, relative to compound (64a) or (64b). The amount of the base to be used is preferably 1 to 1.5 equivalents relative to compound (64a) or (64b). The reaction can be generally performed at âˆ’80Â° C. to 150Â° C., preferably 0Â° C. to 100Â° C. As the inert solvent, ethers such as tetrahydrofuran, 1,4-dioxane and the like, hydrocarbons such as hexane, benzene, toluene and the like, amides such as N,N-dimethylformamide, N-methylpyrrolidone and the like, sulfoxides such as dimethyl sulfoxide and the like, nitriles such as acetonitrile and the like, and the like can be used. These solvents may be mixed at an appropriate rate and used.

Step 47 is an intramolecular cyclization reaction based on reduction of the nitro group and a double bond, which can be performed, for example, under a hydrogen atmosphere, using palladium-carbon as a catalyst in an inert solvent (ethanol, methanol, tetrahydrofuran etc.) at normal pressure or under pressurization at room temperature or under warming.

[Production Method 13 of Compound (1)]

A production method of compound (1) when Ar is (III), from among the compounds of the formula (I), is shown below. When Ar is (III), particularly (III-3a), compound (74) can be obtained by performing a Friedel-Crafts reaction of compound (68) with chloroacetic acid chloride to introduce a chloroacetyl group (Step 48), reacting compound (69) with pyridine (Step 49) to give a carboxylic acid form (71) by alkali decomposition (Step 50), which is followed by conversion of carboxylic acid to ester (Step 51), N-alkylation reaction (Step 52), and ester hydrolysis. Hereafter, the object compound (67a) can be obtained by the method shown in [Production Method 2 of Compound (1)]. The N-alkylation reaction of Step 52 can also be performed prior to Step 48.

[Image Omitted]

wherein R⁹, R²¹, R²³and X are as defined above.

Steps 48, 49 and 50

These steps can be performed according to a known method, for example, the methods described in Journal of Medicinal Chemistry, 1992, 35, 620-628, Chemical & Pharmaceutical Bulletin, 1986, 34, 682-693, and the like, or a method analogous thereto.

For example, Step 48 is a reaction of compound (68) with chloroacetyl chloride in the presence of aluminum chloride in an inert solvent. The amount of chloroacetyl chloride is generally 1 to 10 equivalents, preferably 1 to 3 equivalents, relative to compound (68). The amount of aluminum chloride is generally 1 to 50 equivalents, preferably 1 to 10 equivalents, relative to compound (68). As the inert solvent, carbon disulfide and dichloromethane can be generally used. The reaction temperature is generally 0Â° C.-100Â° C., preferably from 0Â° C. to the refluxing temperature of the solvent. The reaction time is generally 1 hr to 24 hr, preferably 1 to 5 hr.

Step 49 can be performed by heating compound (69) in a pyridine solvent. The reaction is generally performed at 70Â° C.-100Â° C., and the reaction time is generally 1 to 5 hr.

Step 50 can be performed by treating compound (70) in the presence of alkali metal hydroxides such as sodium hydroxide, potassium hydroxide and the like in a solvent such as water and the like. The amount of the alkali metal hydroxides to be used is generally 1 to 100 equivalents, preferably 1 to 20 equivalents, relative to compound (70). The reaction is generally performed at 50Â° C.-100Â° C. The reaction time is generally 1 to 10 hr.

Step 51

In this step, an esterification reaction of carboxylic acid can be performed by a known method, for example, the method described in Protective Groups in Organic Synthesis (third edition) page 373-433.

Step 52

In this step, an N-alkylation reaction can be performed in the same manner as in Step 37.

Step 53

In this step, an ester hydrolysis can be performed in the same manner as in Step 2.

[Production Method 14 of Compound (1)]

A general production method of compound (1) wherein Ar is (III), particularly (III-5a) or (III-6b), from among the compounds of the formula (I), is shown below.

[Image Omitted]

wherein R⁹, R²³and X are as defined above.

A known compound (75a) or (75b), or compound (75a) or (75b) synthesized by the method described in the aforementioned â€œProduction Methods 1, 3 and 7 of compound (1)â€ is acetylated to protect an amino group (Step 54), and compound (78a) or (78b) is synthesized by a Friedel-Crafts reaction (Step 55). Then, ketone is led to oxime (Step 56), which is subjected to a ring-closure reaction to give compound (80a) or (80b) (Step 57). The object compound (81a) or (81b) can be obtained by deprotection of the amino group (Step 58).

[Image Omitted]

wherein R⁹, R²³and X are as defined above.

Step 54 (Acetylation Reaction)

In this step, the synthesis can be performed by a known method, for example, by reacting compound (75a) or (75b) with acetic anhydride or acetyl chloride in the presence of a base in an inert solvent.

Step 55

In this step, an acyl group is introduced into the ortho-position of a methoxy group by a Friedel-Crafts reaction, and a methoxy group is simultaneously converted to a hydroxyl group. This reaction can be performed by using compound (76a) or (76b) and an acid chloride shown by compound (77) as starting materials, and using Lewis acid such as aluminum chloride, ferric chloride, stannic chloride and the like, or acid such as sulfuric acid, polyphosphoric acid and the like as catalyst, without solvent or in an inert solvent such as dichloromethane, 1,2-dichloroethane, nitrobenzene, carbon tetrachloride and the like under cooling, at room or under warming.

Step 56 (Oximation Reaction)

This step can be performed by a known method, for example, in the presence of compound (78a) or (78b), hydroxylamine hydrochloride and a base (e.g., sodium acetate, potassium carbonate, sodium carbonate, sodium hydroxide, potassium hydroxide, triethylamine, pyridine etc.) to neutralize hydrochloric acid of hydroxylamine hydrochloride in an inert solvent (e.g., ethanol, methanol, water or a mixture thereof) under cooling, at room temperature to under warming.

Step 57 (Ring-Closure Reaction)

This step can be performed by a method according to a known method, for example, the intramolecular Mitsunobu reaction described in Synthetic Communications, 27 (1997) 22, 3839-3846, and the like, the method described in Journal of Medicinal Chemistry, 1995, 38, 2802-2808 and the like, that is, a method including acylating a hydroxyl group contained in the oxime group, reacting the compound in the presence of a base (e.g., sodium hydride, potassium tert-butoxide, sodium hydroxide, potassium carbonate, pyridine etc.) in an inert solvent at room temperature or under warming, and subjecting same to a ring-closure reaction, or the method described in Tetrahedron Letters, Vol. 33, No. 8, p 993-996 (1992) and the like, that is, a method including reacting compound (79a) or (79b) with N,N-dimethylformamide dimethylacetal without a solvent or in an inert solvent (e.g., toluene, 1,4-dioxane etc.) with warming (preferably 70Â° C.-120Â° C.), and the like.

Step 58

In this step, deprotection of the amino group can be performed in the same manner as in Step 6. For example, an acetyl group can be deprotected by warming compound (80a) or (80b) in diluted hydrochloric acid.

[Production Method 15 of Compound (1)]

A general production method of compound (1) wherein Ar is (III), particularly (III-5b) or (III-6b), from among the compounds of the formula (I), is shown below.

[Image Omitted]

wherein R⁹and X are as defined above.

The methoxy group of the aforementioned compound (76a) or (76b) is deprotected and converted to a hydroxyl group (Step 59), and compound (83a) or (83b) is synthesized by Duff reaction or an improved method thereof (Step 60). The steps thereafter can be performed in the same manner as in Steps 56-58 of the aforementioned [Production Method 14 of compound (1)], whereby the object compound (84a) or (84b) can be obtained.

[Image Omitted]

wherein R⁹and X are as defined above.

Step 59

This step is a conversion reaction of a methoxy group to a hydroxyl group, which can be performed according to the method described in the section of protection and deprotection of phenol in Protective Groups in Organic Synthesis (third edition) p 249-257, or a method analogous thereto. In addition, compound (82a) or (82b) can also be synthesized by using a compound containing, as a hydroxyl-protecting group, a protecting group other than a methoxy group as starting material.

Step 60

This step is a formylation reaction by a Duff reaction, which can be performed by a known method, for example, the methods described in Chemical & Pharmaceutical Bulletin, 31, 1751-1753 (1983), Synthesis, (1998) 7, 1029-1032, and the like, or a method analogous thereto. For example, the synthesis includes reacting compound (82a) or (82b) with hexamethylenetetramine in a acidic solvent (e.g., trifluoroacetic acid, methanesulfonic acid, polyphosphoric acid etc.) at room temperature or under warming.

[Production Method 16 of Compound (1)]

A general production method of compound (1) wherein Ar is (III), particularly (III-6c), from among the compounds of the formula (I), is shown below.

[Image Omitted]

wherein R⁹and X are as defined above, and R²⁷is hydrogen or an optionally substituted C_1-4alkyl group.

Compound (85) is acylated by a Friedel-Crafts reaction or formylated by a Duff reaction (Step 61), followed by oximation (Step 62) and a ring-closure reaction (Step 63) to synthesize compound (88), and compound (89) is obtained by nitration (Step 64). The object compound (90) can be obtained by reducing the nitro group according to a method similar to those described in [Production Methods 1, 3 and 7 of compound (1)].

[Image Omitted]

wherein R⁹, R²⁷, G and X are as defined above, and R²⁸is hydrogen or a methyl group.

Step 61

This step can be performed in the same manner as in the aforementioned Step 55 or Step 60.

Step 62% This step can be performed in the same manner as in the aforementioned Step 56.

Step 63

This step can be performed in the same manner as in the aforementioned Step 57.

Step 64 (Nitration)

This step can be performed in the same manner as in the aforementioned Step 17, and can be synthesized, for example, according to the methods described in Journal of the American Chemical Society, vol. 126 (2004) No. 26, 8195-8205, U.S. Pat. No. 5,484,763 and the like, or a method analogous thereto.

[Production Method 17 of Compound (1)]

A general production method of compound (1) wherein Ar is (III), from among the compounds of the formula (I), is shown below. A production method of compound (1) when Ar is (III), particularly (III-7), and R⁹is R¹², is described in the following.

[Image Omitted]

wherein R⁹is as defined above, R²⁹and R³⁰are independently selected and each is hydrogen or R¹¹, and R¹¹is as defined above.

The object compound (93) can be obtained by leading compound (91) to compound (92) by a nitration reaction (Step 65), and reducing a nitro group in the same manner as in [Production Method 1 of compound (1)].

[Image Omitted]

wherein R⁹, R²⁹, R³⁰and X are as defined above.

Step 65

In this step, nitration can be performed in the same manner as in Step 17.

[Production Method 18 of Compound (1)]

A general production method of compound (1) wherein Ar is (III), particularly (III-7), and X is a sulfur atom, from among the compounds of the formula (I), is shown below.

The object compound (97) can be obtained by reacting a known compound (94) or a compound (94) easily synthesizable by a known compound with compound (95) (Step 66) to lead to compound (96), and reducing the nitro group in the same manner as in Step 18.

[Image Omitted]

wherein R¹², R²⁹and R³⁰are as defined above.

Step 66

This step can be performed in the same manner as in Step 21, for example, according to the method described in Chemical & Pharmaceutical Bulletin, 42, 500-511 (1994) and the like, or a method analogous thereto. Compound (96) can be obtained by reacting, for example, compound (94) with compound (95) under basic conditions in an inert solvent at room temperature to under heating. As the base, sodium methoxide, potassium tert-butoxide, sodium hydride and the like can be used. As the inert solvent, sulfoxides such as dimethyl sulfoxide and the like, amides such as N,N-dimethylformamide and the like, and the like can be used.

[Production Method 19 of Compound (1)]

A general production method of compound (1) wherein Ar is (III), particularly (III-7), and X is an oxygen atom, from among the compounds of the formula (I), is shown below.

The object compound (100) can be obtained by subjecting a known compound (98) or a compound (98) easily synthesizable by a known method to an alkylation reaction to lead to compound (99) (Step 67), and reducing the nitro group in the same manner as in Step 18.

[Image Omitted]

wherein R¹², R²⁹and R³⁰are as defined above.

Step 67

This step can be performed in the same manner as in Step 23.

[Production Method 20 of Compound (1)]

A general production method of compound (1) wherein Ar is (III), particularly (III-7), X is an oxygen atom, and R¹²is particularly an optionally substituted aryl group, from among the compounds of the formula (I), is shown below.

The object compound (104) can be obtained by subjecting a known compound (101) or a compound (101) easily synthesizable by a known method to an Ullmann reaction to lead to compound (103) (Step 68), and hereafter in the same manner as in [Production method 6 of compound (1)].

[Image Omitted]

wherein R²¹, R²⁹and R³⁰are as defined above, and R¹²is an optionally substituted aryl group.

Step 68

This step can be performed by the method described in Chemical & Pharmaceutical Bulletin, 14, 78-82 (1966) and the like, or a method analogous thereto. For example, the synthesis can be performed by warming (preferably 120Â° C. to 150Â° C.) compound (101) and compound (102) in the presence of potassium carbonate, copper and pyridine.

[Production Method 21 of Compound (1)]

A general production method of compound (1) wherein Ar is (III), particularly (III-8), X is an oxygen atom, and R⁹is R¹², from among the compounds of the formula (I), is shown below.

[Image Omitted]

wherein R⁹and X are as defined above.

The object compound can be synthesized by subjecting a known compound (116) to an alkylation reaction.

[Image Omitted]

wherein R¹²is as defined above.

Step 69

This step can be performed in the same manner as in Step 24.

[Production Method 22 of Compound (1)]

A general production method of compound (1) wherein Ar is (III), particularly (III-8), X is an oxygen atom, and R⁹is R¹², from among the compounds of the formula (I), is shown below.

The object compound (106) can be synthesized by leading a known compound (107) to compound (108) by alkylation, and thereafter in the same manner as in [Production Method 6 of compound (1)].

[Image Omitted]

wherein R¹²and R²¹are as defined above.

Step 70

This step can be performed in the same manner as in Step 25.

[Production Method 23 of Compound (1)]

A general production method of compound (1) wherein Ar is (III), particularly (III-8), X is a â€œbondâ€ , and R⁹is a halogen atom, from among the compounds of the formula (I), is shown below.

The object compound (111) can be synthesized by diazotizing a known compound (109) and halogenating the compound to give compound (110) (Step 71), and thereafter in the same manner as in [Production Method 2 of compound (1)].

[Image Omitted]

wherein G is as defined above.

Step 75

In this step, an amino group is converted to a diazonium salt with sodium nitrite by a known method such as to Sandmeyer reaction and Schiemann reaction, and converted to a halogen atom. In the Sandmeyer reaction, chlorine, bromine and an iodine atom can be introduced using copper chloride, copper bromide and copper iodide, and in the Schiemann reaction, a fluorine atom can be introduced by converting to a diazonium fluoroborate, followed by thermal decomposition. For example, when G is a fluorine atom, the method described in Bioorganic Medicinal Chemistry Letters, 12, 1651-1655 (2002) can be performed.

[Production Method 24 of Compound (1)]

A general production method of compound (1) wherein Ar is (III), particularly (III-8), X is a â€œbondâ€ , and R⁹is R¹², from among the compounds of the formula (I), is shown below.

The object compound (114) can be synthesized by subjecting a known compound (112) to a Stille coupling reaction to introduce R¹²moiety (Step 72), and thereafter treating in the same manner as in [Production Method 9 of compound (1)]. When compound (43) is an alkenyltin derivative, conversion to an alkyl group can be achieved by subjecting the double bond site contained in R¹²to a reduction reaction in an appropriate step.

[Image Omitted]

wherein R¹²and M¹are as defined above.

Step 72

This step can be performed by, for example, using the compound (123) described in Bioorganic Medicinal Chemistry, 10, 779-801 (2002), and the method described therein, or a method analogous thereto. For example, compound (112) and a known compound (43) or a compound (43) easily synthesizable by a known method can be treated according to the method described in Journal of the American Chemical Society, 1987, 109, 5478-5486.

[Production Method 25 of Compound (1)]

A general production method of compound (1) wherein Ar is (III), particularly (III-9), from among the compounds of the formula (I), is shown below.

[Image Omitted]

wherein R⁹, R²⁴, R²⁵and X are as defined above, and q is an integer of 1 to 3.

Compound (120) is obtained by converting a known compound (115) or a compound (115) easily synthesizable by a known method to compound (117) by a Friedel-Crafts reaction (Step 73), and by nitration of the ortho-position of substituent â€”XR⁹(Step 74), reduction of the nitro group (Step 75) and acetylation (Step 76). The object compound (123) is obtained by reducing ketone (Step 77), synthesizing compound (122) by an intramolecular Friedel-Crafts cyclization reaction (Step 78), and performing deacetylation (Step 79).

[Image Omitted]

wherein R⁹, R²⁴, R²⁵, X and q are as defined above.

Step 73

This step is a Friedel-Crafts reaction and the synthesis can be performed by, for example, the method described in Organic Synthesis collective volume II, p 81-82, or a method analogous thereto. For example, synthesis is performed by warming a mixture of compound (115) and compound (116) in the presence of aluminum chloride.

Step 74

In this step, nitration can be performed in the same manner as in Step 17.

Step 75

In this step, a reduction reaction of the nitro group can be performed in the same manner as in Step 18.

Step 76

This step is an acetylation reaction which can be performed in the same manner as in Step 54. In addition, this step can be simultaneously performed with Step 75. That is, the acetylation can be performed by reducing the nitro group in Step 75 under a hydrogen atmosphere and using palladium-carbon as a catalyst, and adding acetic anhydride to a solvent during the conversion reaction to an amino group.

Step 77

In this step, a reduction reaction of ketone can be performed, for example, under a hydrogen atmosphere using palladium-carbon as a catalyst in a solvent (for example, acetic acid) at room temperature or under warming.

Step 78

In this step, an intramolecular Friedel-Crafts cyclization reaction can be performed by a known method, for example, the method described in Journal of Organic Chemistry, 1962, 27, 70-76 and the like, the method described in Synthetic Communications, vol. 34, No. 20, 3751-3762 (2004) and the like, or a method analogous thereto. For example, a method including converting carboxylic acid contained in compound (121) to acid chloride and the like, and reacting same in the presence of aluminum chloride in an inert solvent (e.g., nitrobenzene etc.), a method including reacting same in the presence of trifluoroacetic anhydride in dichloromethane, a method including reacting same in the presence of diphosphorus pentaoxide in methanesulfonic acid, and the like can be performed.

Step 79

This step can be performed in the same manner as in Step 58.

[Production Method 26 of Compound (1)]

A general production method of compound (1) wherein Ar is (III), particularly (III-9), and R²⁴and R²⁵are hydrogen, from among the compounds of the formula (I), is shown below.

[Image Omitted]

wherein R⁹, X and q are as defined above.

Compound (126) is obtained by subjecting a known compound (124) or a compound (124) easily synthesizable by a known method to Wittig reaction and the like to lead to compound (125), and reducing the double bond site. Thereafter, the object compound (138) can be synthesized in the same manner as in [Production Method 27 of compound (1)].

[Image Omitted]

wherein R⁹, X and q are as defined above.

Step 80

In this step, compound (125) can be synthesized by a method shown in i) of Step 46 when q is 1, that is, Knoevenagel reaction and the like, and compound (125) can be synthesized by Wittig reaction using (2-carboxyethyl)triphenylphosphonium bromide and the like when q is 2, and (3-carboxypropyl)triphenylphosphonium bromide and the like when q is 3.

Step 81

In this step, a reduction reaction of a double bond can be performed, for example, under a hydrogen atmosphere using palladium-carbon as a catalyst in an inert solvent (e.g., ethanol, methanol, tetrahydrofuran etc.) under normal pressure or under pressurization conditions at room temperature or under warming.

[Production Method 27 of Compound (1)]

A general production method of compound (1) wherein Ar is (III), particularly (III-9), R²⁴and R²⁵are hydrogen, and q is 2, from among the compounds of the formula (I), is shown below.

Compound (131) can be synthesized by acetylating an amino group of compound (129) easily synthesizable from known compound (128) according to the method of â€œProduction Methods 1, 3 and 7 of compound (1)â€ and the like, and subjecting the compound to Stille coupling reaction with an alkenyltin derivative. Thereafter, the object compound (132) can be synthesized in the same manner as in [Production Method 27 of compound (1)].

[Image Omitted]

wherein R⁹and X are as defined above.

Step 82

This step can be performed in the same manner as in Step 54.

Step 83

This step is a Stille coupling reaction, and compound (131) can be synthesized by reacting compound (130) and an alkenyltin derivative described in Synthetic Communications, vol. 34, No. 20, pp 3751-3762, (2004) and the like using, for example, triphenylphosphinepalladium(0) as a catalyst in toluene under warming, which is followed by a treatment with hydrochloric acid, silica gel or the like.

[Production Method 28 of Compound (1)]

A general production method of compound (1) wherein Ar is (III), particularly (III-10), from among the compounds of the formula (I), is shown below.

[Image Omitted]

wherein R⁹, R²⁴, R²⁵, X and q are as defined above.

Of the compounds (123) easily synthesizable by â€œProduction methods 27, 28 and 29 of compound (1)â€ and the like, particularly, the amino group of a compound (133) wherein X is a â€œbondâ€ and R⁹is hydrogen is converted to a diazonium salt, converted to a halogen atom or a hydroxyl group (Step 84), and nitrated to synthesize compound (135a) or (135b) (Step 85). Thereafter, the object compound (136) can be synthesized according to the introduction method of substituent-XR⁹and the reduction method of the nitro group described in [Production Methods 1, 3, 4 and 7 of compound (1)] and the like.

[Image Omitted]

wherein R⁹, R²⁴, R²⁵, X, G and q are as defined above.

Step 84

Synthesis in this step can be performed by a known method, for example, the methods described in Journal of Organic Chemistry, 1962, 27, 70-76, Bioorganic Medicinal Chemistry, 13, 3309-3320, (2005) and the like, or a method analogous thereto.

Step 85

This step is a nitration reaction which can be performed in the same manner as in Step 17 and, for example, synthesis can be performed according to the method described in U.S. Pat. No. 5,034,311.

[Production Method 29 of Compound (1)]

Introduction and conversion methods of substituent R¹⁰of a compound of the formula (I) wherein Ar is (II) or (IV) are shown below. A compound wherein a substituent of R¹⁰is hydrogen, a halogen atom, an alkyl group, a hydroxyl group, trifluoromethyl, a carbonyl group, a carboxyl group, an amino group, a cyano group, sulfide, sulfoxide, a sulfone group and the like can be synthesized using a known compound as a starting compound, or according to a known method, for example, the method described in Comprehensive Organic Transformations 2^ndEdition VCH Publishers Inc. 1999 and the like, or a method analogous thereto. For example, when the substituent is a halogen atom (chlorine, bromine, iodine etc.), an alkyl group, an alkenyl group, an alkynyl group, a cyano group, an aryl group, a heteroaryl group, a heterocycle group, and the like can be introduced by a cross-coupling reaction using a derivative of boron, tin and the like, and a transition metal catalyst. In addition, hydrolysis of a cyano group results in the conversion to a carboxyl group (carboxylic acid). Furthermore, conversion to an amino group can be performed by subjecting a carboxyl group to a rearrangement reaction, conversion to an aminocarbonyl group (amide) can be performed by amidation, and conversion to aldehyde can be performed by a reduction reaction. Moreover, conversion to a cyano group can be performed by subjecting an aminocarbonyl group to a dehydration reaction, and conversion to a heteroaryl group, a heterocyclic group and the like can be performed by a ring formation reaction using an aminocarbonyl group or a cyano group. In addition, conversion to a hydroxyalkyl group and further to an alkyl group can be performed by reducing a carboxyl group and a carbonyl group. Moreover, an amino group can be converted to an alkylamino group by alkylation, to a carbonylamino group or a sulfonylamino group by amidation, and to a halogen atom, a phenolic hydroxyl group or a cyano group via a diazonium salt. Furthermore, a cross-coupling reaction can also be performed after conversion of a phenolic hydroxyl group to an alkoxy group by an alkylation reaction with alkyl halide or by a Mitsunobu reaction with alkyl alcohol, and conversion of a phenolic hydroxyl group to a trifluoromethylsulfonyloxy group.

Examples of the introduction and conversion methods of the substituent R¹⁰include the following production methods.

[Image Omitted]

wherein R⁹and M¹are as defined above, LG* is chlorine, bromine, iodine or a triflate group, and R³²is an aryl group, a heteroaryl group and the like.

(II-2) wherein R¹⁰is an aryl group, a heteroaryl group or a heterocycle group can be synthesized by a cross-coupling reaction (e.g., Suzuki coupling reaction, Stille coupling reaction etc.) using (II-1) having a halogen atom permitting a cross-coupling reaction such as chlorine, bromine, iodine and the like or a triflate group as a substituent, and compound R³²-M¹which is an atom group (e.g., boron, tin, magnesium etc.) permitting a cross-coupling reaction. The reaction conditions and the like are the same as those in Step 29 of [Production Method 7 of compound (1)].

[Image Omitted]

wherein R⁹is as defined above.

In addition, (II-4) wherein R¹⁰is a cyano group can be synthesized by warming (II-1) and zinc cyanide in the presence of a transition metal catalyst (e.g., tetrakistriphenylphosphinepalladium (0) etc.)

[Image Omitted]

wherein R⁹is as defined above.

In addition, (II-4) can be converted to (II-5) wherein R¹⁰is a tetrazole group by using, for example, sodium azide, trimethyltin azide and the like.

[Image Omitted]

wherein R⁹and R²¹are as defined above.

In addition, (II-4) can be converted to (II-7) wherein R¹⁰is a 1,2,4-oxadiazol-3-yl group by reacting (II-4) with hydroxylamine or a salt thereof for conversion to (II-6), acylating the hydroxyl group, and performing a dehydrating reaction. In addition, (II-6) can also be converted to (II-7*) wherein R¹⁰is a 5-methyl-1,2,4-oxadiazol-3-yl group by reaction with N,N-dimethylacetamide dimethylacetal under warming.

[Image Omitted]

wherein R⁹, R²¹and LG are as defined above.

In addition, (II-6) can be converted to (II-8) by reacting (II-6) with ethyl chloroformate and the like under basic conditions, and can be further converted to (II-9) by an alkylation.

[Image Omitted]

wherein R⁹is as defined above.

In addition, (II-6) can be converted to (II-10) by reacting (II-6) with 1,1â€²-thiocarbonyldiimidazole and the like.

[Image Omitted]

wherein R⁹, R²¹, R²⁷and LG are as defined above.

In addition, (II-11) can be converted to an aminocarbonothioyl group to give (II-12), which can then be converted to (II-13) wherein R¹⁰is a thiazole group.

[Image Omitted]

wherein R⁹and R²⁸are as defined above.

In addition, (II-11) can be converted to (II-15) wherein R¹⁰is a 1,2,4-oxadiazol-5-yl group by reacting (II-11) with N,N-dimethylformamide dimethyl acetal or N,N-dimethylacetamide dimethyl acetal to give (II-14), which is then reacted with hydroxylamine or a salt thereof, and can be converted to (II-16) wherein R¹⁰is a 1,2,4-triazol-3-yl group by a reaction with hydrazine or hydrazinium salt.

[Image Omitted]

wherein R⁹and R²⁷are as defined above.

In addition, (II-17) can be converted to (II-19) wherein R¹⁰is a 2-oxo-1,3,4-oxadiazole group by condensing (II-17) with a hydrazine derivative to give (II-18), which is then cyclized using triphosgene and the like.

[Image Omitted]

wherein R⁹and R²⁷are as defined above.

In addition, (II-17) can be converted to (II-21) wherein R¹⁰is a 1,3,4-thiadiazole group by converting (II-17) to (II-20), and treating (II-20) with a Lawesson reagent and the like.

[Image Omitted]

wherein R⁹and R²⁷are as defined above.

In addition, (II-20) can be converted to (II-22) wherein R¹⁰is a 1,3,4-oxadiazole group using polyphosphoric acid and the like.

[Image Omitted]

wherein R⁹and R²⁷are as defined above, and R³³is hydrogen or a C_1-4alkyl group.

In addition, (II-17) can be converted to (II-25) wherein R¹⁰is an oxazole group by converting compound (II-17) to (II-24) directly or via (II-23), and then using phosphorus oxychloride, a Burgess reagent and the like.

[Image Omitted]

wherein R⁹, R²⁷and R³³are as defined above.

In addition, (II-24) can be converted to (II-26) wherein R¹⁰is a thiazole group by using a Lawesson reagent and the like.

[Production Method 1 of Compound (6)]

An example of a general production method of starting compound (6) for introducing â€”N(A)(R¹) which is a partial structure of the formula (I) is shown below. A is an optionally substituted aryl group, an optionally substituted aryl-C₁-C₄alkyl group, an optionally substituted heteroaryl-C₁-C₄alkyl group, a C₃-C₆alkynyl group, an optionally substituted C₃-C₈cycloalkyl group, or a group represented by the following formula (V), (VI), (VII) or (VIII).

[Image Omitted]

wherein R¹⁵, R¹⁶, W, D, h, i, g and n are as defined above.

Production methods of compounds (6a), (6b) and (6c), which are compounds (6) wherein W for A is â• CHâ€” and R¹is a C₁-C₃alkyl group, are shown below.

[Image Omitted]

wherein A and R²¹are as defined above, and R³⁴is methyl or an ethyl group.

Compound (6a) and (6b) can be obtained by converting compound (148) to an alkylcarbamate form (149a) and an amide form (149b), and converting them to an alkyl group by a reduction reaction (e.g., reduction reaction using lithium aluminum hydride etc.). Compound (6c) wherein an isopropyl group is substituted can be synthesized by subjecting compound (148) to a reductive amination reaction with acetone.

[Production Method 2 of Compound (6)]

[Image Omitted]

wherein A and LG are as defined above, and R³⁵is a C₁-C₃alkyl group.

A production method of compound (6d), which is compound (6) wherein R¹is a C₁-C₃alkyl group, is shown below. In compound (6d), when A is (V)-(VII), then W is â• CHâ€”.

Compound (6d) can be obtained by leading an alcohol form of compound (150) to a ketone or aldehyde form (151a) by an oxidation reaction, and then performing a reductive amination reaction. Compound (6d) can be obtained by converting compound (150) to a halogen atom (e.g., chlorine, bromine, iodine etc.) or a leaving group such as methanesulfonyloxy, paratoluenesulfonyloxy, trifluoromethanesulfonyloxy group and the like, and then performing an alkylation reaction.

[Production Method 3 of Compound (6)]

A production method of compound (6e) wherein the formula A is particularly (V), especially W is â• CHâ€”, R¹is a C_1-3alkyl group, h is 1, and the dotted line shows a double bond, is shown below.

[Image Omitted]

wherein R¹⁵, R³⁵, i and n are as defined above.

[Image Omitted]

wherein R¹⁵, i and n are as defined above.

As a production method of compound (6e), for example, compound (6e) can be produced using compound (152) as a starting material and according to the methods described in Organic Reactions, Vol. VII, Wiley, 1966, 327-377, Journal of Medicinal Chemistry, 1982, 25, 1442-1446, Journal of Medicinal Chemistry, 2001, 44, 4716-4732, Tetrahedron Letters, Vol. 36, No. 25, 4337-4340, 1995 and the like, or a method analogous thereto. For example, compound (152) is treated with alkyl nitrite to convert the Î±-position of ketone to oxyimino to give compound (153), subjecting the compound to a hydrogenation reaction under pressure using a palladium catalyst to give compound (154), and thereafter performing the method of [Production Method 1 of compound (6)].

[Production Method 4 of Compound (6)]

Production methods of compound (6e*) wherein the formula A is particularly (V), especially W is â• CHâ€”, h is 1, the dotted line shows a double bond, and R¹is a methyl group, and (6e**) wherein R¹is an ethyl group or a propyl group, are shown below.

[Image Omitted]

wherein R¹⁵, R²¹, R³⁴, and n are as defined above.

Compounds (6e*) and (6e**) can be produced by protecting the hydroxyl group of compound (153) with a tert-butyldimethylsilyl group (TBS), performing a reduction reaction with boron to lead to compound (156), converting the amino group to a carbamate form or an amide form, reducing the hydroxyl group with triethylsilane and the like in the presence of a Lewis acid to lead to compound (158a) or (158b), and thereafter following the [Production Method 3 of compound (6)].

[Production Method 5 of Compound (6)]

When A of compound (6) is (V), (VI), (VII), or (VIII), W is â• Nâ€”, and R¹is a C_1-3alkyl group, compound (6) is tri-substituted hydrazine (6f). An example of a general production method of tri-substituted hydrazine (6f) is shown below.

[Image Omitted]

(6f)

wherein R³⁵is as defined above.

[Image Omitted]

wherein R³⁵is as defined above.

Secondary amine is indicated as (159) for convenience. Compound (6f) can be synthesized by reacting (159) with sodium nitrite under acidic conditions to give a nitroso form (160), reducing the nitroso group with lithium aluminum hydride, zinc, titanium trichloride or the like to give compound (161), converting the amino group to imine, and introducing the R³⁵group by a reduction reaction.

[Production Method 6 of Compound (6)]

Examples of the synthesis methods of compounds (6g), (6h) and (6i) when R¹is a C₁-C₃alkyl group, A is (V), W is â• Nâ€”, i is 1, h is 1, and the dotted line shows a double bond, or A is (VI) and W is â• Nâ€” or A is (VIII) are shown below.

[Image Omitted]

wherein R¹⁵, R¹⁶, R³⁵and n are as defined above.

[Image Omitted]

wherein R¹⁵, R¹⁶and n are as defined above, and R³⁶is hydrogen, a hydroxyl group or an alkoxy group.

Compound (162a), (162b) or (162c) is converted to an alcohol form (163a), (163b) or (163c) by reduction with lithium aluminum hydride and the like, which can be converted to compound (164a), (164b) or (164c) by a known method, for example, a method including bromination by warming in an aqueous hydrobromic acid solution, a method including bromination with phosphorus tribromide in an inert solvent, a method including bromination with carbon tetrabromide, and the like.

[Image Omitted]

wherein R¹⁵and n are as defined above.

In addition, compound (164a) can also be synthesized by the method described in Journal of Organic Chemistry, 1988, 53, 1775-1779 and the like, that is, by warming an orthoxylene derivative (165) in an inert solvent (e.g., carbon tetrachloride etc.) in the presence of N-bromosuccinimide and a catalytic amount of a radical initiator (e.g., benzoyl peroxide, azobisbutyronitrile etc.) for bromination.

[Image Omitted]

wherein R¹⁵, R¹⁶, R³⁵, n and P are as defined above.

The object compound (6g), (6h) or (6i) can be synthesized using compound (164a), (164b) or (164c) and according to the method described in U.S. Pat. No. 4,272,284, that is, by reacting the compounds with compound (166) with heating in an inert solvent of amide such as N,N-dimethylformamide, N-methylpyrrolidone and the like in the presence of a base such as triethylamine, N,N-diisopropylethylamine and the like at room temperature to 150Â° C. with warming, preferably 40Â° C.-100Â° C. with warming, to convert them to compound (167a), (167b) or (167c), and performing a deprotection reaction.

[Production Method 7 of Compound (6)]

In addition, an example of a production method of compound (6j) wherein A is (VII), R¹is a C₁-C₃alkyl group, W is â• Nâ€”, g is 0, and D is â• CHâ€”R¹⁷(except when R¹⁷is an alkylamino group or an arylamino group), is shown below.

[Image Omitted]

wherein R¹⁶, R³⁵and n are as defined above, and R³⁷is hydrogen, C₁-C₄alkyl, aryl, a C₁-C₆alkoxy group or an aryloxy group.

Compound (6j) can be synthesized by, for example, the method shown below.

[Image Omitted]

wherein R¹⁶, R³⁷, n, P and LG are as defined above.

The object compound (6j) can be synthesized by warming a butane derivative (168) having a leaving group at the 1,4-position with compound (166) in the presence of an organic base such as triethylamine, N,N-diisopropylethylamine and the like at a temperature of not more than the boiling point of the organic base to give compound (169), and then performing a deprotection reaction.

[Production Method 1 of Compounds (8) and (11)]

Examples of the general production methods of starting material compounds (8) and (11) used for introducing â€”N(R³)-L-R², which is a partial structure of the formula (I), are shown below. When the nitrogen contained in R²is primary or secondary amine, compound (8), wherein nitrogen of R²is substituted by an amino-protecting group, is desirably used for producing compound (1), so that the NH(R³) group contained in the starting compound HN(R³)-L-R²will selectively react with compound (7).

[Image Omitted]

wherein R², R³, L, P and P* are as defined above, an amino group contained in R²is a primary or secondary amino group, and P* is an amino-protecting group different from P.

As a production method of compound (8) wherein R²is as defined above, and the nitrogen contained is primary or secondary amine, for example, the amino group of (R³)NHâ€” of the above-mentioned compound (11a) is protected by a protecting group P*, and then the amino group contained in R²is protected by a protecting group P. Thereafter, the object compound (8) can be synthesized by removing the protecting group P. Examples of the 2-nitrobenzenesulfonyl group as P* and a tert-butoxycarbonyl group as P are shown below.

[Image Omitted]

wherein R², R³and L are as defined above, and the amino group contained in R²is primary or secondary amino group.

For example, using compound (11a) and 2-nitrobenzenesulfonyl chloride, the amino group of (R³)NHâ€” is selectively protected with a 2-nitrobenzenesulfonyl group in the presence of a base (triethylamine etc.) in an inert solvent (e.g., dichloromethane, tetrahydrofuran etc.) at âˆ’20Â° C. to room temperature, and then the amino group contained in R²is reacted with di-tert-butyl dicarbonate in an inert solvent (e.g., dichloromethane etc.) at âˆ’20Â° C. to room temperature to give compound (171a). Then, the object compound (8a) can be synthesized by reacting compound (171a) with benzenethiol in an inert solvent (e.g., acetonitrile, dichloromethane, N,N-dimethylformamide etc.) in the presence of a base (potassium carbonate, cesium carbonate, triethylamine etc.) at room temperature or under warming where necessary.

[Production Method 2 of Compounds (8) and (11)]

[Image Omitted]

wherein R², L and P are as defined above.

Compound (8) can be synthesized by condensing a known compound (172) or a compound (172) easily synthesizable by a known method with phthalimide by a Mitsunobu reaction, followed by deprotection with hydrazine and the like.

[Production Method 3 of Compounds (8) and (11)]

Example of the production method of compound (11b), which is compound (11) wherein R²is N(R^2a)(R^2b) and both R^2aand R^2bare substituents other than hydrogen, is shown below.

[Image Omitted]

wherein R^2a, R^2b, L and LG are as defined above.

When R²is â€”N(R^2a)(R^2b), and both R^2aand R^2bare substituents other than hydrogen, compound (11b) can be synthesized by condensing a known compound (177), or compound (177) easily synthesizable by a known method with compound (178) by an alkylation reaction to give compound (179), and then performing a deprotection reaction.

[Production Method 4 of Compounds (8) and (11)]

[Image Omitted]

wherein R^eaand L are as defined above.

In addition, when R²is â€”N(R^2a)(R^2b) and at least one of R^2aand R^2bis hydrogen (for convenience, at least R^2bis hydrogen), compound (8b) substituted by a 2-nitrobenzenesulfonyl group can be synthesized by condensing compound (177) and compound (180) by an alkylation reaction to give compound (181), and deprotecting the phthalimide side.

The compound of the formula (I) obtained as mentioned above and each intermediate are isolated and purified by conventional chemical operations such as extraction, crystallization, recrystallization, various chromatographies and the like.

As a salt of the above-mentioned compound of the formula (I), an acid addition salt or a base addition salt can be used. The kind of the salt is not particularly limited as long as it is physiologically acceptable.

The salt of the compound of the formula (I) and a solvate thereof can be produced from an amine derivative of the formula (I) by a known method.

When the compound of the formula (I) or a salt thereof contains an optically active form, it can be resolved into each optical isomer by a conventional optical resolution means. Alternatively, an optically active form of the compound of the formula (I) or a salt thereof may be synthesized by using an optically pure starting material or a compound having a known steric configuration.

The compound of the present invention and a compound having an SAHH inhibitory action can be used as superior therapeutic drugs for ischemic stroke.

The administration subject of the medicament of the present invention can be, for example, mammals such as human, dog, cat, bovine, horse, swine, monkey, mouse and the like.

While the medicament of the present invention may be an active ingredient as is, it is preferably added with an active ingredient and a pharmacologically and pharmaceutically acceptable additive, and provided as a preparation in a form well known to those of ordinary skill in the art.

For example, the medicament of the present invention can be prepared, together with a suitable diluent and other additives generally used, into a suitable administration form (powder, injection, tablet, capsule, topical external preparation etc.), and administered to human or animal by a suitable administration method (e.g., intravenous administration, oral administration, transdermal administration or topical administration etc.) according to the administration form thereof.

As the pharmacologically and pharmaceutically acceptable additive, excipient, disintegrant, binder, lubricant, coating agent, dye, diluent, base, isotonicity agent and the like can be used.

Examples of the preparation suitable for oral administration include tablet, capsule, powder, fine granules, granules, liquid, syrup and the like, and examples of the preparation suitable for parenteral administration include injection, drip infusion, suppository and the like.

A preparation suitable for oral administration can contain, as additive, excipient, disintegrant, binder, lubricant, coating agent, base and the like. In addition, when the compound of the present invention is administered to a treatment subject patient, other agent suitable for the treatment of the target disease and the compound of the present invention may be used in combination.

The administration route of the medicament of the present invention is not particularly limited, and they can be administered orally or parenterally. The dose is determined depending on the age, body weight, general health condition, sex, meal, administration time, administration method, clearance rate, combination of drugs, and the level of disease state for which the patients are undergoing treatment at that time, or in consideration of them or other factors. The compound of the present invention and an optical isomer thereof are low toxic and can be used safely. While the daily dose thereof varies depending on the condition and body weight of patients, the kind of compound, administration route and the like, it is desirably administered, for example, at about 0.1 to 1000 mg/patient/day, preferably 1 to 500 mg/patient/day, parenterally by subcutaneous, intravenous, intramuscular or intrarectal administration, or orally at about 0.1 to 1000 mg/patient/day, preferably 1 to 500 mg/patient/day.

EXAMPLES

The present invention is explained in more detail in the following by referring to Examples, which are not to be construed as limitative.

The â€œroom temperatureâ€ in the following Reference Examples and Examples shows 0-30Â° C. In addition, the solvent ratio when a mixed solvent is used shows the volume ratio.

MS spectrum was measured according to any of the following methods.

<LC/MS manufactured by SHIMADZU Corporation>
apparatus: LC-2010
column: Chromolith SpeedROD RP-18e (4.6Ï†Ã—50 mm) (manufactured by Merck)
mobile phase: SOLUTION A (0.05% trifluoroacetic acid/water), SOLUTION B (0.05% trifluoroacetic acid/acetonitrile), gradient elution from SOLUTION A:SOLUTION B=95:5 to SOLUTION
A:SOLUTION B=0:100 over 4 min
flow rate: 4.0 ml/min
column temperature: room temperature
MS measurement mode: ESI (electrospray-ionization) method Positive
<LC/MS manufactured by Waters>
apparatus: Acquity HPLC/ZQ
column: Acquity BEH C18 (2.0Ï†Ã—50 mm) (manufactured by Waters)
mobile phase: SOLUTION A (0.05% trifluoroacetic acid/water), SOLUTION B (0.05% trifluoroacetic acid/acetonitrile), gradient elution from SOLUTION A:SOLUTION B=95:5 to SOLUTION A:SOLUTION B=2:98 over 1 min
flow rate: 0.6 ml/min
column temperature: 40Â° C.
MS measurement mode: ESI (electrospray-ionization) method

Positive

¹H-NMR (proton nuclear magnetic resonance spectrum) was measured at 300 MHz or 400 MHz. The chemical shift of ¹H-NMR was measured using tetramethylsilane (TMS) as an internal standard and the relative delta (5) value is shown in ppm. As for the coupling constant (J), obvious multiplicity is shown in hertz (Hz), using s (singlet), d (doublet), t (triplet), q (quartet), quintet (quintet), m (multiplet), dd (double doublet), dt (double triplet), tt (triple triplet), broad showing broad absorption peak, and brs showing broad single absorption peak (broad singlet).

Other abbreviation used in the specification mean the following.

Me: methyl
CDCl₃: deuterated chloroform DMSO-d₆: deuterated dimethyl sulfoxide
TMW (Total Molecular Weight): total molecular weight
LC/MS or LC-MS: liquid chromatography-mass spectrometry
Found: mass spectrometry measurement value (shows [M+H]⁺)
NT (Not Tested): not measured

Reference Example 1tert-butyl (2-aminoethyl)methylcarbamate hydrochloride

According to the method described in Synthetic Communications, 23(17), 2443-2449 (1993), tert-butyl (2-aminoethyl)methylcarbamate from N-methylaminoethanol (10 g). Using 4N hydrochloric acid-dioxane solution to give the hydrochloride salt, the title compound (9 g) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.41 (s, 9H), 2.81 (s, 3H), 2.89 (q, J=6.1, 2H), 3.39 (t, J=6.5, 2H), 8.05 (brs, 3H).

Reference Example 2tert-butyl (2-aminoethyl)ethylcarbamate

N-Ethylethylenediamine (21.02 g, 238 mmol) and triethylamine (51 ml, 366 mmol) were dissolved in dichloromethane (200 ml), 2-nitrobenzenesulfonyl chloride (54.45 g, 246 mmol) was gradually added with stirring under cooling at âˆ’20Â° C., further stirred at 0Â° C. for 8 hr, di-tert-butyl dicarbonate (53.48 g, 245 mmol) was added and the mixture was stood overnight at room temperature. The reaction mixture was diluted with ethyl acetate-hexane 1:1 mixed solvent and water, and the organic layer was extracted. The organic layer was washed with 10% aqueous citric acid solution, saturated aqueous sodium hydrogen carbonate and saturated brine and dried over sodium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure to give tert-butyl ethyl[2-{[(2-nitrophenyl)sulfonyl]amino}ethyl]carbamate (98.05 g) as a crude orange oil. The obtained oil was dissolved in acetonitrile (800 ml), cesium carbonate (157 g, 482 mmol) and benzenethiol (37 ml, 360 mmol) were added and the mixture was stirred at room temperature for 90 min. The reaction mixture was diluted with water, concentrated under reduced pressure to evaporate most part of acetonitrile, and the aqueous layer was extracted with dichloromethane. The obtained organic layer was dried over potassium carbonate, the insoluble material was filtered off, and the solvent was concentrated under reduced pressure. The obtained oil was dissolved in toluene, and the mixture was extracted with 10% aqueous citric acid solution (500 ml). An aqueous sodium hydroxide solution was added to the aqueous layer to give a strong alkaline solution, and the suspending oil was extracted. The aqueous layer was extracted with dichloromethane, mixed with oil and dichloromethane solution, and the mixture was dried over potassium carbonate. The insoluble material was filtered off and the solution was concentrated under reduced pressure to give the title compound as a pale-yellow oil (35.54 g, yield 79%).

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.11 (t, J=7.1, 3H), 1.25 (brs, 2H), 1.46 (s, 9H), 2.82 (t, J=6.7, 2H), 3.2-3.3 (m, 4H).

Reference Example 3tert-butyl (2-aminoethyl)isopropylcarbamateStep Atert-butyl isopropyl[2-{[(2-nitrophenyl)sulfonyl]amino}ethyl]carbamate

N-Isopropylethylenediamine (8.44 g, 82.60 mmol) and triethylamine (18 ml, 129 mmol) were dissolved in dichloromethane (80 ml), and 2-nitrobenzenesulfonyl chloride (18.31 g, 82.62 mmol) was gradually added with stirring under ice-cooling. The mixture was stirred at room temperature for 4 hr, ice-cooled again, di-tert-butyl-dicarbonate (19.35 g, 88.66 mmol) was added with stirring, and the mixture was stood overnight at room temperature. The reaction mixture was diluted with ethyl acetate-hexane=1:1 mixed solvent, washed with water, 10% aqueous citric acid solution, saturated aqueous sodium hydrogen carbonate and saturated brine and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure to give the title compound (34.21 g) as a crude pale-yellow oil.

Step Btert-butyl (2-aminoethyl)isopropylcarbamate

The compound (34.21 g, 82.60 mmol) obtained in step A was dissolved in acetonitrile (300 ml), cesium carbonate (52.38 g, 161 mmol) and benzenethiol (12 ml, 117 mmol) were added and the mixture was stirred at room temperature for one day. The reaction mixture was diluted with water, and the aqueous layer was extracted with dichloromethane. The obtained organic layer was dried over potassium carbonate, the insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was dissolved in toluene, and the mixture was extracted with 1N aqueous hydrogensulfate potassium solution. An aqueous sodium hydroxide solution was added to the aqueous layer to give a strong alkaline solution, and the suspending oil was extracted. The aqueous layer was extracted with dichloromethane, mixed with oil and dichloromethane solution, and the mixture was dried over sodium sulfate. The insoluble material was filtered off and the solution was concentrated under reduced pressure to give the title compound as a pale-yellow oil (15.0 g, yield 79%).

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.0-1.2 (broad, 2H), 1.13 (d, J=6.9, 6H), 1.46 (s, 9H), 2.80 (t, J=7.2, 2H), 3.11 (m, 2H), 4.0-4.4 (broad, 1H).

Reference Example 4N-(3-aminopropyl)-N-isopropyl-2-nitrobenzenesulfonamideStep AN-isopropyl-2-nitrobenzenesulfonamide

Isopropylamine (11.07 g, 68.85 mmol) and triethylamine (13 ml, 93 mmol) were dissolved in dichloromethane (50 ml) and the mixture was stirred under ice-cooling. Thereto was added 2-nitrobenzenesulfonyl chloride (10.11 g, 45.62 mmol), and the mixture was stirred at room temperature for 6 hr. The reaction mixture was diluted with ethyl acetate-hexane=1:1 mixed solvent, and the organic layer was washed with diluted hydrochloric acid and water, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, the solution was concentrated under reduced pressure and the obtained solid was washed with hexane and air-dried to give the title compound (10.73 g, yield 96%) as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.16 (d, J=6.2, 6H), 3.60-3.73 (m, 1H), 5.12 (d, J=7.1, 1H), 7.72-7.78 (m, 2H), 7.85-7.89 (m, 1H), 8.16-8.20 (m, 1H).

Step BN-[3-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)propyl]-N-isopropyl-2-nitrobenzenesulfonamide

The compound (6.29 g, 25.75 mmol) obtained in step A was dissolved in N-methylpyrrolidone (100 ml), and the mixture was stirred under ice-cooling. Thereto was added 60% sodium hydride (1.21 g, 30 mmol) and the mixture was stirred at room temperature for 20 min. After stirring, N-(3-bromopropyl)phthalimide (8.31 g, 31.0 mmol) was added and the mixture was stirred at 70Â° C. for 90 min. The reaction mixture was diluted with ethyl acetate, washed with water, saturated aqueous sodium hydrogen carbonate and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained solid was washed with diethyl ether-hexane mixed solvent, and dried under reduced pressure to give the title compound (8.11 g, yield 73%) as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.17 (d, J=6.6, 6H), 1.97-2.08 (m, 2H), 3.34 (t, J=7.8, 2H), 3.73 (t, J=7.1, 2H), 4.1-4.2 (m, 1H), 7.5-7.8 (m, 5H), 7.84-7.87 (m, 2H), 7.98-8.02 (m, 1H).

Step CN-(3-aminopropyl)-N-isopropyl-2-nitrobenzenesulfonamide

The compound (8.11 g, 18.80 mmol) obtained in step B and hydrazine monohydrate (5 ml) were added to ethanol (200 ml) and the mixture was heated under reflux for 1 hr. The reaction mixture was cooled, and diluted with diethyl ether. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was dissolved in dichloromethane, and the solution was extracted with hydrochloric acid. The aqueous layer was alkalified with aqueous sodium hydroxide solution, extracted with dichloromethane, and the organic layer was dried over potassium carbonate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure to give the title compound (5.62 g, yield 99%) as a yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.18 (d, J=6.6, 6H), 1.38 (brs, 2H), 1.74-1.85 (m, 2H), 2.76 (t, J=6.9, 2H), 3.33 (t, J=7.7, 2H), 4.0-4.2 (m, 1H), 7.5-7.7 (m, 3H), 8.02-8.06 (m, 1H).

Reference Example 5N-(3-aminopropyl)-N-methyl-2-nitrobenzenesulfonamide hydrochlorideStep AN-methyl-2-nitrobenzenesulfonamide

Using methylamine hydrochloride (12.4 g) and according to the method of Reference Example 4, step A, the title compound (7.39 g, yield 32%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.80 (d, J=5.3, 3H), 5.23 (brs, 1H), 7.7-7.9 (m, 3H), 8.1-8.2 (m, 1H).

Step BN-[3-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)propyl]-N-methyl-2-nitrobenzenesulfonamide

Using the compound (3.10 g, 14.34 mmol) obtained in step A and N-(3-bromopropyl)phthalimide (3.80 g, 14.17 mmol), and according to the method of Reference Example 4, step B, the title compound (4.19 g, yield 73%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.93-2.04 (m, 2H), 2.95 (s, 3H), 3.35 (t, J=7.4, 2H), 3.73 (t, J=7.4, 2H), 7.62-7.75 (m, 5H), 7.83-7.87 (m, 2H), 7.96-8.00 (m, 1H).

Step CN-(3-aminopropyl)-N-methyl-2-nitrobenzenesulfonamide hydrochloride

Using the compound (4.18 g, 10.36 mmol) obtained in step B and according to the method of Reference Example 4, step C, N-(3-aminopropyl)-N-methyl-2-nitrobenzenesulfonamide (3.20 g) was obtained as a crude oil. This was dissolved in dichloromethane (50 ml), 4N hydrochloric acid-dioxane solution (3 ml) was added, and diluted with diethyl ether to allow precipitation of a solid. The precipitated solid was filtered, and dried under reduced pressure to give the title compound (3.18 g, yield 99%) as a pale-yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.8-1.9 (m, 2H), 2.7-2.8 (m, 2H), 2.86 (s, 3H), 3.29 (t, J=6.9, 2H), 7.8-8.1 (m, 7H (4H of Ar&NH₃)).

Reference Example 6N-(2-aminoethyl)-N-methyl-2-nitrobenzenesulfonamideStep AN-[2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)ethyl]-N-methyl-2-nitrobenzenesulfonamide

Using the compound (4.26 g, 19.7 mmol) of Reference Example 5, step A, and N-(2-bromoethyl)phthalimide (5.05 g, 19.9 mmol), and according to the method of Reference Example 4, step B, the title compound (1.64 g, yield 21%) was obtained as pale-yellow crystals.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 3.06 (s, 3H), 3.56 (t, J=6.5, 2H), 3.90 (t, J=6.5, 2H), 7.40-7.55 (m, 1H), 7.58-7.62 (m, 2H), 7.68-7.72 (m, 2H), 7.80-7.84 (m, 2H), 7.93-7.97 (m, 1H).

Step BN-(2-aminoethyl)-N-methyl-2-nitrobenzenesulfonamide

Using the compound (1.63 g, 4.19 mmol) obtained in step A and according to the method of Reference Example 4, step C, the title compound (0.95 g, yield 88%) as a yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.90 (t, J=5.4, 2H), 2.92 (s, 3H), 3.30 (t, J=5.4, 2H), 7.61-7.64 (m, 1H), 7.66-7.74 (m, 2H), 8.00-8.04 (m, 1H).

Reference Example 7N-(2-aminoethyl)-N-isopropyl-2-nitrobenzenesulfonamideStep Atert-butyl [2-{[(2-nitrophenyl)sulfonyl]amino}ethyl]carbamate

Using tert-butyl (2-aminoethyl)carbamate (4.61 g) and according to the method of Reference Example 4, step A, the title compound (2.22 g, yield 22%) as a yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.42 (s, 9H), 3.2-3.4 (m, 4H), 4.84 (brs, 1H), 5.71 (brs, 1H), 7.73-7.79 (m, 2H), 7.85-7.90 (m, 1H), 8.11-8.15 (m, 1H).

Step BN-(2-aminoethyl)-N-isopropyl-2-nitrobenzenesulfonamide

The compound (2.22 g, 6.43 mmol) obtained in step A, isopropanol (0.65 ml, 8.46 mmol), and triphenylphosphine (1.85 g, 7.05 mmol) were dissolved in tetrahydrofuran (50 ml) and the mixture was stirred under ice-cooling. Thereto was slowly added 40% diisopropyl azodicarboxylate-toluene solution (5 ml), and the mixture was stirred at the same temperature for 1 hr. The reaction mixture was concentrated under reduced pressure and diluted with diethyl ether, and the precipitated colorless solid was filtered off. The mother liquor was concentrated under reduced pressure and the obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give tert-butyl [2-{isopropyl[(2-nitrophenyl)sulfonyl]amino}ethyl]carbamate (3.75 g) as a colorless crude oil. This was dissolved in dichloromethane (10 ml), 4N hydrochloric acid-dioxane solution 10 ml) was added at room temperature and the mixture was stirred for 1 hr. The reaction mixture was diluted with diethyl ether, and the mixture was extracted with water. The aqueous layer was alkalified with aqueous sodium hydroxide solution, extracted with dichloromethane, dried over sodium sulfate, the insoluble material was filtered off, and the solution was concentrated under reduced pressure to give the title compound (1.39 g, yield 75%) as a yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.16 (d, J=6.9, 6H), 1.32 (brs, 2H), 2.91 (t, J=7.1, 2H), 3.30 (t, J=7.1, 2H), 4.0-4.2 (m, 1H), 7.6-7.8 (m, 3H), 8.0-8.1 (m, 1H).

Reference Example 8[(2R)-1-(2-aminoethyl)pyrrolidin-2-yl]methanolStep A[(2R)-1-glycylpyrrolidin-2-yl]methanol

N-(tert-butoxycarbonyl)glycine (5.00 g, 28.5 mmol) and D-prolinol (3.50 g, 34.2 mmol) was dissolved in N,N-dimethylformamide (10 ml) and dichloromethane (100 ml), and the mixture was stirred at room temperature. At the same temperature, 1-hydroxybenzotriazole.monohydrate (7.70 g, 57.0 mmol) and N-(3-dimethylaminopropyl)-Nâ€²-ethylcarbodiimide hydrochloride (hereinafter to be indicated as WSC) (8.20 g, 42.8 mmol) were added, and the mixture was stirred at room temperature overnight. The reaction mixture was washed with diluted hydrochloric acid, diluted aqueous sodium hydroxide solution, water and saturated brine, and the organic layer was dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure, the obtained oil was purified by silica gel column chromatography (methanol-chloroform) to give a crude product. This was dissolved in ethyl acetate (30 ml) and methanol (20 ml), 4N hydrochloric acid-ethyl acetate solution (20 ml) was added, and the mixture was stirred at room temperature overnight. The solution was concentrated under reduced pressure, and to the obtained concentrate was added a saturated aqueous potassium carbonate solution, and the mixture was extracted with chloroform. The organic layer was dried over anhydrous magnesium sulfate, the insoluble material was filtered off, and the solution was concentrated under reduced pressure to give the title compound (1.00 g, yield 22%) as a pale-yellow oil.

Step B[(2R)-1-(2-aminoethyl)pyrrolidin-2-yl]methanol

To tetrahydrofuran (30 ml) was added lithium aluminum hydride (720 mg, 19.0 mmol) and the mixture was stirred under ice-cooling. Then, a solution (20 ml) of the compound (1.00 g, 6.32 mmol) obtained in step A in tetrahydrofuran was gradually added, and the mixture was heated under reflux for 2 hr. The reaction mixture was cooled, water (0.72 ml), 1N aqueous sodium hydroxide solution (1.44 ml) and water (0.72 ml) were slowly added in this order with stirring, and the mixture was stirred at room temperature for 1 hr. The insoluble material was filtered off through celite, and the solution was concentrated under reduced pressure to give the title compound (718 mg, yield 79%) as a yellow oil.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.22-1.40 (m, 1H), 1.47-1.82 (m, 4H), 2.08-2.20 (m, 1H), 2.21-2.35 (m, 1H), 2.37-2.42 (m, 1H), 2.43-2.60 (m, 2H), 2.61-2.81 (m, 2H), 2.95-3.04 (m, 1H), 3.17-3.25 (m, 1H), 3.30-3.41 (m, 1H).

Reference Example 9tert-butyl 4-aminopiperidine-1-carboxylate hydrochlorideStep Atert-butyl 4-[(methylsulfonyl)oxy]piperidine-1-carboxylate

4-Hydroxypiperidine (4.88 g, 48.2 mmol) was dissolved in dichloromethane (50 ml) and triethylamine (6.7 ml) (48.1 mmol) was added, and the mixture was stirred under ice-cooling. Thereto was added di-tert-butyl dicarbonate (10.11 g, 46.3 mmol) dissolved in dichloromethane (30 ml) was added. The mixture was stirred at the same temperature for 2 hr, triethylamine (8.0 ml, 57.4 mmol) and methanesulfonylchloride (3.8 ml, 49.1 mmol) were added, and the mixture was stirred at room temperature for 3 hr. The reaction mixture was diluted with ethyl acetate-hexane=1:1 solution, washed with aqueous citric acid solution, water, saturated aqueous sodium hydrogen carbonate and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the obtained solution was concentrated under reduced pressure and the obtained solid was washed with hexane to give the title compound (8.60 g) (yield 66%) as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.46 (s, 9H), 1.75-1.90 (m, 2H), 1.91-2.01 (m, 2H), 3.04 (s, 3H), 3.25-3.35 (m, 2H), 3.66-3.74 (m, 2H), 4.85-4.92 (m, 1H).

Step Btert-butyl 4-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)piperidine-1-carboxylate

Using the compound (2.43 g, 8.70 mmol) obtained by the method of step A and potassium phthalimide (2.40 g, 12.96 mmol), and according to the method of Reference Example 4, step B, the title compound (846 mg, yield 29%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.49 (s, 9H), 1.6-1.7 (m, 2H), 2.3-2.5 (m, 2H), 2.7-2.9 (m, 2H), 4.22-4.32 (m, 3H), 7.70-7.74 (m, 2H), 7.81-7.85 (m, 2H).

Step Ctert-butyl 4-aminopiperidine-1-carboxylate hydrochloride

The compound (837 mg, 2.53 mmol) obtained in step B was added to ethanol (20 ml), hydrazine monohydrate (0.31 ml, 6.4 mmol) was added, and the mixture was heated under reflux for 1 hr. The reaction mixture was cooled, and diethyl ether was added to allow precipitation of a solid. The precipitated solid was filtered, and the obtained solution was concentrated under reduced pressure to give a colorless oil. The oil was dissolved in diethyl ether, 4N hydrochloric acid-dioxane solution (1 ml) was added at room temperature and the mixture was diluted with ethyl acetate to allow precipitation of a solid. This was filtered, washed with ethyl acetate, and dried under reduced pressure to give the title compound (598 mg, yield 100%) as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.3-1.5 (m, 2H), 1.39 (s, 9H), 1.8-1.9 (m, 2H), 2.6-2.8 (m, 2H), 3.0-3.2 (m, 1H), 3.9-4.0 (m, 2H), 8.17 (brs, 3H).

Reference Example 10tert-butyl 3-aminopiperidine-1-carboxylate hydrochlorideStep Atert-butyl 3-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)piperidine-1-carboxylate

tert-Butyl 3-hydroxypiperidine-1-carboxylate (4.38 g) (21.76 mmol), phthalimide (4.82 g, 32.76 mmol), and triphenylphosphine (8.62 g, 32.86 mmol) were added to tetrahydrofuran (60 ml), 40% diethyl azodicarboxylate-toluene solution (15 ml) was slowly added at room temperature with stirring, and the mixture was stirred at the same temperature overnight. The reaction mixture was concentrated under reduced pressure, diluted with diethyl ether, and the precipitated colorless solid was filtered off. The mother liquor was concentrated under reduced pressure and the obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (2.04 g, yield 28%) as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.46 (s, 9H), 1.5-1.7 (m, 1H), 1.75-1.90 (m, 2H), 2.2-2.4 (m, 1H), 2.6-2.8 (m, 1H), 3.4-3.6 (m, 1H), 3.9-4.3 (m, 3H), 7.70-7.76 (m, 2H), 7.81-7.86 (m, 2H).

Step Btert-butyl 3-aminopiperidine-1-carboxylate hydrochloride

Using the compound (2.04 g, 6.17 mmol) obtained in step A and according to the method of Reference Example 9, step C, the title compound (1.45 g, yield 99%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.3-1.6 (m, 2H), 1.43 (s, 9H), 1.6-1.8 (m, 1H), 1.9-2.0 (m, 1H), 2.7-3.1 (m, 3H), 3.6-3.8 (m, 1H), 3.9-4.0 (m, 1H), 8.23 (brs, 3H).

Reference Example 11tert-butyl 3-aminopyrrolidine-1-carboxylate hydrochloride

3-(Trifluoroacetamido)pyrrolidine hydrochloride (4.60 g, 21.04 mmol) was added to dichloromethane (60 ml), triethylamine (3.5 ml, 25.1 mmol) and di-tert-butyl dicarbonate (4.61 g, 21.12 mmol) were added under ice-cooling, and the mixture was stirred at room temperature for 7 hr. The reaction mixture was dissolved in ethyl acetate-hexane=1:1 mixed solvent (100 ml), and the organic layer was washed with water, 10% aqueous citric acid solution and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure to give the title compound (6.66 g) as a crude colorless oil. This was dissolved in methanol (70 ml), potassium carbonate (14.46 g) dissolved in water (50 ml) was added under ice-cooling, and the mixture was stirred at room temperature for 5 hr. The reaction mixture was concentrated under reduced pressure, diluted with diethyl ether and washed with saturated brine and dried over sodium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure to give an oil. This was dissolved in diethyl ether (50 ml), and 4N hydrochloric acid-dioxane solution (5.5 ml) was added. Hexane was added to the solution to allow crystallization, and the precipitated solid was filtered and dried under reduced pressure to give the title compound (4.22 g, yield 90%) as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.41 (s, 9H), 1.8-2.0 (m, 1H), 2.0-2.2 (m, 1H), 3.2-3.6 (m, 4H), 3.7-4.0 (m, 1H), 8.40 (brs, 3H).

Reference Example 12tert-butyl (2S)-2-(aminomethyl)pyrrolidine-1-carboxylate hydrochloride

Using tert-butyl (2S)-2-(hydroxymethyl)pyrrolidine-1-carboxylate (4.07 g, 20.22 mmol) and according to the methods of Reference Example 10, steps A and B, the title compound (4.34 g, yield 91%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.41 (s, 9H), 1.6-2.0 (m, 4H), 2.6-2.8 (m, 1H), 2.8-3.0 (m, 1H), 3.1-3.3 (m, 2H), 3.8-4.0 (m, 1H), 8.16 (brs, 3H).

Reference Example 13tert-butyl (2R)-2-(aminomethyl)pyrrolidine-1-carboxylate hydrochloride

Using tert-butyl (2R)-2-(hydroxymethyl)pyrrolidine-1-carboxylate (3.21 g, 15.95 mmol) and according to the methods of Reference Example 10, steps A and B, the title compound (3.31 g, yield 88%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.42 (s, 9H), 1.6-2.0 (m, 4H), 2.6-2.8 (m, 1H), 2.8-3.0 (m, 1H), 3.1-3.3 (m, 2H), 3.8-4.0 (m, 1H), 8.09 (brs, 3H).

Reference Example 14N-(2-aminoethyl)-2,2,2-trifluoro-N-(2,2,2-trifluoroethyl)acetamide hydrochlorideStep Atert-butyl {2-[(trifluoroacetyl)amino]ethyl}carbamate

tert-Butyl (2-aminoethyl)carbamate (5.00 g, 31.2 mmol) and pyridine (3.0 ml, 37 mmol) were added to dichloromethane (100 ml), and the mixture was stirred under ice-cooling. Then, trifluoroacetic acid anhydride (4.9 ml, 34 mmol) was added dropwise. After the completion of the dropwise addition, the reaction mixture was stood at room temperature overnight. Water was added and the mixture was extracted with ethyl acetate, washed with diluted hydrochloric acid, diluted aqueous sodium hydroxide solution and saturated brine, and dried over anhydrous magnesium sulfate. The solution was concentrated under reduced pressure to give the title compound (6.57 g, yield 82%) as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.37 (s, 9H), 3.00-3.10 (m, 2H), 3.15-3.24 (m, 2H), 6.91 (t, J=5.4, 1H), 9.35 (brs, 1H).

Step Btert-butyl {2-[(2,2,2-trifluoroethyl)amino]ethyl}carbamate

The compound (6.57 g, 25.6 mmol) obtained in step A was dissolved in tetrahydrofuran (100 ml), and the mixture was stirred under ice-cooling. Then, a suspension of lithium aluminum hydride (1.94 g, 51.2 mmol) in tetrahydrofuran (50 ml) was slowly added dropwise. Thereafter, the mixture was stood overnight at room temperature. The reaction mixture was ice-cooled again, water (2 ml), 1N aqueous sodium hydroxide solution (4 ml) and water (2 ml) were added in this order with stirring, and the mixture was stirred at room temperature for 5 hr. The insoluble material was filtered off through celite, and the obtained solution was concentrated under reduced pressure to give the title compound (4.56 g, yield 74%) as a yellow oil.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.37 (s, 9H), 2.51-2.68 (m, 2H), 2.98 (q, J=6.3, 2H), 3.15-3.25 (m, 2H), 6.74 (brs, 1H).

Step Ctert-butyl {2-[(trifluoroacetyl)(2,2,2-trifluoroethyl)amino]ethyl}carbamate

Using the compound (4.56 g, 18.8 mmol) obtained in step B and according to the method of Reference Example 14, step A, the title compound (3.05 g, yield 48%) was obtained as a pale-yellow oil.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.36 (s, 9H), 3.20-3.32 (m, 2H), 3.43-3.58 (m, 2H), 4.25-4.40 (m, 2H), 7.04 (brs, 1H).

Step DN-(2-aminoethyl)-2,2,2-trifluoro-N-(2,2,2-trifluoroethyl)acetamide hydrochloride

The compound (3.05 g, 9.02 mmol) obtained in step C was dissolved in ethyl acetate (20 ml), 4N hydrochloric acid-ethyl acetate solution (10 ml) was added, and the mixture was stirred at room temperature for 6 hr. The precipitated solid was collected by filtration, and the obtained solid was washed with ethyl acetate, and dried under reduced pressure to give the title compound (1.51 g, yield 61%) as a pale-bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 3.02-3.19 (m, 2H), 3.68-3.88 (m, 2H), 4.31-4.63 (m, 2H), 8.34 (brs, 3H).

Reference Example 15N-(2-aminoethyl)-N-ethyl-2,2,2-trifluoroacetamide hydrochloride

According to the method described in Synthetic Communications, 23(17), 2443-2449 (1993), tert-butyl N-[2-(ethylamino)ethyl]carbamate (3.06 g, 16.25 mmol) was obtained from N-ethylethylenediamine (8.36 g) and di-tert-butyl dicarbonate (6.25 g). Using this compound, and according to the method of Reference Example 14, step A, tert-butyl {2-[ethyl(trifluoroacetyl)amino]ethyl}carbamate (4.92 g) was obtained as a crude pale-yellow oil. Using this compound and according to the method of Reference Example 14, step D, the title compound (1.91 g, yield 30%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.09 (t, J=7.1, 0.8H), 1.17 (t, J=7.1, 2.2H), 2.9-3.1 (m, 2H), 3.40-3.51 (m, 2H), 3.59-3.69 (m, 2H), 8.12 (brs, 3H).

Reference Example 16N-(tert-butyl)ethane-1,2-diamineStep A[benzyl(tert-butyl)amino]acetonitrile

Benzyl(tert-butyl)amine (10.0 g, 61.3 mmol) was dissolved in acetonitrile (100 ml), and bromoacetonitrile (4.5 ml, 64.6 mmol), potassium carbonate (16.9 g, 122.3 mmol) and sodium iodide (9.2 g, 61.4 mmol) were successively added with stirring at room temperature, and the mixture was stirred at the same temperature overnight. The reaction mixture was diluted with saturated aqueous potassium carbonate solution, extracted with ethyl acetate, washed with saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure, and the obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (10.8 g, yield 87%) as a pale-yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.30 (s, 9H), 3.45 (s, 2H), 3.84 (s, 2H), 7.25-7.37 (m, 5H).

Step BN-benzyl-N-(tert-butyl)ethane-1,2-diamine

The compound (5.00 g, 24.7 mmol) obtained in step A was dissolved in tetrahydrofuran (100 ml), and the mixture was stirred under ice-cooling. Lithium aluminum hydride (1.87 g, 49.4 mmol) was gradually added at the same temperature, and the mixture was stirred at room temperature for 2 hr. After ice-cooling again, water (1.9 ml), 1N aqueous sodium hydroxide solution (3.8 ml) and water (1.9 ml) were gradually added in this order, and the mixture was stirred at room temperature for 1 hr. The insoluble material was filtered off through celite, and the obtained solution was concentrated under reduced pressure to give the title compound (4.89 g, yield 96%) as a pale-yellow oil.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.06 (s, 9H), 2.28 (t, J=6.9, 2H), 2.47-2.53 (m, 2H), 3.33 (brs, 2H), 3.64 (s, 2H), 7.13-7.16 (m, 1H), 7.18-7.33 (m, 4H).

Step CN-(tert-butyl)ethane-1,2-diamine

The compound (2.65 g, 12.8 mmol) obtained in step B was dissolved in ethanol (30 ml), and the mixture was stirred at room temperature. Then, 10% palladium carbon (containing water) (500 mg) was added, and the mixture was stirred under a hydrogen atmosphere at room temperature for 7 hr. The insoluble material was filtered off through celite, and the obtained solution was concentrated under reduced pressure to give the title compound (850 mg, yield 57%) as a pale-yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.00 (s, 9H), 2.40-2.46 (m, 2H), 2.49-2.56 (m, 2H), 2.75-4.00 (broad, 3H).

Reference Example 17N-methyl-1,3-dihydro-2H-isoindol-2-amine hydrochlorideStep Atert-butyl 1-methylhydrazinecarboxylate

According to the method described in Journal of Heterocyclic Chemistry, 2000, 37(1), 47-55, the title compound (122.7 g) was obtained as a colorless oil from N-methylhydrazine (44.1 g).

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.48 (s, 9H), 3.06 (s, 3H), 4.06 (brs, 2H).

Step Btert-butyl 1,3-dihydro-2H-isoindol-2-yl(methyl)carbamate

The step was performed according to the method described in U.S. Pat. No. 4,272,284. Xylylene dibromide (160 g, 606 mmol) and compound (88.52 g, 606 mmol) obtained in step A were dissolved in N-methylpyrrolidone (550 ml). While maintaining the reaction mixture at 50Â° C.-60Â° C., triethylamine (190 ml, 1.36 mol) was gradually added dropwise using infundibulum with stirring and, after the completion of the dropwise addition, the reaction mixture was stood overnight at room temperature. A 5% aqueous citric acid solution (700 ml) was added to the reaction mixture, and the precipitated solid was collected by filtration, washed with water and dried under reduced pressure to give the title compound (126 g, yield 84%) as a crude pale-pink solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.41 (s, 9H), 3.09 (s, 3H), 4.44 (s, 4H), 7.1-7.2 (m, 4H).

Step CN-methyl-1,3-dihydro-2H-isoindol-2-amine hydrochloride

The compound (126 g) obtained in step B was dissolved in a mixed solvent of dichloromethane (150 ml) and ethanol (150 ml). A 4N hydrochloric acid-dioxane solution (500 ml) was added with stirring at room temperature and the mixture was stirred at the same temperature for 5 hr. The reaction mixture was diluted with dichloromethane and water and the aqueous layer was extracted. An ice-cooled aqueous sodium hydroxide solution was added to the ice-cooled aqueous layer to give a strongly-alkaline aqueous layer. The aqueous layer was extracted with dichloromethane. The organic layer was dried over potassium carbonate, and the insoluble material was filtered off. The solvent was evaporated under reduced pressure. The obtained oil was dissolved in diethyl ether (500 ml), and 4N hydrochloric acid-dioxane solution (140 ml) was added with stirring under ice-cooling to allow precipitation of a solid. This was filtered, washed with diethyl ether, and dried under reduced pressure to give the title compound (75.89 g, yield 81%) as a gray solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.77 (s, 3H), 4.43 (s, 4H), 7.2-7.4 (m, 4H), 11.0 (brs, 2H).

Reference Example 184-fluoro-N-methyl-1,3-dihydro-2H-isoindol-2-amine hydrochlorideStep Atert-butyl (4-fluoro-1,3-dihydro-2H-isoindol-2-yl)methylcarbamate

3-Fluoro-ortho-xylene (1.99 g, 16.03 mmol), N-bromosuccinimide (6.98 g, 39.22 mmol) and benzoyl peroxide (0.24 g) were added to carbon tetrachloride (60 ml), and the mixture was heated under reflux for 45 min. The reaction mixture was cooled, diluted with hexane, and the insoluble material was filtered off. The obtained solution was concentrated under reduced pressure. Using the obtained oil, the reaction was performed according to the method of Reference Example 17, step B. After completion of the reaction, 10% aqueous citric acid solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate-hexane=1:1 mixed solvent, washed with water, saturated aqueous sodium hydrogen carbonate and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (826 mg, yield 19%) as a pale-yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.41 (s, 9H), 3.09 (s, 3H), 4.47 (s, 2H), 4.48 (s, 2H), 6.87 (t, J=8.6, 1H), 6.94 (d, J=7.2, 1H), 7.1-7.2 (m, 1H).

Step B4-fluoro-N-methyl-1,3-dihydro-2H-isoindol-2-amine hydrochloride

The compound (806 mg, 3.03 mmol) obtained in step A was dissolved in a dichloromethane (3 ml)-ethanol (0.3 ml) mixed solvent. 4N Hydrochloric acid-dioxane solution (3 ml) was added with stirring at room temperature, and the mixture was stirred at the same temperature for 100 min. Diethyl ether was added to the reaction mixture, and the precipitated solid was filtered, washed with diethyl ether and dried under reduced pressure to give the title compound (433 mg, yield 71%) as a gray solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.80 (s, 3H), 4.48 (s, 2H), 4.50 (s, 2H), 7.14 (t, J=8.9, 1H), 7.21 (d, J=7.2, 1H), 7.33-7.41 (m, 1H), 10.9 (brs, 2H).

Reference Example 195-fluoro-N-methyl-1,3-dihydro-2H-isoindol-2-amine hydrochlorideStep Atert-butyl (5-fluoro-1,3-dihydro-2H-isoindol-2-yl)methylcarbamate

Using 4-fluoro-ortho-xylene (20.05 g, 161.5 mmol) and according to the method of Reference Example 18, step A, the title compound (13.04 g, yield 30%) was obtained as a yellow bistered oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.41 (s, 9H), 3.08 (s, 3H), 4.39 (s, 2H), 4.43 (s, 2H), 6.85-6.95 (m, 2H), 7.07-7.13 (m, 1H).

Step B5-fluoro-N-methyl-1,3-dihydro-2H-isoindol-2-amine hydrochloride

Using the compound (13.04 g, 48.97 mmol) of step A and according to the method of Reference Example 18, step B, the title compound (7.61 g, yield 77%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.77 (s, 3H), 4.39 (s, 2H), 4.42 (s, 2H), 7.09-7.17 (m, 1H), 7.20-7.24 (m, 1H), 7.34-7.40 (m, 1H), 10.9 (brs, 2H).

Reference Example 205-methoxy-N-methyl-1,3-dihydro-2H-isoindol-2-amine hydrochlorideStep Atert-butyl (5-methoxy-1,3-dihydro-2H-isoindol-2-yl)methylcarbamate

Using 4-methoxy-ortho-xylene (6.85 g, 50.3 mmol) and according to the method of Reference Example 18, step A, the title compound (2.11 g, yield 15%) was obtained as a brown oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.41 (s, 9H), 3.08 (s, 3H), 3.78 (s, 3H), 4.36 (brs, 2H), 4.41 (brs, 2H), 6.7-6.8 (m, 2H), 7.06 (d, J=8.1, 1H).

Step B5-methoxy-N-methyl-1,3-dihydro-2H-isoindol-2-amine hydrochloride

Using the compound (2.10 g, 7.54 mmol) obtained in step A and according to the method of Reference Example 18, step B, the title compound (1.23 g, yield 76%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.76 (s, 3H), 3.74 (s, 3H), 4.36 (brs, 2H), 4.40 (brs, 2H), 6.86 (d, J=8.4, 1H), 6.93 (s, 1H), 7.24 (d, J=8.3, 1H), 10.9 (brs, 2H).

Reference Example 215-cyano-N-methyl-1,3-dihydro-2H-isoindol-2-amine hydrochlorideStep Atert-butyl (5-cyano-1,3-dihydro-2H-isoindol-2-yl)methylcarbamate

Using 4-bromo-ortho-xylene (5.88 g, 31.77 mmol) and according to the method of Reference Example 18, step A, 5-bromo-1,3-dihydro-2H-isoindol-2-yl(methyl)carbamate (2.52 g) was obtained as a crude brown oil. This oil, zinc cyanide (734 mg, 6.25 mmol), and tetrakis(triphenylphosphine)palladium(0) (1.74 g) were added to N,N-dimethylformamide (25 ml), and the reaction mixture was stirred with heating at 100Â° C. for 7 hr. The reaction mixture was cooled, diluted with ethyl acetate, and the insoluble material was filtered off. The filtrate was washed with aqueous ammonia and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (390 mg, yield 4%) as a colorless oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.41 (s, 9H), 3.09 (s, 3H), 4.49 (brs, 2H), 4.50 (brs, 2H), 7.27 (d, J=7.7, 1H), 7.46 (s, 1H), 7.50 (d, J=7.7, 1H).

Step B5-cyano-N-methyl-1,3-dihydro-2H-isoindol-2-amine hydrochloride

Using the compound (370 mg, 1.35 mmol) of step A and according to the method of Reference Example 18, step B, the title compound (200 mg, yield 70%) was obtained as a gray solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.77 (s, 3H), 4.49 (brs, 2H), 4.52 (brs, 2H), 7.57 (d, J=7.8, 1H), 7.78 (d, J=7.8, 1H), 7.84 (s, 1H), 11.11 (brs, 2H).

Reference Example 22N-ethyl-1,3-dihydro-2H-isoindol-2-amine hydrochlorideStep Atert-butyl 1-ethylhydrazinecarboxylate

According to the method described in Journal of Heterocyclic Chemistry, 2000, 37(1), 47-55, the title compound (64.8 g) was obtained as a colorless oil from N-ethylhydrazine (25.0 g).

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.12 (t, J=7.2, 3H), 1.47 (s, 9H), 3.06 (q, J=7.2, 2H), 3.96 (brs, 2H).

Step Btert-butyl 1,3-dihydro-2H-isoindol-2-yl(ethyl)carbamate

Using the compound (6.0 g, 38 mmol) obtained in step A and according to the method of Reference Example 17, step B, the title compound (6.5 g, yield 66%) was obtained as a crude pale-brown solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.21 (t, J=6.9, 3H), 1.38 (s, 9H), 3.47 (q, J=6.9, 2H), 4.48 (s, 4H), 7.12-7.26 (m, 4H).

Step CN-ethyl-1,3-dihydro-2H-isoindol-2-amine hydrochloride

Using the compound (6.10 g, 23 mmol) obtained in step B and according to the method of Reference Example 18, step B, the title compound (4.15 g, yield 90%) was obtained as a gray solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.26 (brs, 3H), 3.19 (brs, 2H), 4.43 (s, 4H), 7.3-7.4 (m, 4H), 10.9 (brs, 2H).

Reference Example 23N-methylindan-2-amine hydrochlorideStep Atert-butyl (2,3-dihydro-1H-inden-2-yl)carbamate

2-Aminoindane (3.10 g, 23.3 mmol) was dissolved in dichloromethane (50 ml), di-tert-butyl-dicarbonate (5.20 g, 23.8 mmol) and triethylamine (5 ml) were added under ice-cooling, and the mixture was stirred at room temperature for 2 hr. The reaction mixture was diluted with ethyl acetate-hexane=1:1 mixed solvent (100 ml), and the organic layer was washed with 10% aqueous citric acid solution, saturated aqueous sodium hydrogen carbonate and saturated brine and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure to give the title compound (4.68 g, yield 86%) as a colorless oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.45 (s, 9H), 2.78 (dd, J=4.8, 15.9, 2H), 3.28 (dd, J=7.1, 15.9, 2H), 4.3-4.6 (broad, 1H), 4.6-4.9 (broad, 1H), 7.15-7.24 (m, 4H).

Step BN-methylindan-2-amine hydrochloride

Lithium aluminum hydride (2.56 g, 67.46 mmol) and the compound (4.63 g, 19.84 mmol) obtained in step A were added to tetrahydrofuran (100 ml), and the mixture was heated under reflux for 3 hr. The reaction mixture was ice-cooled, and water (2.56 ml), 15% aqueous sodium hydroxide solution (2.56 ml), water (7.68 ml) and anhydrous magnesium sulfate were successively added with stirring. The insoluble material was filtered off through celite, and the solution was concentrated under reduced pressure to give an oil (3.15 g). This was dissolved in diethyl ether (50 ml), 4N hydrochloric acid-dioxane solution (6 ml) was added, and the precipitated solid was filtered, washed with diethyl ether and dried under reduced pressure to give the title compound (3.53 g, yield 97%) as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.58 (t, J=5.3, 3H), 3.09 (dd, J=6.6, 16.2, 2H), 3.28 (dd, J=8.0, 16.4, 2H), 3.9-4.0 (m, 1H), 7.18-7.23 (m, 2H), 7.24-7.29 (m, 2H), 9.25 (brs, 2H).

Reference Example 24N-ethylindan-2-amine hydrochlorideStep AN-(2,3-dihydro-1H-inden-2-yl)acetamide

2-Aminoindane (1.07 g, 8.03 mmol) was dissolved in dichloromethane (20 ml), and acetic anhydride (0.76 ml, 8.04 mmol) and triethylamine (1.7 ml) were added under ice-cooling, and the mixture was stirred at room temperature for 50 min. The reaction mixture was diluted with ethyl acetate-hexane=1:1 mixed solvent (80 ml), and the organic layer was washed with diluted hydrochloric acid, saturated aqueous sodium hydrogen carbonate and saturated brine and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained solid was washed with diethyl ether-hexane=1:5 mixed solvent, and dried under reduced pressure to give the title compound (961 mg, yield 68%) as a pale-yellow solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.94 (s, 3H), 2.80 (dd, J=3.9, 16.2, 2H), 3.31 (dd, J=3.9, 16.2, 2H), 4.7-4.8 (m, 1H), 5.70 (brs, 1H), 7.15-7.30 (m, 4H).

Step BN-ethylindan-2-amine hydrochloride

Using the compound (960 mg, 5.48 mmol) obtained in step A and according to the method of Reference Example 23, step B, the title compound (1.01 g, yield 94%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.24 (t, J=7.2, 3H), 2.9-3.2 (m, 4H), 3.2-3.4 (m, 2H), 3.9-4.1 (m, 1H), 7.1-7.3 (m, 4H), 9.1-9.5 (broad, 2H).

Reference Example 255,N-dimethylindan-2-amine hydrochlorideStep A6-methyl-1H-inden-1,2(3H)-dione 2-oxime

6-Methylindan-1-one (5.00 g, 34.2 mmol) and 4N hydrochloric acid-dioxane solution (2 ml) were added to ethanol (30 ml), isoamyl nitrite (5.1 ml, (37.6 mmol) was added under ice-cooling, and the mixture was stirred at room temperature for 3 hr. The precipitated solid was collected by filtration and washed with diisopropyl ether to give the title compound (5.36 g, yield 89%) as a pale-yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.39 (s, 3H), 3.72 (s, 2H), 7.45-7.60 (m, 3H), 12.59 (s, 1H).

Step B6-methyl-1H-inden-1,2(3H)-dione 2-{O-[tert-butyl(dimethyl)silyl]oxime}

To N,N-dimethylformamide (50 ml) were added at room temperature the compound (4.36 g, 24.9 mmol) obtained in step A, imidazole (5.10 g, 74.7 mmol) and tert-butyldimethylsilyl chloride (5.60 g, 37.4 mmol), and the mixture was stirred at 95Â° C. for 2 hr. After cooling to room temperature, water was added to the reaction solution with stirring and the precipitated solid was filtered, washed with water, and dried under reduced pressure to give the title compound (6.00 g, yield 83%) as a pale-bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 0.25 (s, 6H), 0.96 (s, 9H), 2.40 (s, 3H), 3.80 (s, 2H), 7.48-7.62 (m, 3H).

Step Cethyl (1-hydroxy-6-methyl-2,3-dihydro-1H-inden-2-yl)carbamate

The compound (6.00 g, 20.7 mmol) obtained in step B was dissolved in tetrahydrofuran (100 ml), and the mixture was stirred with heating at 63Â° C. At the same temperature, 1 mol/L borane-tetrahydrofuran complex/tetrahydrofuran solution (41.4 ml, 41.4 mmol) was slowly added dropwise. The mixture was stirred at the same temperature for 2.5 hr, cooled to room temperature and methanol was slowly added dropwise with stirring. The reaction solution was concentrated under reduced pressure, methanol and toluene were added again, and the solution was concentrated under reduced pressure. This was repeated 4 times, and the obtained colorless solid and triethylamine (3.5 ml, 24.8 mmol) were dissolved in dichloromethane (50 ml) and the mixture was stirred under ice-cooling. Then, ethyl chloroformate (2.2 ml, 22.8 mmol) was added, and the mixture was stood at room temperature overnight. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic layer was washed with diluted hydrochloric acid and saturated brine, and dried over anhydrous magnesium sulfate. The solution was concentrated under reduced pressure, and the obtained oil was purified by silica gel column chromatography (methanol-chloroform) to give the title compound (3.30 g, yield 67%) as a colorless oil.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.21 (t, J=7.2, 3H), 2.33 (s, 3H), 2.76-3.05 (m, 2H), 4.00-4.17 (m, 3H), 4.83 (t, J=5.8, 1H), 5.20 (d, J=5.8, 1H), 6.75 (d, J=7.3, 1H), 7.02-7.19 (m, 3H).

Step Dethyl (5-methyl-2,3-dihydro-1H-inden-2-yl)carbamate

With stirring at room temperature, the compound (3.30 g, 13.9 mmol) obtained in step C, triethylsilane (4.4 ml, (27.8 mmol) and boron trifluoride-diethyl ether complex (3.4 ml, 27.8 mmol) dissolved in 1,2-dichloroethane (20 ml) were added to 1,2-dichloroethane (90 ml), and the mixture was stirred at 83Â° C. for 1 hr. After cooling to room temperature, the reaction mixture was diluted with water, and extracted with dichloromethane. The organic layer was washed with diluted aqueous sodium hydroxide solution, diluted hydrochloric acid and saturated brine, and dried over anhydrous magnesium sulfate. The solution was concentrated under reduced pressure to give the title compound (2.76 g, yield 91%) as a pale-yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.18 (t, J=6.9, 3H), 2.25 (s, 3H), 2.63-2.78 (m, 2H), 3.01-3.12 (m, 2H), 3.92-4.05 (m, 2H), 4.13-4.28 (m, 1H), 6.93 (d, J=7.8, 1H), 6.99 (s, 1H), 7.05 (d, J=7.5, 1H), 7.41 (d, J=6.6, 1H).

Step E5,N-dimethylindan-2-amine hydrochloride

Using the compound (2.76 g, 12.6 mmol) obtained in step D and according to the method of Reference. Example 23, step B, the title compound (1.52 g, yield 61%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.27 (s, 3H), 2.57 (t, J=5.4, 3H), 2.91-3.12 (m, 2H), 3.15-3.29 (m, 2H), 3.82-4.00 (m, 1H), 7.01 (d, J=7.5, 1H), 7.07 (s, 1H), 7.14 (d, J=7.5, 1H), 9.18 (brs, 2H).

Reference Example 264,N-dimethylindan-2-amine hydrochlorideStep A4-methyl-1H-inden-1,2(3H)-dione 2-oxime

Using 4-methylindan-1-one (5.00 g, 34.2 mmol) and according to the method of Reference Example 25, step A, the title compound (4.03 g, yield 67%) was obtained as a pale-bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.35 (s, 3H), 3.69 (s, 2H), 7.39 (t, J=7.5, 1H), 7.52-7.60 (m, 2H), 12.66 (s, 1H).

Step B4-methyl-1H-inden-1,2(3H)-dione 2-{O-[tert-butyl(dimethyl)silyl]oxime}

Using the compound (4.03 g, 23.0 mmol) obtained in step A and according to the method of Reference Example 25, step B, the title compound (6.24 g, yield 94%) was obtained as a pale-bistered solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 0.27 (s, 6H), 1.04 (s, 9H), 2.38 (s, 3H), 3.70 (s, 2H), 7.34 (t, J=7.5, 1H), 7.46 (d, J=7.5, 1H), 7.73 (d, J=7.5, 1H).

Step Cethyl (1-hydroxy-4-methyl-2,3-dihydro-1H-inden-2-yl)carbamate

Using the compound (6.24 g, 21.6 mmol) obtained in step B and according to the method of Reference Example 25, step C, the title compound (2.73 g, yield 54%) was obtained as a pale-bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.22 (t, J=7.2, 3H), 2.24 (s, 3H), 2.71-2.83 (m, 1H), 2.94-3.10 (m, 1H), 3.99-4.16 (m, 3H), 4.87 (t, J=6.0, 1H), 5.20 (d, J=6.0, 1H), 6.73 (d, J=7.2, 1H), 7.05-7.21 (m, 3H).

Step Dethyl (4-methyl-2,3-dihydro-1H-inden-2-yl)carbamate

Using the compound (2.73 g, 11.6 mmol) obtained in step C and according to the method of Reference Example 25, step D, the title compound (2.36 g, yield 93%) was obtained as a pale-bistered solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.23 (t, J=6.9, 3H), 2.24 (s, 3H), 2.65-2.85 (m, 2H), 3.18-3.33 (m, 2H), 4.05-4.19 (m, 2H), 4.50 (brs, 1H), 4.88 (brs, 1H), 6.93-7.12 (m, 3H).

Step E4,N-dimethylindan-2-amine hydrochloride

Using the compound (2.36 g, 10.8 mmol) obtained in step D and according to the method of Reference Example 23, step B, the title compound (1.85 g, yield 87%) was obtained as a pale-bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.22 (s, 3H), 2.57 (t, J=5.3, 3H), 2.95-3.32 (m, 4H), 3.85-3.96 (m, 1H), 6.95-7.14 (m, 3H), 9.47 (brs, 2H).

Reference Example 275-fluoro-N-methylindan-2-amine hydrochlorideStep A5-fluoro-1H-inden-1,2(3H)-dione 2-oxime

Using 5-fluoroindan-1-one (5.00 g, 33.3 mmol) and according to the method of Reference Example 25, step A, the title compound (4.45 g, yield 75%) was obtained as a pale-bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 3.78 (s, 2H), 7.21-7.37 (m, 1H), 7.40-7.51 (m, 1H), 7.75-7.90 (m, 1H), 12.67 (s, 1H).

Step B5-fluoro-1H-inden-1,2(3H)-dione 2-{O-[tert-butyl(dimethyl)silyl]oxime}

Using the compound (4.45 g, 24.8 mmol) obtained in step A and according to the method of Reference Example 25, step B, the title compound (5.15 g, yield 71%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 0.27 (s, 6H), 0.97 (s, 9H), 3.82 (s, 2H), 7.02-7.18 (m, 2H), 7.85-7.98 (m, 1H).

Step Cethyl (1-hydroxy-5-fluoro-2,3-dihydro-1H-inden-2-yl)carbamate

Using the compound (5.15 g, 17.6 mmol) obtained in step B and according to the method of Reference Example 25, step C, the title compound (1.84 g, yield 44%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.18 (t, J=7.2, 3H), 2.85-3.04 (m, 2H), 3.95-4.15 (m, 3H), 4.81 (d, J=5.4, 1H), 5.23 (brs, 1H), 6.77 (d, J=6.9, 1H), 6.96-7.07 (m, 2H), 7.35 (dd, J=5.1, 8.4, 1H).

Step D5-fluoro-N-methylindan-2-amine hydrochloride

Using the compound (1.84 g, 7.69 mmol) obtained in step C and according to the method of Reference Example 25, step D, Reference Example 23, step B, the title compound (1.06 g, yield 68%) was obtained as a pale-bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.57 (s, 3H), 3.09 (dt, J=6.6, 16.2, 2H), 3.20-3.33 (m, 2H), 3.90-4.01 (m, 1H), 6.95-7.05 (m, 1H), 7.09-7.14 (m, 1H), 7.28 (dd, J=6.6, 8.1, 1H), 9.35 (brs, 2H).

Reference Example 285-chloro-N-methylindan-2-amine hydrochlorideStep A5-chloro-1H-inden-1,2(3H)-dione 2-oxime

Using 5-chloroindan-1-one (5.00 g, 30.0 mmol) and according to the method of Reference Example 25, step A, the title compound (4.67 g, yield 80%) was obtained as a pale-bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 3.78 (s, 2H), 7.54 (d, J=7.8, 1H), 7.74-7.78 (m, 2H), 12.74 (s, 1H).

Step Bethyl (1-hydroxy-5-chloro-2,3-dihydro-1H-inden-2-yl)carbamate

Using the compound (4.45 g, 24.8 mmol) obtained in step A and according to the methods of Reference Example 25, steps B and C, the title compound (2.78 g, yield 39%) was obtained as a bistered oil.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.17 (t, J=7.2, 3H), 2.84-3.02 (m, 2H), 3.95-4.15 (m, 3H), 4.82 (t, J=5.1, 1H), 5.30 (d, J=5.4, 1H), 6.78 (d, J=7.5, 1H), 7.21-7.36 (m, 3H).

Step Cethyl (5-chloro-2,3-dihydro-1H-inden-2-yl)carbamate

Using the compound (2.78 g, 10.87 mmol) obtained in step B and according to the method of Reference Example 25, step D, the title compound (2.31 g, yield 89%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.20-1.28 (m, 3H), 2.70-2.85 (m, 2H), 3.15-3.32 (m, 2H), 4.02-4.21 (m, 2H), 4.43-4.52 (m, 1H), 4.85 (brs, 1H), 7.11-7.22 (m, 3H).

Step D5-chloro-N-methylindan-2-amine hydrochloride

Using the compound (2.31 g, 9.64 mmol) obtained in step C and according to the method of Reference Example 23, step B, the title compound (1.79 g, yield 85%) was obtained as a pale-green solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.56 (t, J=5.3, 3H), 3.05-3.34 (m, 4H), 3.89-4.00 (m, 1H), 7.20-7.37 (m, 3H), 9.43 (brs, 2H).

Reference Example 295-methoxy-N-methylindan-2-amine hydrochlorideStep A5-methoxy-1H-inden-1,2(3H)-dione 2-oxime

Using 5-methoxyindan-1-one (5.00 g, 30.8 mmol) and according to the method of Reference Example 25, step A, the title compound (5.35 g, yield 91%) was obtained as a bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 3.73 (s, 2H), 3.89 (s, 3H), 7.02 (dd, J=2.1, 8.7, 1H), 7.15 (d, J=1.8, 1H), 7.69 (d, J=8.7, 1H), 12.45 (s, 1H).

Step B5-methoxy-1H-inden-1,2(3H)-dione 2-{O-[tert-butyl(dimethyl)silyl]oxime}

Using the compound (3.40 g, 17.8 mmol) obtained in step A and according to the method of Reference Example 25, step B, the title compound (4.91 g, yield 90%) was obtained as a pale-bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 0.01 (s, 6H), 0.72 (s, 9H), 3.56 (s, 2H), 3.66 (s, 3H), 6.80 (dd, J=2.1, 8.4, 1H), 6.93 (d, J=1.8, 1H), 7.49 (d, J=8.7, 1H).

Step Cethyl (1-hydroxy-5-methoxy-2,3-dihydro-1H-inden-2-yl)carbamate

Using the compound (4.91 g, 16.1 mmol) obtained in step B and according to the method of Reference Example 25, step C, the title compound (3.05 g, yield 81%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.17 (t, J=7.2, 3H), 2.79-3.00 (m, 2H), 3.72 (s, 3H), 3.95-4.10 (m, 3H), 4.75 (t, J=5.4, 1H), 5.07 (d, J=5.4, 1H), 6.72-6.80 (m, 3H), 7.23 (d, J=8.4, 1H).

Step Dethyl (5-methoxy-2,3-dihydro-1H-inden-2-yl)carbamate

Using the compound (3.05 g, 13.0 mmol) obtained in step C and according to the method of Reference Example 25, step D, the title compound (2.35 g, yield 77%) was obtained as a pale-bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=6.9, 3H), 2.71 (dt, J=6.9, 16.2, 2H), 3.06 (dt, J=7.5, 13.8, 2H), 3.70 (s, 3H), 3.99 (q, J=7.2, 2H), 4.23 (q, J=7.2, 1H), 6.69 (dd, J=2.4, 8.4, 1H), 6.77 (s, 1H), 7.07 (d, J=8.4, 1H), 7.39 (d, J=6.3, 1H).

Step E5-methoxy-N-methylindan-2-amine hydrochloride

Using the compound (2.35 g, 9.99 mmol) obtained in step D and according to the method of Reference Example 23, step B, the title compound (1.98 g, yield 93%) was obtained as a pale-bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.56 (t, J=5.4, 3H), 3.03-3.29 (m, 4H), 3.72 (s, 3H), 3.88-3.95 (m, 1H), 6.76 (dd, J=2.1, 8.1, 1H), 6.85 (d, J=1.8, 1H), 7.15 (d, J=8.4, 1H), 9.40 (brs, 2H).

Reference Example 305,6-dimethoxy-N-methylindan-2-amine hydrochlorideStep A 5,6-dimethoxy-1H-inden-1,2(3H)-dione 2-oxime

Using 5,6-dimethoxyindan-1-one (10.0 g, 52.0 mmol) and according to the method of Reference Example 25, step A, the title compound (11.64 g, yield 100%) was obtained as a pale-bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 3.66 (s, 2H), 3.83 (s, 3H), 3.90 (s, 3H), 7.18 (s, 1H), 7.19 (s, 1H), 12.40 (s, 1H).

Step B5,6-dimethoxy-1H-inden-1,2(3H)-dione 2-{O-[tert-butyl(dimethyl)silyl]oxime}

Using the compound (11.64 g, 52.0 mmol) obtained in step A and according to the method of Reference Example 25, step B, the title compound (16.70 g, yield 96%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 0.29 (s, 6H), 0.98 (s, 9H), 3.75 (s, 2H), 3.93 (s, 3H), 3.99 (s, 3H), 6.90 (s, 1H), 7.32 (s, 1H).

Step Cethyl (5,6-dimethoxy-2,3-dihydro-1H-inden-2-yl)carbamate

Using the compound (10.0 g, 29.8 mmol) obtained in step B and according to the methods of Reference Example 25, steps C and D, the title compound (3.31 g, yield 42%) was obtained as a bistered solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.23 (t, J=6.9, 3H), 2.73 (dd, J=4.8, 15.6, 2H), 3.24 (dd, J=7.2, 15.9, 2H), 3.85 (s, 6H), 4.11 (q, J=6.9, 2H), 4.50 (brs, 1H), 4.88 (brs, 1H), 6.73 (s, 2H).

Step D5,6-dimethoxy-N-methylindan-2-amine hydrochloride

Using the compound (3.31 g, 12.48 mmol) obtained in step C and according to the method of Reference Example 23, step B, the title compound (3.03 g, yield 100%) was obtained as a pale-bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.95-3.06 (m, 2H), 3.19 (dd, J=7.8, 15.9, 2H), 3.72 (s, 6H), 3.83-3.98 (m, 1H), 6.87 (s, 2H), 9.22 (brs, 2H).

The compounds of Reference Examples 1-30 are shown below.

TABLE 1ReferenceStructuralExampleFormula1 [Image Omitted]

2

3

4

5

6

7

8

9

10

11

12

13

14

15

16

17

18

19

20

21

22

23

24

25

26

27

28

29

30

Reference Example 313,4-dichloro-N-methylaniline hydrochlorideStep Atert-butyl (3,4-dichlorophenyl)carbamate

Using 3,4-dichloroaniline (5.00 g, 30.9 mmol) and according to the method of Reference Example 23, step A, the title compound (4.62 g, yield 59%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.47 (s, 9H), 7.38 (dd, J=2.3, 8.8, 1H), 7.50 (d, J=8.9, 1H), 7.78 (d, J=2.2, 1H), 9.71 (s, 1H).

Step B3,4-dichloro-N-methylaniline hydrochloride

Using the compound (4.62 g, 17.6 mmol) obtained in step A and according to the method of Reference Example 23, step B, the title compound (3.38 g, yield 100%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.67-2.71 (m, 3H), 6.51-7.18 (m, 2H), 7.25-7.40 (m, 1H), 9.2-10.9 (broad, 2H).

Reference Example 32N-methylindane-5-amine hydrochlorideStep Atert-butyl (2,3-dihydro-1H-inden-5-yl)carbamate

Using 5-aminoindane (4.10 g, 30.9 mmol) and according to the method of Reference Example 23, step A, the title compound (6.98 g, yield 97%) was obtained as a bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.63 (s, 9H), 2.08-2.21 (m, 2H), 2.90-2.99 (m, 4H)., 7.23 (d, J=8.1, 1H), 7.32 (d, J=8.1, 1H), 7.53 (s, 1H), 9.34 (s, 1H).

Step BN-methylindan-5-amine hydrochloride

Using the compound (6.98 g, 29.9 mmol) obtained in step A and according to the method of Reference Example 23, step B, the title compound (3.91 g, yield 71%) was obtained as a bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.97-2.09 (m, 2H), 2.79-2.93 (m, 4H), 2.86 (s, 3H), 7.23-7.41 (m, 3H), 11.10 (brs, 2H).

Reference Example 33trans-N-methyl-4-phenylcyclohexanamine hydrochlorideStep Atert-butyl (trans-4-phenylcyclohexyl)carbamate

Using hydrochloride (3.42 g, 16.15 mmol) of trans-4-phenylcyclohexylamine, which is the compound described in Journal of Organic Chemistry, 1952, 17, 1017-1022 and triethylamine (4.8 ml, 34 mmol), and according to the method of Reference Example 23, step A, the title compound (4.06 g, yield 91%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.2-1.4 (m, 2H), 1.46 (s, 9H), 1.5-1.6 (m, 2H), 1.9-2.0 (m, 2H), 2.1-2.2 (m, 2H), 2.4-2.5 (m, 1H), 3.49 (brs, 1H), 4.42 (brs, 1H), 7.15-7.21 (m, 3H), 7.25-7.32 (m, 2H)

Step Btrans-N-methyl-4-phenylcyclohexanamine hydrochloride

Using the compound (3.92 g, 14.23 mmol) obtained in step A and according to the method of Reference Example 23, step B, the title compound (3.11 g, yield 97%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.4-1.6 (m, 4H), 1.8-2.0 (m, 2H), 2.0-2.2 (m, 2H), 2.4-2.6 (m, 1H), 2.54 (t, J=5.4, 3H), 2.9-3.1 (m, 1H), 7.16-7.32 (m, 5H), 8.89 (brs, 2H).

Reference Example 34N-methyl-1,2,3,4-tetrahydronaphthalen-2-amine hydrochlorideStep Atert-butyl (1,2,3,4-tetrahydronaphthalen-2-yl)carbamate

Using hydrochloride (2.50 g, 13.61 mmol) of 1,2,3,4-tetrahydro-2-naphthylamine, which is the compound described in Journal of Medicinal Chemistry, 1980, 23, 745-749 and triethylamine (2.01 ml, 15.0 mmol), and according to the method of Reference Example 23, step A, the title compound (3.06 g, yield 91%) was obtained as a pale-bistered solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.28 (s, 9H), 1.65-1.80 (m, 1H), 1.95-2.15 (m, 1H), 2.62 (dd, J=8.3, 16.3, 1H), 2.84-2.90 (m, 2H), 3.12 (dd, J=5.0, 16.3, 1H), 3.98 (brs, 1H), 4.59 (brs, 1H), 7.04-7.15 (m, 4H).

Step BN-methyl-1,2,3,4-tetrahydronaphthalen-2-amine hydrochloride

Using the compound (3.00 g, 12.13 mmol) obtained in step A and according to the method of Reference Example 23, step B, the title compound (1.66 g, yield 69%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.71-1.85 (m, 1H), 2.20-2.30 (m, 1H), 2.60 (s, 3H), 2.73-2.95 (m, 3H), 3.13-3.24 (m, 1H), 3.31-3.41 (m, 1H), 7.09-7.19 (m, 4H), 9.36 (brs, 2H).

Reference Example 35N-methylpyrrolidin-1-amine hydrochlorideStep Atert-butyl methyl(pyrrolidin-1-yl)carbamate

To N,N-diisopropylethylamine (25 ml, 144 mmol) were added the compound (5.00 g, 34.2 mmol) obtained in Reference Example 17, step A and 1,4-dibromobutane (7.40 g, 34.2 mmol), and the mixture was stirred with heating at 130Â° C. for 5 hr. The reaction mixture was cooled, diluted with ethyl acetate, and the precipitated solid was filtered off, and the obtained solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (3.43 g, yield 50%) as a colorless oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.47 (s, 9H), 1.73-1.82 (m, 4H), 2.96 (s, 3H), 2.97-3.21 (m, 4H).

Step BN-methylpyrrolidin-1-amine hydrochloride

The compound (3.43 g, 17.1 mmol) obtained in step A was dissolved in ethyl acetate (40 ml), and 4N hydrochloric acid-ethyl acetate solution (20 ml, 80.0 mmol) was added at room temperature. The mixture was stood at the same temperature overnight, and the solvent was concentrated under reduced pressure to give the title compound (3.42 g, yield>100%) as a bistered oil.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.83-1.92 (m, 4H), 2.64 (s, 3H), 3.19 (brs, 4H), 5.4-6.8 (br, 2H).

Reference Example 36N-methyl-2,5-dihydro-1H-pyrrol-1-amine hydrochlorideStep Atert-butyl 2,5-dihydro-1H-pyrrol-1-yl(methyl)carbamate

Using tert-butyl 1-methylhydrazinecarboxylate (5.00 g, 34.2 mmol) and (2Z)-1,4-dichloro-2-butene (3.6 ml, 34.2 mmol), and according to the method of Reference Example 35, step A, the title compound (5.85 g, yield 86%) was obtained as a yellow oil.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.39 (s, 9H), 2.90 (s, 3H), 3.77 (s, 4H), 5.74 (s, 2H).

Step BN-methyl-2,5-dihydro-1H-pyrrol-1-amine hydrochloride

Using the compound (5.85 g, 29.5 mmol) obtained in step A and according to the method of Reference Example 35, step B, the title compound (3.07 g, yield 77%) as a red bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.64 (s, 3H), 3.95 (s, 4H), 5.87 (s, 2H), 7.83 (brs, 2H).

Reference Example 37(3aR,7aS)-N-methyloctahydro-2H-isoindol-2-amineStep A(3aR,7aS)-nitrosooctahydro-1H-isoindole

cis-Octahydro-1H-isoindole (1.81 g, 14.5 mmol), which is the compound described in Tetrahedron, 55 (1999) 9439-9454, was dissolved in 1N hydrochloric acid (16 ml), and the mixture was stirred under ice-cooling, sodium nitrite (6.22 g, 90.1 mmol) dissolved in water (20 ml) was gradually added, and the mixture was stirred at the same temperature for 3 hr. The reaction mixture was extracted with diethyl ether, and the organic layer was washed with saturated aqueous sodium hydrogen carbonate and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure to give the title compound (1.22 g, yield 55%) as a bistered oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.3-1.7 (m, 8H), 2.3-2.4 (m, 2H), 3.4-3.6 (m, 2H), 4.1-4.3 (m, 2H).

Step B(3aR,7aS)â€”N-methyleneoctahydro-2H-isoindol-2-amine

To lithium aluminum hydride (0.89 g, 23 mmol) was added diethyl ether (50 ml), the compound (1.20 g, 7.78 mmol) of step A was added under ice-cooling with stirring, and the mixture was stirred at room temperature for 4 hr. The reaction mixture was ice-cooled, and water (0.89 ml), 15% aqueous sodium hydroxide solution (0.89 ml), water (2.67 ml) and sodium sulfate were successively added with stirring. The insoluble material was filtered off through celite, and the solution was concentrated under reduced pressure to give (3a,7a)-cis-octahydro-2H-isoindol-2-amine (1.14 g) as a crude pale-yellow oil. To the obtained oil were added water (10 ml) and acetic acid (0.49 ml), 37% formalin (0.7 ml) was added under ice-cooling with stirring, and the mixture was stirred for 10 min. To the reaction mixture was added diluted aqueous sodium hydroxide solution. The reaction mixture was extracted with diethyl ether, and the organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (956 mg, yield 81%) as a colorless oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.3-1.6 (m, 8H), 2.1-2.3 (m, 2H), 3.16 (dd, J=5.3, 9.8, 2H), 3.29 (dd, J=6.8, 9.6, 2H), 5.84 (d, J=11.6, 1H), 5.93 (d, J=11.6, 1H).

Step C(3aR,7aS)-N-methyloctahydro-2H-isoindol-2-amine

To lithium aluminum hydride (204 mg, 5.38 mmol) was added diethyl ether (50 ml) and the mixture was stirred under ice-cooling. Thereto was added the compound (505 mg, 3.39 mmol) obtained in step B and the mixture was heated under reflux for 1 hr. The reaction mixture was ice-cooled, and water (0.204 ml), 15% aqueous sodium hydroxide solution (0.204 ml), water (0.615 ml) and sodium sulfate were successively added with stirring. The insoluble material was filtered off through celite, and the solution was concentrated under reduced pressure to give the title compound (436 mg, yield 85%) as a colorless oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.2-1.7 (m, 8H), 2.0-2.3 (m, 2H), 2.60 (s, 3H), 2.70 (dd, J=5.9, 9.8, 2H), 3.00 (dd, J=7.4, 9.8, 2H).

Reference Example 38(3aR,6aS)-cis-N-methylhexahydrocyclopenta[c]pyrrol-2(1H)-amineStep A(3aR,6aS)-cis-N-methylenehexahydrocyclopenta[c]pyrrol-2(1H)-amine

To 3-amino-3-azabicyclo[3.3.0]octane hydrochloride (2.50% g, 15.4 mmol) were added water (4.5 ml) and sodium acetate (1.26 g, 15.4 mmol) and the mixture was stirred under ice-cooling. Thereto was added 37% formalin (1.37 ml) and the mixture was stirred for 5 min. To the reaction mixture was added diluted aqueous sodium hydroxide solution. The reaction mixture was extracted with dichloromethane, and the organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (2.12 g, yield>100%) as a colorless oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.4-1.9 (m, 6H), 2.6-2.7 (m, 2H), 2.87 (dd, J=3.6, 9.6, 2H), 3.23 (t, J=8.6, 2H), 6.15 (s, 2H).

Step B

(3aR,6aS)-cis-N-methylhexahydrocyclopenta[c]pyrrol-2(1H)-amine

Using the compound (2.12 g) obtained in step A and according to the method of Reference Example 37, step C, the title compound (2.53 g, yield>100%) was obtained as a colorless oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.4-1.7 (m, 6H), 2.19-2.23 (m, 2H), 2.51-2.60 (m, 2H), 2.61 (s, 3H), 3.00 (t, J=9.0, 2H).

Reference Example 39N-methylmorpholin-4-amineStep AN-methylenemorpholin-4-amine

Using N-aminomorpholine (2.50 g, 24.5 mmol) and according to the method of Reference Example 38, step A, the title compound (1.89 g, yield 68%) was obtained as a pale-yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 3.01 (t, J=4.9, 4H), 3.83 (t, J=4.9, 4H), 6.35 (d, J=10.9, 1H), 6.52 (d, J=10.9, 1H).

Step BN-methylmorpholin-4-amine

Using the compound (0.90 g, 7.9 mmol) obtained in step A and according to the method of Reference Example 37, step C, the title compound (0.89 g, yield 98%) as a red-bistered oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.59 (s, 3H), 2.61-2.73 (m, 4H), 3.74 (t, J=4.7, 4H).

Reference Example 40N-methylthiomorpholin-4-amineStep A4-nitrosothiomorpholine

Using thiomorpholine (11.53 g, 111.7 mmol) and according to the method of Reference Example 37, step A, the title compound (7.26 g, yield 49%) was obtained as a yellow solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.57-2.61 (m, 2H), 2.4-2.89 (m, 2H), 4.05-4.10 (m, 2H), 4.49-4.53 (m, 2H).

Step BN-methylenethiomorpholin-4-amine

Using the compound (3.00 g, 22.7 mmol) obtained in step A and according to the method of Reference Example 37, step B, the title compound (3.38 g, yield>100%) was obtained as a yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.74 (t, J=5.2, 4H), 3.39 (t, J=5.2, 4H), 6.34 (d, J=10.8, 1H), 6.49 (d, J=10.9, 1H).

Step CN-methylthiomorpholin-4-amine

Using the compound (3.38 g) obtained in step B and according to the method of Reference Example 37, step C, the title compound (3.50 g, yield>100%) was obtained as a pale-yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.57 (s, 3H), 2.75 (d, J=3.6, 4H), 2.92 (t, J=2.8, 4H).

Reference Example 41N-methylpiperidin-1-amineStep AN-methylenepiperidin-1-amine

Using N-nitrosopiperidine (2.50 g, 21.9 mmol) and according to the method of Reference Example 37, step B, the title compound (1.63 g, yield 66%) was obtained as a pale-yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.46-1.55 (m, 2H), 1.66-1.74 (m, 4H), 2.99 (t, J=5.6, 4H), 6.27 (d, J=11.1, 1H), 6.46 (d, J=11.1, 1H).

Step BN-methylpiperidin-1-amine

Using the compound (1.63 g, 14.5 mmol) obtained in step A and according to the method of Reference Example 37, step C, the title compound (1.65 g, yield>100%) was obtained as a yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.39-1.42 (m, 2H), 1.60-1.68 (m, 4H), 1.83-1.90 (m, 4H), 2.59 (s, 3H).

Reference Example 42N-methyl-3,4-dihydroisoquinolin-2(1H)-amineStep A2-nitroso-1,2,3,4-tetrahydroisoquinoline

Using 1,2,3,4-tetrahydroisoquinoline (5.0 g, 37.5 mmol) and according to the method of Reference Example 37, step A, the title compound (3.33 g, yield 55%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 3.11 (t, J=5.9, 2H), 4.55 (t, J=5.9, 2H), 4.84 (s, 2H), 7.15-7.30 (m, 4H).

Step B

Using N-methylene-3,4-dihydroisoquinolin-2(1H)-amine and the compound (3.00 g, 18.5 mmol) obtained in step A, and according to the method of Reference Example 37, step B, the title compound (2.86 g, yield 95%) was obtained as a pale-yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.89 (t, J=5.8, 2H), 3.48 (t, J=5.8, 2H), 4.19 (s, 2H), 6.27 (d, J=10.8, 1H), 6.47 (d, J=10.8, 1H), 7.10-7.19 (m, 4H).

Step CN-methyl-3,4-dihydroisoquinolin-2(1H)-amine

Using the compound (2.86 g, 17.9 mmol) obtained in step B and according to the method of Reference Example 37, step C, the title compound (2.65 g, yield 92%) was obtained as a yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.68 (s, 3H), 2.98 (s, 4H), 3.87 (s, 2H), 7.01-7.27 (m, 4H).

Reference Example 43N-methylazepan-1-amine hydrochlorideStep AN-methyleneazepan-1-amine

Using 1-aminohomopiperidine (2.00 g, 17.5 mmol) and according to the method of Reference Example 38, step A, the title compound (1.88 g, yield 85%) was obtained as a red-bistered oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.54-1.59 (m, 4H), 1.68-1.72 (m, 4H), 3.35 (t, J=5.5, 4H), 5.77 (d, J=11.1, 1H), 5.95 (d, J=11.1, 1H)

Step BN-methylazepan-1-amine hydrochloride

A pale-yellow oil obtained using the compound (1.20 g, 9.5 mmol) obtained in step A and according to the method of Reference Example 37, step C was dissolved in diethyl ether (15 ml), 4N hydrochloric acid-dioxane solution (1.8 ml) was added with stirring under ice-cooling, and the solution was concentrated under reduced pressure to give the title compound (0.85 g, yield 53%) as a pale-yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.66 (brs, 4H), 1.87 (brs, 4H), 2.83 (s, 3H), 3.38 (t, J=5.4, 4H), 9.36 (brs, 2H).

Reference Example 44N-methyl-4-phenylpiperazin-1-amineStep AN-nitroso-4-phenylpiperazin-1-amine

Using 1-phenylpiperazine (5.00 g, 30.8 mmol) and according to the method of Reference Example 37, step A, the title compound (1.10 g, yield 19%) was obtained as a pale-yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 3.19 (t, J=5.4, 2H), 3.42 (t, J=5.4, 2H), 3.98 (t, J=5.4, 2H), 4.42 (t, J=5.4, 2H), 6.92-6.98 (m, 3H), 7.2-7.4 (m, 2H).

Step BN-methylene-4-phenylpiperazin-1-amine

Using the compound (1.10 g, 5.8 mmol) obtained in step A and according to the method of Reference Example 37, step B, the title compound (1.35 g, yield>100%) was obtained as a yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 3.15-3.18 (m, 4H), 3.31-3.35 (m, 4H), 6.37 (d, J=10.9, 1H), 6.35 (d, J=10.9, 1H), 6.85-6.97 (m, 3H), 7.24-7.30 (m, 2H).

Step CN-methyl-4-phenylpiperazin-1-amine

Using the compound (1.35 g) obtained in step B and according to the method of Reference Example 37, step C, the title compound (1.0 g, yield 90%) was obtained as a red-bistered oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.63 (s, 3H), 2.81 (t, J=4.8, 4H), 3.25 (t, J=4.8, 4H), 6.82-6.94 (m, 3H), 7.2-7.3 (m, 2H).

Reference Example 45(2-fluorobenzyl)methylamine

To tetrahydrofuran (5 ml) was added under ice-cooling with stirring 40% aqueous methylamine solution (5 ml) and 2-fluorobenzylbromide (1.00 g, 5.29 mmol) dissolved in tetrahydrofuran (2 ml), and the mixture was stirred at the same temperature for 1 hr. The reaction mixture was diluted with ethyl acetate, and the organic layer was washed with water and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography to give the title compound (0.65 g, yield 87%) as a colorless oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.43 (s, 3H), 3.79 (s, 2H), 7.01-7.12 (m, 2H), 7.21-7.25 (m, 1H), 7.29-7.33 (m, 1H).

Reference Example 46tert-butyl 4-(methylamino)piperidine-1-carboxylate

To tert-butyl 4-oxo-1-piperidinecarboxylate (3.99 g, 20 mmol) was added ethanol (30 ml), and methylamine hydrochloride (2.70 g, 40 mmol), triethylamine (5.6 ml, 40 mmol) and titanium(IV)isopropoxide (11.8 ml, 40 mmol) were added under ice-cooling with stirring, and the mixture was stirred at room temperature for 8 hr. Then, to the reaction mixture was added sodium borohydride (1.14 g, 30 mmol), and the mixture was stirred at room temperature for 15 hr. To the reaction mixture was added 28% aqueous ammonia, and the reaction solution was filtered off through celite. The filtrate was concentrated under reduced pressure, water was added to the residue, and the mixture was extracted with dichloromethane-ethanol=5:1 mixed solvent, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (dichloromethane-methanol) to give the title compound (2.46 g, yield 57%) as a pale-yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.16-1.29 (m, 2H), 1.46 (s, 9H), 1.83-1.87 (m, 2H), 2.44 (s, 3H), 2.46-2.53 (m, 1H), 2.80 (t, J=11.7, 2H), 4.02-4.05 (m, 2H).

Reference Example 47N-methyl-4-[(2-nitrophenyl)sulfonyl]piperazin-1-amineStep A1-benzylideneamino-piperazine

According to the method described in West Germany patent application publication No. 2127171, the title compound (5.9 g) was obtained as a pale-yellow solid from piperazine (20.0 g).

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 3.05-3.09 (m, 4H), 3.14-3.19 (m, 4H), 7.2-7.4 (m, 3H), 7.57-7.62 (m, 3H).

Step B1-benzylideneamino-4-[(2-nitrophenyl)sulfonyl]piperazine

The compound (3.45 g, 18.24 mmol) obtained in step A was dissolved in dichloromethane (50 ml), triethylamine (3.8 ml, 27 mmol) and 2-nitrobenzenesulfonyl chloride (4.45 g, 20.1 mmol) were added, and the mixture was stirred at room temperature for 8 hr and directly stood overnight. The reaction mixture was diluted with diluted aqueous sodium hydroxide solution (200 ml), and extracted with diethyl ether (200 ml). The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure to give the title compound (6.61 g, yield 97%) as a yellow green amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 3.28 (t, J=5.5, 4H), 3.52 (t, J=5.3, 4H), 7.28-7.35 (m, 3H), 7.57-7.75 (m, 6H), 8.00-8.05 (m, 1H).

Step C4-[(2-nitrophenyl)sulfonyl]piperazin-1-amine

To the compound (6.61 g, 17.67 mmol) obtained in step B was added 1N hydrochloric acid, and generated benzaldehyde was evaporated by azeotropic distillation in a flask mounted with Dean-Stark water removing apparatus (Dean-Stark trap) for 6 hr. The reaction mixture was cooled, washed with diethyl ether, and the aqueous layer was alkalified with potassium carbonate. The layer was extracted twice with ethyl acetate (150 ml), and the organic layer was combined. The mixture was washed with saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solvent was concentrated under reduced pressure to give the title compound (4.85 g, yield 96%) as a yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.70 (t, J=4.8, 4H), 3.19 (brs, 2H), 3.38 (t, J=4.5, 4H), 7.61-7.75 (m, 3H), 7.96-8.00 (m, 1H).

Step DN-methylene-4-[(2-nitrophenyl)sulfonyl]piperazin-1-amine

Using the compound (4.85 g, 16.94 mmol) obtained in step C and according to the method of Reference Example 38, step A, the title compound (4.93 g, yield 98%) was obtained as a pale-yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 3.13 (t, J=5.1, 4H), 3.48 (t, J=4.8, 4H), 6.39 (d, J=10.8, 1H), 6.52 (d, J=10.5, 1H), 7.62-7.75 (m, 3H), 7.99-8.02 (m, 1H).

Step EN-methyl-4-[(2-nitrophenyl)sulfonyl]piperazin-1-amine

To a methanol (50 ml)-tetrahydrofuran (30 ml) mixed solvent was added the compound (4.93 g, 16.53 mmol) obtained in step D, sodium cyanoborohydride (1.35 g, 21.49 mmol) was added under ice-cooling with stirring, and acetic acid (1 ml) and methanol (10 ml) solution were added dropwise by a small amount. After the completion of the dropwise addition, the mixture was further stirred at the same temperature for 30 min. The reaction mixture was poured into diluted aqueous sodium hydroxide solution, and the mixture was extracted with chloroform. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (chloroform-methanol) to give the title compound (2.77 g, yield 56%) as a pale-yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.56 (s, 3H), 2.74 (t, J=4.9, 4H), 3.38 (t, J=4.9, 4H), 7.60-7.75 (m, 3H), 7.95-7.98 (m, 1H).

Reference Example 48N-methyl-4-(methylsulfonyl)piperazin-1-amineStep A1-benzyl-4-(methylsulfonyl)piperazine

To dichloromethane (50 ml) was added 1-benzylpiperazine (10.0 g, 56.73 mmol), methanesulfonyl chloride (4.4 ml, 56.85 mmol) was added under ice-cooling with stirring, and the mixture was stirred at the same temperature for 1 hr. The reaction mixture was diluted with 10% aqueous sodium carbonate solution, and extracted with dichloromethane. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure to give the title compound (9.58 g, yield 66%) as a pale-yellow solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.55 (t, J=5.0, 4H), 2.77 (s, 3H), 3.24 (t, J=5.0, 4H), 3.55 (s, 2H), 7.24-7.36 (m, 5H).

Step B1-(methylsulfonyl)piperazine hydrochloride

To dichloromethane (70 ml) was added the compound (9.58 g, 37.66 mmol) obtained in step A and 1-chloroethyl chloroformate (4.53 ml, 41.43 mmol) was added under ice-cooling with stirring, and the mixture was stirred at room temperature for 1 hr. The reaction mixture was concentrated under reduced pressure, the residue was dissolved in methanol (70 ml), and the mixture was heated under reflux for 30 min. The reaction mixture was cooled to room temperature, and the precipitated solid was filtered and washed with a small amount of methanol. The filtrate was concentrated under reduced pressure, and the precipitated solid was filtered, and washed with a small amount of methanol. The obtained solid was combined, and the mixture was washed with diethyl ether to give the title compound (6.65 g, yield 88%) as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.99 (s, 3H), 3.16 (t, J=5.4, 4H), 3.38 (t, J=5.7, 4H), 9.59 (brs, 1H), 9.90 (brs, 1H).

Step C1-(methylsulfonyl)-4-nitrosopiperazine

Using the compound (6.65 g, 33.14 mmol) obtained in step B and according to the method of Reference Example 37, step A, the title compound (3.75 g, yield 59%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.85 (s, 3H), 3.25 (t, J=5.4, 2H), 3.51 (t, J=5.1, 2H), 3.96 (t, J=5.4, 2H), 4.39-4.56 (m, 2H).

Step DN-methylene-4-(methylsulfonyl)piperazin-1-amine

Using the compound (3.75 g, 19.41 mmol) obtained in step C and according to the method of Reference Example 37, step B, the title compound (2.12 g, yield 57%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.82 (s, 3H), 3.16 (t, J=4.9, 4H), 3.39 (t, J=4.9, 4H), 6.41 (d, J=10.5, 1H), 6.53 (d, J=10.6, 1H).

Step EN-methyl-4-(methylsulfonyl)piperazin-1-amine

Using the compound (2.12 g, 11.08 mmol) obtained in step D and according to the method of Reference Example 37, step C, the title compound (1.73 g, yield 81%) was obtained as a yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.39 (s, 3H), 2.78 (t, J=4.2, 4H), 2.80 (s, 3H), 3.33 (t, J=4.8, 4H).

Reference Example 49methyl[2-(2-thienyl)ethyl]amine hydrochlorideStep Atert-butyl [2-(2-thienyl)ethyl]carbamate

Using [2-(2-thienyl)ethyl]amine (2.00 g, 15.72 mmol) and according to the method of Reference Example 23, step A, the title compound (3.86 g) was obtained as a yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.44 (s, 9H), 3.12 (t, J=6.6, 2H), 3.39 (q, J=6.6, 2H), 4.65 (brs, 1H), 6.83 (dt, J=1.2, 3.6, 1H), 6.94 (dd, J=3.6, 5.1, 1H), 7.15 (dd, J=1.2, 5.1, 1H).

Step Bmethyl[2-(2-thienyl)ethyl]amine hydrochloride

Using the compound (3.86 g) obtained in step A and according to the method of Reference Example 23, step B, the title compound (2.44 g, total yield from step A 87%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.55 (s, 3H), 3.09-3.24 (m, 4H), 6.97-7.01 (m, 2H), 7.42 (d, J=4.1, 1H), 9.23 (brs, 2H).

Reference Example 50[2-(2-furyl)ethyl]methylamineStep A[2-(2-furyl)ethyl]amine

Tetrahydrofuran (50 ml) was added to lithium aluminum hydride (2.05 g, 53.91 mmol), and the mixture was stirred under ice-cooling. Thereto was added a solution of 2-(2-nitrovinyl)furan (2.50 g, 17.97 mmol) in tetrahydrofuran (30 ml) and the mixture was heated under reflux for 1 hr. The reaction mixture was ice-cooled, water-containing diethyl ether (80 ml), tetrahydrofuran (80 ml) and saturated aqueous sodium sulfate solution (14 ml) were successively added with stirring. The insoluble material was filtered off through celite, and the solution was concentrated under reduced pressure to give the title compound (1.87 g, yield 94%) as a red-bistered oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.77 (t, J=6.5, 2H), 2.98 (t, J=6.5, 2H), 6.06 (d, J=3.1, 1H), 6.29 (dd, J=2.5, 4.8, 1H), 7.33 (d, J=1.7, 1H).

Step Btert-butyl [2-(2-furyl)ethyl]carbamate

Using the compound (1.87 g, 16.83 mmol) obtained in step A and according to the method of Reference Example 23, step A, the title compound (3.94 g) was obtained as a red-bistered oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.44 (s, 9H), 2.82 (t, J=6.6, 2H), 3.41 (q, J=6.6, 2H), 4.67 (brs, 1H), 6.07 (d, J=3.3, 1H), 6.30 (dd, J=2.4, 5.1, 1H), 7.33 (d, J=1.2, 1H).

Step C[2-(2-furyl)ethyl]methylamine

To lithium aluminum hydride (1.79 g, 47.16 mmol) was added tetrahydrofuran (40 ml) and the mixture was stirred under ice-cooling. Thereto was added a solution of the compound (3.94 g) obtained in step B in tetrahydrofuran (20% ml) and the mixture was heated under reflux for 3 hr. The reaction mixture was ice-cooled, water-containing diethyl ether (60 ml), tetrahydrofuran (60 ml) and saturated aqueous sodium sulfate solution (12 ml) were successively added with stirring. The insoluble material was filtered off through celite, and the solution was concentrated under reduced pressure to give the title compound (1.76 g, total yield from step B 84%) as a red-bistered oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.44 (s, 3H), 2.82-2.83 (m, 4H), 6.04 (d, J=2.4, 1H), 6.29 (dd, J=2.1, 3.0, 1H), 7.31 (t, J=1.5, 1H).

Reference Example 51[2-(2-methoxyphenyl)ethyl]methylamine hydrochlorideStep Atert-butyl [2-(2-methoxyphenyl)ethyl]carbamate

Using [2-(2-methoxyphenyl)ethyl]amine (2.00 g, 13.23 mmol) and according to the method of Reference Example 23, step A, the title compound (4.44 g) was obtained as a pale-yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.42 (s, 9H), 2.81 (t, J=6.8, 2H), 3.31-3.40 (m, 2H), 3.82 (s, 3H), 6.87 (t, J=8.4, 1H), 6.90 (t, J=7.6, 1H), 7.13 (d, J=7.4, 1H), 7.22 (dt, J=1.6, 8.0, 1H).

Step B[2-(2-methoxyphenyl)ethyl]methylamine hydrochloride

Using the compound (4.44 g) obtained in step A and according to the method of Reference Example 23, step B, the title compound (2.47 g, total yield from step A 93%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.52-2.56 (m, 3H), 2.89-3.08 (m, 4H), 3.80 (s, 3H), 6.91 (t, J=7.6, 1H), 7.00 (d, J=8.1, 1H), 7.18 (dd, J=1.4, 7.5, 1H), 7.26 (dt, J=1.5, 8.1, 1H), 9.15 (brs, 2H).

Reference Example 52[2-(3-methoxyphenyl)ethyl]methylamine hydrochlorideStep Atert-butyl [2-(3-methoxyphenyl)ethyl]carbamate

Using [2-(3-methoxyphenyl)ethyl]amine (2.00 g, 13.23 mmol) and according to the method of Reference Example 23, step A, the title compound (4.53 g) was obtained as a pale-yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.46 (s, 9H), 2.77 (t, J=7.0, 2H), 3.38 (q, J=6.5, 2H), 3.80 (s, 3H), 4.55 (brs, 1H), 6.73-6.80 (m, 3H), 7.22 (t, J=7.7, 1H).

Step B[2-(3-methoxyphenyl)ethyl]methylamine hydrochloride

Using the compound (4.53 g) obtained in step A and according to the method of Reference Example 23, step B, the title compound (2.15 g, total yield from step A 81%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.50-2.54 (m, 3H), 2.93 (t, J=6.8, 2H), 3.02-3.18 (m, 2H), 3.75 (s, 3H), 6.80-6.85 (m, 3H), 7.25 (t, J=8.0, 1H), 9.15 (brs, 2H).

Reference Example 53[2-(4-methoxyphenyl)ethyl]methylamine hydrochlorideStep Atert-butyl [2-(4-methoxyphenyl)ethyl]carbamate

Using [2-(4-methoxyphenyl)ethyl]amine (2.00 g, 13.23 mmol) and according to the method of Reference Example 23, step A, the title compound (3.98 g) was obtained as a pale-yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.43 (s, 9H), 2.73 (t, J=7.0, 2H), 3.34 (q, J=6.5, 2H), 3.79 (s, 3H), 4.54 (brs, 1H), 6.85 (d, J=8.6, 2H), 7.11 (d, J=8.6, 2H).

Step B[2-(4-methoxyphenyl)ethyl]methylamine hydrochloride

Using the compound (3.98 g) obtained in step A and according to the method of Reference Example 23, step B, the title compound (2.15 g, total yield from step A 81%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.50-2.55 (m, 3H), 2.88 (t, J=6.7, 2H), 2.95-3.15 (m, 2H), 3.73 (s, 3H), 6.89 (d, J=8.5, 2H), 7.18 (d, J=8.7, 2H), 9.12 (brs, 2H).

Reference Example 54[2-(2-methylphenyl)ethyl]methylamine hydrochlorideStep A1-methyl-2-(2-nitrovinyl)benzene

Ortho-tolualdehyde (10.00 g, 83.23 mmol) was dissolved in acetic acid (50 ml), ammonium acetate (6.93 g, 89.89 mmol) and nitromethane (7 ml, 129 mmol) were added, and the mixture was stirred at 110Â° C. for 8 hr and stood at room temperature overnight. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure to give the title compound (12.71 g, yield 94%) as a bistered oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.49 (s, 3H), 7.23-7.29 (m, 2H), 7.36-7.42 (m, 1H), 7.48-7.53 (m, 2H), 8.30 (d, J=13.5, 1H).

Step B[2-(2-methylphenyl)ethyl]amine hydrochloride

Using the compound (12.71 g, 77.89 mmol) obtained in step A and according to the method of Reference Example 50, step A, [2-(2-methylphenyl)ethyl]amine was obtained as a crude product. This was dissolved in ethyl acetate (200 ml), 4N hydrochloric acid-dioxane solution (20 ml) was added, and the precipitated solid was filtered, washed with diisopropyl ether, and dried under reduced pressure to give the title compound (4.30 g, yield 32%) as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.30 (s, 3H), 2.92 (brs, 4H), 7.12-7.20 (m, 4H), 8.23 (brs, 3H).

Step Ctert-butyl [2-(2-methylphenyl)ethyl]carbamate

Using the compound (2.50 g, 14.56 mmol) obtained in step B and triethylamine (3 ml) (21.8 mmol), and according to the method of Reference Example 23, step A, the title compound (3.73 g) was obtained as a pale-yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.44 (s, 9H), 2.33 (s, 3H), 2.81 (t, J=7.1, 2H), 3.34 (q, J=6.7, 2H), 4.58 (brs, 1H), 7.05-7.15 (m, 4H).

Step D[2-(2-methylphenyl)ethyl]methylamine hydrochloride

Using the compound (3.73 g) obtained in step C and according to the method of Reference Example 23, step B, the title compound (2.35 g, total yield from step C 87%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.31 (s, 3H), 2.56 (s, 3H), 2.93-3.04 (m, 4H), 7.13-7.20 (m, 4H), 9.24 (brs, 2H).

Reference Example 55[2-(3-methylphenyl)ethyl]methylamine hydrochlorideStep A1-methyl-3-(2-nitrovinyl)benzene

Using meta-tolualdehyde (10.00 g, 83.23 mmol) and according to the method of Reference Example 54, step A, the title compound (12.75 g, yield 94%) was obtained as a bistered oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.40 (s, 3H), 7.30-7.36 (m, 4H), 7.58 (d, J=13.8, 1H), 7.98 (d, J=13.8, 1H).

Step B[2-(3-methylphenyl)ethyl]amine hydrochloride

Using the compound (12.75 g, 78.14 mmol) obtained in step A and according to the method of Reference Example 50, step A, [2-(3-methylphenyl)ethyl]amine was obtained as a crude product. This was dissolved in ethyl acetate (100 ml), 4N hydrochloric acid-dioxane solution (21 ml) was added, and the precipitated solid was filtered, washed with diethyl ether, and dried under reduced pressure to give the title compound (3.27 g, yield 24%) as a pale-yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.29 (s, 3H), 2.84-3.05 (m, 4H), 7.03-7.07 (m, 3H), 7.21 (t, J=7.9, 1H), 8.20 (brs, 3H).

Step Ctert-butyl [2-(3-methylphenyl)ethyl]carbamate

Using the compound (2.50 g, 14.56 mmol) obtained in step B and triethylamine (3 ml) (21.9 mmol), and according to the method of Reference Example 23, step A, the title compound (3.78 g) was obtained as a yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.44 (s, 9H), 2.33 (s, 3H), 2.76 (t, J=7.0, 2H), 3.37 (q, J=6.7, 2H), 4.54 (brs, 1H), 6.98-7.05 (m, 3H), 7.20 (t, J=7.4, 1H).

Step D[2-(3-methylphenyl)ethyl]methylamine hydrochloride

Using the compound (3.78 g) obtained in step C and according to the method of Reference Example 23, step B, the title compound (2.24 g, total yield from step C 83%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.29 (s, 3H), 2.54 (s, 3H), 2.89-2.95 (m, 2H), 3.05-3.11 (m, 2H), 7.03-7.08 (m, 3H), 7.22 (t, J=7.6, 1H), 9.15 (brs, 2H).

Reference Example 56[2-(4-methylphenyl)ethyl]methylamine hydrochlorideStep Atert-butyl [2-(4-methylphenyl)ethyl]carbamate

Using [2-(4-methylphenyl)ethyl]amine (3.63 g, 26.85 mmol) and according to the method of Reference Example 23, step A, the title compound (7.13 g) was obtained as a yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.43 (s, 9H), 2.33 (s, 3H), 2.75 (t, J=6.9, 2H), 3.35 (q, J=6.6, 2H), 4.53 (brs, 1H), 7.06-7.13 (m, 4H).

Step B[2-(4-methylphenyl)ethyl]methylamine hydrochloride

Using the compound (7.13 g) obtained in step A and according to the method of Reference Example 23, step B, the title compound (3.85 g, total yield from step A 77%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.28 (s, 3H), 2.53 (s, 3H), 2.87-2.94 (m, 2H), 3.03-3.09 (m, 2H), 7.14 (s, 4H), 9.13 (brs, 2H).

Reference Example 57trans-N-methyl-2-phenylcyclopropaneamineStep AN-(trans-2-phenylcyclopropyl)formamide

trans-2-Phenylcyclopropylamine hydrochloride (2.74 g, 16.15 mmol) was dissolved in water (50 ml), and the solution was alkalified with potassium carbonate. The mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. To the residue was added formic acid (18.5 ml), and the mixture was ice-cooled, and acetic anhydride (7 ml) was added dropwise with stirring. The reaction mixture was stood at room temperature overnight, ice-cooled again. Water (7 ml) was added, and the mixture was concentrated under reduced pressure. The residue was diluted with ethyl acetate, washed with 5% aqueous potassium carbonate solution and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure to give the title compound (2.36 g, yield 91%) as a pale-bistered solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.17-1.35 (m, 2H), 2.04-2.21 (m, 1H), 2.80-2.95 (m, 1H), 5.87 (brs, 0.6H), 6.52 (brs, 0.4H), 7.05-7.35 (m, 5H), 8.19 (s, 0.6H), 8.30 (d, J=11.7, 0.4H).

Step Btrans-N-methyl-2-phenylcyclopropanamine

To a suspension of sodium borohydride (0.66 g, 17.57 mmol) in tetrahydrofuran (55 ml) was added dropwise at room temperature a solution of the compound (2.36 g, 14.64 mmol) obtained in step A in tetrahydrofuran (32 ml). Then, a solution of iodine (1.86 g, 7.33 mmol) in tetrahydrofuran (63 ml) was added dropwise, and the mixture was heated under reflux overnight. The reaction mixture was ice-cooled, methanol (125 ml) was added, and the mixture was concentrated under reduced pressure. To the residue was added 10% aqueous potassium carbonate solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (chloroform-methanol) to give the title compound (1.23 g, yield 57%) as a pale-yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 0.94-1.00 (m, 1H), 1.05-1.10 (m, 1H), 1.87-1.95 (m, 1H), 2.29-2.35 (m, 1H), 2.51 (s, 3H), 7.04-7.35 (m, 5H).

Reference Example 58methyl(3-phenylpropyl)amineStep Atert-butyl (trans-2-phenylcyclopropyl)carbamate

Using trans-2-phenylcyclopropylamine hydrochloride (1.12 g, 6.60 mmol) and triethylamine (1.0 ml, 7.17 mmol), and according to the method of Reference Example 23, step A, the title compound (944 mg, yield 61%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.10-1.19 (m, 2H), 1.45 (s, 9H), 2.00-2.07 (m, 1H), 2.73 (brs, 1H), 4.85 (brs, 1H), 7.11-7.29 (m, 5H).

Step Bmethyl(3-phenylpropyl)amine

Using the compound (930 mg, 3.99 mmol) obtained in step A and according to the method of Reference Example 50, step C, the title compound (605 mg, yield>100%) was obtained as a pale-yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.68-1.89 (m, 2H), 2.43 (s, 3H), 2.61 (t, J=7.5, 2H), 2.66 (t, J=7.5, 2H), 7.51-7.35 (m, 5H).

Reference Example 59N-methyl-4,6-dihydro-5H-thieno[2,3-c]pyrrol-5-amine hydrochlorideStep Atert-butyl 4,6-dihydro-5H-thieno[2,3-c]pyrrol-5-yl(methyl)carbamate

2,3-bis(Bromomethyl)thiophene (3.59 g, 13.3 mmol) synthesized according to the method described in Journal of organic Chemistry, 1966, 31, 592-3595 and the compound (1.94 g, 13.3 mmol) of Reference Example 17, step A, were dissolved in N-methylpyrrolidone (100 ml), and triethylamine (5.0 ml, 35.9 mmol) was slowly added with stirring while keeping the reaction mixture at 80-85Â° C. The mixture was stirred by heating at the same temperature for 10 hr, and the mixture was stood overnight at room temperature. The reaction mixture was diluted with water and extracted with ethyl acetate-hexane=1:1 mixed solvent, and the organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel chromatography (ethyl acetate-hexane) to give the title compound (1.31 g, yield 39%) as an orange oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.40 (brs, 9H), 3.10 (s, 3H), 4.30 (brs, 2H), 4.42 (brs, 2H), 6.80 (d, J=4.8, 1H), 7.20 (d, J=4.8, 1H).

Step BN-methyl-4,6-dihydro-5H-thieno[2,3-c]pyrrol-5-amine hydrochloride

Using the compound (1.31 g, 5.15 mmol) obtained in step A and according to the method of Reference Example 18, step B, the title compound (764 mg, yield 78%) was obtained as a pale-purple solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.75 (s, 3H), 4.32 (brs, 2H), 4.46 (brs, 2H), 6.97 (d, J=4.8, 1H), 7.55 (d, J=4.8, 1H), 11.05 (brs, 2H).

Reference Example 60N,5-dimethyl-1,3-dihydro-2H-isoindol-2-amine hydrochlorideStep A(4-methyl-1,2-phenylene)dimethanol

To tetrahydrofuran (200 ml) was added lithium aluminum hydride (4.91 g, 129 mmol), and the mixture was stirred under ice-cooling. Then, a solution (100 ml) of 4-methylphthalic anhydride (10.4 g, 64.1 mmol) in tetrahydrofuran was added and the mixture was heated under reflux for 90 min. The reaction mixture was ice-cooled, and water (4.91 ml), 15% aqueous sodium hydroxide solution (4.91 ml), water (14.7 ml) and anhydrous magnesium sulfate were successively added with stirring. The insoluble material was filtered off through celite, and the solution was concentrated under reduced pressure to give the title compound (9.34 g, yield 96%) as a colorless oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.35 (s, 3H), 2.8-2.9 (m, 1H), 2.9-3.0 (m, 1H), 4.69 (s, 2H), 4.71 (2H, s), 7.12 (d, J=7.6, 1H), 7.17 (s, 1H), 7.23 (d, J=7.6, 1H).

Step B1,2-bis(bromomethyl)-4-methylbenzene

To the compound (9.34 g, 61.4 mmol) obtained in step A was added 47% hydrobromic acid (60 ml), and the mixture was stirred with heating at 100Â° C. for 90 min. The reaction mixture was cooled, diluted with water, and extracted with ethyl acetate-hexane=1:1 mixed solvent. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure to give the title compound (16.7 g, yield 98%) as an orange solid.

¹H-NMR (300 MHz, CDCl₃); Î´(Ppm) 2.33 (s, 3H), 4.63 (s, 2H), 4.64 (2H, s), 7.10 (d, J=7.7, 1H), 7.17 (s, 1H), 7.25 (d, J=7.7, 1H).

Step Ctert-butyl methyl(5-methyl-1,3-dihydro-2H-isoindol-2-yl)carbamate

Using the compound (16.6 g, 59.7 mmol) obtained in step B and according to the method of Reference Example 17, step B, the title compound (13.8 g) was obtained as a crude red oil.

This was directly used for the next step.

Step DN,5-dimethyl-1,3-dihydro-2H-isoindol-2-amine hydrochloride

The compound (13.8 g) obtained in step C was dissolved in ethanol (65 ml), 4N hydrochloric acid-dioxane solution (65 ml) was added at room temperature, and the mixture was stirred at the same temperature for one day. To the reaction mixture was added activated carbon, the insoluble material was filtered off through celite, and the solution was concentrated under reduced pressure. The obtained solid was washed with an acetone-diethyl ether mixed solvent, dried under reduced pressure to give the title compound (5.68 g, yield from step C 48%) as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.31 (s, 3H), 2.77 (brs, 3H), 4.36 (brs, 4H), 7.11 (d, J=7.5, 1H), 7.15 (s, 1H), 7.22 (d, J=7.5, 1H), 10.82 (brs, 2H).

The compounds of Reference Examples 31-60 are shown below.

TABLE 2ReferenceExampleStructural Formula31 [Image Omitted]

32

33

34

35

36

37

38

39

40

41

42

43

44

45

46

47

48

49

50

51

52

53

54

55

56

57

58

59

60

Reference Example 61N-(5-cyano-2-methylphenyl)iminodiacetic acidStep A4-methyl-3-nitrobenzoic acid tert-butyl ester

4-methyl-3-nitrobenzoic acid (40.0 g, 221 mmol), 4-dimethylaminopyridine (54.5 g, 446 mmol) and WSC (84.4 g, 440 mmol) were dissolved in dichloromethane (450 ml). tert-Butanol (34.4 g, 464 mmol) was added with stirring at room temperature, and the mixture was stirred at the same temperature overnight. The reaction mixture was concentrated under reduced pressure, and diluted with ethyl acetate-hexane=1:1 mixed solvent (500 ml). The organic layer was washed with water, 10% aqueous citric acid solution, saturated aqueous sodium hydrogen carbonate and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure to give the title compound (48.7 g, yield 93%) as a pale-yellow solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.61 (s, 9H), 2.65 (s, 3H), 7.40 (d, J=8.0, 1H), 8.09 (dd, J=1.4, 8.0, 1H), 8.52 (dd, J=1.4, 1H).

Step B4-methyl-3-aminobenzoic acid tert-butyl ester

The compound (29.3 g, 123 mmol) of step A was dissolved in methanol (500 ml), ferric chloride (FeCl₃) (1.73 g, 10.7 mmol) and activated carbon (4.5 g) were added and the mixture was stirred at room temperature. Then, hydrazine monohydrate (20 ml, 412 mmol) was added, and the mixture was heated under reflux for 45 min. The reaction mixture was cooled, filtered through celite, and the solution was concentrated under reduced pressure. The obtained oil was diluted with an ethyl acetate-hexane=1:1 mixed solvent (300 ml), washed with saturated aqueous sodium hydrogen carbonate and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure to give the title compound (26.2 g) as a pale-yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.57 (s, 9H), 2.20 (s, 3H), 3.67 (brs, 2H), 7.07 (d, J=7.6, 1H), 7.29 (d, J=1.5, 1H), 7.33 (dd, J=1.5, 7.6, 1H).

Step CN-(5-tert-butoxycarbonyl-2-methylphenyl)iminodiacetic acid diethyl ester

The compound (26.2 g) obtained in step B, ethyl bromoacetate (80 ml, 719 mmol) and N,N-diisopropylethylamine (130 ml, 764 mmol) were mixed, and the mixture was stirred by heating at 140Â° C. for 200 min. The reaction mixture was cooled, diluted with an ethyl acetate-hexane=1:1 mixed solvent, and the organic layer was washed with 10% aqueous citric acid solution, saturated aqueous sodium hydrogen carbonate and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (46.3 g, yield from step B 99%) as a pale-yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.25 (t, J=7.2, 6H), 1.58 (s, 9H), 2.38 (s, 3H), 4.03 (s, 4H), 4.15 (q, J=7.2, 4H), 7.19 (d, J=7.8, 1H), 7.60 (dd, J=1.7, 7.8, 1H), 7.78 (d, J=1.7, 1H).

Step DN-(5-carboxy-2-methylphenyl)iminodiacetic acid diethyl ester

The compound (38.8 g, 102 mmol) obtained in step C was dissolved in dichloromethane (100 ml), trifluoroacetic acid (100 ml) was added under ice-cooling, and the mixture was stood for one day at room temperature. The reaction mixture was concentrated under reduced pressure, water was added to the obtained oil to allow precipitation of a solid. This was filtered, washed with water, and dried under reduced pressure to give the title compound (29.3 g, yield 89%) as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.14 (t, J=7.2, 6H), 2.32 (s, 3H), 4.03 (s, 4H), 4.05 (q, J=7.2, 4H), 7.26 (d, J=8.1, 1H), 7.52 (dd, J=1.2, 8.1, 1H), 7.70 (d, J=1.2, 1H), 12.75 (brs, 1H).

Step EN-[5-(aminocarbonyl)-2-methylphenyl]iminodiacetic acid diethyl ester

The compound (8.03 g, 24.8 mmol) obtained in step D was added to dichloromethane (160 ml), oxalyl chloride (3.0 ml, 35 mmol) and a catalytic amount of N,N-dimethylformamide were added under ice-cooling with stirring, and the mixture was stirred at room temperature for 2 hr. The reaction mixture was concentrated under reduced pressure, dissolved in tetrahydrofuran (100 ml), 28% aqueous ammonia (20 ml) was added under ice-cooling with stirring, and the mixture was stirred at the same temperature for 1 hr. The reaction mixture was diluted with ethyl acetate, washed with water and saturated brine, and the organic layer was dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure to give the title compound (8.77 g) as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.24 (t, J=7.2, 6H), 2.39 (s, 3H), 4.04 (s, 4H), 4.14 (q, J=7.2, 4H), 5.4-6.2 (broad, 2H), 7.23 (d, J=7.8, 1H), 7.41 (dd, J=1.8, 7.8, 1H), 7.69 (d, J=1.8, 1H).

Step FN-(5-cyano-2-methylphenyl)iminodiacetic acid diethyl ester

The compound (8.77 g) obtained in step E was dissolved in dichloromethane (150 ml), and the mixture was stirred under ice-cooling. Then, trichloroacetyl chloride (3.2 ml, 29 mmol) and triethylamine (8.0 ml, 57 mmol) were successively added, and the mixture was stirred at the same temperature for 40 min. To the reaction mixture was added saturated aqueous sodium hydrogen carbonate, and the organic layer was extracted and the organic layer was washed with 10% aqueous citric acid solution and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained solid was washed with hexane, and dried under reduced to pressure to give the title compound (6.03 g, yield from step E 80%) as a pale-yellow solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.25 (t, J=7.2, 6H), 2.39 (s, 3H), 4.02 (s, 4H), 4.16 (q, J=7.2, 4H), 7.25-7.27 (m, 2H), 7.46 (s, 1H).

Step GN-(5-cyano-2-methylphenyl)iminodiacetic acid

The compound (6.02 g, 19.8 mmol) obtained in step F was dissolved in a methanol-tetrahydrofuran=1:1 mixed solvent (100 ml). 1N sodium hydroxide (100 ml) was added with stirring at room temperature, and the mixture was stirred at the same temperature for 2 hr. The reaction mixture was concentrated under reduced pressure, 1N hydrochloric acid (110 ml) was added, and the aqueous layer was extracted 4 times with chloroform. The organic layer was mixed, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure, and the obtained solid was washed with diethyl ether-hexane mixed solvent, and dried under reduced pressure to give the title compound (4.26 g, yield 87%) as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.32 (s, 3H), 3.95 (s, 4H), 7.33-7.37 (m, 2H), 7.42 (s, 1H), 12.54 (brs, 2H).

Reference Example 62N-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]iminodiacetic acidStep AN-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]iminodiacetic acid diethyl ester

To an ethanol (350 ml)-water (100 ml) mixed solvent were added the compound (12.97 g, 42.62 mmol) obtained in Reference Example 61, step F, sodium acetate (17.54 g, 214 mmol) and hydroxylammonium chloride (14.85 g, 214 mmol) and the mixture was heated under reflux for 2 hr. The reaction mixture was cooled, diluted with ethyl acetate (1000 ml), washed with saturated aqueous sodium hydrogen carbonate and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure to give a yellow oil. This was dissolved in toluene (50 ml), N,N-dimethylacetamide-dimethylacetal (26 ml) was added, and the mixture was stirred with heating at 100Â° C. for 45 min. The reaction mixture was cooled, diluted with an ethyl acetate-hexane=1:1 mixed solvent, and the organic layer was washed with water and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure, and the obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane). The obtained solid was washed with a diethyl ether-hexane=1:1 mixed solvent, and dried under reduced pressure to give the title compound (10.38 g, yield 67%) as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.24 (t, J=7.2, 6H), 2.40 (s, 3H), 2.63 (s, 3H), 4.07 (s, 4H), 4.15 (q, J=7.2, 4H), 7.26 (d, J=7.8, 1H), 7.68 (dd, J=1.5, 7.8, 1H), 7.90 (d, J=1.5, 1H).

Step BN-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]iminodiacetic acid

The compound (10.32 g, 28.56 mmol) obtained in step A was dissolved in a methanol (100 ml)-tetrahydrofuran (40 ml) mixed solvent. 1N sodium hydroxide (110 ml) was added with stirring at room temperature, and the mixture was stirred at the same temperature for 3 hr. The reaction mixture was concentrated under reduced pressure, 1N hydrochloric acid (150 ml) was added, and the precipitated solid was filtered, washed with water, and dried under reduced pressure to give the title compound (8.64 g, yield 99%) as a colorless solid. ¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.32 (s, 3H), 2.65 (s, 3H), 3.98 (s, 4H), 7.30 (d, J=8.1, 1H), 7.54 (dd, J=1.4, 8.1, 1H), 7.70 (d, J=1.4, 1H), 12.50 (brs, 2H).

Reference Example 63N-(2-methylphenyl)iminodiacetic acid

Using o-toluidine (10.0 g, 93.3 mmol) and according to the methods of Reference Example 61, step C, Reference Example 62, step B, the title compound (19.12 g, yield 92%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.24 (s, 3H), 3.91 (s, 4H), 6.87-6.93 (m, 1H), 7.04-7.13 (m, 3H), 12.43 (brs, 2H).

Reference Example 64N-(3-chloro-2-methylphenyl)iminodiacetic acid

Using 3-chloro-2-methylaniline (1.88 g, 13.28 mmol) and according to the methods of Reference Example 61, step C, Reference Example 62, step B, the title compound (2.92 g, yield 85%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.30 (s, 3H), 3.92 (s, 4H), 7.10 (brs, 3H), 12.45 (brs, 2H).

Reference Example 65N-(5-chloro-2-methylphenyl)iminodiacetic acid

Using 5-chloro-2-methylaniline hydrochloride (5.03 g, 28.25 mmol) and according to the methods of Reference Example 61, step C, Reference Example 62, step B, the title compound (5.98 g, yield 82%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.21 (s, 3H), 3.92 (s, 4H), 6.95 (dd, J=2.1, 8.1, 1H), 7.04 (d, J=2.1, 1H), 7.14 (d, J=8.1, 1H), 12.51 (brs, 2H).

Reference Example 66N-(4-chloro-2-methylphenyl)iminodiacetic acid

Using 4-chloro-2-methylaniline (5.00 g, 35.3 mmol) and according to the methods of Reference Example 61, step C, Reference Example 62, step B, the title compound (3.88 g, yield 43%) was obtained as a pale-bistered solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.31 (s, 3H), 4.00 (s, 4H), 7.08-7.18 (m, 3H).

Reference Example 67N-(5-acetyl-2-methylphenyl)iminodiacetic acidStep A2-methyl-5-(2-methyl-1,3-dioxolan-2-yl)aniline

To a flask mounted with Dean-Stark water removing apparatus (Dean-Stark trap) were added toluene (200 ml), 4-methyl-3-nitroacetophenone (9.77 g, 54.53 mmol), ethylene glycol (4.6 ml) and p-toluenesulfonic acid.monohydrate (0.79 g), and the mixture was heated under reflux for 100 min. The reaction mixture was cooled, washed with diluted aqueous sodium hydroxide solution and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure to give a crude brown oil (13.0 g). Using the crude oil and according to the method of Reference Example 61, step B, the title compound (9.89 g, yield 94%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.63 (s, 3H), 2.15 (s, 3H), 3.61 (brs, 2H), 3.76-3.82 (m, 2H), 3.98-4.04 (m, 2H), 6.80 (s, 1H), 6.82 (d, J=7.4, 1H), 7.02 (d, J=7.4, 1H).

Step BN-(5-acetyl-2-methylphenyl)iminodiacetic acid diethyl ester

The compound (9.87 g, 51.08 mmol) obtained in step A, ethyl bromoacetate (23 ml, 207 mmol) and N,N-diisopropylethylamine (45 ml, 265 mmol) were mixed, and the mixture was stirred with heating at 140Â° C. for 200 min. The reaction mixture was cooled, diluted with an ethyl acetate-hexane=1:1 mixed solvent, and the organic layer was washed with 10% aqueous citric acid solution, saturated aqueous sodium hydrogen carbonate and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was dissolved in tetrahydrofuran (160 ml), 6N aqueous hydrochloric acid solution (25 ml) was added, and the mixture was stirred at room temperature for 30 min. To the reaction mixture were added water and an ethyl acetate-hexane=1:1 mixed solvent, and the organic layer was washed with saturated aqueous sodium hydrogen carbonate and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (16.30 g, yield 99%) as a yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.24 (t, J=7.2, 6H), 2.40 (s, 3H), 2.55 (s, 3H), 4.04 (s, 4H), 4.14 (q, J=7.2, 4H), 7.24 (d, J=8.1, 1H), 7.57 (dd, J=1.8, 8.1, 1H), 7.80 (d, J=2.1, 1H).

Step CN-(5-acetyl-2-methylphenyl)iminodiacetic acid

Using the compound (4.22 g, 13.13 mmol) obtained in step B and according to the method of Reference Example 61, step G, the title compound (2.63 g, yield 76%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.32 (s, 3H), 2.50 (s, 3H), 3.96 (s, 4H), 7.28 (d, J=7.8, 1H), 7.54 (d, J=7.8, 1H), 7.63 (s, 1H), 12.46 (brs, 2H).

Reference Example 68N-(4-cyano-2-methylphenyl)iminodiacetic acidStep A 4-amino-3-methylbenzonitrile

To an ethanol (500 ml)-water (60 ml)-acetic acid (30 ml) mixed solvent were added 3-methyl-4-nitrobenzonitrile (8.40 g, 51.8 mmol) and reduced iron (18 g, 322 mmol), and the mixture was stirred with heating at 85Â° C. for 3 hr. The reaction mixture was cooled, filtered through celite, and the solution was concentrated under reduced pressure. The obtained residue was diluted with ethyl acetate, washed with diluted aqueous sodium hydroxide solution and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure to give the title compound (6.37 g, yield 93%) as a pale-yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.04 (s, 3H), 5.89 (brs, 2H), 6.64 (d, J=8.1, 1H), 7.26-7.31 (m, 2H).

Step BN-(4-cyano-2-methylphenyl)iminodiacetic acid

Using the compound (4.47 g, 33.8 mmol) obtained in step A and according to the methods of Reference Example 61, steps C and G, the title compound (2.60 g, yield 31%) was obtained as a pale-pink solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.26 (s, 3H), 4.01 (s, 4H), 7.01 (d, J=8.4, 1H), 7.49-7.55 (m, 2H), 12.64 (brs, 2H).

Reference Example 69N-[2-methyl-4-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]iminodiacetic acidStep A3-methyl-4-nitrobenzoic acid tert-butyl ester

Using 3-methyl-4-nitrobenzoic acid (50.0 g, 276 mmol) and according to the method of Reference Example 61, step A, the title compound (55.6 g, yield 85%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.61 (s, 9H), 2.62 (s, 3H), 7.88-7.97 (m, 3H).

Step B4-amino-3-methylbenzoic acid tert-butyl ester

The compound (55.6 g, 234 mmol) obtained in step A was dissolved in an ethanol (200 ml)-tetrahydrofuran (100 ml) mixed solvent. Then, 10% palladium carbon (containing water) (10 g) suspended in ethanol (20 ml) was added. Under a hydrogen atmosphere and at room temperature, the reaction mixture was stirred for 5 hr, and filtered off through celite. The obtained solution was concentrated under reduced pressure to give the title compound (51.5 g) as a bistered oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.57 (s, 9H), 2.17 (s, 3H), 3.95 (brs, 2H), 6.62 (d, J=8.1, 1H), 7.66-7.70 (m, 2H).

Step CN-(4-tert-butoxycarbonyl-2-methylphenyl)iminodiacetic acid diethyl ester

The compound (51.5 g) obtained in step B, ethyl bromoacetate (160 ml, 1.44 mol) and N,N-diisopropylethylamine (250 ml, 1.47 mol) were mixed, and the mixture was stirred with heating at 140Â° C. for 10 hr. The reaction mixture was cooled, diluted with ethyl acetate, and the organic layer was washed with 20% aqueous citric acid solution and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give a mixture of the title compound and N-(4-tert-butoxycarbonyl-2-methyl)phenylglycine ethyl ester. To this mixture were added ethyl bromoacetate (80 ml, 719 mmol) and N,N-diisopropylethylamine (125 ml, 735 mmol), and the mixture was stirred again with heating at 140Â° C. for 11 hr, which was followed by the purification similar to the above to give the title compound (95.3 g) as a yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.24 (t, J=7.3, 6H), 1.57 (s, 9H), 2.34 (s, 3H), 4.06 (s, 4H), 4.15 (q, J=7.3, 4H), 7.10 (d, J=8.3, 1H), 7.74 (dd, J=2.1, 8.3, 1H), 7.78 (d, J=2.1, 1H).

Step DN-(4-carboxy-2-methylphenyl)iminodiacetic acid diethyl ester

Using the compound (15.0 g, 39.5 mmol) obtained by the method of step C and according to the method of Reference Example 61, step D, the title compound (14.1 g) was obtained as a pale-yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.25 (t, J=7.2, 6H), 2.36 (s, 3H), 4.10 (s, 4H), 4.17 (q, J=6.9, 4H), 7.10 (d, J=8.4, 1H), 7.86 (dd, J=1.9, 8.4, 1H), 7.90 (d, J=1.9, 1H), 9.77 (brs, 1H)

Step EN-[4-(aminocarbonyl)-2-methylphenyl]iminodiacetic acid diethyl ester

Using the compound (14.1 g) obtained in step D and according to the method of Reference Example 61, step E, the title compound (11.2 g, yield from step D 88%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.24 (t, J=6.9, 6H), 2.36 (s, 3H), 4.06 (s, 4H), 4.14 (q, J=6.9, 4H), 5.90-5.99 (broad, 2H), 7.14 (d, J=8.4, 1H), 7.55 (dd, J=2.1, 8.4, 1H), 7.65 (d, J=2.1, 1H).

Step FN-(4-cyano-2-methylphenyl)iminodiacetic acid diethyl ester

Using the compound (11.2 g, 34.8 mmol) obtained in step E and according to the method of Reference Example 61, step F, the title compound (9.64 g, yield 91%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.25 (t, J=7.5, 6H), 2.33 (s, 3H), 4.06 (s, 4H), 4.17 (q, J=7.5, 4H), 7.12 (d, J=8.2, 1H), 7.38-7.43 (m, 2H).

Step GN-[2-methyl-4-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]iminodiacetic acid diethyl ester

Using the compound (9.64 g, 31.67 mmol) obtained in step F and according to the method of Reference Example 62, step A, the title compound (8.03 g, yield 71%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.24 (t, J=7.2, 6H), 2.38 (s, 3H), 2.64 (s, 3H), 4.08 (s, 4H), 4.15 (q, J=7.5, 4H), 7.21 (d, J=8.4, 1H), 7.81 (dd, J=2.1, 8.4, 1H), 7.86 (d, J=2.1, 1H).

Step HN-[2-methyl-4-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]iminodiacetic acid

Using the compound (8.03 g, 22.22 mmol) obtained in step G and according to the method of Reference Example 62, step B, the title compound (7.74 g, yield>100%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.31 (s, 3H), 2.63 (s, 3H), 3.99 (s, 4H), 7.10 (d, J=8.4, 1H), 7.69 (dd, J=1.8, 8.4, 1H), 7.74 (d, J=1.8, 1H), 12.58 (brs, 2H).

Reference Example 70N-[4-{[2-(tert-butoxycarbonyl)-2-methylhydrazino]carbonyl}-2-methylphenyl]iminodiacetic acidStep AN-[4-{[2-(tert-butoxycarbonyl)-2-methylhydrazino]carbonyl}-2-methylphenyl]iminodiacetic acid diethyl ester

The compound (2.50 g, 7.7 mmol) of Reference Example 69, step D, was dissolved in dichloromethane (85 ml), oxalyl chloride (1.00 ml, 11.6 mmol) and a catalytic amount of N,N-dimethylformamide were added with stirring under ice-cooling, and the mixture was stirred at room temperature for 2 hr. The reaction mixture was concentrated, the obtained oil was dissolved in dichloromethane (85 ml), tert-butyl 1-methylhydrazine carboxylate (1.70 g, 11.6 mmol) and triethylamine (4.3 ml, 31 mmol) were added with stirring under ice-cooling, and the mixture was stirred at room temperature for 2 hr. The reaction mixture was concentrated, and the obtained oil was dissolved in ethyl acetate, washed with water and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (methanol-chloroform) to give the title compound (3.15 g, yield 81%) as a pale-yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.24 (t, J=7.1, 6H), 1.46 (brs, 9H), 2.27 (brs, 3H), 3.17 (brs, 3H), 4.03 (brs, 4H), 4.13 (q, J=6.8, 4H), 6.95-7.09 (m, 1H), 7.53-7.56 (m, 1H), 7.63 (s, 1H), 8.7-9.22 (m, 1H).

Step BN-[4-{[2-(tert-butoxycarbonyl)-2-methylhydrazino]carbonyl}-2-methylphenyl]iminodiacetic acid

Using the compound (3.15 g, 6.97 mmol) obtained in step A and according to the method of Reference Example 61, step G, the title compound (2.29 g, yield 83%) was obtained as a colorless oil.

35 ¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.33 (s, 9H), 2.28 (s, 3H), 3.09 (s, 3H), 3.98 (s, 4H), 7.00 (d, J=8.4, 1H), 7.52-7.60 (m, 2H), 10.4 (s, 1H), 12.5 (brs, 2H).

Reference Example 71N-[4-{[2-(tert-butoxycarbonyl)-2-ethylhydrazino]carbonyl}-2-methylphenyl]iminodiacetic acidStep AN-[4-{[2-(tert-butoxycarbonyl)-2-ethylhydrazino]carbonyl}-2-methylphenyl]iminodiacetic acid diethyl ester

Using the compound (2.50 g, 7.7 mmol) of Reference Example 69, step D and tert-butyl 1-ethylhydrazinecarboxylate (1.86 g, 11.6 mmol), and according to the method of Reference Example 70, step A, the title compound (2.60 g, yield 72%) was obtained as a pale-yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.14 (t, J=4.2, 3H), 1.24 (t, J=7.5, 6H), 1.46 (brs, 9H), 2.30 (brs, 3H), 3.60 (q, J=7.2, 2H), 4.04 (brs, 4H), 4.14 (q, J=7.2, 4H), 7.09 (brs, 1H), 7.53 (d, J=8.1, 1H), 7.62 (s, 1H).

Step BN-[4-{[2-(tert-butoxycarbonyl)-2-ethylhydrazino]carbonyl}-2-methylphenyl]iminodiacetic acid

Using the compound (2.60 g, 5.58 mmol) obtained in step A and according to the method of Reference Example 61, step G, the title compound (1.9 g, yield 83%) was obtained as a colorless oil.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.00-1.07 (m, 3H), 1.33 (s, 9H), 2.28 (s, 3H), 3.43 (q, J=7.2, 2H), 3.98 (s, 4H), 7.02 (d, J=8.4, 1H), 7.55-7.68 (m, 2H), 10.3 (s, 1H), 12.2 (brs, 2H).

Reference Example 72N-[5-(tert-butoxycarbonyl)-2-methylphenyl]iminodiacetic acid

Using the compound (7.44 g, 19.6 mmol) of Reference Example 61, step C, and according to the method of Reference Example 62, step B, the title compound (5.46 g, yield 86%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.52 (s, 9H), 2.30 (s, 3H), 3.94 (s, 4H), 7.23 (d, J=8.1, 1H), 7.44 (dd, J=0.9, 8.1, 1H), 7.62 (d, J=0.9, 1H), 12.48 (brs, 2H).

Reference Example 73N-[5-(aminocarbonyl)-2-methylphenyl]iminodiacetic acid

Using the compound (3.16 g, 9.80 mmol) of Reference Example 61, step E, and according to the method of Reference Example 62, step B, the title compound (2.56 g, yield 98%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.28 (s, 3H), 3.94 (s, 4H), 7.17 (d, J=7.8, 1H), 7.18 (brs, 1H), 7.41 (d, J=7.8, 1H), 7.60 (s, 1H), 7.85 (brs, 1H), 12.41 (brs, 2H).

Reference Example 74N-[5-{[2-(tert-butoxycarbonyl)-2-methylhydrazino]carbonyl}-2-methylphenyl]iminodiacetic acidStep AN-[5-{[2-(tert-butoxycarbonyl)-2-methylhydrazino]carbonyl}-2-methylphenyl]iminodiacetic acid diethyl ester

Using the compound (15.92 g, 49.24 mmol) of Reference Example 61, step D, and tert-butyl 1-methylhydrazinecarboxylate (9.93 g, 67.93 mmol), and according to the method of Reference Example 70, step A, the title compound (24.27 g) was obtained as a crude orange oil. This was directly used for the next step.

Step BN-[5-{[2-(tert-butoxycarbonyl)-2-methylhydrazino]carbonyl}-2-methylphenyl]iminodiacetic acid

Using the compound (24.27 g) obtained in step A and according to the method of Reference Example 62, step B, the title compound (16.51 g, yield from step A 85%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.33 (s, 5.4H), 1.45 (s, 3.6H), 2.30 (s, 3H), 3.02 (s, 1.2H), 3.08 (s, 1.8H), 3.96 (s, 4H), 7.22 (d, J=7.8, 1H), 7.32-7.43 (m, 1H), 7.5-7.6 (m, 1H), 10.50 (s, 0.6H), 10.54 (s, 0.4H), 12.45 (brs, 2H).

Reference Example 75N-[5-{[2-(tert-butoxycarbonyl)-2-ethylhydrazino]carbonyl}-2-methylphenyl]iminodiacetic acidStep AN-[5-{[2-(tert-butoxycarbonyl)-2-ethylhydrazino]carbonyl}-2-methylphenyl]iminodiacetic acid diethyl ester

Using the compound (1.50 g, 4.63 mmol) of Reference Example 61, step D, and tert-butyl 1-ethylhydrazinecarboxylate (1.12 g, 7 mmol), and according to the method of Reference Example 70, step A, the title compound (2.10 g, yield 98%) was obtained as a colorless oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.09-1.28 (m, 9H), 1.47 (s, 9H), 2.37 (s, 3H), 3.62 (q, J=7.1, 2H), 4.02 (s, 4H), 4.14 (q, J=7.1, 4H), 7.18 (brs, 1H), 7.38 (d, J=7.6, 1H), 7.65 (s, 1H).

Step BN-[5-{[2-(tert-butoxycarbonyl)-2-ethylhydrazino]carbonyl}-2-methylphenyl]iminodiacetic acid

Using the compound (2.10 g, 4.5 mmol) obtained in step A and according to the method of Reference Example 61, step G, the title compound (1.71 g, yield 93%) was obtained as a colorless oil.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.08 (t, J=6.9, 3H), 1.33-1.43 (m, 9H), 2.29 (s, 3H), 3.36-3.45 (m, 2H), 3.95 (s, 4H), 7.21 (d, J=7.8, 1H), 7.34-7.41 (m, 1H), 7.53-7.66 (m, 1H), 10.38-10.43 (m, 1H), 12.45 (brs, 2H).

Reference Example 76N-[5-(tert-butoxycarbonylamino)-2-methylphenyl]iminodiacetic acidStep AN-[5-(tert-butoxycarbonylamino)-2-methylphenyl]iminodiacetic acid diethyl ester

To toluene (20 ml) were added the compound (3.06 g, 9.46 mmol) of Reference Example 61, step D, diphenylphosphoryl azide (2.24 ml, 10.4 mmol) and triethylamine (1.45 ml, 10.4 mmol), and the mixture was heated under reflux for 90 min. Then, to the reaction mixture was added tert-butanol (9.0 ml), and the mixture was further heated under reflux for 7 hr. The reaction mixture was cooled to room temperature and concentrated under reduced pressure. The residue was diluted with dichloromethane, and the organic layer was washed with water and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained crude product was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (3.39 g, yield 85%) as a pale-yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.24 (t, J=6.9, 6H), 1.50 (s, 9H), 2.27 (s, 3H), 4.01 (s, 4H), 4.14 (q, J=6.9, 4H), 6.35 (brs, 1H), 7.04 (m, 2H), 7.15 (s, 1H).

Step BN-[5-(tert-butoxycarbonylamino)-2-methylphenyl]iminodiacetic acid

Using the compound (3.38 g, 8.00 mmol) obtained by the method of step A and according to the method of Reference Example 62, step B, the title compound (2.39 g, yield 81%) was obtained as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.45 (s, 9H), 2.15 (s, 3H)_r3.88 (s, 4H), 6.94-6.98 (m, 2H), 7.22 (s, 1H), 9.12 (s, 1H), 12.4 (brs, 2H).

Reference Example 77N-[5-(ethoxycarbonyl)-2-methylphenyl]iminodiacetic acidStep AN-[5-(ethoxycarbonyl)-2-methylphenyl]iminodiacetic acid diethyl ester

Using the compound (1.00 g, 3.1 mmol) of Reference Example 61, step D, and ethanol (0.4 ml, 6.2 mmol), and according to the method of Reference Example 61, step A, the title compound (1.20 g, yield>100%) was obtained as a pale-yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.25 (t, J=7.5, 6H), 1.37 (t, J=7.5, 3H), 2.39 (s, 3H), 4.05 (s, 4H), 4.15 (q, J=7.2, 4H), 4.35 (q, J=7.2, 2H), 7.22 (d, J=7.8, 1H), 7.66 (dd, J=7.8, 1.2, 1H), 7.85 (d, J=1.2, 1H).

Step BN-[5-(ethoxycarbonyl)-2-methylphenyl]iminodiacetic acid

The compound (0.62 g, 1.76 mmol) obtained in step A was dissolved in a ethanol (10 ml)-tetrahydrofuran (5 ml) mixed solvent, 1N sodium hydroxide (3.53 ml, 3.53 mmol) was added at room temperature with stirring, and the mixture was stirred at the same temperature for 90 min. To the reaction mixture was added 1N hydrochloric acid (5 ml), and the mixture was extracted with ethyl acetate. The organic layer was washed with diluted hydrochloric acid and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure to give the title compound (0.52 g) as a crude colorless oil.

Reference Example 78N-[2-methyl-5-(5-methyl-1,3-oxazol-2-yl)phenyl]iminodiacetic acidStep AN-[2-methyl-5-{[(2-oxopropyl)amino]carbonyl}phenyl]iminodiacetic acid diethyl ester

The compound (2.00 g, 6.18 mmol) of Reference Example 61, step D, was dissolved in dichloromethane (60 ml), oxalyl chloride (0.80 ml, 9.28 mmol) and a catalytic amount of N,N-dimethylformamide were added under ice-cooling with stirring, and the mixture was stirred at room temperature for 2 hr. The reaction mixture was concentrated, the obtained oil was dissolved again in dichloromethane (60 ml), 1-aminopropan-2-one hydrochloride (1.10 g, 9.89 mmol) and triethylamine (2.8 ml, 20 mmol) were added under ice-cooling with stirring, and the mixture was stirred at room temperature for 2 hr. The reaction mixture was concentrated, and the obtained oil was diluted with ethyl acetate, washed with water and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained crude product was purified by silica gel column chromatography (methanol-dichloromethane) to give the title compound (2.60 g, yield>100%) as a pale-yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.24 (t, J=6.9, 6H), 2.26 (s, 3H), 2.38 (s, 3H), 4.04 (s, 4H), 4.15 (q, J=6.9, 4H), 4.33 (d, J=4.5, 2H), 6.87 (brs, 1H), 7.22 (d, J=7.9, 1H), 7.41 (dd, J=1.5, 7.9, 1H), 7.67 (d, J=1.5, 1H).

Step BN-[2-methyl-5-(5-methyl-1,3-oxazol-2-yl)phenyl]iminodiacetic acid diethyl ester

To the compound (555 mg, 1.47 mmol) obtained in step A was added phosphorus oxychloride (8.00 g), and the mixture was stirred at 120Â° C. for 3 hr. The reaction mixture was cooled to room temperature and slowly added to ice water. The solution was extracted with ethyl acetate, and washed with water, saturated aqueous sodium hydrogen carbonate and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel chromatography (ethyl acetate-hexane) to give the title compound (0.30 g, yield 57%) as a yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.23 (t, J=7.2, 6H), 2.37 (s, 3H), 2.38 (s, 3H), 4.07 (s, 4H), 4.14 (q, J=7.2, 4H), 6.79 (s, 1H), 7.22 (d, J=7.8, 1H), 7.62 (dd, J=1.5, 7.8, 1H), 7.82 (s, 1H).

Step CN-[2-methyl-5-(5-methyl-1,3-oxazol-2-yl)phenyl]iminodiacetic acid

Using the compound (0.30 g, 0.83 mmol) obtained in step B and according to the method of Reference Example 62, step B, the title compound (0.21 g, yield 84%) was obtained as a yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.29 (s, 3H), 2.37 (s, 3H), 3.98 (s, 4H), 6.94 (s, 1H), 7.254 (d, J=7.8, 1H), 7.47 (dd, J=1.2, 7.8, 1H), 7.63 (d, J=1.2, 1H), 12.5 (brs, 2H).

Reference Example 79N-[2-methyl-5-(4-methyl-1,3-thiazol-2-yl)phenyl]iminodiacetic acidStep AN-[5-(aminocarbonothioyl)-2-methylphenyl]iminodiacetic acid diethyl ester

The compound (0.84 g, 2.6 mmol) of Reference Example 61, step E, and Lawesson reagent (1.20 g, 3.4 mmol) were dissolved in 1,4-dioxane (36 ml), and the mixture was stirred at 80Â° C. for 1 hr. The reaction mixture was concentrated under reduced pressure, and the obtained oil was purified by silica gel chromatography (NH silica gel use, methanol-chloroform) to give the title compound (0.80 g, yield 91%) as a yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.26 (t, J=7.2, 6H), 2.36 (s, 3H), 4.04 (s, 4H), 4.14 (q, J=7.2, 4H), 7.16 (d, J=8.1, 1H), 7.4-7.6 (broad, 1H), 7.47 (d, J=8.1, 1H), 7.78 (s, 1H), 7.95 (brs, 1H).

Step BN-[2-methyl-5-(4-methyl-1,3-thiazol-2-yl)phenyl]iminodiacetic acid

The compound (0.70 g, 2.1 mmol) obtained in step A was dissolved in a ethanol (14 ml)-N,N-dimethylformamide (4 ml) mixed solvent. Then, chloroacetone (0.18 ml, 2.3 mmol) was added, and the mixture was stirred at 80Â° C. for 3 hr. The reaction mixture was concentrated under reduced pressure, and the obtained oil was diluted with dichloromethane, washed with water, saturated aqueous sodium hydrogen carbonate and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure to give a crude oil of the title compound containing N,N-dimethylformamide. Using this oil and according to the method of Reference Example 62, step B, the title compound (0.56 g, yield 83%) was obtained as a pale-yellow oil.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.36 (s, 3H), 2.48 (s, 3H), 4.08 (s, 4H), 6.84 (s, 1H), 7.18 (d, J=7.8, 1H), 7.45 (d, J=7.8, 1H), 7.77 (s, 1H), 12.0 (brs, 2H).

Reference Example 80N-[2-methyl-5-(5-methyl-1,3-thiazol-2-yl)phenyl]iminodiacetic acidStep AN-[2-methyl-5-(5-methyl-1,3-thiazol-2-yl)phenyl]iminodiacetic acid diethyl ester

The compound (1.30 g, 3.43 mmol) of Reference Example 78, step A, and a Lawesson reagent (1.84 g, 4.56 mmol) were dissolved in 1,4-dioxane (30 ml), and the mixture was stirred at 80Â° C. for 3 hr. The reaction mixture was concentrated under reduced pressure, and the obtained oil was purified by silica gel chromatography (ethyl acetate-hexane) to give the title compound (1.28 g, yield 100%) as a yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.23 (t, J=7.3, 6H), 2.37 (s, 3H), 2.49 (s, 3H), 4.07 (s, 4H), 4.15 (q, J=7.0, 4H), 7.20 (d, J=7.9, 1H), 7.45-7.52 (m, 2H), 7.73 (d, J=1.7, 1H).

Step BN-[2-methyl-5-(5-methyl-1,3-thiazol-2-yl)phenyl]iminodiacetic acid

Using the compound (0.80 g, 2.12 mmol) obtained in step A and according to the method of Reference Example 62, step B, the title compound (0.68 g, yield 100%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.28 (s, 3H), 2.49 (s, 3H), 3.97 (s, 4H), 7.11 (d, J=7.5, 1H), 7.22 (d, J=8.1, 1H), 7.54 (s, 1H), 7.59 (s, 1H), 12.5 (brs, 2H).

Reference Example 81N-[2-methyl-5-(4-ethyl-1,3-thiazol-2-yl)phenyl]iminodiacetic acid

Using the compound (1.44 g, 4.26 mmol) of Reference Example 79, step A, and 1-bromo-2-butanone (0.5 ml, 4.90 mmol), and according to the method of Reference Example 79, step B, the title compound (0.91 g, yield 64%) was obtained as a yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.26 (t, J=7.5, 3H), 2.29 (s, 3H), 2.77 (q, J=7.5, 2H), 3.98 (s, 4H), 7.22-7.27 (m, 2H), 7.44 (d, J=8.1, 1H), 7.62 (s, 1H), 12.5 (brs, 2H).

Reference Example 82N-[2-methyl-5-(4-tert-butyl-1,3-thiazol-2-yl)phenyl]iminodiacetic acid

Using the compound (1.44 g, 4.26 mmol) of Reference Example 79, step A, and 1-chloropinacolone (0.61 ml, 4.7 mmol), and according to the method of Reference Example 79, step B, the title compound (0.95 g, yield 62%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.33 (s, 9H), 2.29 (s, 3H), 3.98 (s, 4H), 7.22-7.25 (m, 2H), 7.45 (dd, J=1.2, 7.5, 1H), 7.59 (d, J=1.2, 1H), 12.5 (brs, 2H).

Reference Example 83N-[2-methyl-5-(5-methyl-1,3,4-oxadiazol-2-yl)phenyl]iminodiacetic acidStep ANâ€²-acetyl-4-methyl-3-nitrobenzohydrazide

4-Methyl-3-nitrobenzoic acid (3.00 g, 16.5 mmol) was added to dichloromethane (50 ml), triethylamine (3.0 ml, 21.3 mmol) and isobutyl chloroformate (2.80 ml, 21.5 mmol) were added under ice-cooling with stirring, and the mixture was stirred at room temperature for 3 hr. The reaction mixture was ice-cooled again, acetohydrazide (2.45 g, 33.1 mmol) was added with stirring, and the mixture was stirred at room temperature for about 3 hr. The reaction mixture was diluted with ethyl acetate, washed with 10% aqueous citric acid solution, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained solid was washed with diethyl ether and hexane to give the title compound (1.72 g, yield 44%) as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.94 (s, 3H), 2.59 (s, 3H), 7.66 (d, J=8.1, 1H), 8.10 (dd, J=1.8, 8.1, 1H), 8.47 (d, J=1.8, 1H), 10.01 (s, 1H), 10.6 (s, 1H).

Step B2-methyl-5-(4-methyl-3-nitrophenyl)-1,3,4-oxadiazole

The compound (0.70 g, 2.95 mmol) obtained in step A and polyphosphoric acid (8.0 g) were mixed, and the mixture was stirred with heating at 120Â° C. After cooling to room temperature, the reaction mixture was poured into ice water, and diluted with ethyl acetate. The mixture was washed with water and saturated aqueous sodium hydrogen carbonate, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure to give the title compound (0.91 g) as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.66 (s, 3H), 2.67 (s, 3H), 7.52 (d, J=8.1, 1H), 8.19 (dd, J=1.8, 8.1, 1H), 8.59 (d, J=1.8, 1H).

Step C2-methyl-5-(5-methyl-1,3,4-oxadiazol-2-yl)aniline

Using the compound (0.91 g) obtained in step B and according to the method of Reference Example 61, step B, the title compound (0.71 g) was obtained as a colorless oil. This was directly used for the next step.

Step DN-[2-methyl-5-(5-methyl-1,3,4-oxadiazol-2-yl)phenyl]iminodiacetic acid diethyl ester

Using the compound (0.71 g) obtained in step C and according to the method of Reference Example 61, step C, the title compound (0.68 g, yield from step B 64%) was obtained as a pale-yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.24 (t, J=7.4, 6H), 2.41 (s, 3H), 2.60 (s, 3H), 4.00-4.21 (m, 8H), 7.29 (d, J=8.0, 1H), 7.65 (dd, J=1.3, 8.0, 1H), 7.85 (d, J=1.3, 1H).

Step EN-[2-methyl-5-(5-methyl-1,3,4-oxadiazol-2-yl)phenyl]iminodiacetic acid

Using the compound (0.68 g, 1.9 mmol) obtained in step D and according to the method of Reference Example 61, step G, the title compound (0.51 g, yield 89%) was obtained as a colorless oil.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.32 (s, 3H), 2.77 (s, 3H), 4.00 (s, 4H), 7.29 (d, J=7.8, 1H), 7.43 (d, J=7.8, 1H), 7.64 (s, 1H), 12.5 (brs, 2H).

Reference Example 84N-[2-methyl-5-(5-methyl-1,3,4-thiadiazol-2-yl)phenyl]iminodiacetic acidStep AN-{[5-(2-acetylhydrazino)carbonyl]-2-methylphenyl}iminodiacetic acid diethyl ester

The compound (3.00 g, 9.27 mmol) of Reference Example 61, step D, was dissolved in dichloromethane (100 ml), and the mixture was stirred under ice-cooling. Then, oxalyl chloride (1.25 ml, 14.6 mmol) and a catalytic amount of N,N-dimethylformamide were added, and the mixture was stirred at room temperature for 2 hr. The reaction mixture was concentrated under reduced pressure, and the obtained oil was dissolved in dichloromethane (100 ml) again. While stirring the solution under ice-cooling, acetohydrazide (1.20 g, 16.2 mmol) and triethylamine (5.8 ml, 42 mmol) were successively added, and the mixture was stirred at room temperature overnight. The reaction mixture was concentrated under reduced pressure, and the obtained oil was dissolved in ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (methanol-dichloromethane) to give the title compound (2.61 g, yield 74%) as a pale-yellow oil.

Step BN-[2-methyl-5-(5-methyl-1,3,4-thiadiazol-2-yl)phenyl]iminodiacetic acid diethyl ester

Using the compound (2.61 g, 6.88 mmol) obtained in step A and according to the method of Reference Example 80, step A, the title compound (2.36 g, yield 91%) was obtained as a yellow oil.

Step CN-[2-methyl-5-(5-methyl-1,3,4-thiadiazol-2-yl)phenyl]iminodiacetic acid

Using the compound (2.36 g, 6.25 mmol) obtained in step B and according to the method of Reference Example 62, step B, the title compound (1.40 g, yield 70%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.31 (s, 3H), 2.76 (s, 3H), 3.99 (s, 4H), 7.29 (d, J=7.8, 1H), 7.36-7.44 (m, 1H), 7.63 (s, 1H), 12.5 (brs, 2H).

Reference Example 85N-[2-methyl-5-(5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)phenyl]iminodiacetic acidStep AN-[5-{[2-(methoxycarbonyl)hydrazino]carbonyl}-2-methylphenyl]iminodiacetic acid diethyl ester

Using the compound (3.00 g, 9.28 mmol) of Reference Example 61, step D, and methyl carbazate (1.25 g, 13.9 mmol), and according to the method of Reference Example 84, step A, the title compound (3.67 g, yield 100%) was obtained as a pale-yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.21 (t, J=6.5, 6H), 2.35 (s, 3H), 3.62 (s, 3H), 4.00 (s, 4H), 4.12 (q, J=6.5, 4H), 7.14 (d, J=7.6, 1H), 7.45 (d, J=7.6, 1H), 7.74 (s, 1H).

Step BN-[2-methyl-5-(5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)phenyl]iminodiacetic acid diethyl ester

To the compound (3.67 g, 9.28 mmol) obtained in step A was added phosphorus oxychloride (30 g), and the mixture was stirred at 110Â° C. for 2.5 hr. After cooling to room temperature, the reaction mixture was poured into ice water, and the solution was extracted with ethyl acetate. The organic layer was washed with water, saturated aqueous sodium hydrogen carbonate and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure to give the title compound (2.00 g, yield 59%) as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.25 (t, J=6.9, 6H), 2.39 (s, 3H), 4.06 (s, 4H), 4.16 (q, J=6.9, 4H), 7.25 (d, J=8.1, 1H), 7.46 (dd, J=1.5, 8.1, 1H), 7.68 (d, J=1.5, 1H), 9.94 (brs, 1H).

Step CN-[2-methyl-5-(5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)phenyl]iminodiacetic acid

Using the compound (1.20 g, 3.30 mmol) obtained by the method of step B and according to the method of Reference Example 62, step B, the title compound (0.94 g, yield 92%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.31 (s, 3H), 3.97 (s, 4H), 7.27-7.35 (m, 2H), 7.45 (s, 1H), 12.40-12.65 (broad, 1H), 12.5 (brs, 2H).

Reference Example 86N-(4-bromo-2-methylphenyl)iminodiacetic acid

Using 4-bromo-2-methylaniline (10.0 g, 53.7 mmol) and according to the methods of Reference Example 61, step C, and Reference Example 62, step B, the title compound (10.89 g, yield 67%) was obtained as a pale-bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.4. (s, 3H), 3.90 (s, 4H), 7.01 (d, J=8.4, 1H), 7.24 (dd, J=2.4, 8.4, 1H), 7.31 (d, J=2.4, 1H), 12.45 (brs, 2H).

Reference Example 87N-(2,6-dimethylphenyl)iminodiacetic acid

Using 2,6-dimethylaniline (5.00 g, 41.3 mmol) and according to the methods of Reference Example 61, step C, and Reference Example 62, step B, the title compound (8.16 g, yield 83%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.35 (s, 6H), 3.81 (s, 4H), 6.88-6.99 (m, 3H), 12.42 (brs, 2H).

Reference Example 88N-(4-bromo-2,6-dimethylphenyl)iminodiacetic acid

Using 4-bromo-2,6-dimethylaniline (10.00 g, 50.0 mmol) and according to the methods of Reference Example 61, step C, Reference Example 62, step B, the title compound (8.90 g, yield 56%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.35 (s, 6H), 3.80 (s, 4H), 7.17 (s, 2H), 12.45 (brs, 2H).

Reference Example 89N-(5-bromo-2-methylphenyl)iminodiacetic acidStep AN-(5-bromo-2-methylphenyl)iminodiacetic acid diethyl ester

Using 5-bromo-2-methylaniline (10.27 g, 55.22 mmol) and according to the method of Reference Example 69, step C, the title compound (18.90 g, yield 96%) was obtained as a pale-yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.25 (t, J=7.2, 6H), 2.28 (s, 3H), 4.00 (s, 4H), 4.15 (q, J=7.2, 4H), 7.01 (d, J=8.1, 1H), 7.11 (dd, J=1.8, 8.1, 1H), 7.32 (d, J=1.8, 1H).

Step BN-(5-bromo-2-methylphenyl)iminodiacetic acid

Using the compound (7.03 g, 19.62 mmol) obtained in step A and according to the method of Reference Example 62, step B, the title compound (4.40 g, yield 74%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.20 (s, 3H), 3.92 (s, 4H), 7.08 (brs, 2H), 7.17 (s, 1H), 12.51 (brs, 2H).

Reference Example 90N-(2-methyl-5-pyrimidin-2-ylphenyl)iminodiacetic acidStep A2-(4-methyl-3-nitrophenyl)pyrimidine

To a toluene (40 ml)-ethanol (40 ml) mixed solvent were added 4-methyl-3-nitrophenylboronic acid (2.66 g, 14.7 mmol), 2-bromopyrimidine (3.15 g, 19.81 mmol), tetrakis(triphenylphosphine)palladium(0) (1.01 g, 0.874 mmol) and sodium carbonate (3.93 g, 37.08 mmol), and the mixture was heated under reflux for 24 hr. The reaction mixture was cooled, diluted with ethyl acetate, washed with diluted aqueous sodium hydroxide solution and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure to give a solid. This was purified by silica gel column chromatography (ethyl acetate-dichloromethane) to give the title compound (1.74 g, yield 55%) as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.67 (s, 3H), 7.24-7.28 (t, J=4.8, 1H), 7.47 (d, J=8.1, 1H), 8.58 (dd, J=1.8, 8.1, 1H), 8.83 (d, J=4.8, 2H), 9.07 (d, J=1.8, 1H).

Step B2-methyl-5-pyrimidin-2-ylaniline

Using the compound (1.72 g, 7.99 mmol) obtained in step A and according to the method of Reference Example 61, step B, the title compound (1.43 g, yield 97%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.24 (s, 3H), 3.72 (brs, 2H), 7.14 (d, J=4.8, 1H), 7.18 (d, J=8.1, 1H), 7.77-7.81 (m, 2H), 8.77 (d, J=4.8, 2H).

Step CN-(2-methyl-5-pyrimidin-2-ylphenyl)iminodiacetic acid

Using the compound (1.01 g, 5.45 mmol) obtained in step B and according to the methods of Reference Example 61, step C, and Reference Example 62, step B, the title compound (1.22 g, yield 74%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.33 (s, 3H), 4.00 (s, 4H), 7.28 (d, J=8.1, 1H), 7.41 (t, J=5.1, 1H), 7.97 (dd, J=1.5, 8.1, 1H), 8.17 (d, J=1.5, 1H), 8.88 (d, J=5.1, 2H), 12.47 (brs, 2H).

The compounds of Reference Examples 61-90 are shown below.

TABLE 3Ref-erenceEx-StructuralampleFormula61 [Image Omitted]

62

63

64

65

66

67

68

69

70

71

72

73

74

75

76

77

78

79

80

81

82

83

84

85

86

87

88

89

90

Reference Example 91N-(2-methyl-5-pyrimidin-4-ylphenyl)iminodiacetic acidStep AN-[2-methyl-(5-tri-n-butylstanyl)phenyl]iminodiacetic acid diethyl ester

To toluene (70 ml) were added the compound (3.92 g, 10.94 mmol) of Reference Example 89, step A, bis(tri-n-butyltin) (9.0 ml, 17.8 mmol), and tetrakis(triphenylphosphine)palladium(0) (574 mg, 0.497 mmol), and the mixture was heated under reflux for 2 hr. The reaction mixture was cooled, water was added, and the mixture was vigorously stirred. The precipitated solid was filtered off through celite, and the organic layer was extracted and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (3.56 g, yield 57%) as a colorless oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 0.88 (t, J=7.2, 9H), 0.98-1.05 (m, 6H), 1.23 (t, J=7.1, 6H), 1.28-1.34 (m, 6H), 1.5-1.6 (m, 6H), 2.32 (s, 3H), 4.04 (s, 4H), 4.14 (q, J=7.1, 4H), 7.06 (d, J=7.4, 1H), 7.12 (d, J=7.4, 1H), 7.24 (s, 1H).

Step BN-[5-(6-chloropyrimidin-4-yl)-2-methylphenyl]iminodiacetic acid diethyl ester

To toluene (40 ml) were added the compound (1.40 g, 2.46 mmol) obtained in step A, 4,6-dichloropyrimidine (606 mg, 4.07 mmol) and bis(triphenylphosphine)palladium(II) dichloride (138 mg, 0.261 mmol), and the mixture was heated under reflux for 3 hr. The reaction mixture was cooled, diluted with an ethyl acetate-hexane=1:1 mixed solvent, washed with water and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (747 mg, yield 77%) as a pale-yellow solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.24 (t, J=7.2, 6H), 2.42 (s, 3H), 4.10 (s, 4H), 4.15 (q, J=7.2, 4H), 7.30 (d, J=8.1, 1H), 7.68 (dd, J=1.5, 8.1, 1H), 7.68 (s, 1H), 7.98 (d, J=1.5, 1H), 8.99 (s, 1H).

Step CN-(2-methyl-5-pyrimidin-4-ylphenyl)iminodiacetic acid diethyl ester

The compound (696 mg, 1.78 mmol) obtained in step B was dissolved in a ethanol (25 ml)-tetrahydrofuran (2 ml) mixed solvent. Then, sodium acetate (164 mg, 2.00 mmol) and 10% palladium carbon (containing water) (0.68 g) were added, and the mixture was stirred at room temperature for 5 hr under a hydrogen atmosphere. The insoluble material was filtered off through celite, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (466 mg, yield 73%) as a colorless oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.24 (t, J=7.2, 6H), 2.42 (s, 3H), 4.10 (s, 4H), 4.15 (q, J=7.2, 4H), 7.30 (d, J=8.1, 1H), 7.67 (dd, J=1.2, 5.4, 1H), 7.71 (dd, J=1.5, 8.1, 1H), 8.01 (d, J=1.5, 1H), 8.72 (d, J=5.4, 1H), 9.23 (d, J=1.2, 1H).

Step DN-(2-methyl-5-pyrimidin-4-ylphenyl)iminodiacetic acid

Using the compound (450 mg, 1.26 mmol) obtained in step C and according to the method of Reference Example 62, step B, the title compound (378 mg, yield 100%) was obtained as a yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.29 (s, 3H), 4.01 (s, 4H), 7.31 (d, J=7.8, 1H), 7.74 (d, J=7.8, 1H), 7.96 (s, 1H), 8.00 (d, J=5.3, 1H), 8.82 (d, J=5.3, 1H), 9.21 (s, 1H), 12.48 (brs, 2H).

Reference Example 92N-(2-methyl-5-pyrimidin-5-ylphenyl)iminodiacetic acidStep AN-(2-methyl-5-pyrimidin-5-ylphenyl)iminodiacetic acid diethyl ester

Using the compound (685 mg, 1.21 mmol) of Reference Example 91, step A, and 5-bromopyrimidine (316 mg, 1.99 mmol), and according to the method of Reference Example 91, step B, the title compound (334 mg, yield 77%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.23 (t, J=7.2, 6H), 2.41 (s, 3H), 4.09 (s, 4H), 4.15 (q, J=7.2, 4H), 7.20 (dd, J=1.7, 7.8, 1H), 7.31 (d, J=7.8, 1H), 7.43 (d, J=1.7, 1H), 8.91 (s, 2H), 9.18 (s, 1H).

Step BN-(2-methyl-5-pyrimidin-5-ylphenyl)iminodiacetic acid

Using the compound (329 mg, 0.921 mmol) obtained in step A and according to the method of Reference Example 62, step B, the title compound (270 mg, yield 97%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.31 (s, 3H), 4.00 (s, 4H), 7.29 (d, J=8.0, 1H), 7.34 (d, J=8.0, 1H), 7.42 (s, 1H), 9.06 (s, 2H), 9.16 (s, 1H).

Reference Example 93N-(2-methyl-5-pyridin-3-ylphenyl)iminodiacetic acidStep AN-(2-methyl-5-pyridin-3-ylphenyl)iminodiacetic acid diethyl ester

Using the compound (2.90 g, 5.10 mmol) of Reference. Example 91, step A, and 3-bromopyridine (0.75 ml, 7.79 mmol), and according to the method of Reference Example 91, step B, the title compound (1.08 g, yield 59%) was obtained as a colorless oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.23 (t, J=7.2, 6H), 2.39 (s, 3H), 4.09 (s, 4H), 4.15 (q, J=7.2, 4H), 7.19-7.23 (m, 1H), 7.26-7.36 (m, 2H), 7.43 (d, J=1.8, 1H), 7.81-7.84 (m, 1H), 8.55-8.58 (m, 1H), 8.81 (d, J=2.1, 1H).

Step BN-(2-methyl-5-pyridin-3-ylphenyl)iminodiacetic acid

Using the compound (1.06 g, 2.97 mmol) obtained in step B and according to the method of Reference Example 62, step B, the title compound (740 mg, yield 83%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.30 (s, 3H), 4.00 (s, 4H), 7.26 (s, 2H), 7.35 (s, 1H), 7.45-7.50 (m, 1H), 7.96-8.00 (m, 1H), 8.53-8.56 (m, 1H), 8.80 (d, J=2.1, 1H), 12.49 (brs, 2H).

Reference Example 94N-(5-cyano-2-ethylphenyl)iminodiacetic acidStep A3-nitro-4-vinylbenzonitrile

To N,N-dimethylformamide (50 ml) were added 4-chloro-3-nitrobenzonitrile (2.81 g, 15.39 mmol), tri-n-butylvinyltin (5.23 g, 16.49 mmol) and bis(triphenylphosphine)palladium(II) dichloride (701 mg, 0.999 mmol), and the mixture was stirred with heating at 100Â° C. for 160 min. The reaction mixture was cooled, diluted with an ethyl acetate-hexane=1:1 mixed solvent, washed with water and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (2.21 g, yield 82%) as a yellow solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 5.69 (d, J=11.3, 1H), 5.90 (d, J=17.3, 1H), 7.20 (dd, J=11.3, 17.3, 1H), 7.78 (d, J=8.1, 1H), 7.85 (dd, J=1.5, 8.1, 1H), 8.24 (d, J=1.5, 1H).

Step B3-amino-4-ethylbenzonitrile

The compound (1.90 g, 10.9 mmol) obtained in step A was dissolved in ethanol (100 ml). Then, 10% palladium carbon (containing water) (1.93 g) was added, and the mixture was stirred at room temperature for 3 hr under a hydrogen atmosphere. The insoluble material was filtered off through celite, and the solution was concentrated under reduced pressure to give the title compound (1.56 g, yield 98%) as a pale-yellow solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.26 (t, J=7.5, 3H), 2.53 (q, J=7.5, 2H), 3.82 (brs, 2H), 6.90 (d, J=1.5, 1H), 7.02 (dd, J=1.5, 7.7, 1H), 7.13 (d, J=7.7, 1H).

Step CN-(5-cyano-2-ethylphenyl)iminodiacetic acid

Using the compound (1.70 g, 11.63 mmol) obtained in step B and according to the methods of Reference Example 61, steps C and G, the title compound (2.26 g, yield 74%) as a pale-yellow oil.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.19 (t, J=7.5, 3H), 2.72 (q, J=7.5, 2H), 3.93 (s, 4H), 7.38 (d, J=7.8, 1H), 7.44 (dd, J=1.2, 7.8, 1H), 7.52 (d, J=1.2, 1H), 12.52 (brs, 2H).

Reference Example 95N-(2-benzylphenyl)iminodiacetic acid

Using 2-benzylaniline (8.00 g, 43.7 mmol) and according to the methods of Reference Example 61, steps C and G, the title compound (15.0 g, yield>100%) was obtained as a colorless oil.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 3.88 (s, 4H), 4.07 (s, 2H), 6.91-6.95 (m, 2H), 7.09-7.29 (m, 7H), 12.4 (brs, 2H).

Reference Example 96N-(2-chlorophenyl)iminodiacetic acid

Using 2-chloroaniline (10.0 g, 78.4 mmol) and according to the methods of Reference Example 69, step C, and Reference Example 62, step B, the title compound (4.13 g, yield 22%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 4.07 (s, 4H), 6.98 (dd, J=1.5, 7.8, 1H), 7.12 (dd, J=1.5, 8.4, 1H), 7.21 (dd, J=1.5, 7.2, 1H), 7.35 (dd, J=1.5, 7.8, 1H), 12.54 (brs, 2H).

Reference Example 97N-(3-chlorophenyl)iminodiacetic acid

Using 3-chloroaniline (1.00 g, 7.84 mmol) and according to the methods of Reference Example 61, step C, and Reference Example 62, step B, the title compound (1.70 g, yield 89%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 4.02 (s, 4H), 6.41-6.43 (m, 2H), 6.67 (d, J=8.4, 1H), 7.16 (t, J=8.1, 1H).

Reference Example 98N-(2,5-dichlorophenyl)iminodiacetic acidStep AN-(2,5-dichlorophenyl)iminodiacetic acid diethyl ester

Using 2,5-dichloroaniline (1.00 g, 6.17 mmol) and according to the method of Reference Example 69, step C, the title compound (648 mg, yield 31%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.26 (t, J=7.1, 6H), 4.15-4.22 (m, 8H), 6.94 (dd, J=2.3, 8.4, 1H), 7.14 (d, J=2.3, 1H), 7.24-7.26 (m, 1H).

Step BN-(2,5-dichlorophenyl)iminodiacetic acid

Using the compound (647 mg, 1.94 mmol) obtained in step A and according to the method of Reference Example 62, step B, the title compound (474 mg, yield 88%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 4.08 (s, 4H), 7.03 (dd, J=2.4, 8.4, 1H), 7.10 (d, J=2.7, 1H), 7.38 (d, J=8.7, 1H), 12.59 (brs, 2H).

Reference Example 99N-(2,4-dichlorophenyl)iminodiacetic acid

Using 2,4-dichloroaniline (5.00 g, 30.9 mmol) and according to the methods of Reference Example 61, step C, and Reference Example 62, step B, the title compound (480 mg, yield 6%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 4.10 (s, 4H), 7.18-7.26 (m, 2H), 7.41 (d, J=2.1, 1H).

Reference Example 100N-(2-chloro-5-cyanophenyl)iminodiacetic acidStep A3-amino-4-chlorobenzonitrile

Using 4-chloro-3-nitrobenzonitrile (11.40 g, 62.45 mmol) and according to the method of Reference Example 61, step B, the title compound (8.00 g, yield 84%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 4.28 (brs, 2H), 6.95 (dd, J=1.5, 8.1, 1H), 7.00 (d, J=1.5, 1H), 7.33 (d, J=8.1, 1H).

Step BN-(2-chloro-5-cyanophenyl)iminodiacetic acid

Using the compound (8.00 g, 52.43 mmol) obtained in step A and according to the methods of Reference Example 69, step C, and Reference Example 62, step B, the title compound (1.92 g, yield 14%) was obtained as a pale-pink solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 4.11 (s, 4H), 7.41 (dd, J=2.1, 8.4, 1H), 7.55 (d, J=2.1, 1H), 7.57 (d, J=8.4, 1H), 12.66 (brs, 2H).

Reference Example 101N-(5-tert-butoxycarbonyl-2-chlorophenyl)iminodiacetic acidStep A4-chloro-3-nitrobenzoic acid tert-butyl ester

Using 4-chloro-3-nitrobenzoic acid (18.0 g, 89.3 mmol) and according to the method of Reference Example 61, step A, the title compound (13.62 g, yield 59%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.61 (s, 9H), 7.62 (d, J=8.7, 1H), 8.11 (dd, J=2.1, 8.4, 1H), 8.43 (d, J=1.8, 1H).

Step BN-(5-tert-butoxycarbonyl-2-chlorophenyl)iminodiacetic acid diethyl ester

Using the compound (6.00 g, 23.3 mmol) obtained in step A and according to the methods of Reference Example 61, steps B and C, the title compound (2.21 g, yield 24%) was obtained as a yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.26 (t, J=7.2, 6H), 1.57 (s, 9H), 4.08-4.22 (m, 8H), 7.36 (d, J=8.3, 1H), 7.56 (dd, J=2.0, 8.3, 1H), 7.86 (d, J=2.0, 1H).

Step CN-(5-tert-butoxycarbonyl-2-chlorophenyl)iminodiacetic acid

Using the compound (2.21 g, 5.53 mmol) obtained in step B and according to the method of Reference Example 62, step B, the title compound (1.19 g, yield 63%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.53 (s, 9H), 4.09 (s, 4H), 7.40-7.51 (m, 2H), 7.62 (s, 1H), 12.66 (brs, 2H).

Reference Example 102N-(5-chloro-2-fluorophenyl)iminodiacetic acid

Using 5-chloro-2-fluoroaniline (5.0 g, 34.4 mmol) and according to the methods of Reference Example 61, step C, and Reference Example 62, step B, the title compound (1.94 g, yield 22%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 4.06 (s, 4H), 6.70-6.83 (m, 2H), 7.10 (dd, J=8.7, 14.1, 1H), 12.65 (brs, 2H).

Reference Example 103N-(5-cyano-2-fluorophenyl)iminodiacetic acidStep A3-amino-4-fluorobenzonitrile

Using 4-fluoro-3-nitrobenzonitrile (13.64 g, 82.11 mmol) and according to the method of Reference Example 68, step A, the title compound (10.16 g, yield 91%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 3.94 (brs, 2H), 7.00-7.09 (m, 3H).

Step BN-(5-cyano-2-fluorophenyl)iminodiacetic acid

Using the compound (10.16 g, 74.63 mmol) obtained in step A and according to the methods of Reference Example 69, step C, and Reference Example 62, step B, the title compound (5.42 g, yield 29%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 4.11 (s, 4H), 7.19-7.33 (m, 3H), 12.69 (brs, 2H).

Reference Example 104N-biphenyl-3-yliminodiacetic acidStep AN-biphenyl-3-yliminodiacetic acid diethyl ester

Using biphenyl-3-ylamine (5.00 g, 29.5 mmol) and according to the method of Reference Example 61, step C, the title compound (10.0 g, yield 99%) was obtained as a pale-yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.26 (t, J=7.2, 6H), 4.12-4.25 (m, 8H), 6.61 (d, J=8.1, 1H), 6.82 (s, 1H), 7.00 (d, J=7.8, 1H), 7.25-7.42 (m, 4H), 7.53 (d, J=7.8, 2H).

Step BN-(biphenyl-3-yl)iminodiacetic acid

Using the compound (10.0 g, 29.3 mmol) obtained by the method of step A and according to the method of Reference Example 62, step B, the title compound (8.39 g, yield>100%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 4.17 (s, 4H), 6.51 (d, J=8.1, 1H), 6.71 (s, 1H), 6.94 (d, J=7.5, 1H), 7.25 (t, J=8.1, 1H), 7.34 (t, J=7.2, 1H), 7.44 (t, J=7.8, 2H), 7.58 (d, J=7.5, 2H), 12.7 (brs, 2H).

Reference Example 105N-biphenyl-2-yliminodiacetic acidStep AN-biphenyl-2-yliminodiacetic acid diethyl ester

Using biphenyl-2-ylamine (5.00 g, 29.5 mmol) and according to the method of Reference Example 61, step C, the title compound (9.51 g, yield 94%) was obtained as a colorless oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.18 (t, J=7.2, 6H), 3.85 (s, 4H), 4.08 (q, J=7.2, 4H), 7.05-7.14 (m, 2H), 7.21-7.32 (m, 3H), 7.39 (t, J=7.8, 2H), 7.66 (d, J=7.0, 2H).

Step BN-biphenyl-2-yliminodiacetic acid

Using the compound (0.91 g, 29.3 mmol) obtained by the method of step A and according to the method of Reference Example 62, step B, the title compound (0.72 g, yield 95%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 3.74 (s, 4H), 7.01 (t, J=7.5, 1H), 7.12 (q, J=7.8, 2H), 7.22 (t, J=7.5, 1H), 7.32 (d, J=7.2, 1H), 7.41 (t, J=7.2, 2H), 7.71 (d, J=7.8, 2H), 12.4 (s, 2H). % Reference Example 106:

N-(4-cyanobiphenyl-2-yl)iminodiacetic acidStep A2-nitrobiphenyl-4-carbonitrile

To N-methylpyrrolidone (25 ml) were added 4-chloro-3-nitrobenzonitrile (1.79 g, 9.80 mmol), phenylboronic acid (1.53 g, 12.5 mmol), cesium fluoride (3.90 g, 25.7 mmol) and bis(triphenylphosphine)palladium(II) dichloride (447 mg, 0.637 mmol), and the mixture was stirred with heating at 100Â° C. for 9 hr. The reaction mixture was cooled, diluted with ethyl acetate and water, and the insoluble material was filtered off through celite. The organic layer was extracted and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (1.74 g, yield 79%) as a yellow solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 7.30-7.34 (m, 2H), 7.45-7.49 (m, 3H), 7.61 (d, J=8.2, 1H), 7.90 (dd, J=1.5, 8.2, 1H), 8.14 (d, J=1.5, 1H).

Step B2-aminobiphenyl-4-carbonitrile

Using the compound (1.72 g, 7.67 mmol) obtained in step A and according to the method of Reference Example 61, step B, the title compound (1.59 g) was obtained as a colorless oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 3.95 (brs, 2H), 6.99 (d, J=1.5, 1H), 7.08 (dd, J=1.5, 7.5, 1H), 7.18 (d, J=7.5, 1H), 7.40-7.51 (m, 5H).

Step CN-(4-cyanobiphenyl-2-yl)iminodiacetic acid

Using the compound (1.59 g) obtained in step B and according to the methods of Reference Example 69, step C, and Reference Example 62, step B, the title compound (483 mg, yield from step B 20%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 3.78 (s, 4H), 7.33 (d, J=8.1, 1H), 7.36-7.49 (m, 5H), 7.72 (d, J=8.1, 2H), 12.49 (brs, 2H).

Reference Example 107N-1-naphthyliminodiacetic acid

Using 1-naphthylamine (10.0 g, 69.84 mmol) and according to the methods of Reference Example 61, step C, and Reference Example 62, step B, the title compound (16.64 g, yield 92%) was obtained as a pale-green solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 4.24 (s, 4H), 7.37-7.40 (m, 2H), 7.42-7.55 (m, 2H), 7.60-70 (m, 1H), 7.85 (dd, J=1.5, 8.6, 1H), 8.14 (dd, J=1.2, 9.1, 1H) 8.85 (brs, 2H).

Reference Example 108N-(4-chloro-1-naphthyl)iminodiacetic acid

Using 1-amino-4-chloronaphthalene (3.0 g, 16.89 mmol) and according to the methods of Reference Example 61, step C, and Reference Example 62, step B, the title compound (4.56 g, yield 92%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 4.11 (s, 4H), 7.25 (d, J=8.2, 1H), 7.60 (d, J=8.2, 1H), 7.62-7.71 (m, 2H), 8.15 (dd, J=1.7, 7.6, 1H), 8.24 (dd, J=1.7, 7.8, 1H), 12.58 (brs, 2H).

Reference Example 109N-(3-methoxy-2-naphthyl)iminodiacetic acidStep A(3-methoxy-2-naphthylamine

3-Amino-2-naphthol (7.96 g, 50.0 mmol) was dissolved in N-methylpyrrolidone (190 ml), and the mixture was stirred under ice-cooling. Then, 60% sodium hydride (2.08 g, 52 mmol) was added, and the mixture was stirred at the same temperature for 40 min. Then, ethyl iodide (3.3 ml, 53 mmol) was added, and the mixture was stirred at the same temperature for 2 hr. To the reaction mixture was added diluted aqueous sodium hydroxide solution, and the mixture was extracted with an ethyl acetate-hexane=1:1 mixed solvent. The organic layer was washed with diluted aqueous sodium hydroxide solution, water and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane), and the obtained solid was washed with hexane and dried under reduced pressure to give the title compound (4.53 g, yield 52%) as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 3.98 (s, 3H), 4.07 (brs, 2H), 7.00 (s, 1H), 7.05 (s, 1H), 7.18-7.29 (m, 2H), 7.55 (dd, J=1.5, 7.5, 1H), 7.63 (dd, J=1.5, 7.5, 1H).

Step BN-(3-methoxy-2-naphthyl)iminodiacetic acid

Using the compound (4.51 g, 26.0 mmol) obtained in step A and according to the methods of Reference Example 61, step C, and Reference Example 62, step B, the title compound (6.06 g, yield 80%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 3.86 (s, 3H), 4.12 (s, 4H), 7.03 (s, 1H), 7.25 (s, 1H), 7.22-7.29 (m, 2H), 7.59-7.64 (m, 1H), 7.65-7.71 (m, 1H), 12.45 (brs, 2H).

Reference Example 110N-(5,6,7,8-tetrahydronaphthalen-1-yl)iminodiacetic acid

Using 5,6,7,8-tetrahydronaphthalen-1-ylamine (5.34 g, 36.27 mmol) and according to the methods of Reference Example 61, step C, and Reference Example 62, step B, the title compound (8.28 g, yield 87%) was obtained as a pale-showy pink solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.55-1.75 (m, 4H), 2.64-2.73 (m, 4H), 3.86 (s, 4H), 6.75 (dd, J=1.2, 7.1, 1H), 6.92-7.01 (m, 2H), 12.40 (brs, 2H).

Reference Example 111N-(2,3-dihydro-1H-inden-4-yl)iminodiacetic acid

Using 4-aminoindane (5.0 g, 37.54 mmol) and according to the methods of Reference Example 61, step C, and Reference Example 62, step B, the title compound (8.53 g, yield 91%) was obtained as a pale-bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.85-2.00 (m, 2H), 2.75-2.82 (m, 4H), 3.99 (s, 4H), 6.49 (d, J=7.8, 1H), 6.75 (d, J=7.2, 1H), 6.96 (t, J=7.5, 1H), 12.51 (brs, 2H).

Reference Example 112N-(5-cyano-2,3-dihydro-1-benzofuran-7-yl)iminodiacetic acidStep Atert-butyl (5-bromo-2,3-dihydro-1-benzofuran-7-yl)carbamate

To toluene (30 ml) were added 5-bromo-2,3-dihydro-1-benzofuran-7-carboxylic acid (5.00 g, 20.6 mmol), N,N-diisopropylethylamine (4.3 ml, 24.7 mmol), diphenylphosphorylazide (6.36 g, 22.7 mmol) and tert-butanol (25 ml), and the mixture was heated under reflux for 10 hr. The reaction mixture was concentrated under reduced pressure, diluted with ethyl acetate, washed with diluted hydrochloric acid, diluted aqueous sodium hydroxide solution and saturated brine, and dried over anhydrous magnesium sulfate. The solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (6.27 g, yield 97%) as a pale-yellow oil.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.44 (s, 9H), 3.20 (t, J=8.7, 2H), 4.55 (t, J=8.7, 2H), 7.12 (d, J=1.5, 1H), 7.50 (s, 1H), 8.60 (s, 1H).

Step B(5-bromo-2,3-dihydro-1-benzofuran-7-yl)amine hydrochloride

The compound (6.27 g, 20.0 mmol) obtained in step A was dissolved in ethyl acetate, 4N hydrochloric acid-ethyl acetate solution (25 ml, 100 mmol) was added at room temperature with stirring, and the mixture was stirred at the same temperature overnight. The precipitated solid was filtered, washed with ethyl acetate, and dried under reduced pressure to give the title compound (4.65 g, yield 93%) as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 3.23 (t, J=8.7, 2H), 4.62 (t, J=8.7, 2H), 7.13-7.22 (m, 2H), 8.00 (brs, 3H).

Step CN-(5-bromo-2,3-dihydro-1-benzofuran-7-yl)iminodiacetic acid diethyl ester

Using the compound (4.65 g, 18.6 mmol) obtained in step B and according to the method of Reference Example 69, step C, the title compound (6.04 g, yield 84%) was obtained as a yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.27 (t, J=7.1, 6H), 3.13 (t, J=8.8, 2H), 4.15 (s, 4H), 4.20 (q, J=7.1, 4H), 4.52 (t, J=8.8, 2H), 6.62 (d, J=1.6, 1H), 6.85 (s, 1H).

Step DN-(5-cyano-2,3-dihydro-1-benzofuran-7-yl)iminodiacetic acid diethyl ester

To N,N-dimethylformamide (50 ml) were added the compound (6.04 g, 15.6 mmol) obtained in step C, zinc cyanide (1.84 g, 15.6 mmol) and tetrakis(triphenylphosphine)palladium(0) (3.61 g, 3.12 mmol), and the mixture was stirred with heating at 100Â° C. for 5 hr. The reaction mixture was cooled to room temperature, diluted aqueous ammonia was added, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (1.91 g, yield 37%) as a pale-bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.18 (t, J=7.1, 6H), 3.16 (t, J=8.9, 2H), 4.10 (q, J=6.9, 4H), 4.19 (s, 4H), 4.55 (t, J=8.9, 2H), 6.84 (s, 1H), 7.16 (s, 1H).

Step EN-(5-cyano-2,3-dihydro-1-benzofuran-7-yl)iminodiacetic acid

Using the compound (1.91 g, 5.75 mmol) obtained in step D and according to the method of Reference Example 62, step B, the title compound (1.58 g, yield 99%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 3.16 (t, J=8.4, 2H), 4.12 (s, 4H), 4.57 (t, J=8.4, 2H), 6.77 (s, 1H), 7.14 (s, 1H), 12.54 (brs, 2H).

Reference Example 113N-(1,7-dimethyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-yl)iminodiacetic acidStep A7-methyl-6-nitro-3,4-dihydroquinolin-2(1H)-one

7-Methyl-3,4-dihydroquinolin-2(1H)-one (10.0 g, 62.0 mmol) obtained by the method described in Chemical & Pharmaceutical Bulletin, 367 (1968) was suspended in nitromethane (200 ml), and the suspension was stirred under ice-cooling. Then, an ice-cooled nitric acid (8.3 ml)-water (18.2 ml)-sulfuric acid (116 ml) mixed solution was slowly added dropwise, and thereafter added dropwise at room temperature. The mixture was stirred for 2 hr. To the reaction mixture was added ice water, the solution was extracted with ethyl acetate, and the organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solution was concentrated under reduced pressure, and the precipitated solid was washed with ethyl acetate and dried under reduced pressure to give the title compound (3.14 g, yield 25%) as a pale-bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.48-2.55 (m, 5H), 2.96 (t, J=7.8, 2H), 6.82 (s, 1H), 7.96 (s, 1H), 10.55 (brs, 1H).

Step B6-amino-1,7-dimethyl-3,4-dihydroquinolin-2(1H)-one

The compound (3.14 g, 15.2 mmol) obtained in step A was dissolved in N,N-dimethylformamide (30 ml), 60% sodium hydride (730 mg, 18.2 mmol) was added under ice-cooling with stirring, and thereafter the mixture was stirred at room temperature for 30 min. The reaction mixture was ice-cooled again, methyl iodide (1.9 ml, 30.4 mmol) was added with stirring, and the mixture was stirred at room temperature for 1 hr. To the reaction mixture was added water, and the precipitated solid was collected by filtration, washed with water, and dried under reduced pressure to give a bistered solid. Using this solid and according to the method of Reference Example 116, step B, the title compound (1.76 g, yield 61%) was obtained as a pale-bistered solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.17 (s, 3H), 2.55-2.61 (m, 2H), 2.75-2.80 (m, 2H), 3.31 (s, 3H), 3.51 (brs, 2H), 6.50 (s, 1H), 6.69 (s, 1H).

Step CN-(1,7-dimethyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-yl)iminodiacetic acid diethyl ester

Using the compound (1.50 g, 7.88 mmol) obtained in step B and according to the method of Reference Example 61, step C, the title compound (1.85 g, yield 65%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.2, 6H), 2.27 (s, 3H), 2.44-2.54 (m, 2H), 2.75 (t, J=7.4, 2H), 3.20 (s, 3H), 3.94 (s, 4H), 4.05 (q, J=7.2, 4H), 6.87 (s, 1H), 7.02 (s, 1H).

Step DN-(1,7-dimethyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-yl)iminodiacetic acid

Using the compound (1.85 g, 5.10 mmol) obtained in step C and according to the method of Reference Example 62, step B, the title compound (1.05 g, yield 67%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.26 (s, 3H), 2.43-2.55 (m, 2H), 2.75 (t, J=7.4, 2H), 3.20 (s, 3H), 3.87 (s, 4H), 6.87 (s, 1H), 6.99 (s, 1H), 12.35 (brs, 2H).

Reference Example 114N-(1-ethyl-7-methyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-yl)iminodiacetic acidStep A7-methyl-2-oxo-1,2,3,4-tetrahydroquinoline-6-carboxylic acid

7-Methyl-3,4-dihydroquinolin-2(1H)-one (80.0 g, 500 mmol) obtained by the method described in Chemical & Pharmaceutical Bulletin, 367 (1968), and chloroacetylchloride (85.0 g, 750 mmol) were dissolved in 1,2-dichloroethane (800 ml), aluminum chloride (165 g, 1.25 mol) was gradually added at room temperature with stirring, and thereafter the mixture was stirred at 40Â° C. for 1 hr. The reaction mixture was slowly poured into ice water, the precipitated solid was collected by filtration, and the obtained solid was washed with water and dried under reduced pressure to give a colorless solid. This solid was added to pyridine (750 ml) at room temperature, and then the mixture was stirred at 90Â° C. for 30 min. The reaction mixture was cooled to room temperature, and the precipitated solid was collected by filtration, and dried under reduced pressure. The obtained solid was added to 10% aqueous sodium hydroxide solution (1000 ml), and the mixture was stirred at 90Â° C. for 2.5 hr. The reaction mixture was cooled to room temperature, activated carbon was added, and the insoluble material was filtered off through celite. Concentrated hydrochloric acid was added to adjust the obtained solution to pH 1, and the precipitated solid was collected by filtration, washed with water, and dried under reduced pressure to give the title compound (78.0 g, yield 76%) as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.43-2.53 (m, 5H), 2.87 (t, J=7.5, 2H), 6.71 (s, 1H), 7.70 (s, 1H), 10.28 (s, 1H), 12.48 (brs, 1H).

Step B7-methyl-2-oxo-1,2,3,4-tetrahydroquinoline-6-carboxylic acid ethyl ester

To the compound (40.0 g, 195 mmol) obtained in step A were added ethanol (600 ml) and concentrated sulfuric acid (60 ml), and the mixture was heated under reflux for 24 hr. After cooling to room temperature, the solution was concentrated under reduced pressure. The obtained oil was diluted with water, and extracted with chloroform. The organic layer was washed with diluted aqueous sodium hydroxide solution, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained solid was recrystallized from ethanol to give the title compound (32.0 g, yield 70%) as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.30 (t, J=6.9, 3H), 2.43-2.52 (m, 2H), 2.45 (s, 3H), 2.89 (t, J=7.4, 2H), 4.24 (q, J=6.9, 2H), 6.73 (s, 1H), 7.69 (s, 1H), 10.34 (brs, 1H).

Step C1-ethyl-7-methyl-2-oxo-1,2,3,4-tetrahydroquinoline-6-carboxylic acid ethyl ester

Using the compound (10.0 g, 42.9 mmol) obtained in step B and ethyl iodide (6.86 ml, 85.8 mmol), and according to the method of Reference Example 113, step B, the title compound (9.54 g, yield 85%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.27 (t, J=7.2, 3H), 1.39 (t, J=7.2, 3H), 2.61-2.67 (m, 2H), 2.62 (s, 3H), 2.86-2.92 (m, 2H), 4.00 (q, J=7.2, 2H), 4.35 (q, J=7.2, 2H), 6.84 (s, 1H), 7.76 (s, 1H).

Step D1-ethyl-7-methyl-2-oxo-1,2,3,4-tetrahydroquinoline-6-carboxylic acid

The compound (9.54 g, 36.5 mmol) obtained in step C was dissolved in methanol (100 ml), 1N sodium hydroxide (100 ml) was added at room temperature with stirring, and the mixture was stirred at the same temperature overnight. The reaction mixture was concentrated under reduced pressure, 1N hydrochloric acid (160 ml) was added, and the solution was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained solid was washed with a diisopropyl ether-isopropanol mixed solvent, and dried under reduced pressure to give the title compound (8.17 g, yield 96%) as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.13 (t, J=6.9, 3H), 2.50-2.56 (m, 2H), 2.55 (s, 3H), 2.85 (t, J=7.2, 2H), 3.92 (q, J=6.9, 2H), 7.03 (s, 1H), 7.71 (s, 1H), 12.58 (brs, 1H).

Step Etert-butyl (1-ethyl-7-methyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-yl)carbamate

Using the compound (4.65 g, 18.6 mmol) obtained in step D and according to the method of Reference Example 112, step A, the title compound (6.07 g, yield 57%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.11 (t, J=6.9, 3H), 1.45 (s, 9H), 2.18 (s, 3H), 2.44-2.51 (m, 2H), 2.73-2.79 (m, 2H), 3.87 (q, J=6.9, 2H), 6.93 (s, 1H), 7.11 (s, 1H), 8.46 (brs, 1H).

Step F6-amino-1-ethyl-7-methyl-3,4-dihydroquinolin-2(1H)-one hydrochloride

Using the compound (6.07 g, 19.9 mmol) obtained in step E and according to the method of Reference Example 112, step B, the title compound (4.41 g, yield 92%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.12 (t, J=6.9, 3H), 2.35 (s, 3H), 2.48-2.54 (m, 2H), 2.76-2.84 (m, 2H), 3.90 (q, J=6.9, 2H), 7.09 (s, 1H), 07.23 (s, 1H), 9.61-10.39 (broad, 3H).

Step GN-(1-ethyl-7-methyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-yl)iminodiacetic acid

Using the compound (4.41 g, 18.3 mmol) obtained in step F and according to the methods of Reference Example 61, step C, and Reference Example 62, step B, the title compound (3.81 g, yield 65%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.11 (t, J=6.9, 3H), 2.26 (s, 3H), 2.43-2.52 (m, 2H), 2.70-2.76 (m, 2H), 3.80-3.89 (m, 2H), 3.88 (s, 4H), 6.90 (s, 1H), 6.98 (s, 1H), 12.39 (brs, 2H).

Reference Example 115N-(3-methoxy-8-oxo-5,6,7,8-tetrahydronaphthalen-2-yl)iminodiacetic acidStep A6-methoxy-7-nitro-3,4-dihydronaphthalen-1(2H)-one

6-Methoxy-1-tetralone (12.0 g, 68.1 mmol) was dissolved in acetic anhydride (60 ml), a fuming nitric acid (4.8 ml)-acetic acid (4.2 ml) mixed solvent was slowly added dropwise under ice-cooling with stirring, and thereafter the mixture was stirred at the same temperature for 2 hr. The reaction mixture was diluted with ether, and the precipitated solid was collected by filtration and dried under reduced pressure. The obtained solid was recrystallized from benzene (100 ml), and the precipitated solid was filtered, dried under reduced to pressure to give the title compound (3.62 g, yield 24%) as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.17 (m, 2H), 2.66 (t, J=6.2, 2H), 3.01 (t, J=6.0, 2H), 4.01 (s, 3H), 6.90 (s, 1H), 8.50 (s, 1H).

Step B7-amino-6-methoxy-3,4-dihydronaphthalen-1(2H)-one

Using the compound (0.50 g, 2.26 mmol) obtained in step A and according to the method of Reference Example 68, step A, the title compound (0.50 g) was obtained as a red-bistered oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.08 (m, 2H), 2.56 (t, J=6.3, 2H), 2.85 (t, J=6.3, 2H), 3.80 (brs, 2H), 3.90 (s, 3H), 6.58 (s, 1H), 7.35 (s, 1H).

Step CN-(3-methoxy-8-oxo-5,6,7,8-tetrahydronaphthalen-2-yl)iminodiacetic acid diethyl ester

Using the compound (0.50 g) obtained in step B and according to the method of Reference Example 61, step C, the title compound (0.94 g) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.27 (t, J=7.2, 6H), 2.04-2.11 (m, 2H), 2.55 (t, J=6.3, 2H), 2.86 (t, J=6.0, 2H), 3.87 (s, 3H), 4.12 (s, 4H), 4.19 (q, J=7.2, 4H), 6.63 (s, 1H), 7.51 (s, 1H).

Step DN-(3-methoxy-8-oxo-5,6,7,8-tetrahydronaphthalen-2-yl)iminodiacetic acid

Using the compound (0.94 g) obtained by the method of step C and according to the method of Reference Example 62, step B, the title compound (0.70 g, yield from step B>100%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.96-2.01 (m, 2H), 2.45-2.52 (m, 2H), 2.82-2.87 (m, 2H), 3.82 (s, 3H), 3.99 (s, 4H), 6.84 (s, 1H), 7.22 (s, 1H), 12.42 (brs, 2H).

Reference Example 116N-(3,6-dimethyl-1,2-benzisoxazol-5-yl)iminodiacetic acidStep AN-(4-methoxy-2-methylphenyl)acetamide

4-Methoxy-2-methylaniline (26.06 g, 190 mmol) and triethylamine (43 ml, 309 mmol) were dissolved in dichloromethane, acetic anhydride (25 ml, 265 mmol) was added under ice-cooling, and the mixture was stirred at the same temperature for 80 min. To the reaction mixture was added 10% aqueous citric acid solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with diluted hydrochloric acid, saturated aqueous sodium hydrogen carbonate and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained solid was filtered, washed with hexane, and dried under reduced pressure to give the title compound (30.78 g, yield 90%) as a pale-pink solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.00 (s, 3H), 2.14 (s, 3H), 3.71 (s, 3H), 6.71 (dd, J=3.0, 8.7, 1H), 6.77 (d, J=3.0, 1H), 7.18 (d, J=8.7, 1H), 9.16 (s, 1H).

Step BN-(5-acetyl-4-hydroxy-2-methylphenyl)acetamide

The compound (31.43 g, 175.4 mmol) obtained by the method of step A was dissolved in dichloromethane (500 ml). Acetyl chloride (40 ml, 561 mmol) and aluminum chloride (93.3 g, 700 mmol) were successively added thereto under ice-cooling with stirring, and the mixture was heated under reflux for 2 hr. The reaction mixture was cooled, poured into ice water, directly stirred for 2 hr, and extracted with dichloromethane. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained solid was filtered, and washed with hexane to give the title compound (35.46 g, yield 98%) as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.03 (s, 3H), 2.19 (s, 3H), 2.57 (s, 3H), 6.83 (s, 1H), 7.77 (s, 1H), 9.32 (s, 1H), 11.81 (s, 1H).

Step CN-[4-hydroxy-5-(N-hydroxyethaneimidoyl)-2-methylphenyl]acetamide

To an ethanol (560 ml)-water (180 ml) mixed solvent were added the compound (35.46 g, 171.1 mmol) obtained in step B, hydroxylammonium chloride (19.41 g, 279.3 mmol) and sodium acetate (22.83 g, 278.3 mmol), and the mixture was heated under reflux for 70 min. The reaction mixture was cooled, water (500 ml) was added, and the solution was concentrated under reduced pressure (about 300 ml) to allow precipitation of a solid. Water (500 ml) was added hereto again, and the precipitated solid was filtered, washed with water, and dried under reduced pressure to give the title compound (32.7 g, yield 86%) as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.01 (s, 3H), 2.12 (s, 3H), 2.19 (s, 3H), 6.72 (s, 1H), 7.35 (s, 1H), 9.22 (s, 1H), 11.37 (s, 1H), 11.48 (s, 1H).

Step D3,6-dimethyl-1,2-benzisoxazol-5-amine

To N,N-dimethylformamide-dimethylacetal (90 ml) was added the compound (32.7 g, 147 mmol) obtained in step C, and the mixture was stirred with heating at 100Â° C. for 7 min. The reaction mixture was cooled, water (700 ml) was added, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure to give a brown solid (20.45 g). This was added to 3N aqueous hydrochloric acid solution (600 ml), and the mixture was heated under reflux for 80 min. The reaction mixture was ice-cooled, and an aqueous solution of sodium hydroxide (80 g) was added at the same temperature. The precipitated solid was collected by filtration, washed with water, and dried under reduced pressure to give the title compound (12.6 g, yield 53%) as a yellow bistered solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.32 (s, 3H), 2.50 (s, 3H), 3.64 (brs, 2H), 6.81 (s, 1H), 7.26 (s, 1H).

Step EN-(3,6-dimethyl-1,2-benzisoxazol-5-yl)iminodiacetic acid diethyl ester

Using the compound (11.5 g, 71.0 mmol) obtained in step D and according to the method of Reference Example 61, step C, the title compound (19.8 g, yield 83%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.22 (t, J=7.2, 6H), 2.51 (s, 3H), 2.53 (s, 3H), 4.05 (s, 4H), 4.13 (q, J=7.2, 4H), 7.35 (s, 1H), 7.55 (s, 1H).

Step FN-(3,6-dimethyl-1,2-benzisoxazol-5-yl)iminodiacetic acid

Using the compound (16.59 g, 49.62 mmol) obtained in step E and according to the method of Reference Example 62, step B, the title compound (13.58 g, yield 98%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.44 (s, 3H), 2.48 (s, 3H), 3.95 (s, 4H), 7.49 (s, 1H), 7.58 (s, 1H), 12.40 (brs, 2H).

Reference Example 117N-(3,5-dimethyl-1,2-benzisoxazol-6-yl)iminodiacetic acidStep AN-(5-methoxy-2-methylphenyl)acetamide

Using 5-methoxy-2-methylaniline (10.22 g, 74.5 mmol) and according to the method of Reference Example 116, step A, the title compound (10.88 g, yield 81%) was obtained as a yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.99 (s, 3H), 2.11 (s, 3H), 3.69 (s, 3H), 6.65 (dd, J=2.4, 8.3, 1H), 7.07 (d, J=2.4, 1H), 7.08 (d, J=8.3, 1H), 9.18 (brs, 1H).

Step BN-(4-acetyl-5-hydroxy-2-methylphenyl)acetamide

Using the compound (3.58 g, 19.98 mmol) obtained in step A and according to the method of Reference Example 116, step B, the title compound (3.00 g, yield 72%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.13 (s, 3H), 2.22 (s, 3H), 2.58 (s, 3H), 7.47 (s, 1H), 7.70 (s, 1H), 9.21 (s, 1H), 11.96 (s, 1H).

Step CN-[5-hydroxy-4-(N-hydroxyethaneimidoyl)-2-methylphenyl]acetamide

Using the compound (2.99, 14.43 mmol) obtained in step B and according to the method of Reference Example 116, step C, the title compound (2.94 g, yield 92%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.07 (s, 3H), 2.16 (s, 3H), 2.22 (s, 3H), 7.17 (s, 1H), 7.27 (s, 1H), 9.13 (s, 1H), 11.35 (s, 1H), 11.38 (s, 1H).

Step D3,5-dimethyl-1,2-benzisoxazol-6-amine

Using the compound (2.94 g, 13.23 mmol) obtained in step C and according to the method of Reference Example 116, step D, the title compound (1.14 g, yield 53%) was obtained as a dark green solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.25 (s, 3H), 2.47 (s, 3H), 3.99 (brs, 2H), 6.74 (s, 1H), 7.24 (s, 1H).

Step EN-(3,5-dimethyl-1,2-benzisoxazol-6-yl)iminodiacetic acid diethyl ester

Using the compound (1.13 g, 6.97 mmol) obtained in step D and according to the method of Reference Example 69, step C, the title compound (1.02 g, yield 44%) was obtained as a pale-yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.24 (t, J=7.2, 6H), 2.43 (s, 3H), 2.51 (s, 3H), 4.10 (s, 4H), 4.15 (q, J=7.2, 4H), 7.31 (s, 1H), 7.38 (s, 1H).

Step FN-(3,5-dimethyl-1,2-benzisoxazol-6-yl)iminodiacetic acid

Using the compound (1.02 g, 3.05 mmol) obtained in step E and according to the method of Reference Example 62, step B, the title compound (698 mg, yield 82%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.35 (s, 3H), 2.46 (s, 3H), 4.02 (s, 4H), 7.22 (s, 1H), 7.55 (s, 1H), 12.57 (brs, 2H).

Reference Example 118N-(6-methyl-1,3-benzodioxol-5-yl)iminodiacetic acidStep A5-methyl-6-nitro-1,3-benzodioxole

5-Methyl-1,3-benzodioxole (8.00 g, 58.8 mmol) was dissolved in chloroform (160 ml), and the mixture was stirred under ice-cooling. To this solution was gradually added 60% nitric acid (20 ml), and the mixture was stirred at room temperature for 30 min. The reaction mixture was diluted with dichloromethane, washed with water and saturated aqueous sodium hydrogen carbonate, and dried over potassium carbonate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure to give the title compound (9.58 g, yield 90%) as a pale-yellow solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.55 (s, 3H), 6.08 (s, 2H), 6.70 (s, 1H), 7.50 (s, 1H).

Step B6-methyl-1,3-benzodioxol-5-amine

Using the compound (9.58 g, 52.9 mmol) obtained in step A and according to the method of Reference Example 61, step B, the title compound (8.00 g, yield 100%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.08 (s, 3H), 3.31 (brs, 2H), 5.81 (s, 2H), 6.28 (s, 1H), 6.56 (s, 1H).

Step CN-(6-methyl-1,3-benzodioxol-5-yl)iminodiacetic acid diethyl ester

Using the compound (8.00 g, 52.9 mmol) obtained in step B and according to the method of Reference Example 61, step C, the title compound (15.8 g, yield 92%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.23 (t, J=7.2, 6H), 2.27 (s, 3H), 3.93 (s, 4H), 4.13 (q, J=7.2, 4H), 5.87 (s, 2H), 6.63 (s, 1H), 6.87 (s, 1H).

Step DN-(6-methyl-1,3-benzodioxol-5-yl)iminodiacetic acid

Using the compound (5.00 g, 15.5 mmol) obtained in step C and according to the method of Reference Example 62, step B, the title compound (3.11 g, yield 75%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.18 (s, 3H), 3.82 (s, 4H), 5.90 (s, 2H), 6.71 (s, 1H), 6.81 (s, 1H), 12.4 (brs, 2H).

Reference Example 119N-(3,6-dimethyl-2-oxo-2,3-dihydro-1,3-benzoxazol-5-yl)iminodiacetic acidStep A3,6-dimethyl-1,3-benzoxazol-2(3H)-one

3-Methyl-2-oxo-2,3-dihydro-1,3-benzoxazole-6-carbaldehyde (4.41 g, 24.9 mmol) obtained by the method described in JP-A-10-139780 was dissolved in ethyl acetate (100 ml), 10% palladium carbon (containing water) (2.0 g) and acetic acid (20 ml) were added, and the mixture was stirred at room temperature for 12 hr under a hydrogen atmosphere. The insoluble material was filtered off through celite, and the solution was concentrated under reduced pressure to give the title compound (3.33 g, yield 82%) as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.34 (s, 3H), 3.31 (s, 3H), 7.04 (d, J=8.1, 1H), 7.13 (d, J=8.1, 1H), 7.17 (s, 1H).

Step B3,6-dimethyl-5-nitro-1,3-benzoxazol-2(3H)-one

The compound (3.33 g, 20.4 mmol) obtained in step A was dissolved in trifluoroacetic acid (60 ml), sodium nitrite (1.41 g, 20.4 mmol) was gradually added under ice-cooling with stirring, and the mixture was stirred at room temperature for 3 hr. The reaction solution was poured into ice water, and the precipitated solid was collected by filtration, washed with water, and dried under reduced pressure to give the title compound (2.75 g, yield 65%) as a pale-bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.54 (s, 3H), 3.38 (s, 3H), 7.51 (s, 1H), 8.00 (s, 1H).

Step C5-amino-3,6-dimethyl-1,3-benzoxazol-2(3H)-one

Using the compound (2.75 g, 13.2 mmol) obtained in step B and according to the method of Reference Example 69, step B, the title compound (1.95 g, yield 83%) was obtained as a pale-pink solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.06 (s, 3H), 3.23 (s, 3H), 4.83 (brs, 2H), 6.43 (s, 1H), 6.92 (s, 1H).

Step DN-(3,6-dimethyl-2-oxo-2,3-dihydro-1,3-benzoxazol-5-yl)iminodiacetic acid

Using the compound (1.95 g, 10.94 mmol) obtained in step C and according to the methods of Reference Example 61, step C, and Reference Example 62, step B, the title compound (2.45 g, yield 76%) was obtained as a bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.29 (s, 3H), 3.28 (s, ³H), 3.91 (s, 4H), 7.09 (s, 1H), 7.13 (s, 1H), 12.39 (brs, 2H).

Reference Example 120N-(3,5-dimethyl-2-oxo-2,3-dihydro-1,3-benzoxazol-6-yl)iminodiacetic acidStep A5-methyl-1,3-benzoxazol-2(3H)-one

2-Amino-4-methylphenol (5.00 g, 40.6 mmol) and triethylamine (17 ml, 122 mmol) were dissolved in chloroform (100 ml), ethyl chloroformate (5.8 ml, 61 mmol) was added at room temperature with stirring, and thereafter the mixture was stood at the same temperature overnight. Water was added to the reaction mixture, the mixture was extracted with chloroform, and the organic layer was dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. N,N-Dimethylformamide (35 ml) and potassium carbonate (11.2 g, 81.2 mmol) were added to the obtained residue, and the mixture was stirred at 70Â° C. for 9 hr. The reaction mixture was cooled to room temperature, and 3N hydrochloric acid was added with stirring. The precipitated solid was filtered, washed with water, and dried under reduced pressure to give the title compound (4.94 g, yield 82%) as a pale-bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.31 (s, 3H), 6.85-6.90 (m, 2H), 7.14 (d, J=7.8, 1H), 11.53 (brs, 1H).

Step B5-methyl-6-nitro-1,3-benzoxazol-2(3H)-one

Using the compound (3.94 g, 26.4 mmol) obtained in the same manner as in step A and according to the method of Reference Example 119, step B, the title compound (2.60 g, yield 51%) was obtained as a pale-bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.56 (s, 3H), 7.17 (s, 1H), 8.03 (s, 1H), 12.28 (brs, 1H).

Step C3,5-dimethyl-6-nitro-1,3-benzoxazol-2(3H)-one

Using the compound (3.26 g, 16.8 mmol) obtained by the method of step B and methyl iodide (2.09 ml, 33.6 mmol), and according to the method of Reference Example 113, step B, the title compound (3.21 g, yield 92%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.60 (s, 3H), 3.37 (s, 3H), 7.40 (s, 1H), 8.09 (s, 1H).

Step D6-amino-3,5-dimethyl-1,3-benzoxazol-2(3H)-one

Using the compound (3.21 g, 15.4 mmol) obtained by the method of step C and according to the method of Reference Example 69, step B, the title compound (764 mg, yield 28%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆): Î´(ppm) 2.08 (s, 3H), 3.23 (s, 3H), 4.78 (brs, 2H), 6.60 (s, 1H), 6.83 (s, 1H).

Step EN-(3,5-dimethyl-2-oxo-2,3-dihydro-1,3-benzoxazol-6-yl)iminodiacetic acid

Using the compound (764 mg, 4.29 mmol) obtained in step D and according to the methods of Reference Example 61, step C, and Reference Example 62, step B, the title compound (678 mg, yield 54%) was obtained as a bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.32 (s, 3H), 3.28 (s, 3H), 3.88 (s, 4H), 7.04 (s, 1H), 7.19 (s, 1H), 12.42 (brs, 2H).

The compounds of Reference Examples 91-120 are shown below.

TABLE 4ReferenceStructuralExampleFormula91 [Image Omitted]

92

93

94

95

96

97

98

99

100

101

102

103

104

105

106

107

108

109

110

111

112

113

114

115

116

117

118

119

120

Reference Example 121N-(4-iodo-2-methylphenyl)iminodiacetic acidStep AN-(4-iodo-2-methylphenyl)iminodiacetic acid diethyl ester

Using 4-iodo-2-methylaniline (4.66 g, 20.0 mmol) and according to the method of Reference Example 61, step C, the title compound (8.05 g, yield 99%) was obtained as a brown oil.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.14 (t, J=7.0, 6H), 2.21 (s, 3H), 3.98 (s, 4H), 4.04 (q, J=7.1, 4H), 6.90 (d, J=8.5, 1H), 7.40 (dd, J=8.4, 2.0, 1H), 7.49 (d, J=1.8, 1H).

Step BN-(4-iodo-2-methylphenyl)iminodiacetic acid

Using the compound (8.05 g, 1.99 mmol) obtained in step A and according to the method of Reference Example 61, step G, the title compound (6.93 g, yield 100%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 2.20 (s, 3H), 3.90 (s, 4H), 6.86 (d, J=8.5, 1H), 7.40 (dd, J=8.5, 2.0, 1H), 7.47 (d, J=1.9, 1H), 12.45 (brs, 2H).

Reference Example 122N-[2-methyl-4-(3-methylisoxazol-5-yl)phenyl]iminodiacetic acidStep AN-[2-methyl-4-(3-methylisoxazol-5-yl)phenyl]iminodiacetic acid diethyl ester

To toluene (4 ml) were added the compound (810 mg, 2.00 mmol) of Reference Example 121, step A, 5-(tri-n-butylstanyl)-3-methylisoxazole (1.12 g, 3.01 mmol), which is the compound described in Tetrahedron, 47 (1991) 5111-5118, bis(triphenylphosphine)palladium(II)dichloride (140 mg, 0.199 mmol) and lithium chloride (170 mg, 4.01 mmol), and the mixture was heated under reflux for 2 hr. The reaction mixture was cooled, diluted with ethyl acetate, washed with water and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (428 mg, yield 59%) as a brown oil.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.2, 6H), 2.26 (s, 3H), 2.30 (s, 3H), 4.06 (s, 4H), 4.07 (q, J=7.2, 4H), 6.71 (s, 1H), 7.13 (d, J=8.5, 1H), 7.54 (dd, J=8.4, 2.0, 1H), 7.60 (d, J=1.6, 1H).

Step BN-[2-methyl-4-(3-methylisoxazol-5-yl)phenyl]iminodiacetic acid

Using the compound (428 mg, 1.19 mmol) obtained in step A and according to the method of Reference Example 61, step G, the title compound (388 mg, yield>100%) was obtained as a brown solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 2.25 (s, 3H), 2.30 (s, 3H), 3.98 (s, 4H), 6.69 (s, 1H), 7.08 (d, J=8.4, 1H), 7.52-7.54 (m, 1H), 7.58 (d, J=1.7, 1H), 12.55 (brs, 2H).

Reference Example 123N-[2-methyl-5-(3-methylisoxazol-5-yl)phenyl]iminodiacetic acidStep AN-[2-methyl-5-(3-methylisoxazol-5-yl)phenyl]iminodiacetic acid diethyl ester

Using the compound (716 mg, 2.00 mmol) of Reference Example 89, step A, and 5-(tri-n-butylstanyl)-3-methylisoxazole (819 mg, 2.20 mmol), and according to the method of Reference Example 122, step A, the title compound (388 mg, yield 54%) was obtained as a pale-yellow oil.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.13 (t, J=7.1, 6H), 2.27 (s, 3H), 2.30 (s, 3H), 4.05 (q, J=7.2, 4H), 4.06 (s, 4H), 6.78 (s, 1H), 7.28 (d, J=7.9, 1H), 7.39-7.41 (m, 1H), 7.53 (s, 1H).

Step BN-[2-methyl-5-(3-methylisoxazol-5-yl)phenyl]iminodiacetic acid

Using the compound (388 mg, 1.08 mmol) obtained in step A and according to the method of Reference Example 61, step G, the title compound (333 mg, yield>100%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 2.27 (s, 3H), 2.30 (s, 3H), 3.98 (s, 4H), 6.76 (s, 1H), 7.27 (d, J=7.9, 1H), 7.36 (dd, J=7.8, 1.2, 1H), 7.48 (d, J=1.2, 1H), 12.50 (brs, 2H).

Reference Example 124N-(4-acetyl-2-methylphenyl)iminodiacetic acidStep A1-(4-amino-3-methylphenyl)ethanone

Using 1-(3-methyl-4-nitrophenyl)ethanone (5.46 g, 30.5 mmol) and according to the method of Reference Example 68, step A, the title compound (4.33 g, yield 95%) was obtained as a yellow solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 2.19 (s, 3H), 2.51 (s, 3H), 4.07 (brs, 2H), 6.64 (d, J=8.2, 1H), 7.68 (d, J=2.0, 1H), 7.71 (dd, J=2.0, 8.2, 1H).

Step BN-(4-acetyl-2-methylphenyl)iminodiacetic acid diethyl ester

Using the compound (4.33 g, 29.0 mmol) obtained in step A and according to the method of Reference Example 61, step C, the title compound (5.87 g, yield 63%) was obtained as a yellow oil.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.25 (t, J=7.1, 6H), 2.36 (s, 3H), 2.54 (s, 3H), 4.09 (s, 4H), 4.17 (q, J=7.1, 4H), 7.10 (d, J=8.4, 1H), 7.72 (dd, J=1.8, 8.4, 1H), 7.78 (d, J=1.8, 1H).

Step CN-(4-acetyl-2-methylphenyl)iminodiacetic acid

Using the compound (5.86 g, 18.2 mmol) obtained in step B and according to the method of Reference Example 61, step G, the title compound (3.43 g, yield 71%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 2.29 (s, 3H), 2.48 (s, 3H), 4.01 (s, 4H), 6.97 (d, J=8.4, 1H), 7.67 (d, J=1.9, 1H), 7.70 (dd, J=1.9, 8.4, 1H), 12.61 (brs, 2H).

Reference Example 125N-(6-methyl-1-oxo-2,3-dihydro-1H-inden-5-yl)iminodiacetic acidStep AN-(5-iodo-2-methylphenyl)iminodiacetic acid diethyl ester

Using 5-iodo-2-methylaniline (4.66 g, 20 mmol) and according to the method of Reference Example 61, step C, the title compound (8.31 g, yield>100%) was obtained as a pale-yellow oil.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.1, 6H), 2.20 (s, 3H), 3.98 (s, 4H), 4.06 (q, J=7.1, 4H), 6.93 (d, J=8.0, 1H), 7.28 (dd, J=7.9, 1.5, 1H), 7.39 (d, J=1.4, 1H).

Step BN-[5-(3-tert-butoxy-3-oxopropyl)-2-methylphenyl]iminodiacetic acid diethyl ester

To N,N-dimethylformamide (43 ml) were added the compound (2.03 g, 5.00 mmol) obtained in step A, tert-butyl acrylate (3.20 g, 25.00 mmol), [1,1â€²-bis(diphenylphosphino)ferrocene]palladium(II)dichloride-dichloromethane complex (1:1) (204 mg, 0.250 mmol), tetra-n-butylammoniumiodide (2.78 g, 7.50 mmol), water (6.9 ml) and triethylamine (6.9 ml), and the mixture was heated at 80Â° C. for 2 hr. The reaction mixture was cooled, diluted with ethyl acetate, washed with water and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, the solution was concentrated under reduced pressure, and the obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane). To the obtained colorless oil (1.86 g) in ethanol (23 ml) was added 10% palladium carbon (containing water) (186 mg), and the mixture was stirred at room temperature for 3 hr. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (1.79 g, yield 88%) as a colorless oil.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.14 (t, J=7.2, 6H), 1.37 (s, 9H), 2.20 (s, 3H), 2.43 (t, J=7.6, 2H), 2.70 (t, J=7.5, 2H), 3.96 (s, 4H), 4.05 (q, J=7.1, 4H), 6.78 (dd, J=7.7, 1.1, 1H), 6.94 (d, J=1.1, 1H), 7.02 (d, J=7.7, 1H).

Step CN-[5-(2-carboxyethyl)-2-methylphenyl]iminodiacetic acid diethyl ester

To dichloromethane (8.8 ml) were added the compound (1.79 g, 4.40 mmol) obtained in step B and 4N hydrochloric acid-dioxane solution (8.8 ml), and the mixture was stirred at room temperature for 2 hr. The reaction mixture was diluted with dichloromethane, washed with water, and dried over sodium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (1.21 g, yield 79%) as a colorless oil.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.14 (t, J=7.1, 6H), 2.20 (s, ³H), 2.45 (t, J=7.7, 2H), 2.71 (t, J=7.7, 2H), 3.97 (s, 4H), 4.05 (q, J=7.1, 4H), 6.78 (dd, J=7.8, 1.1, 1H), 6.94 (d, J=1.1, 1H), 7.02 (d, J=7.7, 1H), 12.11 (brs, 1H).

Step DN-(6-methyl-1-oxo-2,3-dihydro-1H-inden-5-yl)iminodiacetic acid diethyl ester

To dichloromethane (68 ml) were added the compound (4.79 g, 13.6 mmol) obtained in step C, N,N-dimethylformamide (5 drops) and oxalyl chloride (2.59 g, 20.4 mmol), and the mixture was stirred at 40Â° C. for 3 hr. The reaction mixture was concentrated under reduced pressure, and the obtained oil was diluted with dichloroethane (68 ml) and cooled in an ice water bath. To this solution was added aluminum chloride (2.54 g, 19.0 mmol) by small portions, and the mixture was stirred at 90Â° C. for 4 hr. The reaction mixture was diluted with dichloromethane, washed with water and saturated brine, and dried over sodium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (2.59 g, yield 57%) as a colorless oil.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.17 (t, J=7.1, 6H), 2.27 (s, 3H), 2.54 (t, J=5.8, 2H), 2.96 (t, J=5.6, 2H), 4.08-4.12 (m, 8H), 7.07 (s, 1H), 7.39 (s, 1H).

Step EN-(6-methyl-1-oxo-2,3-dihydro-1H-inden-5-yl)iminodiacetic acid

Using the compound (1.59 g, 7.77 mmol) obtained in step D and according to the method of Reference Example 61, step G, the title compound (1.91 g, yield 89%) was obtained as a yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 2.27 (s, 3H), 2.52-2.55 (m, 2H), 2.96 (t, J=5.2, 2H), 4.03 (s, 4H), 7.00 (s, 1H), 7.38 (s, 1H), 12.59 (brs, 2H).

Reference Example 126N-(6-methyl-3-oxo-2,3-dihydro-1H-inden-5-yl)iminodiacetic acidStep A5-methyl-6-nitroindan-1-one

This step was performed according to the method described in Journal of Medicinal Chemistry, 2006, 49, 7502-7512. 5-Methylindan-1-one (3.27 g, 22.4 mmol) was dissolved in concentrated sulfuric acid (27 ml), a solution of potassium nitrate (2.28 g, 22.6 mmol) in concentrated sulfuric acid (5 ml) was added dropwise over 10 min under ice-cooling with stirring, and the mixture was stirred at the same temperature for 2 hr. The reaction mixture was added to ice water, and extracted with an ethyl acetate-hexane=1:1 mixed solvent. The organic layer was washed with saturated aqueous sodium hydrogen carbonate and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (2.37 g, yield 55%) as a colorless solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 2.68 (s, 3H), 2.77-2.81 (m, 2H), 3.18-3.22 (m, 2H), 7.47 (s, 1H), 8.31 (s, 1H).

Step B6-amino-5-methylindan-1-one

Using the compound (2.36 g, 12.3 mmol) obtained in step A and according to the method of Reference Example 68, step A, the title compound (1.51 g, yield 76%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 2.25 (s, 3H), 2.62-2.66 (m, 2H), 2.98-3.02 (m, 2H), 3.71 (brs, 2H), 7.00 (s, 1H), 7.17 (s, 1H).

Step CN-(6-methyl-3-oxo-2,3-dihydro-1H-inden-5-yl)iminodiacetic acid

Using the compound (1.50 g, 9.31 mmol) obtained in step B and according to the methods of Reference Example 61, steps C and G, the title compound (2.28 g, yield 88%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 2.36 (s, 3H), 2.56-2.60 (m, 2H), 2.95-2.99 (m, 2H), 3.94 (s, 4H), 7.31 (s, 1H), 7.35 (s, 1H), 12.47 (brs, 2H).

Reference Example 127N-(3-methyl-8-oxo-5,6,7,8-tetrahydronaphthalen-2-yl)iminodiacetic acidStep A6-methyl-7-nitro-3,4-dihydronaphthalen-1(2H)-one

Using 6-methyl-3,4-dihydronaphthalen-1(2H)-one (4.74 g, 29.6 mmol) and according to the method of Reference Example 126, step A, the title compound (3.02 g, yield 50%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 2.14-2.21 (m, 2H), 2.63 (s, 3H), 2.67-2.71 (m, 2H), 3.00 (t, J=6.1, 2H), 7.25 (s, 1H), 8.61 (s, 1H).

Step B7-amino-6-methyl-3,4-dihydronaphthalen-1(2H)-one

Using the compound (3.00 g, 14.6 mmol) obtained in step A and according to the method of Reference Example 68, step A, the title compound (2.32 g, yield 91%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 2.04-2.12 (m, 2H), 2.20 (s, 3H), 2.57-2.61 (m, 2H), 2.83 (t, J=6.1, 2H), 3.62 (brs, 2H), 6.95 (s, 1H), 7.31 (s, 1H).

Step CN-(3-methyl-8-oxo-5,6,7,8-tetrahydronaphthalen-2-yl)iminodiacetic acid

Using the compound (2.31 g, 13.2 mmol) obtained in step B and according to the methods of Reference Example 61, steps C and G, the title compound (3.15 g, yield 82%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.95-2.02 (m, 2H), 2.29 (s, 3H), 2.40-2.55 (m, 2H), 2.82 (t, J=5.8, 2H), 3.92 (s, 4H), 7.12 (s, 1H), 7.59 (s, 1H), 12.44 (brs, 2H).

Reference Example 128N-(5-cyano-4-fluoro-2-methylphenyl)iminodiacetic acidStep AN-(5-bromo-4-fluoro-2-methylphenyl)iminodiacetic acid diethyl ester

Using 1-bromo-2-fluoro-4-methyl-5-nitrobenzene (5.00 g, 21.4 mmol) and according to the methods of Reference Example 61, steps B and C, the title compound (6.82 g, yield 85%) as a pale-yellow oil.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.14 (t, J=7.0, 6H), 2.24 (s, 3H), 3.97 (s, 4H), 4.05 (q, J=7.2, 4H), 7.19 (d, J=9.8, 1H), 7.41 (d, J=6.5, 1H).

Step BN-(5-cyano-4-fluoro-2-methylphenyl)iminodiacetic acid diethyl ester

Using the compound (5.74 g, 15.3 mmol) obtained in step A and according to the method of Reference Example 112, step D, the title compound (4.03 g, yield 82%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.1, 6H), 2.36 (s, 3H), 4.00-4.08 (m, 8H), 7.36 (d, J=10.2, 1H), 7.66 (d, J=6.2, 1H).

Step CN-(5-cyano-4-fluoro-2-methylphenyl)iminodiacetic acid

Using the compound (4.03 g, 12.5 mmol) obtained in step B and according to the method of Reference Example 61, step G, the title compound (3.31 g, yield 99%) was obtained as a colorless solid.

35 ¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 2.35 (s, 3H), 3.92 (s, 4H), 7.35 (d, J=10.2, 1H), 7.57 (d, J=6.1, 1H), 12.54 (brs, 2H).

Reference Example 129N-[2-methyl-4-(3-methyl-1,2,4-oxadiazol-5-yl)phenyl]iminodiacetic acid

The compound (5.40 g, 16.8 mmol) of Reference Example 69, step E was dissolved in toluene (10 ml), then N,N-dimethylacetamide dimethylacetal (10 ml) was added, and the mixture was stirred at 100Â° C. for 1 hr. The reaction mixture was concentrated under reduced pressure, and the obtained oil was dissolved in 1,4-dioxane (50 ml). Hydroxylammonium chloride (2.30 g, 33.1 mmol), sodium acetate (2.72 g, 33.2 mmol) and acetic acid (5 ml) were added, and the mixture was stirred with heating at 90Â° C. for 110 min. The reaction mixture was cooled to room temperature, and diluted with an ethyl acetate-hexane=1:1 mixed solvent. The organic layer was washed with water, 10% aqueous citric acid solution, saturated aqueous sodium hydrogen carbonate and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give a colorless oil (6.52 g). Using this oil and according to the method of Reference Example 62, step B, the title compound (3.98 g, yield 78%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.32 (s, 3H), 2.38 (s, 3H), 4.04 (s, 4H), 7.08 (d, J=8.5, 1H), 7.79 (dd, J=2.0, 8.5, 1H), 7.83 (d, J=2.0, 1H), 12.65 (brs, 2H).

Reference Example 130N-[2-methyl-4-(4-methyl-1,3-thiazol-2-yl)phenyl]iminodiacetic acidStep AN-[4-(aminocarbonothioyl)-2-methylphenyl]iminodiacetic acid diethyl ester

Using the compound (3.68 g, 11.4 mmol) of Reference Example 69, step E and according to the method of Reference Example 79, step A, the title compound (2.13 g, yield 55%) was obtained as a yellow oil.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.25 (t, J=7.2, 6H), 2.36 (s, 3H), 4.07 (s, 4H), 4.16 (q, J=7.2, 4H), 7.08 (d, J=8.4, 1H), 7.09 (brs, 1H), 7.46 (brs, 1H), 7.62 (dd, J=2.3, 8.4, 1H), 7.77 (d, J=2.3, 1H).

Step BN-[2-methyl-4-(4-methyl-1,3-thiazol-2-yl)phenyl]iminodiacetic acid

Using the compound (2.21 g, 6.53 mmol) obtained in step A and according to the method of Reference Example 79, step B, the title compound (1.58 g, yield 76%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 2.30 (s, 3H), 2.39 (d, J=0.8, 3H), 3.98 (s, 4H), 7.06 (d, J=8.4, 1H), 7.21 (d, J=0.8, 1H), 7.61 (dd, J=2.2, 8.4, 1H), 7.66 (d, J=2.2, 1H), 12.54 (brs, 2H).

Reference Example 131N-[2-methyl-4-(5-methyl-1,3-thiazol-2-yl)phenyl]iminodiacetic acidStep AN-[4-{[(2-hydroxypropyl)amino]carbonyl}-2-methylphenyl]iminodiacetic acid diethyl ester

Using the compound (2.97 g, 9.19 mmol) of Reference Example 69, step D, and 1-amino-2-propanol (1.4 ml), and according to the method of Reference Example 70, step A, the title compound (3.47 g, yield 99%) was obtained as a yellow oil.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.15-1.30 (m, 3H), 1.24 (t, J=7.2, 6H), 2.35 (s, 3H), 2.74 (d, J=4.4, 1H), 3.25-3.32 (m, 1H), 3.59-3.66 (m, 1H), 3.95-4.05 (m, 1H), 4.06 (s, 4H), 4.15 (q, J=7.2, 4H), 6.55 (t, J=5.4, 1H), 7.14 (d, J=8.4, 1H), 7.52 (dd, J=2.1, 8.4, 1H), 7.62 (d, J=2.1, 1H).

Step BN-[2-methyl-4-{[(2-oxopropyl)amino]carbonyl}phenyl]iminodiacetic acid diethyl ester

The compound (3.11 g, 8.17 mmol) obtained in step B was dissolved in dichloromethane (40 ml), Dess-Martin Periodinane (5.07 g, 12.0 mmol) was added at room temperature, and the mixture was stirred at the same temperature for 3 hr. To the reaction mixture was added saturated aqueous sodium hydrogen carbonate (80 ml) containing sodium sulfite (20 g), the mixture was stirred at room temperature and diluted with dichloromethane, and the organic layer was extracted. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (2.39 g, yield 77%) as a yellow oil.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.24 (t, J=7.2, 6H), 2.26 (s, 3H), 2.36 (s, 3H), 4.06 (s, 4H), 4.15 (q, J=7.2, 4H), 4.34 (d, J=4.4, 2H), 6.83 (broad t, 1H), 7.15 (d, J=8.4, 1H), 7.57 (dd, J=2.2, 8.4, 1H), 7.64 (d, J=2.2, 1H).

Step CN-[2-methyl-4-(5-methyl-1,3-thiazol-2-yl)phenyl]iminodiacetic acid diethyl ester

Using the compound (1.24 g, 3.28 mmol) obtained in step B and according to the method of Reference Example 80, step A, the title compound (859 mg, yield 70%) was obtained as a pale-yellow oil.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.24 (t, J=7.2, 6H), 2.38 (s, 3H), 2.49 (s, 3H), 4.06 (s, 4H), 4.15 (q, J=7.2, 4H), 7.18 (d, J=8.4, 1H), 7.44 (s, 1H), 7.61 (dd, J=2.2, 8.4, 1H), 7.72 (d, J=2.2, 1H).

Step DN-[2-methyl-4-(5-methyl-1,3-thiazol-2-yl)phenyl]iminodiacetic acid

Using the compound (833 mg, 2.21 mmol) obtained in step C and according to the method of Reference Example 62, step B, the title compound (589 mg, yield 83%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 2.30 (s, 3H), 2.46 (d, J=1.1, 3H), 3.97 (s, 4H), 7.07 (d, J=8.4, 1H), 7.51 (d, J=1.1, 1H), 7.57 (dd, J=2.2, 8.4, 1H), 7.62 (d, J=2.2, 1H), 12.53 (brs, 2H).

Reference Example 132N-[2-methyl-4-(5-methyl-1,3,4-thiadiazol-2-yl)phenyl]iminodiacetic acidStep AN-{4-[(2-acetylhydrazino)carbonyl]-2-methylphenyl}iminodiacetic acid diethyl ester

Using the compound (3.08 g, 9.53 mmol) of Reference Example 69, step D, and acetohydrazide (1.18 g, 15.9 mmol), and according to the method of Reference Example 84, step A, the title compound (3.13 g, yield 87%) was obtained as a pale-yellow oil.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.24 (t, J=7.2, 6H), 2.07 (s, 3H), 2.31 (s, 3H), 4.06 (s, 4H), 4.15 (q, J=7.2, 4H), 7.09 (d, J=8.4, 1H), 7.60 (dd, J=2.0, 8.4, 1H), 7.65 (d, J=2.0, 1H), 9.35 (d, J=5.2, 1H), 9.48 (d, J=5.2, 1H).

Step BN-[2-methyl-4-(5-methyl-1,3,4-thiadiazol-2-yl)phenyl]iminodiacetic acid diethyl ester

Using the compound (3.12 g, 8.22 mmol) obtained in step A and according to the method of Reference Example 80, step A, the title compound (2.42 g, yield 78%) was obtained as a yellow oil.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.25 (t, J=7.2, 6H), 2.39 (s, 3H), 2.79 (s, 3H), 4.08 (s, 4H), 4.16 (q, J=7.2, 4H), 7.19 (d, J=8.3, 1H), 7.65 (dd, J=2.2, 8.3, 1H), 7.77 (d, J=2.2, 1H).

Step CN-[2-methyl-4-(5-methyl-1,3,4-thiadiazol-2-yl)phenyl]iminodiacetic acid

Using the compound (2.40 g, 6.36 mmol) obtained in step B and according to the method of Reference Example 62, step B, the title compound (1.92 g, yield 94%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 2.31 (s, 3H), 2.74 (s, 3H), 4.00 (s, 4H), 7.09 (d, J=8.4, 1H), 7.63 (dd, J=2.0, 8.4, 1H), 7.68 (d, J=2.0, 1H), 12.57 (brs, 2H).

The compounds of Reference Examples 121-132 are shown below.

TABLE 5ReferenceStructuralExampleFormula121 [Image Omitted]

122

123

124

125

126

127

128

129

130

131

132

Reference Example 133N-[6-methyl-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-5-yl]iminodiacetic acidStep A6-methyl-5-nitro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole

6-Methyl-5-nitro-1H-indazole (15.1 g, 85.2 mmol), 2,3-dichloro-5,6-dicyano-p-benzoquinone (DDQ) (1.94 g, 8.55 mmol) and 3,4-dihydro-2H-pyran (9.0 ml, 98.4 mmol) were dissolved in acetonitrile (300 ml), and the mixture was heated under reflux for 4.5 hr. The reaction mixture was concentrated under reduced pressure, and the residue was diluted with an ethyl acetate-hexane=1:1 mixed solvent, washed with saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (16.0 g, yield 72%) as an orange solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.6-1.9 (m, 3H), 2.0-2.2 (m, 2H), 2.4-2.6 (m, 1H), 2.75 (s, 3H), 3.74-3.81 (m, 1H), 4.00-4.04 (m, 1H), 5.73 (dd, J=2.5, 9.1, 1H), 7.49 (s, 1H), 8.13 (s, 1H), 8.50 (s, 1H).

Step B6-methyl-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-5-amine

Using the compound (16.0 g, 61.2 mmol) of step A and according to the method of Reference Example 61, step B, the title compound (11.7 g, yield 83%) was obtained as a colorless solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.5-1.8 (m, 3H), 2.0-2.2 (m, 2H), 2.34 (s, 3H), 2.5-2.6 (m, 1H), 3.55 (brs, 2H), 3.70-3.77 (m, 1H), 4.01-4.04 (m, 1H), 5.63 (dd, J=2.5, 9.4, 1H), 6.93 (s, 1H), 7.31 (s, 1H), 7.80 (s, 1H).

Step CN-[6-methyl-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-5-yl]iminodiacetic acid

Using the compound (11.7 g, 50.6 mmol) of step B and according to the methods of Reference Example 61, steps C and G, the title compound (12.9 g, yield 73%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.5-1.7 (m, 2H), 1.7-1.8 (m, 1H), 1.89-2.05 (m, 2H), 2.3-2.5 (m, 1H), 2.42 (s, 3H), 3.68-3.75 (m, 1H), 3.85-3.90 (m, 1H), 3.93 (s, 4H), 5.73 (dd, J=2.2, 9.6, 1H), 7.49 (s, 1H), 7.52 (s, 1H), 7.94 (s, 1H), 12.35 (brs, 2H).

Reference Example 134N-[5-methyl-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-6-yl]iminodiacetic acidStep A5-methyl-6-nitro-1H-indazole

Using 2,4-dimethylaniline (49.6 g, 409 mmol), and according to the method described in WO2003/068754, the title compound (66.2 g, yield 91%) was obtained as a red bistered solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 2.54 (s, 3H), 7.85 (s, 1H), 8.20 (s, 1H), 8.22 (s, 1H), 13.57 (brs, 1H).

Step B5-methyl-6-nitro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole

Using the compound (8.47 g, 47.8 mmol) of step A and according to the method of Reference Example 133, step A, the title compound (11.5 g, yield 92%) was obtained as a red bistered solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.7-1.9 (m, 3H), 2.0-2.2 (m, 2H), 2.45-2.60 (m, 1H), 2.65 (s, 3H), 3.74-3.81 (m, 1H), 4.00-4.06 (m, 1H), 5.75 (dd, J=2.7, 9.2, 1H), 7.65 (s, 1H), 8.04 (s, 1H), 8.27 (s, 1H).

Step C5-methyl-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-6-amine

Using the compound (11.5 g, 44.0 mmol) of step B and according to the method of Reference Example 61, step B, the title compound (9.62 g, yield 95%) was obtained as a yellow amorphous solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.5-1.8 (m, 3H), 2.0-2.2 (m, 2H), 2.25 (s, 3H), 2.5-2.6 (m, 1H), 3.68-3.75 (m, 1H), 3.83 (brs, 2H), 3.99-4.04 (m, 1H), 5.56 (dd, J=2.7, 9.4, 1H), 6.77 (s, 1H), 7.36 (s, 1H), 7.80 (s, 1H).

Step DN-[5-methyl-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-6-yl]iminodiacetic acid

Using the compound (9.62 g, 41.6 mmol) of step C and according to the methods of Reference Example 61, step C, and Reference Example 62, step B, the title compound (7.34 g, yield 51%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.5-1.6 (m, 2H), 1.65-1.80 (m, 1H), 1.80-1.95 (m, 1H), 1.95-2.05 (m, 1H), 2.3-2.4 (m, 1H), 2.34 (s, 3H), 3.66-3.74 (m, 1H), 3.8-3.9 (m, 1H), 3.99 (s, 4H), 5.70 (dd, J=2.4, 9.6, 1H), 7.35 (s, 1H), 7.49 (s, 1H), 7.88 (s, 1H), 12.47 (brs, 2H).

Reference Example 135N-(3-iodo-1,5-dimethyl-1H-indazol-6-yl)iminodiacetic acidStep A3-iodo-5-methyl-6-nitro-1H-indazole

The compound (34.9 g, 197 mmol) of Reference Example 134, step A was dissolved in N,N-dimethylformamide (400 ml), iodine (103 g, 406 mmol) and potassium hydroxide pellet (52 g, 927 mmol) were successively added under ice-cooling with stirring, and the mixture was stirred at room temperature for 1 hr. The reaction mixture was poured into 10% aqueous sodium bisulfite solution (2000 ml), and the precipitated solid was collected by filtration, washed with water, and dried under reduced pressure to give the title compound (45.1 g, yield 76%) as a brown solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 2.56 (s, 3H), 7.54 (s, 1H), 8.25 (s, 3H), 13.98 (s, 1H).

Step B3-iodo-1,5-dimethyl-6-nitro-1H-indazole

The compound (16.1 g, 53.1 mmol) of step A was dissolved in N,N-dimethylformamide (200 ml), 60% sodium hydride (2.41 g, 60.3 mmol) was added under ice-cooling with stirring, and the mixture was stirred at 0Â° C. for 45 min. Then, methyl iodide (5.0 ml, 80.3 mmol) was added, and the mixture was stirred at the same temperature for 100 min. To the reaction mixture was added diluted hydrochloric acid, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated. The obtained solid was purified by silica gel column chromatography (hexane:dichloromethane:ethyl acetate=10:1:1) to give the title compound (6.09 g, yield 36%) as a yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 2.56 (s, 3H), 4.14 (s, 3H), 7.52 (s, 1H), 8.49 (s, 1H).

Step C3-iodo-1,5-dimethyl-1H-indazol-6-amine

Using the compound (6.09 g, 19.2 mmol) of step B and according to the method of Reference Example 61, step B, the title compound (4.68 g, yield 85%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 2.28 (s, 3H), 3.91 (brs, 2H), 3.95 (s, 3H), 6.51 (s, 1H), 7.10 (s, 1H).

Step DN-(3-iodo-1,5-dimethyl-1H-indazol-6-yl)iminodiacetic acid diethyl ester

Using the compound (4.68 g, 16.3 mmol) of step C and according to the method of Reference Example 61, step C, the title compound (3.99 g, yield 53%) was obtained as a colorless solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.23 (t, J=7.0, 6H), 2.45 (s, 3H), 4.02 (s, 3H), 4.12 (s, 4H), 4.14 (q, J=7.0, 4H), 7.18 (s, 1H), 7.23 (s, 1H).

Step EN-(3-iodo-1,5-dimethyl-1H-indazol-6-yl)iminodiacetic acid

Using the compound (3.74 g, 8.14 mmol) of step D and according to the method of Reference Example 62, step B, the title compound (3.15 g, yield 96%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 2.37 (s, 3H), 3.96 (s, 3H), 4.00 (s, 4H), 7.14 (s, 1H), 7.25 (s, 1H), 12.48 (brs, 2H).

Reference Example 136N-(3-iodo-1,6-dimethyl-1H-indazol-5-yl)iminodiacetic acidStep A3-iodo-6-methyl-5-nitro-1H-indazole

Using 6-methyl-5-nitro-1H-indazole (5.15 g, 29.1 mmol) and according to the method of Reference Example 135, step A, the title compound (8.65 g, yield 98%) was obtained as a yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 2.64 (s, 3H), 7.63 (s, 1H), 8.15 (s, 1H), 13.94 (brs, 1H).

Step B3-iodo-1,6-dimethyl-5-nitro-1H-indazole

Using the compound (6.07 g, 20.0 mmol) of step A and according to the method of Reference Example 135, step B, the title compound (3.36 g, yield 51%) was obtained as a yellow bistered solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 2.65 (s, 3H), 4.09 (s, 3H), 7.80 (s, 1H), 8.13 (s, 1H).

Step C3-iodo-1,6-dimethyl-1H-indazol-5-amine

Using the compound (3.36 g, 10.6 mmol) of step B and according to the method of Reference Example 61, step B, the title compound (2.61 g, yield 86%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 2.34 (s, 3H), 3.63 (brs, 2H), 4.01 (s, 3H), 6.66 (s, 1H), 7.09 (s, 1H).

Step DN-(3-iodo-1,6-dimethyl-1H-indazol-5-yl)iminodiacetic acid diethyl ester

Using the compound (2.59 g, 9.02 mmol) of step C and according to the method of Reference Example 61, step C, the title compound (2.59 g, yield 63%) was obtained as an orange oil.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.25 (t, J=7.1, 6H), 2.53 (s, 3H), 4.02 (s, 3H), 4.06 (s, 4H), 4.14 (q, J=7.1, 4H), 7.17 (s, 1H), 7.31 (s, 1H).

Step EN-(3-iodo-1,6-dimethyl-1H-indazol-5-yl)iminodiacetic acid

Using the compound (2.58 g, 5.62 mmol) of step D and according to the method of Reference Example 62, step B, the title compound (1.97 g, yield 87%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 2.43 (s, 3H), 3.95 (s, 4H). 3.98 (s, 3H), 7.13 (s, 1H), 7.45 (s, 1H), 12.42 (brs, 2H).

Reference Example 137N-(2,3,5-trimethyl-2H-indazol-6-yl)iminodiacetic acidStep A3-iodo-5-methyl-6-nitro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole

Using the compound (18.0 g, 59.4 mmol) of Reference Example 135, step A and according to the method of Reference Example 133, step A, the title compound (17.0 g, yield 74%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.6-1.8 (m, 3H), 2.0-2.2 (m, 2H), 2.4-2.6 (m, 1H), 2.66 (s, 3H), 3.72-3.79 (m, 1H), 3.99-4.04 (m, 1H), 5.72 (dd, J=2.8, 9.2, 1H), 7.40 (s, 1H), 8.24 (s, 1H).

Step B3,5-dimethyl-6-nitro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole

The compound (5.60 g, 14.5 mmol) of step A, trimethylboroxine (2.20 ml, 15.8 mmol), bis(tricyclohexylphosphine)palladium(II)dichloride (926 mg, 1.25 mmol) and 1.27 mol/l aqueous potassium phosphate solution (35.0 ml, 44.5 mmol) were added to 1,4-dioxane (150 ml), and the mixture was heated under reflux for 18 hr. The reaction mixture was cooled to room temperature, and the solution was concentrated under reduced pressure. The residue was diluted with ethyl acetate, and the organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (2.73 g, yield 68%) as a yellow solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.6-1.9 (m, 3H), 2.0-2.2 (m, 2H), 2.46-2.56 (m, 1H), 2.58 (s, 3H), 2.65 (s, 3H), 3.72-3.79 (m, 1H), 4.04-4.09 (m, 1H), 5.64 (dd, J=2.6, 9.9, 1H), 7.54 (s, 1H), 8.18 (s, 1H).

Step C3,5-dimethyl-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-6-amine

Using the compound (2.71 g, 9.84 mmol) of step B and according to the method of Reference Example 61, step B, the title compound (1.85 g, yield 77%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.5-1.8 (m, 3H), 1.97-2.02 (m, 1H), 2.09-2.13 (m, 1H), 2.25 (s, 3H), 2.47 (s, 3H), 2.48-2.59 (m, 1H), 3.66-3.73 (m, 1H), 3.80 (brs, 2H), 4.03-4.08 (m, 1H), 5.47 (dd, J=2.6, 10.0, 1H), 6.70 (s, 1H), 7.27 (s, 1H).

Step DN-[3,5-dimethyl-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-6-yl]iminodiacetic acid ethyl ester

Using the compound (1.82 g, 7.42 mmol) of step C and according to the method of Reference Example 61, step C, the title compound (2.53 g, yield 82%) was obtained as a yellow oil.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.23 (t, J=7.1, 6H), 1.55-1.65 (m, 1H), 1.7-1.8 (m, 2H), 1.95-2.00 (m, 1H), 2.05-2.15 (m, 1H), 2.43 (s, 3H), 2.50 (s, 3H), 2.5-2.6 (m, 1H), 3.68-3.76 (m, 1H), 4.0-4.1 (m, 1H), 4.11 (s, 4H), 4.14 (q, J=7.1, 4H), 5.52 (dd, J=2.5, 10.1, 1H), 7.29 (s, 1H), 7.39 (s, 1H).

Step EN-(3,5-dimethyl-1H-indazol-6-yl)iminodiacetic acid ethyl ester

The compound (2.53 g, 6.06 mmol) of step D was dissolved in ethanol (75 ml), concentrated sulfuric acid (0.5 ml) was added at room temperature, and thereafter the mixture was heated under reflux for 70 min. The reaction mixture was concentrated under reduced pressure, and the residue was diluted with ethyl acetate. The organic layer was washed with sodium bicarbonate water and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, the solution was concentrated under reduced pressure, and the obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (1.72 g, yield 85%) as a yellow oil.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.22 (t, J=7.2, 6H), 2.44 (s, 3H), 2.51 (s, 3H), 4.09 (s, 4H), 4.13 (q, J=7.2, 4H), 7.27 (s, 1H), 7.44 (s, 1H), 9.46 (brs, 1H).

Step FN-(2,3,5-trimethyl-2H-indazol-6-yl)iminodiacetic acid diethyl ester

The compound (500 mg, 1.50 mmol) of step E was dissolved in dichloromethane (10 ml), trimethyloxonium tetrafluoroborate (290 mg, 1.96 mmol) was added at room temperature, and the mixture was stirred at the same temperature for 140 min. Water was added to the reaction mixture, and the organic layer was extracted with dichloromethane, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (248 mg, yield 48%) as a pale-yellow oil.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.23 (t, J=7.2, 6H), 2.41 (s, 3H), 2.53 (s, 3H), 4.03 (s, 3H), 4.07 (s, 4H), 4.13 (q, J=7.2, 4H), 7.30 (s, 1H), 7.34 (s, 1H).

Step GN-(2,3,5-trimethyl-2H-indazol-6-yl)iminodiacetic acid

Using the compound (243 mg, 0.699 mmol) of step F and according to the method of Reference Example 62, step B, the title compound (152 mg, yield 75%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 2.31 (s, 3H), 2.51 (s, 3H), 3.93 (s, 4H), 3.95 (s, 3H), 7.08 (s, 1H), 7.35 (s, 1H), 12.41 (brs, 2H).

Reference Example 138N-(2-ethyl-3,5-dimethyl-2H-indazol-6-yl)iminodiacetic acidStep AN-(2-ethyl-3,5-dimethyl-2H-indazol-6-yl)iminodiacetic acid diethyl ester

Using the compound (503 mg, 1.51 mmol) of Reference Example 137, step E, and 1 mol/l triethyloxonium tetrafluoroborate dichloromethane solution (1.8 ml), and according to the method of Reference Example 137, step F, the title compound (205 mg, yield 38%) was obtained as a yellow oil.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.24 (t, J=7.2, 6H), 1.50 (t, J=7.3, 3H), 2.41 (s, 3H), 2.54 (s, 3H), 4.07 (s, 4H), 4.14 (q, J=7.2, 4H), 4.33 (q, J=7.3, 2H), 7.32 (s, 1H), 7.36 (s, 1H).

Step BN-(2-ethyl-3,5-dimethyl-2H-indazol-6-yl)iminodiacetic acid

Using the compound (267 mg, 0.739 mmol) of step A and according to the method of Reference Example 62, step B, the title compound (185 mg, yield 82%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.37 (t, J=7.2, 3H), 2.30 (s, ³H), 2.52 (s, 3H), 3.93 (s, 4H), 4.28 (q, J=7.2, 2H), 7.10 (s, 1H), 7.36 (s, 1H), 12.40 (brs, 2H).

Reference Example 139N-(1-ethyl-3,5-dimethyl-1H-indazol-6-yl)iminodiacetic acidStep AN-(1-ethyl-3,5-dimethyl-1H-indazol-6-yl)iminodiacetic acid diethyl ester

Using the compound (193 mg, 0.579 mmol) of Reference Example 137, step E, and ethyl iodide (0.10 ml, 1.25 mmol), and according to the method of Reference Example 135, step B, the title compound (119 mg, yield 57%) was obtained as a pale-yellow oil.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.22 (t, J=7.1, 6H), 1.44 (t, J=7.2, 3H), 2.43 (s, 3H), 2.50 (s, 3H), 4.11 (s, 4H), 4.13 (q, J=7.1, 4H), 4.28 (q, J=7.2, 2H), 7.17 (s, 1H), 7.41 (s, 1H).

Step BN-(1-ethyl-3,5-dimethyl-1H-indazol-6-yl)iminodiacetic acid

Using the compound (117 mg, 0.324 mmol) of step A and according to the method of Reference Example 62, step B, the title compound (86 mg, yield 87%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); 1.30 (t, J=7.2, 3H), 2.33 (s, 3H), 2.38 (s, 3H), 3.98 (s, 4H), 4.22 (q, J=7.2, 2H), 7.16 (s, 1H), 7.40 (s, 1H), 12.44 (brs, 2H).

Reference Example 140N-[2-(2,2-difluoroethyl)-3,5-dimethyl-2H-indazol-6-yl]iminodiacetic acidStep AN-[2-(2,2-difluoroethyl)-3,5-dimethyl-2H-indazol-6-yl]iminodiacetic acid diethyl ester

The compound (664 mg, 1.99 mmol) of Reference Example 137, step E, 2,2-difluoroethyl trifluoromethanesulfonate (654 mg, 3.05 mmol) and N,N-dicyclohexylmethylamine (0.70 ml, 3.30% mmol) were dissolved in tetrahydrofuran (15 ml), and the mixture was heated under reflux for 6 hr. The reaction mixture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (541 mg, yield 68%) as a colorless oil.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.24 (t, J=7.1, 6H), 2.41 (s, 3H), 2.57 (s, 3H), 4.08 (s, 4H), 4.14 (q, J=7.1, 4H), 4.62 (dt, J=4.4, 13, 2H), 6.22 (tt, J=4.4, 57, 1H), 7.31 (s, 1H), 7.33 (s, 1H).

Step BN-[2-(2,2-difluoroethyl)-3,5-dimethyl-2H-indazol-6-yl]iminodiacetic acid

Using the compound (525 mg, 1.32 mmol) of step A and according to the method of Reference Example 62, step B, the title compound (387 mg, yield 86%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); 2.31 (s, 3H), 2.55 (s, 3H), 3.94 (s, 4H), 4.79 (dt, J=3.9, 15, 2H), 6.46 (tt, J=3.9, 55, 1H), 7.09 (s, 1H), 7.40 (s, 1H), 12.42 (brs, 2H).

Reference Example 141N-(3-ethyl-2,5-dimethyl-2H-indazol-6-yl)iminodiacetic acidStep A5-methyl-6-nitro-1-(tetrahydro-2H-pyran-2-yl)-3-vinyl-1H-indazole

To toluene (160 ml) were added the compound (8.78 g, 22.7 mmol) of Reference Example 137, step A, tri-n-butylvinyltin (8.7 ml, 29.6 mmol), bis(triphenylphosphine)palladium(II)dichloride (1.47 g, 2.09 mmol) and lithium chloride (3.92 g, 92.5 mmol), and the mixture was heated under reflux for 210 min. The reaction mixture was cooled, diluted with ethyl acetate, washed with saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give an orange solid (7.09 g). This was washed with hexane and dried under reduced pressure to give the title compound (5.42 g, yield 83%) as a yellow solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.6-1.9 (m, 3H), 2.0-2.2 (m, 2H), 2.46-2.57 (m, 1H), 2.67 (s, 3H), 3.73-3.80 (m, 1H), 4.02-4.07 (m, 1H), 5.59 (dd, J=1.0, 11, 1H), 5.72 (dd, J=2.8, 9.3, 1H), 6.11 (dd, J=1.0, 18, 1H), 7.01 (dd, J=11, 18, 1H), 7.81 (s, 1H), 8.24 (s, 1H).

Step B3-ethyl-5-methyl-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-6-amine

The compound (3.04 g, 10.6 mmol) of step A was dissolved in an ethanol (100 ml)-tetrahydrofuran (10 ml) mixed solvent, and the mixture was stirred at room temperature. Then, 10% palladium carbon (containing water) (3.20 g) was added, and the mixture was stirred at room temperature for 5 hr under a hydrogen atmosphere. The insoluble material was filtered off through celite, and the obtained solution was concentrated under reduced pressure to give the title compound (2.69 g, yield 98%) as a pale-yellow oil.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.36 (t, J=7.6, 3H), 1.5-1.8 (m, 3H), 1.96-2.01 (m, 1H), 2.09-2.13 (m, 1H), 2.25 (s, 3H), 2.50-2.55 (m, 1H), 2.90 (q, J=7.6, 2H), 3.5-4.0 (broad, 2H), 3.66-3.73 (m, 1H), 4.03-4.09 (m, 1H), 5.48 (dd, J=2.6, 10, 1H), 6.71 (s, 1H), 7.31 (s, 1H).

Step CN-(3-ethyl-5-methyl-1H-indazol-6-yl)iminodiacetic acid diethyl ester

Using the compound (2.67 g, 10.3 mmol) of step B and according to the methods of Reference Example 61, step C, and Reference Example 137, step E, the title compound (2.60 g, yield 75%) was obtained as an orange oil.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.22 (t, J=7.1, 6H), 1.38 (t, J=7.6, 3H), 2.44 (s, 3H), 2.94 (q, J=7.6, 2H), 4.09 (s, 4H), 4.13 (q, J=7.1, 4H), 7.28 (s, 1H), 7.48 (s, 1H), 9.56 (brs, 1H).

Step DN-(3-ethyl-2,5-dimethyl-2H-indazol-6-yl)iminodiacetic acid diethyl ester

Using the compound (722 mg, 2.08 mmol) of step C, and trimethyloxonium tetrafluoroborate (527 mg, 3.56 mmol), and according to the method of Reference Example 137, step F, the title compound (248 mg, yield 33%) was obtained as a yellow oil.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.23 (t, J=7.1, 6H), 1.31 (t, J=7.6, 3H), 2.41 (s, 3H), 2.97 (q, J=7.6, 2H), 4.05 (s, 3H), 4.07 (s, 4H), 4.13 (q, J=7.1, 4H), 7.34-7.36 (m, 2H).

Step EN-(3-ethyl-2,5-dimethyl-2H-indazol-6-yl)iminodiacetic acid

Using the compound (241 mg, 0.667 mmol) of step D and according to the method of Reference Example 62, step B, the title compound (128 mg, yield 63%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); 1.22 (t, J=7.6, 3H), 2.30 (s, 3H), 2.97 (q, J=7.6, 2H), 3.93 (s, 4H), 3.98 (s, 3H), 7.09 (s, ¹H), 7.39 (s, 1H), 12.41 (brs, 2H).

Reference Example 142N-(2,3-diethyl-5-methyl-2H-indazol-6-yl)iminodiacetic acidStep AN-(2,3-diethyl-5-methyl-2H-indazol-6-yl)iminodiacetic acid ethyl ester

Using the compound (692 mg, 1.99 mmol) of Reference Example 141, step C, and 1 mol/l triethyloxonium tetrafluoroborate dichloromethane solution (2.3 ml), and according to the method of Reference Example 137, step F, the title compound (298 mg, yield 40%) was obtained as a yellow oil.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.24 (t, J=7.1, 6H), 1.33 (t, J=7.6, 3H), 1.53 (t, J=7.3, 3H), 2.41 (s, 3H), 2.97 (q, J=7.6, 2H), 4.07 (s, 4H), 4.14 (q, J=7.1, 4H), 4.33 (q. J=7.3, 2H), 7.36 (s, 1H), 7.37 (s, 1H).

Step BN-(2,3-diethyl-5-methyl-2H-indazol-6-yl)iminodiacetic acid

Using the compound (375 mg, 0.999 mmol) of step A and according to the method of Reference Example 62, step B, the title compound (266 mg, yield 63%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); 1.23 (t, J=7.6, 3H), 1.40 (t, J=7.2, 3H), 2.31 (s, 3H), 2.98 (q, J=7.6, 2H), 3.93 (s, 4H), 4.28 (q, J=7.2, 2H), 7.11 (s, 1H), 7.39 (s, 1H), 12.40 (brs, 2H).

Reference Example 143N-[2-(2,2-difluoroethyl)-3-ethyl-5-methyl-2H-indazol-6-yl]iminodiacetic acidStep AN-[2-(2,2-difluoroethyl)-3-ethyl-5-methyl-2H-indazol-6-yl]iminodiacetic acid diethyl ester

Using the compound (721 mg, 2.07 mmol) of Reference Example 141, step C and according to the method of Reference Example 140, step A, the title compound (538 mg, yield 63%) was obtained as an orange oil.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.24 (t, J=7.2, 6H), 1.33 (t, J=7.6, 3H), 2.41 (s, 3H), 3.01 (q, J=7.6, 2H), 4.08 (s, 4H), 4.13 (q, J=7.2, 4H), 4.61 (dt, J=4.4, 13, 2H), 6.27 (tt, J=4.4, 56, 1H), 7.32 (s, 1H), 7.38 (s, 1H).

Step BN-[2-(2,2-difluoroethyl)-3-ethyl-5-methyl-2H-indazol-6-yl]iminodiacetic acid

Using the compound (533 mg, 1.30 mmol) of step A and according to the method of Reference Example 62, step B, the title compound (410 mg, yield 89%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); 1.23 (t, J=7.6, 3H), 2.31 (s, 3H), 3.02 (q, J=7.6, 2H), 3.94 (s, 4H), 4.79 (dt, J=4.0, 15, 2H), 6.48 (tt, J=4.0, 55, 1H), 7.10 (s, 1H), 7.44 (s, 1H), 12.42 (brs, 2H).

Reference Example 144N-[1-(2,2-difluoroethyl)-3-ethyl-5-methyl-1H-indazol-6-yl]iminodiacetic acidStep AN-[1-(2,2-difluoroethyl)-3-ethyl-5-methyl-1H-indazol-6-yl]iminodiacetic acid diethyl ester

Using the compound (312 mg, 0.898 mmol) of Reference Example 141, step C, and 2,2-difluoroethyl trifluoromethanesulfonate (264 mg, 1.23 mmol), and according to the method of Reference Example 135, step B, the title compound (254 mg, yield 69%) was obtained as a pale-yellow oil.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.23 (t, J=7.2, 6H), 1.36 (t, J=7.6, 3H), 2.44 (s, 3H), 2.91 (q, J=7.6, 2H), 4.11 (s, 4H), 4.14 (q, J=7.2, 4H), 4.56 (dt, J=4.4, 14, 2H), 6.08 (tt, J=4.4, 56, 1H), 7.19 (s, 1H), 7.46 (s, 1H).

Step BN-[1-(2,2-difluoroethyl)-3-ethyl-5-methyl-1H-indazol-6-yl]iminodiacetic acid

Using the compound (253 mg, 0.615 mmol) of step A and according to the method of Reference Example 62, step B, the title compound (182 mg, yield 89%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); 1.27 (t, J=7.6, 3H), 2.34 (s, 3H), 2.84 (q, J=7.6, 2H), 3.98 (s, 4H), 4.70 (dt, J=3.7, 15, 2H), 6.32 (tt, J=3.7, 55, 1H), 7.29 (s, 1H), 7.48 (s, 1H), 12.43 (brs, 2H).

Reference Example 145N-[1-(2,2-difluoroethyl)-7-methyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-yl]iminodiacetic acidStep A1-(2,2-difluoroethyl)-7-methyl-2-oxo-1,2,3,4-tetrahydroquinoline-6-carboxylic acid ethyl ester

The compound (4.57 g, 19.6 mmol) of Reference Example 114, step B was dissolved in N,N-dimethylformamide (70 ml), 60% sodium hydride (970 mg, 24.3 mmol) was added under ice-cooling with stirring, and thereafter the mixture was stirred at room temperature for 30 min. The reaction mixture was ice-cooled again, 2,2-difluoroethyl trifluoromethanesulfonate (5.98 g, 27.9 mmol) was added with stirring, and the mixture was stirred at 0Â° C. for 100 min. To the reaction mixture was added 10% citric acid water, and the mixture was extracted with an ethyl acetate:hexane=1:1 mixed solvent. The organic layer was washed with saturated aqueous sodium hydrogen carbonate and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (4.73 g, yield 81%) as a colorless solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.39 (t, J=7.2, 3H), 2.62 (s, 3H), 2.68-2.72 (m, 2H), 2.92-2.96 (m, 2H), 4.27 (dt, J=4.6, 13, 2H), 4.35 (q, J=7.2, 2H), 6.10 (tt, J=4.6, 56, 1H), 6.96 (s, 1H), 7.78 (s, 1H).

Step B1-(2,2-difluoroethyl)-7-methyl-2-oxo-1,2,3,4-tetrahydroquinoline-6-carboxylic acid

Using the compound (4.73 g, 15.9 mmol) of step A and according to the method of Reference Example 114, step D, the title compound (4.31 g, yield 100%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 2.53 (s, 3H), 2.59-2.64 (m, 2H), 2.86-2.91 (m, 2H), 4.41 (dt, J=4.1, 15, 2H), 6.22 (tt, J=4.1, 56, 1H), 7.19 (s, 1H), 7.73 (s, 1H), 12.64 (brs, 1H).

Step Ctert-butyl [1-(2,2-difluoroethyl)-7-methyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-yl]carbamate

Using the compound (4.30 g, 16.0 mmol) of step B and according to the method of Reference Example 112, step A, the title compound (2.38 g, yield 44%) was obtained as a pale-yellow oil.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.53 (s, 9H), 2.26 (s, 3H), 2.62-2.68 (m, 2H), 2.86-2.92 (m, 2H), 4.21 (dt, J=4.5, 14, 2H), 6.09 (tt, J=4.5, 56, 1H), 6.20 (brs, 1H), 6.90 (s, 1H), 7.66 (s, 1H).

Step D6-amino-1-(2,2-difluoroethyl)-7-methyl-3,4-dihydroquinolin-2(1H)-one

The compound (2.29 g, 6.73 mmol) of step C was dissolved in dichloromethane (15 ml), 4N hydrochloric acid-dioxane solution (15 ml, 60 mmol) was added at room temperature, and the mixture was stirred at the same temperature for 2 hr. To the reaction mixture was added saturated aqueous sodium hydrogen carbonate, the mixture was extracted with ethyl acetate, and the organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure to give the title compound (1.43 g, yield 88%) as a colorless solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 2.18 (s, 3H), 2.60-2.65 (m, 2H), 2.78-2.83 (m, 2H), 3.51 (brs, 2H), 4.19 (dt, J=4.7, 13, 2H), 6.09 (tt, J=4.7, 57, 1H), 6.50 (s, 1H), 6.82 (s, 1H).

Step EN-[1-(2,2-difluoroethyl)-7-methyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-yl]iminodiacetic acid

Using the compound (1.42 g, 5.91 mmol) of step D and according to the methods of Reference Example 61, step C, and Reference Example 62, step B, the title compound (1.64 g, yield 79%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 2.25 (s, 3H), 2.53-2.56 (m, 2H), 2.75-2.80 (m, 2H), 3.88 (s, 4H), 4.30 (dt, J=4.1, 14, 2H), 6.19 (tt, J=4.1, 53, 1H), 6.99 (s, 1H), 7.03 (s, 1H), 12.39 (brs, 2H).

Reference Example 146N-[2-(2,2-difluoroethyl)-6-methyl-3-oxo-2,3-dihydro-1H-isoindol-5-yl]iminodiacetic acidStep A4-bromo-2-methylbenzoic acid ethyl ester

4-Bromo-2-methylbenzoic acid (9.97 g, 46.4 mmol) and concentrated sulfuric acid (1.0 ml) were dissolved in ethanol (170 ml), and the mixture was heated under reflux for 33 hr. The reaction mixture was concentrated under reduced pressure, and the residue was diluted with an ethyl acetate-hexane=1:1 mixed solvent, washed with water, saturated aqueous sodium hydrogen carbonate and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure to give the title compound (10.5 g, yield 93%) as a colorless oil.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.39 (t, J=7.1, 3H), 2.58 (s, 3H), 4.35 (q, J=7.1, 2H), 7.38 (dd, J=1.8, 8.4, 1H), 7.41 (d, J=1.8, 1H), 7.78 (d, J=8.4, 1H).

Step B5-bromo-2-(2,2-difluoroethyl)isoindolin-1-one

To carbon tetrachloride (160 ml) were added the compound (10.5 g, 43.2 mmol) of step A, N-bromosuccinimide (8.08 g, 45.4 mmol) and benzoyl peroxide (724 mg), and the mixture was heated under reflux for 50 min. The reaction mixture was cooled and diluted with hexane, the insoluble material was filtered off, and the obtained solution was concentrated under reduced pressure. The obtained oil (18.0 g) was dissolved in N,N-dimethylformamide (180 ml), 2,2-difluoroethylamine (5.99 g, 73.9 mmol) and triethylamine (12.0 ml, 86.1 mmol) were added, and the mixture was stirred at room temperature for 14 hr. The reaction mixture was diluted with an ethyl acetate-hexane=1:1 mixed solvent, washed with water, 10% aqueous citric acid solution, saturated aqueous sodium hydrogen carbonate and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (5.80 g, yield 49%) as a colorless oil.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 3.96 (dt, J=4.2, 15, 2H), 4.53 (s, 2H), 5.99 (tt, J=4.2, 56, 1H), 7.63 (d, J=8.7, 1H), 7.64 (s, 1H), 7.74 (d, J=8.7, 1H).

Step C2-(2,2-difluoroethyl)-5-methylisoindolin-1-one

The compound (5.77 g, 20.9 mmol) of step B, trimethylboroxine (3.00 ml, 21.6 mmol), bis(tricyclohexylphosphine)palladium(II) dichloride (1.53 g, 2.07 mmol) and 1.27 mol/l aqueous potassium phosphate solution (50 ml, 63.5 mmol) were added to 1,4-dioxane (200 ml), and the mixture was heated under reflux for 110 min. The reaction mixture was cooled to room temperature, and concentrated under reduced pressure. The residue was diluted with ethyl acetate, and the organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (NH silica gel use, ethyl acetate-hexane) to give the title compound (4.39 g, yield 99%) as a pale-yellow solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 2.47 (s, 3H), 3.95 (dt, J=4.2, 15, 2H), 4.49 (s, 2H), 5.98 (tt, J=4.2, 56, 1H), 7.26 (s, 1H), 7.29 (d, J=7.8, 1H), 7.75 (d, J=7.8, 1H).

Step D6-amino-2-(2,2-difluoroethyl)-5-methylisoindolin-1-one

The compound (4.31 g, 20.4 mmol) of step C was dissolved in concentrated sulfuric acid (40 ml), 70% nitric acid (d=1.42) (1.50 ml, 23.7 mmol) was added dropwise over 5 min under ice-cooling with stirring, and the mixture was stirred at the same temperature for 1 hr. The reaction mixture was poured into ice water, and extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium hydrogen carbonate and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give a colorless solid (4.79 g). This was dissolved in methanol (150 ml), then ferric chloride (FeCl₃) (733 mg, 4.52 mmol) and activated carbon (1.6 g) were added, and the mixture was stirred at room temperature. Hydrazine (monohydrate 5.0 ml) was added, and the mixture was heated under reflux for 30 min. The reaction mixture was cooled and filtered through celite, and concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (3.36 g, yield 73%) as a colorless solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 2.25 (s, 3H), 3.78 (brs, 2H), 3.93 (dt, J=4.2, 15, 2H), 4.40 (s, 2H), 5.97 (tt, J=4.2, 56, 1H), 7.12 (s, 1H), 7.13 (s, 1H).

Step EN-[2-(2,2-difluoroethyl)-6-methyl-3-oxo-2,3-dihydro-1H-isoindol-5-yl]iminodiacetic acid

Using the compound (3.36 g, 14.8 mmol) of step D and according to the methods of Reference Example 61, step C, and Reference Example 62, step B, the title compound (4.57 g, yield 90%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 2.36 (s, 3H), 3.93 (dt, J=3.6, 16, 2H), 3.96 (s, 4H), 4.46 (s, 2H), 6.26 (tt, J=3.6, 55, 1H), 7.38 (s, 1H), 7.41 (s, 1H), 12.47 (brs, 2H).

Reference Example 147N-(2-ethyl-6-methyl-3-oxo-2,3-dihydro-1H-isoindol-5-yl)iminodiacetic acidStep A5-bromo-2-ethylisoindolin-1-one

Using the compound (7.83 g, 32.2 mmol) of Reference Example 146, step A, and 70% aqueous ethylamine solution (4.0 ml), and according to the method of Reference Example 146, step B, the title compound (2.37 g, yield 31%) was obtained as a colorless solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.27 (t, J=7.2, 3H), 3.67 (q, J=7.2, 2H), 4.37 (s, 2H), 7.59 (dd, J=1.6, 8.3, 1H), 7.61 (d, J=1.6, 1H), 7.70 (d, J=8.3, 1H).

Step B2-ethyl-5-methylisoindolin-1-one

Using the compound (2.32 g, 10.5 mmol) of step A and according to the method of Reference Example 146, step C, the title compound (1.71 g, yield 93%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.26 (t, J=7.2, 3H), 2.45 (s, 3H), 3.66 (q, J=7.2, 2H), 4.33 (s, 2H), 7.26 (d, J=7.7, 1H), 7.27 (s, 1H), 7.72 (d, J=7.7, 1H).

Step C6-amino-2-ethyl-5-methylisoindolin-1-one

Using the compound (1.68 g, 9.59 mmol) of step B and according to the method of Reference Example 146, step D, the title compound (572 mg, yield 31%) was obtained as a colorless solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.24 (t, J=7.2, 3H), 2.25 (s, 3H), 3.64 (q, J=7.2, 2H), 3.74 (brs, 2H), 4.25 (s, 2H), 7.11 (s, 2H).

Step DN-(2-ethyl-6-methyl-3-oxo-2,3-dihydro-1H-isoindol-5-yl)iminodiacetic acid

Using the compound (557 mg, 2.93 mmol) of step C and according to the methods of Reference Example 61, step C, and Reference Example 62, step B, the title compound (682 mg, yield 76%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.14 (t, J=7.2, 3H), 2.35 (s, 3H), 3.50 (q, J=7.2, 2H), 3.95 (s, 4H), 4.34 (s, 2H), 7.34 (s, 1H), 7.36 (s, 1H), 12.45 (brs, 2H).

Reference Example 148N-(2-methyl-8,9,10,11-tetrahydro-7H-azepino[1,2-b]indazol-3-yl)iminodiacetic acidStep A3-iodo-5-methyl-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-6-amine

Using the compound (32.3 g, 83.4 mmol) of Reference Example 137, step A and according to the method of Reference Example 61, step B, the title compound (24.5 g, yield 82%) was obtained as a colorless solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.6-1.8 (m, 3H), 1.98-2.06 (m, 1H), 2.07-2.18 (m, 1H), 2.27 (s, 3H), 2.47-2.57 (m, 1H), 3.65-3.74 (m, 1H), 3.90 (brs, 2H), 3.98-4.06 (m, 1H), 5.52 (dd, J=3.1, 9.2, 1H), 6.72 (s, 1H), 7.10 (s, 1H).

Step BN-[3-iodo-5-methyl-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-6-yl]glycine diethyl ester

Using the compound (24.5 g, 68.6 mmol) of step A and according to the method of Reference Example 61, step C, the title compound (37.9 g) was obtained as a yellow oil.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.23 (t, J=7.2, 6H), 1.6-1.8 (m, 3H), 1.97-2.05 (m, 1H), 2.08-2.17 (m, 1H), 2.44 (s, 3H), 2.48-2.60 (m, 1H), 3.68-3.76 (m, 1H), 3.98-4.05 (m, 1H), 4.11 (s, 4H), 4.14 (q, J=7.2, 4H), 5.59 (dd, J=3.1, 9.7, 1H), 7.22 (s, 1H), 7.33 (s, 1H).

Step CN-[3-(5-chloropentyl)-5-methyl-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-6-yl]glycine diethyl ester

Using the compound (5.52 g, 10.4 mmol) of step B, and trans-5-chloro-1-penten-1-ylboronic acid pinacol ester (2.94 g, 12.8 mmol), and according to the methods of Reference Example 137, step B, and Reference Example 141, step B, the title compound (2.35 g, yield 44%) was obtained as a pale-yellow oil.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.24 (t, J=7.2, 6H), 1.5-1.7 (m, 3H), 1.7-1.9 (m, 6H), 1.93-2.01 (m, 1H), 2.06-2.17 (m, 1H), 2.43 (s, 3H), 2.47-2.57 (m, 1H), 2.90 (t, J=7.7, 2H), 3.53 (t, J=6.6, 2H), 3.68-3.77 (m, 1H), 4.03-4.08 (m, 1H), 4.11 (s, 4H), 4.14 (q, J=7.2, 4H), 5.54 (dd, J=2.6, 9.7, 1H), 7.30 (s, 1H), 7.41 (s, 1H).

Step DN-[3-(5-chloropentyl)-5-methyl-1H-indazol-6-yl]glycine diethyl ester

Using the compound (2.33 g, 4.59 mmol) of step C and according to the method of Reference Example 137, step E, the title compound (1.80 g, yield 93%) was obtained as a colorless oil.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.22 (t, J=7.2, 6H), 1.5-1.6 (m, 2H), 1.78-1.89 (m, 4H), 2.44 (s, 3H), 2.93 (t, J=7.7, 2H), 3.54 (t, J=6.6, 2H), 4.10 (s, 4H), 4.13 (q, J=7.2, 4H), 7.28 (s, 1H), 7.45 (s, 1H), 9.57 (brs, 1H).

Step EN-(2-methyl-8,9,10,11-tetrahydro-7H-azepino[1,2-b]indazol-3-yl)iminodiacetic acid diethyl ester

The compound (1.78 g, 4.20 mmol) of step D was dissolved in N,N-dimethylformamide (120 ml), 60% sodium hydride (206 mg, 5.15 mmol) was added under ice-cooling with stirring, and the mixture was stirred at room temperature for 3 hr. The reaction mixture was diluted with an ethyl acetate-hexane=1:1 mixed solvent of, and the organic layer was washed with water and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (1.31 g, yield 80%) as an orange oil.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.23 (t, J=7.2, 6H), 1.69-1.78 (m, 2H), 1.81-1.89 (m, 2H), 1.89-1.98 (m, 2H), 2.41 (s, 3H), 3.01-3.05 (m, 2H), 4.07 (s, 4H), 4.13 (q, J=7.2, 4H), 4.46-4.52 (m, 2H), 7.30 (s, 1H), 7.36 (s, 1H).

Step FN-(2-methyl-8,9,10,11-tetrahydro-7H-azepino[1,2-b]indazol-3-yl)iminodiacetic acid

Using the compound (1.30 g, 3.36 mmol) of step E and according to the method of Reference Example 62, step B, the title compound (847 mg, yield 76%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.55-1.66 (m, 2H), 1.66-1.76 (m, 2H), 1.82-1.94 (m, 2H), 2.30 (s, 3H), 3.01-3.06 (m, 2H), 3.93 (s, 4H), 4.41-4.44 (m, 2H), 7.10 (s, 1H), 7.36 (s, 1H), 12.40 (brs, 2H).

Reference Example 149N-(2-methyl-7,8,9,10-tetrahydropyrido[1,2-b]indazol-3-yl)iminodiacetic acidStep AN-<3-[4-{[tert-butyl(dimethyl)silyl]oxy}butyl]-5-methyl-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-6-yl>glycine diethyl ester

Using the compound (7.19 g, 13.6 mmol) of Reference Example 148, step B, and trans-4-(tert-butyldimethylsiloxy)-1-buten-1-ylboronic acid pinacol ester (4.93 g, 15.8 mmol), and according to the methods of Reference Example 137, step B, and Reference Example 141, step B, the title compound (4.37 g, yield 54%) was obtained as a colorless oil.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 0.04 (s, 6H), 0.88 (s, 9H), 1.24 (t, J=7.2, 6H), 1.55-1.67 (m, 3H), 1.70-1.86 (m, 4H), 1.92-2.00 (m, 1H), 2.06-2.17 (m, 1H), 2.42 (s, 3H), 2.46-2.58 (m, 1H), 2.90 (t, J=7.7, 2H), 3.64 (t, J=6.4, 2H), 3.68-3.76 (m, 1H), 4.01-4.08 (m, 1H), 4.11 (s, 4H), 4.14 (q, J=7.2, 4H), 5.53 (dd, J=2.6, 9.9, 1H), 7.30 (s, 1H), 7.42 (s, 1H).

Step BN-[3-(4-hydroxybutyl)-5-methyl-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-6-yl]glycine diethyl ester

The compound (4.36 g, 7.39 mmol of step A was dissolved in tetrahydrofuran (60 ml), 1 mol/l tetrabutylammonium fluoride-tetrahydrofuran solution (9.0 ml) was added at room temperature with stirring, and the mixture was stirred at the same temperature for 22 hr. The reaction mixture was diluted with an ethyl acetate-hexane=1:1 mixed solvent, and the organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (2.95 g, yield 84%) as a colorless oil.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.24 (t, J=7.2, 6H), 1.55-1.93 (m, 8H), 1.93-2.03 (m, 1H), 2.06-2.17 (m, 1H), 2.43 (s, 3H), 2.45-2.57 (m, 1H), 2.94 (t, J=7.4, 2H), 3.65 (t, J=6.2, 2H), 3.68-3.77 (m, 1H), 4.03-4.08 (m, 1H), 4.11 (s, 4H), 4.14 (q, J=7.2, 4H), 5.53 (dd, J=2.6, 10.2, 1H), 7.30 (s, 1H), 7.42 (s, 1H).

Step CN-[3-(4-chlorobutyl)-5-methyl-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-6-yl]glycine diethyl ester

The compound (2.91 g, 6.12 mmol) of step B was dissolved in a dichloromethane (20 ml)-carbon tetrachloride (10 ml) mixed solvent, triphenylphosphine (2.55 g, 9.72 mmol) was added at room temperature, and the mixture was stirred with heating at 50Â° C. for 2 hr. The reaction mixture was concentrated, and the obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (2.04 g, yield 67%) as a colorless oil.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.24 (t, J=7.2, 6H), 1.6-2.0 (m, 8H), 2.06-2.18 (m, 1H), 2.43 (s, 3H), 2.46-2.60 (m, 1H), 2.92 (t, J=7.7, 2H), 3.57 (t, J=6.4, 2H), 3.67-3.77 (m, 1H), 4.01-4.08 (m, 1H), 4.11 (s, 4H), 4.14 (q, J=7.2, 4H), 5.54 (dd, J=2.6, 9.8, 1H), 7.30 (s, 1H), 7.41 (s, 1H).

Step DN-(2-methyl-7,8,9,10-tetrahydropyrido[1,2-b]indazol-3-yl)iminodiacetic acid diethyl ester

Using the compound (2.02 g, 4.09 mmol) of step C and according to the methods of Reference Example 148, steps D and E, the title compound (1.26 g, yield 82%) was obtained as an orange oil.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.23 (t, J=7.2, 6H), 1.94-2.02 (m, 2H), 2.09-2.18 (m, 2H), 2.41 (s, 3H), 3.04 (t, J=6.4, 2H), 4.08 (s, 4H), 4.13 (q, J=7.2, 4H), 4.39 (t, J=5.6, 2H), 7.33 (s, 1H), 7.36 (s, 1H).

Step EN-(2-methyl-7,8,9,10-tetrahydropyrido[1,2-b]indazol-3-yl)iminodiacetic acid

Using the compound (1.25 g, 3.35 mmol) of step D and according to the method of Reference Example 62, step B, the title compound (924 mg, yield 87%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.84-1.95 (m, 2H), 1.97-2.08 (m, 2H), 2.30 (s, 3H), 2.98 (t, J=6.2, 2H), 3.93 (s, 4H), 4.27 (t, J=5.8, 2H), 7.10 (s, 1H), 7.34 (s, 1H), 12.40 (brs, 2H).

Reference Example 150N-(8-methyl-2,3-dihydro-1H-pyrrolo[1,2-b]indazol-7-yl)iminodiacetic acidStep AN-[3-(3-hydroxypropyl)-5-methyl-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-6-yl]glycine diethyl ester

Using the compound (9.50 g, 17.9 mmol) of Reference Example 148, step B, and trans-2-chloromethylvinylboronic acid (4.93 g, 15.8 mmol), and according to the methods of Reference Example 137, step B, and Reference Example 141, step B, the title compound (584 mg, yield 7%) was obtained as a yellow oil.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.24 (t, J=7.2, 6H), 1.55-1.85 (m, 3H), 1.95-2.20 (m, 4H), 2.42 (s, 3H), 2.45-2.55 (m, 1H), 3.03 (t, J=7.0, 2H), 3.65-3.80 (m, 3H), 4.00-4.08 (m, 1H), 4.11 (s, 4H), 4.14 (q, J=7.2, 4H), 5.54 (dd, J=2.5, 9.7, 1H), 7.30 (s, 1H), 7.43 (s, 1H).

Step BN-(8-methyl-2,3-dihydro-1H-pyrrolo[1,2-b]indazol-7-yl)iminodiacetic acid diethyl ester

Using the compound (584 mg, 1.27 mmol) of step A and according to the methods of Reference Example 149, steps C and D, the title compound (302 mg, yield 66%) was obtained as a red-bistered oil.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.23 (t, J=7.2, 6H), 2.41 (s, 3H), 2.68-2.77 (m, 2H), 3.13 (t, J=7.2, 2H), 4.08 (s, 4H), 4.13 (q, J=7.2, 4H), 4.38 (t, J=7.2, 2H), 7.35 (s, 1H), 7.40 (s, 1H).

Step CN-(8-methyl-2,3-dihydro-1H-pyrrolo[1,2-b]indazole-7-yl)iminodiacetic acid

Using the compound (291 mg, 0.810 mmol) of step B and according to the method of Reference Example 62, step B, the title compound (190 mg, yield 77%) was obtained as a colorless solid.

35 ¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 2.30 (s, 3H), 2.60-2.69 (m, 2H), 3.07 (t, J=7.2, 2H), 3.93 (s, 4H), 4.29 (t, J=7.4, 2H), 7.15 (s, 1H), 7.35 (s, 1H), 12.41 (brs, 2H).

Reference Example 151N-{5-[4-(aminocarbonyl)-1,3-thiazol-2-yl]-2-methylphenyl}iminodiacetic acidStep A2-{3-[bis(2-ethoxy-2-oxoethyl)amino]-4-methylphenyl}-1,3-thiazole-4-carboxylic acid

To N,N-dimethylformamide (80 ml) were added the compound (7.93 g, 23.4 mmol) of Reference Example 79, step A, and 3-bromopyruvic acid (4.10 g, 24.6 mmol), and the mixture was stirred at 80Â° C. for 30 min. The reaction mixture was cooled, water was added, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (9.19 g, yield 97%) as a brown oil.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.2, 6H), 2.32 (s, 3H), 4.06 (q, J=7.2, 4H), 4.08 (s, 4H), 7.30 (d, J=8.2, 1H), 7.54 (dd, J=2.0, 8.2, 1H), 7.70 (d, J=2.0, 8.2, 1H), 8.45 (s, 1H), 13.11 (brs, 1H).

Step BN-{5-[4-(aminocarbonyl)-1,3-thiazol-2-yl]-2-methylphenyl}iminodiacetic acid diethyl ester

The compound (4.59 g, 11.3 mmol) of step A was dissolved in N,N-dimethylformamide (60 ml), 3H-[1,2,3]triazolo[4,5-b]pyridin-3-ol (1.97 g, 14.5 mmol) and WSC (2.80 g, 14.6 mmol) were added at room temperature, and the mixture was stirred at the same temperature for 70 min. Then, to the reaction mixture was added 28% aqueous ammonia (10 ml), and the mixture was further stirred at room temperature for 2 hr. The reaction mixture was diluted with ethyl acetate and water, and the organic layer was extracted. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, the insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained solid was washed with a diethyl ether-hexane=1:1 mixed solvent, and dried under reduced pressure to give the title compound (4.23 g, yield 92%) as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.2, 6H), 2.32 (s, 3H), 4.06 (q, J=7.2, 4H), 4.08 (s, 4H), 7.29 (d, J=8.2, 1H), 7.61 (d, J=7.7, 1H), 7.68 (brs, 1H), 7.74 (s, 1H), 7.85 (brs, 1H), 8.23 (s, 1H).

Step CN-{5-[4-(aminocarbonyl)-1,3-thiazol-2-yl]-2-methylphenyl}iminodiacetic acid

Using the compound (1.82 g, 4.49 mmol) of step B and according to the method of Reference Example 62, step B, the title compound (1.50 g, yield 96%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 2.31 (s, 3H), 3.17 (s, 3H), 4.00 (s, 4H), 7.28 (d, J=7.7, 1H), 7.58 (d, J=7.7, 1H), 7.69 (brs, 1H), 7.70 (s, 1H), 7.84 (brs, 1H), 8.23 (s, 1H), 12.53 (brs, 2H).

Reference Example 152N-[2-methyl-5-{4-[(methylamino)carbonyl]-1,3-thiazol-2-yl}phenyl]iminodiacetic acid

Using the compound (2.29 g, 5.63 mmol) of Reference Example 151, step A, and 40% aqueous methylamine solution (5.0 ml), and according to the methods of Reference Example 151, step B, and Reference Example 62, step B, the title compound (1.45 g, yield 71%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 2.32 (s, 3H), 2.83 (d, J=5.1, 3H), 4.00 (s, 4H), 7.29 (d, J=7.7, 1H), 7.60 (d, J=7.7, 1H), 7.68 (s, 1H), 8.21 (s, 1H), 8.42 (broad q, 1H), 12.53 (brs, 2H).

Reference Example 153N-[5-{4-[(dimethylamino)carbonyl]-1,3-thiazol-2-yl}-2-methylphenyl]iminodiacetic acid

Using the compound (2.29 g, 5.63 mmol) of Reference Example 151, step A, and 50% aqueous dimethylamine solution (5.0 ml), and according to the methods of Reference Example 151, step B, and Reference Example 62, step B, the title compound (1.65 g, yield 78%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 2.30 (s, 3H), 3.02 (s, 3H), 3.17 (s, 3H), 3.99 (s, 4H), 7.27 (d, J=8.2, 1H), 7.49 (d, J=7.7, 1H), 7.66 (s, 1H), 8.05 (s, 1H), 12.54 (brs, 2H).

The compounds of Reference Examples 133-153 are shown below.

TABLE 6ReferenceStructuralExampleFormula133 [Image Omitted]

134

135

136

137

138

139

140

141

142

143

144

145

146

147

148

149

150

151

152

153

Example 1N²-(5-cyano-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-(5-cyano-2-methylphenyl)-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine

The compound (3.00 g, 12.1 mmol) of Reference Example 61 was dissolved in a dichloromethane (60 ml)-N,N-dimethylformamide (3 ml) mixed solvent, WSC (4.71 g, 24.6 mmol) was added at room temperature, and the mixture was stirred at the same temperature overnight. The reaction mixture was diluted with an ethyl acetate-hexane=1:1 mixed solvent, washed with water and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the reaction mixture was concentrated under reduced pressure. The obtained oil was dissolved in dichloromethane (100 ml), the compound of Reference Example 17 (3.00 g, 16.2 mmol) and 1,8-diazabicyclo[5.4.0]undeca-7-ene (4.8 ml, 32 mmol) were added under ice-cooling with stirring, and the mixture was stirred at room temperature for 7 hr. The reaction mixture was acidified with diluted hydrochloric acid, and the organic layer was extracted with dichloromethane, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (chloroform) to give the title compound (3.38 g, yield 74%) as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.37 (s, 3H), 3.08 (s, 3H), 3.95 (s, 2H), 4.19 (d, J=11.7, 2H), 4.31 (d, J=11.7, 2H), 4.32 (s, 2H), 7.21-7.34 (m, 6H), 7.47 (d, J=1.1, 1H), 13.3 (brs, 1H).

Step BN²-(5-cyano-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

The compound (2.32 g, 6.13 mmol) obtained in step A, the compound of Reference Example 3 (1.67 g, 8.26 mmol) and 1-hydroxybenzotriazole (1.19 g, 8.81 mmol) were dissolved in an N,N-dimethylformamide (3 ml)-dichloromethane (40 ml) mixed solvent, WSC (1.80 g, 9.39 mmol) was added under ice-cooling, and the mixture was stirred at room temperature overnight. The reaction mixture was diluted with an ethyl acetate-hexane=1:1 (250 ml) mixed solvent, washed with water, 10% aqueous citric acid solution, diluted aqueous sodium hydroxide solution and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained solid was washed with a diethyl ether-hexane=1:1 mixed solvent, and dried under reduced pressure to give the title compound (2.81 g, yield 81%) as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.11 (d, J=6.6, 6H), 1.43 (brs, 9H), 2.40 (s, 3H), 2.96 (s, 3H), 3.0-3.2 (m, 2H), 3.34-3.42 (m, 2H), 3.84 (s, 2H), 3.9-4.3 (broad, 1H), 4.15 (d, J=11.7, 2H), 4.24 (s, 2H), 4.27 (d, J=11.7, 2H), 7.19-7.33 (m, 6H), 7.50 (s, 1H), 7.8-8.5 (broad, 1H).

Step CN²-(5-cyano-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

The compound (2.81 g, 4.99 mmol) obtained in step B was dissolved in dichloromethane (15 ml), 4N hydrochloric acid-dioxane solution (15 ml, 60 mmol) was added at room temperature, and the mixture was stirred at the same temperature for 2 hr. Diethyl ether was added to the reaction mixture, and the precipitated solid was collected by filtration, washed with diethyl ether, and dried under reduced pressure to give the title compound (2.60 g, yield 97%) as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.18 (d, J=6.3, 6H), 2.33 (s, 3H), 2.8-3.0 (m, 2H), 2.89 (s, 3H), 3.1-3.4 (m, 3H), 3.90 (s, 2H), 4.13 (d, J=11.7, 2H), 4.26 (d, J=11.7, 2H), 4.30 (s, 2H), 7.25-7.35 (m, 6H), 7.45 (s, 1H), 8.27 (t, J=5.7, 1H), 8.60 (brs, 2H).

Example 2N²-(5-cyano-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-(5-cyano-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (1.73 g, 4.57 mmol) of Example 1, step A, and the compound of Reference Example 2 (1.12 g, 5.95 mmol), and according to the method of Example 1, step B, the title compound (2.11 g, yield 84%) was obtained as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.05 (t, J=6.9, 3H), 1.41 (brs, 9H), 2.39 (s, 3H), 2.97 (s, 3H), 3.16 (q, J=6.9, 2H), 3.2-3.3 (m, 2H), 3.38-3.45 (m, 2H), 3.82 (s, 2H), 4.16 (d, J=11.7, 2H), 4.24 (s, 2H), 4.27 (d, J=11.7, 2H), 7.19-7.30 (m, 6H), 7.49 (s, 1H), 7.9-8.5 (broad, 1H).

Step BN²-(5-cyano-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (469 mg, 0.855 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (443 mg, yield 99%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.17 (t, J=7.2, 3H), 2.34 (s, 3H), 2.8-3.0 (m, 4H), 2.88 (s, 3H), 3.34-3.41 (m, 2H), 3.90 (s, 2H), 4.14 (d, J=11.7, 2H), 4.26 (d, J=11.7, 2H), 4.32 (s, 2H), 7.23-7.34 (m, 6H), 7.45 (s, 1H), 8.32 (broad, 1H), 9.01 (brs, 2H).

Example 3N²-(5-cyano-2-methylphenyl)-N²-{2-[(5-methoxy-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-(5-cyano-2-methylphenyl)-N-{2-[(5-methoxy-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}glycine

Using the compound (401 mg, 1.62 mmol) of Reference Example 61, and the compound (529 mg, 2.46 mmol) of Reference Example 20, and according to the method of Example 1, step A, the title compound (430 mg, yield 65%) was obtained as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.37 (s, 3H), 3.07 (s, 3H), 3.80 (s, 3H), 3.94 (s, 2H), 4.0-4.3 (m, 4H), 4.31 (s, 2H), 6.7-6.9 (m, 2H), 7.12 (d, J=8.4, 1H), 7.2-7.4 (m, 2H), 7.46 (s, 1H), 13.4 (brs, 1H).

Step BN²-(5-cyano-2-methylphenyl)-N²-{2-[(5-methoxy-1,3-dihydro-2H-isoindol-2-yl](methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (411 mg, 1.01 mmol) obtained in step A, and the compound (318 mg, 1.57 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (280 mg, yield 47%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.11 (d, J=6.8, 6H), 1.43 (brs, 9H), 2.40 (s, 3H), 2.95 (s, 3H), 3.0-3.2 (m, 2H), 3.34-3.42 (m, 2H), 3.80 (s, 3H), 3.83 (s, 2H), 4.0-4.3 (m, 5H), 4.24 (s, 2H), 6.77 (d, J=2.1, 1H), 6.82 (dd, J=2.1, 8.3, 1H), 7.12 (d, J=8.3, 1H), 7.2-7.3 (m, 2H), 7.49 (s, 1H), 7.8-8.6 (broad, 1H).

Step CN²-(5-cyano-2-methylphenyl)-N²-{2-[(5-methoxy-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (280 mg, 0.472 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (214 mg, yield 80%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.19 (d, J=6.5, 6H), 2.33 (s, 3H), 2.8-3.0 (m, 2H), 2.87 (s, 3H), 3.1-3.4 (m, 3H), 3.73 (s, 3H), 3.89 (s, 2H), 4.0-4.3 (m, 4H), 4.30 (s, 2H), 6.81 (dd, J=2.1, 8.3, 1H), 6.86 (d, J=2.1, 1H), 7.16 (d, J=8.3, 1H), 7.30 (broad, 2H), 7.45 (s, 1H), 8.27 (m, 1H), 8.68 (brs, 2H).

Example 4N²-(5-cyano-2-methylphenyl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-(5-cyano-2-methylphenyl)-N-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}glycine

To an N,N-dimethylformamide (0.5 ml)-dichloromethane (20 ml) mixed solvent were added the compound (970 mg, 3.91 mmol) of Reference Example 61 and WSC (786 mg, 4.10 mmol), and the mixture was stirred at room temperature for 150 min. The reaction mixture was ice-cooled, the compound (1.05 g, 5.18 mmol) of Reference Example 19 and 1,8-diazabicyclo[5.4.0]undeca-7-ene (1.8 ml, 12 mmol) were added, and the mixture was stirred at room temperature for 7 hr. The reaction mixture was acidified with diluted hydrochloric acid, and the organic layer was extracted with dichloromethane, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (methanol-dichloromethane) to give the title compound (946 mg, yield 61%) as a colorless amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.31 (s, 3H), 2.87 (s, 3H), 3.99 (s, 2H), 4.10-4.24 (m, 4H), 4.30 (s, 2H), 7.0-7.2 (m, 2H), 7.27-7.33 (m, 3H), 7.42 (s, 1H), 12.51 (brs, 1H).

Step BN²-(5-cyano-2-methylphenyl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl) (methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (944 mg, 2.38 mmol) obtained in step A, and the compound (665 mg, 3.29 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (1.28 g, yield 93%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.11 (d, J=6.9, 6H), 1.43 (brs, 9H), 2.40 (s, 3H), 2.96 (s, 3H), 3.0-3.2 (m, 2H), 3.34-3.42 (m, 2H), 3.83 (s, 2H), 3.9-4.3 (m, 5H), 4.23 (s, 2H), 6.9-7.0 (m, 2H), 7.15-7.27 (m, 3H), 7.49 (s, 1H), 7.8-8.4 (broad, 1H).

Step CN²-(5-cyano-2-methylphenyl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (422 mg, 0.727 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (384 mg, yield 95%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.19 (d, J=6.3, 6H), 2.34 (s, 3H), 2.8-3.0 (m, 2H), 2.88 (s, 3H), 3.1-3.5 (m, 3H), 3.89 (s, 2H), 4.0-4.3 (m, 4H), 4.30 (s, 2H), 7.0-7.2 (m, 2H), 7.27-7.33 (m, 3H), 7.45 (s, 1H), 8.27 (broad t, 1H), 8.73 (brs, 2H).

Example 5N²-(5-cyano-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(ethyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-(5-cyano-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(ethyl)amino]-2-oxoethyl}glycine

Using the compound (0.80 g, 3.22 mmol) of Reference Example 61, and the compound (0.96 g, 4.83 mmol) of Reference Example 22, and according to the method of Example 1, step A, the title compound (0.81 g, yield 64%) was obtained as a gray amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.36 (t, J=6.9, 3H), 2.36 (s, 3H), 3.59 (q, J=7.2, 2H), 3.97 (s, 2H), 4.19-4.35 (m, 6H), 7.20-7.30 (m, 6H), 7.45 (s, 1H).

Step BN²-(5-cyano-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(ethyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (0.40 g, 1.02 mmol) obtained in step A, and the compound (0.30 g, 1.59 mmol) of Reference Example 2, and according to the method of Example 1, step B, the title compound (0.42 g, yield 73%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.05 (t, J=6.8, 3H), 1.29 (t, J=7.1, 3H), 1.42 (s, 9H), 2.39 (s, 3H), 3.14-3.29 (m, 4H), 3.40-3.53 (m, 4H), 3.83 (s, 2H), 4.15-4.32 (m, 6H), 7.24-7.30 (m, 6H), 7.48 (s, 1H), 8.12 8.20 (2brs, 1H).

Step CN²-(5-cyano-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(ethyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (0.42 g, 0.75 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (0.30 g, yield 82%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.06-1.21 (m, 6H), 2.33 (s, 3H), 2.8-3.1 (m, 4H), 3.3-3.5 (m, 4H), 3.91 (s, 2H), 4.08-4.28 (m, 6H), 7.20-7.48 (m, 7H), 8.29 (m, 1H), 8.79 (brs, 2H).

Example 6N²-(5-cyano-2-methylphenyl)-N²-{2-[methyl(5-methyl-2,3-dihydro-1H-inden-2-yl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochlorideStep AN-(5-cyano-2-methylphenyl)-N-{2-[methyl(5-methyl-2,3-dihydro-1H-inden-2-yl)amino]-2-oxoethyl}glycine

Using the compound (1.27 g, 5.11 mmol) of Reference Example 61, and the compound (1.50 g, 7.67 mmol) of Reference Example 25, and according to the method of Example 4, step A, the title compound (1.20 g, yield 60%) was obtained as a pale-bistered amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.26 (s, 3H), 2.32 (s, 3H), 2.64 (s, 1.2H), 2.74 (s, 1.8H), 2.74-3.08 (m, 4H), 3.94-3.96 (m, 2H), 4.09 (s, 1.2H), 4.23 (s, 0.8H), 4.82-4.86 (m, 0.4H), 5.25-5.28 (m, 0.6H), 6.95 (d, J=7.8, 1H), 7.02 (s, 1H), 7.09 (d, J=7.8, 1H), 7.29-7.36 (m, 2H), 7.47 (d, J=9.0, 1H), 12.62 (brs, 1H).

Step BN²-(5-cyano-2-methylphenyl)-N²-{2-[methyl(5-methyl-2,3-dihydro-1H-inden-2-yl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (600 mg, 1.53 mmol) obtained in step A, and the compound (464 mg, 2.30 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (819 mg, yield 93%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.03 (d, J=6.3, 6H), 1.39 (s, 9H), 2.26 (s, 3H), 2.34 (s, 3H), 2.50 (s, 1.2H), 2.66 (s, 1.8H), 2.66-3.22 (m, 8H), 3.79-3.81 (m, 2H), 3.89-4.20 (m, 1H), 4.08 (s, 1.2H), 4.23 (s, 0.8H), 4.76-4.84 (m, 0.4H), 5.25-5.33 (m, 0.6H), 6.95 (d, J=7.8, 1H), 7.02 (s, 1H), 7.08 (d, J=7.5, 1H), 7.28-7.35 (m, 2H), 7.48 (d, J=8.7, 1H), 8.12-8.18 (m, 1H).

Step CN²-(5-cyano-2-methylphenyl)-N²-{2-[methyl(5-methyl-2,3-dihydro-1H-inden-2-yl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochloride

Using the compound (300 mg, 0.52 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (212 mg, yield 80%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.21 (d, J=6.3, 6H), 2.26 (s, 3H), 2.75 (s, 3H), 2.66 (s, 1.2H), 2.75 (s, 1.8H), 2.75-3.18 (m, 6H), 3.24-3.28 (m, 1H), 3.34-3.42 (m, 2H), 3.85-3.88 (m, 2H), 4.09 (s, 1.2H), 4.25 (s, 0.8H), 4.77-4.85 (m, 0.4H), 5.25-5.32 (m, 0.6H), 6.96 (d, J=7.5, 1H), 7.02 (s, 1H), 7.09 (d, J=7.5, 1H), 7.28-7.35 (m, 2H), 7.49 (d, J=9.0, 1H), 8.35-8.39 (m, 1H), 8.79 (brs, 2H).

Example 7N²-(5-cyano-2-methylphenyl)-N²-{2-[methyl(5-methyl-2,3-dihydro-1H-inden-2-yl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochlorideStep AN²-(5-cyano-2-methylphenyl)-N²-{2-[methyl(5-methyl-2,3-dihydro-1H-inden-2-yl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (600 mg, 1.53 mmol) obtained in Example 6, step A, and the compound (432 mg, 2.30 mmol) of Reference Example 2, and according to the method of Example 1, step B, the title compound (819 mg, yield 95%) was obtained as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 0.96 (t, J=6.6, 3H), 1.37 (s, 9H), 2.25 (s, 3H), 2.34 (s, 3H), 2.65 (s, 1.2H), 2.74 (s, 1.8H), 2.74-3.20 (m, 10H), 3.77-3.81 (m, 2H), 4.07 (s, 1.2H), 4.23 (s, 0.8H), 4.76-4.84 (m, 0.4H), 5.23-5.32 (m, 0.6H), 6.95 (d, J=7.8, 1H), 7.02 (s, 1H), 7.09 (d, J=7.8, 1H), 7.28-7.34 (m, 2H), 7.47 (d, J=8.7, 1H), 8.10-8.13 (m, 1H).

Step BN²-(5-cyano-2-methylphenyl)-N²-{2-[methyl(5-methyl-2,3-dihydro-1H-inden-2-yl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (300 mg, 0.53 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (242 mg, yield 92%) was obtained as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.18 (t, J=7.2, 3H), 2.26 (s, 3H), 2.35 (s, 3H), 2.58-3.17 (m, 8H), 2.66 (s, 1.2H), 2.75 (s, 1.8H), 3.34-3.41 (m, 2H), 3.84-3.88 (m, 2H), 4.10 (s, 1.2H), 4.25 (s, 0.8H), 4.78-4.85 (m, 0.4H), 5.25-5.32 (m, 0.6H), 6.96 (d, J=7.5, 1H), 7.03 (s, 1H), 7.09 (d, J=7.8, 1H), 7.29-7.35 (m, 2H), 7.49 (d, âˆ’J=9.0, 1H), 8.34-8.37 (m, 1H), 8.77-9.01 (broad, 2H).

Example 8N²-(5-cyano-2-methylphenyl)-N²-{2-[methyl(5-methoxy-2,3-dihydro-1H-inden-2-yl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochlorideStep AN-(5-cyano-2-methylphenyl)-N-{2-[methyl(5-methoxy-2,3-dihydro-1H-inden-2-yl)amino]-2-oxoethyl}glycine

Using the compound (1.53 g, 6.17 mmol) of Reference Example 61, and the compound (1.98 g, 9.26 mmol) of Reference Example 29, and according to the method of Example 4, step A, the title compound (1.60 g, yield 64%) was obtained as a pale-bistered amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.33 (s, 3H), 2.51-3.10 (m, 7H), 3.71 (s, 3H), 3.94-3.96 (m, 2H), 4.09 (s, 1.2H), 4.23 (s, 0.8H), 4.83-4.86 (m, 0.4H), 5.24-5.31 (m, 0.6H), 6.71 (d, J=7.8, 1H), 6.80 (s, 1H), 7.10 (d, J=8.1, 1H), 7.29-7.33 (m, 2H), 7.45-7.50 (m, 1H), 12.60 (brs, 1H).

Step BN²-(5-cyano-2-methylphenyl)-N²-{2-[methyl(5-methoxy-2,3-dihydro-1H-inden-2-yl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (800 mg, 1.96 mmol) obtained in step A, and the compound (595 mg, 2.94 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (1.11 g, yield 96%) was obtained as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.03 (d, J=6.6, 6H), 1.37-1.41 (m, 9H), 2.34 (s, 3H), 2.60-3.22 (m, 12H), 3.71 (s, 3H), 3.79-3.81 (m, 2H), 4.08 (s, 1.2H), 4.23 (s, 0.8H), 4.77-4.85 (m, 0.4H), 5.26-5.34 (m, 0.6H), 6.71 (d, J=8.1, 1H), 6.80 (s, 1H), 7.10 (d, J=8.1, 1H), 7.28-7.34 (m, 2H), 7.47 (d, J=9.0, 1H), 8.14 (brs, 1H).

Step CN²-(5-cyano-2-methylphenyl)-N²-{2-[methyl(5-methoxy-2,3-dihydro-1H-inden-2-yl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochloride

Using the compound (500 mg, 0.84 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (386 mg, yield 87%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.21 (d, J=6.6, 6H), 2.35 (s, 3H), 2.66 (s, 1.2H), 2.76 (s, 1.8H), 2.76-3.17 (m, 6H), 3.20-3.43 (m, 3H), 3.71 (s, 3H), 3.84-3.88 (m, 2H), 4.10 (s, 1.2H), 4.26 (s, 0.8H), 4.79-4.85 (m, 0.4H), 5.26-5.30 (m, 0.6H), 6.71 (d, J=8.2, 1H), 6.80 (s, 1H), 7.10 (d, J=8.2, 1H), 7.29-7.35 (m, 2H), 7.47-7.51 (m, 1H), 8.37-8.40 (m, 1H), 8.89 (brs, 2H).

Example 9N²-(5-cyano-2-methylphenyl)-N²-{2-[methyl(5-methoxy-2,3-dihydro-1H-inden-2-yl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochlorideStep AN²-(5-cyano-2-methylphenyl)-N²-{2-[methyl(5-methoxy-2,3-dihydro-1H-inden-2-yl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (800 mg, 1.96 mmol) obtained in Example 8, step A, and the compound (554 mg, 2.94 mmol) of Reference Example 2, and according to the method of Example 1, step B, the title compound (1.10 g, yield 97%) was obtained as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 0.94-0.99 (m, 3H), 1.36-1.39 (m, 9H), 2.33 (s, 3H), 2.65-3.24 (m, 13H), 3.71 (s, 3H), 3.79 3.80 (2s, 2H), 4.07 (s, 1.2H), 4.23 (s, 0.8H), 4.77-4.83 (m, 0.4H), 5.27-5.33 (m, 0.6H), 6.71 (d, J=8.4, 1H), 6.80 (s, 1H), 7.10 (d, J=8.1, 1H), 7.28-7.35 (m, 2H), 7.47 (d, J=9.0, 1H), 8.11 (brs, 1H).

Step BN²-(5-cyano-2-methylphenyl)-N²-{2-[methyl(5-methoxy-2,3-dihydro-1H-inden-2-yl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (500 mg, 0.87 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (409 mg, yield 91%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.18 (t, J=7.2, 3H), 2.35 (s, 3H), 2.57-3.19 (m, 11H), 3.34-3.41 (m, 2H), 3.71 (s, 3H), 3.85-3.88 (m, 2H), 4.10 (s, 1.2H), 4.26 (s, 0.8H), 4.79-4.86 (m, 0.4H), 5.26-5.30 (m, 0.6H), 6.72 (d, J=8.4, 1H), 6.80 (s, 1H), 7.10 (d, J=8.1, 1H), 7.28-735 (m, 2H), 7.47-7.51 (m, 1H), 8.35-8.37 (m, 1H), 8.89 (brs, 2H).

Example 10N²-(5-cyano-2-methylphenyl)-N²-{2-[(5-fluoro-2,3-dihydro-1H-inden-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochlorideStep AN²-(5-cyano-2-methylphenyl)-N²-{2-[(5-fluoro-2,3-dihydro-1H-inden-2-yl)(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (870 mg, 3.50 mmol) of Reference Example 61, the compound (1.06 g, 5.26 mmol) of Reference Example 27, and the compound (756 mg, 3.74 mmol) of Reference Example 3, and according to the methods of Example 4, step A, and Example 1, step B, the title compound (1.40 g, yield 69%) was obtained as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.03 (d, J=6.6, 6H), 1.38 (s, 9H), 2.34 (s, 3H), 2.64-3.18 (m, 11H), 3.78-3.81 (m, 2H), 3.89-4.20 (m, 1H), 4.09 (s, 1.2H), 4.24 (s, 0.8H), 4.82-4.89 (m, 0.4H), 5.27-5.34 (m, 0.6H), 6.96 (t, J=8.7, 1H), 7.05 (d, J=9.3, 1H), 7.19-7.25 (m, 1H), 7.28-7.34 (m, 2H), 7.48 (d, J=9.9, 1H), 8.09-8.14 (m, 1H).

Step BN²-(5-cyano-2-methylphenyl)-N²-{2-[(5-fluoro-2,3-dihydro-1H-inden-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochloride

Using the compound (700 mg, 1.21 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (609 mg, yield 97%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.21 (d, J=6.3, 6H), 2.36 (s, 3H), 2.65-3.19 (m, 9H), 3.20-3.43 (m, 3H), 3.85-3.87 (m, 2H), 4.26 (s, 1.2H), 4.38 (s, 0.8H), 4.84-4.87 (m, 0.4H), 5.27-5.34 (m, 0.6H), 6.96 (t, J=8.7, 1H), 7.05 (d, J=9.1, 1H), 7.20-7.25 (m, 1H), 7.29-7.32 (m, 2H), 7.49 (d, J=10.2, 1H), 8.38 (t, J=5.6, 1H), 8.86 (brs, 2H).

Example 11N²-{2-[(5-chloro-2,3-dihydro-1H-inden-2-yl)(methyl)amino]-2-oxoethyl}-N²-(5-cyano-2-methylphenyl)-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochlorideStep AN²-{2-[(5-chloro-2,3-dihydro-1H-inden-2-yl)(methyl)amino]-2-oxoethyl]-N²-(5-cyano-2-methylphenyl) [(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (1.36 g, 5.48 mmol) of Reference Example 61, the compound (1.79 g, 8.21 mmol) of Reference Example 28, and the compound (1.07 g, 5.28 mmol) of Reference Example 3, and according to the methods of Example 4, step A, and Example 1, step B, the title compound (2.00 g, yield 61%) was obtained as a bistered amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.03 (d, J=6.5, 6H), 1.39 (s, 9H), 2.34 (s, 3H), 2.65-2.77 (m, 3H), 2.80-3.19 (m, 8H), 3.79-3.81 (m, 2H), 3.89-4.20 (m, 1H), 4.09 (s, 1.2H), 4.23 (s, 0.8H), 4.83-4.90 (m, 0.4H), 5.26-5.34 (m, 0.6H), 7.16-7.34 (m, 5H), 7.46-7.50 (m, 1H), 8.11-8.13 (m, 1H).

Step BN²-{2-[(5-chloro-2,3-dihydro-1H-inden-2-yl)(methyl)amino]-2-oxoethyl}-N²-(5-cyano-2-methylphenyl)-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochloride

Using the compound (1.00 g, 1.68 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (853 mg, yield 95%) was obtained as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.21 (d, J=6.6, 6H), 2.35 (s, 3H), 2.66-2.76 (m, 3H), 2.84-3.19 (m, 6H), 3.21-3.45 (m, 3H), 3.84-3.87 (m, 2H), 4.10 (s, 1.2H), 4.25 (s, 0.8H), 4.82-4.87 (m, 0.4H), 5.26-5.35 (m, 0.6H), 7.16-7.36 (m, 5H), 7.47-7.51 (m, 1H), 8.32-8.36 (m, 1H), 8.73 (brs, 2H).

Example 12N²-(5-cyano-2-methylphenyl)-N²-{2-[methyl(4-methyl-2,3-dihydro-1H-inden-2-yl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochlorideStep AN²-(5-cyano-2-methylphenyl)-N²-{2-[methyl (4-methyl-2,3-dihydro-1H-inden-2-yl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (1.55 g, 6.24 mmol) of Reference Example 61, the compound (1.85 g, 9.36 mmol) of Reference Example 26, and the compound (1.32 g, 6.51 mmol) of Reference Example 3, and according to the methods of Example 4, step A, and Example 1, step B, the title compound (2.52 g, yield 70%) was obtained as a bistered oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.03 (d, J=6.6, 6H), 1.39 (s, 9H), 2.19 (s, 3H), 2.35 (s, 3H), 2.58-3.21 (m, 11H), 3.79-3.82 (m, 2H), 3.90-4.19 (m, 1H), 4.09 (s, 1.2H), 4.25 (s, 0.8H), 4.80-4.86 (m, 0.4H), 5.28-5.35 (m, 0.6H), 6.94-7.08 (m, 3H), 7.28-7.35 (m, 2H), 7.46-7.51 (m, 1H), 8.13-8.15 (m, 1H).

Step BN²-(5-cyano-2-methylphenyl)-N²-{2-[methyl(4-methyl-2,3-dihydro-1H-inden-2-yl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochloride

Using the compound (1.25 g, 2.17 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (1.04 g, yield 94%) was obtained as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.22 (d, J=6.4, 6H), 2.19 (s, 3H), 2.36 (s, 3H), 2.60-3.48 (m, 12H), 3.86-3.89 (m, 2H), 4.12 (s, 1.2H), 4.28 (s, 0.8H), 4.81-4.88 (m, 0.4H), 5.27-5.34 (m, 0.6H), 6.94-7.08 (m, 3H), 7.28-7.32 (m, 2H), 7.47-7.52 (m, 1H), 8.42-8.45 (m, 1H), 9.06 (brs, 2H).

Example 13N²-(5-cyano-2-methylphenyl)-N²-{2-[methyl(1,2,3,4-tetrahydronaphthalen-2-yl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochlorideStep AN-(5-cyano-2-methylphenyl)-N-{2-[methyl(1,2,3,4-tetrahydronaphthalen-2-yl)amino]-2-oxoethyl}glycine

Using the compound (1.00 g, 4.03 mmol) of Reference Example 61, and the compound (1.20 g, 6.05 mmol) of Reference Example 34, and according to the method of Example 4, step A, the title compound (1.02 g, yield 64%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.65-1.98 (m, 2H), 2.29 2.34 (2s, 3H), 2.58-3.05 (m, 7H), 3.90 3.96 (2s, 2H), 4.10-4.80 (m, 3H), 7.08 (s, 4H), 7.30-7.33 (m, 2H), 7.48 (d, J=11.4, 1H), 12.62 (brs, 1H).

Step BN²-(5-cyano-2-methylphenyl)-N²-{2-[methyl(1,2,3,4-tetrahydronaphthalen-2-yl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (1.02 g, 2.60 mmol) obtained in step A, and the compound (789 mg, 3.90 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (1.40 g, yield 93%) was obtained as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.21 (d, J=6.9, 6H), 1.43 (s, 9H), 1.75-2.05 (m, 2H), 2.39 2.42 (2s, 3H), 2.64-3.48 (m, 12H), 3.86 (brs, 2H), 3.97-4.02 (m, 2H), 4.00-4.18 (m, 0.4H), 4.84-4.91 (m, 0.6H), 7.03-7.18 (m, 4H), 7.26 (s, 3H), 7.48 (s, 1H).

Step CN²-(5-cyano-2-methylphenyl)-N²-{2-[methyl(1,2,3,4-tetrahydronaphthalen-2-yl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochloride

Using the compound (700 mg, 1.22 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (480 mg, yield 77%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.20 (d, J=6.3, 6H), 1.62-2.00 (m, 2H), 2.33 2.37 (2s, 3H), 2.64-3.08 (m, 9H), 3.17-3.42 (m, 3H), 3.56-4.71 (m, 5H), 7.09 (s, 4H), 7.28-7.33 (m, 2H), 7.49 (d, J=9.0, 1H), 8.38-8.41 (m, 1H), 8.82 (brs, 2H).

Example 14N²-(5-cyano-2-methylphenyl)-N²-[2-{methyl[4-(methylsulfonyl)piperazin-1-yl]amino}-2-oxoethyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN²-(5-cyano-2-methylphenyl)-N²-[2-{methyl[4-(methylsulfonyl)piperazin-1-yl]amino}-2-oxoethyl]-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (267 mg, 1.08 mmol) of Reference Example 61, the compound (222 mg, 1.15 mmol) of Reference Example 48, and the compound (328 mg, 1.62 mmol) of Reference Example 3, and according to the methods of Example 4, step A, and Example 1, step B, the title compound (476 mg, yield 73%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.12 (d, J=6.9, 6H), 1.44 (brs, 9H), 2.38 (s, 3H), 2.7-2.8 (m, 2H), 2.84 (s, 3H), 2.90-3.05 (m, 7H), 3.1-3.2 (m, 2H), 3.3-3.4 (m, 2H), 3.7-3.9 (m, 2H), 3.79 (s, 2H), 3.9-4.3 (broad, 1H), 4.16 (s, 2H), 7.2-7.3 (m, 2H), 7.44 (s, 1H), 7.7-8.4 (broad, 1H).

Step BN²-(5-cyano-2-methylphenyl)-N²-[2-{methyl[4-(methylsulfonyl)piperazin-1-yl]amino}-2-oxoethyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (475 mg, 0.782 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (375 mg, yield 83%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.21 (d, J=6.6, 6H), 2.32 (s, 3H), 2.7-3.0 (m, 8H), 2.84 (s, 3H), 2.92 (s, 3H), 3.1-3.4 (m, 3H), 3.5-3.6 (m, 2H), 3.90 (s, 2H), 4.25 (s, 2H), 7.30 (broad, 2H), 7.42 (s, 1H), 8.35 (t, J=5.7, 1H), 8.81 (brs, 2H).

Example 15N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]glycine

Using the compound (2.66 g, 8.71 mmol) of Reference Example 62, and the compound (2.47 g, 13.4 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (3.46 g, yield 91%) was obtained as a gray amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.38 (s, 3H), 2.63 (s, 3H), 3.06 (s, 3H), 3.94 (s, 2H), 4.17 (d, J=11.7, 2H), 4.28 (d, J=11.7, 2H), 4.31 (s, 2H), 7.19-7.31 (m, 5H), 7.75 (dd, J=1.2, 7.8, 1H), 7.92 (d, J=1.2, 1H), 13.53 (brs, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (3.45 g, 7.92 mmol) obtained in step A, and the compound (2.33 g, 11.5 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (4.07 g, yield 83%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.11 (d, J=6.9, 6H), 1.46 (brs, 9H), 2.41 (s, 3H), 2.62 (s, 3H), 2.94 (s, 3H), 3.0-3.2 (m, 2H), 3.37-3.45 (m, 2H), 3.82 (s, 2H), 3.9-4.3 (broad, 1H), 4.15 (d, J=11.7, 2H), 4.23 (d, J=11.7, 2H), 4.27 (s, 2H), 7.18-7.29 (m, 5H), 7.69 (d, J=7.2, 1H), 7.94 (d, J=1.5, 1H), 8.1-8.7 (broad, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (4.05 g, 6.53 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (3.57 g, yield 92%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.18 (d, J=6.5, 6H), 2.34 (s, 3H), 2.65 (s, 3H), 2.8-3.0 (m, 2H), 2.88 (s, 3H), 3.1-3.3 (m, 1H), 3.35-3.42 (m, 2H), 3.92 (s, 2H), 4.13 (d, J=11.7, 2H), 4.27 (d, J=11.7, 2H), 4.35 (s, 2H), 7.2-7.3 (m, 5H), 7.51 (d, J=7.6, 1H), 7.75 (s, 1H), 8.36 (t, J=5.7, 1H), 8.72 (brs, 2H).

Example 16N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (1.63 g, 2.97 mmol) of Example 2, step A and according to the method of Reference Example 62, step A, the title compound (1.26 g, yield 70%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.04 (t, J=7.2, 3H), 1.44 (brs, 9H), 2.40 (s, 3H), 2.62 (s, 3H), 2.95 (s, 3H), 3.0-3.2 (m, 2H), 3.2-3.3 (m, 2H), 3.4-3.5 (m, 2H), 3.81 (s, 2H), 4.16 (d, J=11.7, 2H), 4.24 (d, J=11.7, 2H), 4.28 (s, 2H), 7.18-7.29 (m, 5H), 7.68 (dd, J=1.2, 8.4, 1H), 7.94 (d, J=1.2, 1H), 8.38 8.63 (2brs, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (1.25 g, 2.06 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (1.12 g, yield 94%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.2, 3H), 2.33 (s, 3H), 2.65 (s, 3H), 2.8-3.0 (m, 4H), 2.88 (s, 3H), 3.3-3.4 (m, 2H), 3.92 (s, 2H), 4.13 (d, J=11.7, 2H), 4.26 (d, J=11.7, 2H), 4.35 (s, 2H), 7.2-7.3 (m, 5H), 7.51 (dd, J=1.2, 7.6, 1H), 7.75 (d, J=1.2, 1H), 8.34 (t, J=5.7, 1H), 8.70 (brs, 2H).

Example 17N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(4-hydroxypiperidin-1-yl)ethyl]glycinamide dihydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-(2-bromoethyl)glycinamide

Using the compound (1.24 g, 2.85 mmol) of Example 15, step A, 2-bromoethylamine hydrobromide (786 mg, 3.84 mmol), and N,N-diisopropylethylamine (0.70 ml, 4.1 mmol), and according to the method of Example 1, step B, the title compound (1.08 g, yield 70%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.44 (s, 3H), 2.62 (s, 3H), 2.96 (s, 3H), 3.47 (t, J=6.3, 2H), 3.7-3.8 (m, 2H), 3.80 (s, 2H), 4.17 (d, J=11.7, 2H), 4.24 (d, J=11.7, 2H), 4.33 (s, 2H), 7.18-7.31 (m, 5H), 7.71 (dd, J=1.2, 7.8, 1H), 7.95 (d, J=1.2, 1H), 8.87 (t, J=5.7, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(4-hydroxypiperidin-1-yl)ethyl]glycinamide

The compound (1.08 g, 1.99 mmol) obtained in step A and 4-hydroxypiperidine (1.44 g, 14.2 mmol) were dissolved in N,N-dimethylformamide (15 ml), and the mixture was stirred with heating at 60Â° C. for 100 min. The reaction mixture was cooled, diluted with water, and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ammonia-containing methanol-dichloromethane) to give the title compound (967 mg, yield 87%) as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.37 (d, J=4.8, 1H), 1.4-1.6 (m, 2H), 1.8-1.9 (m, 2H), 2.0-2.2 (m, 2H), 2.4-2.5 (m, 2H), 2.44 (s, 3H), 2.62 (s, 3H), 2.7-2.8 (m, 2H), 2.94 (s, 3H), 3.35-3.42 (m, 2H), 3.5-3.7 (m, 1H), 3.85 (s, 2H), 4.15 (d, J=11.7, 2H), 4.24 (d, J=11.7, 2H), 4.26 (s, 2H), 7.18-7.29 (m, 5H), 7.68 (dd, J=1.2, 7.7, 1H), 7.95 (d, J=1.2, 1H), 8.24 (broad t, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(4-hydroxypiperidin-1-yl)ethyl]glycinamide dihydrochloride

The compound (927 mg, 1.65 mmol) obtained in step B was dissolved in ethyl acetate (10 ml), and 4N hydrochloric acid-dioxane solution (1.0 ml, 4.0 mmol) was added at room temperature with stirring. The reaction mixture was diluted with ethyl acetate, and the precipitated solid was filtered, and dried under reduced pressure to give the title compound (901 mg, yield 86%) as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.5-2.0 (m, 4H), 2.34 (s, 3H), 2.65 (s, 3H), 2.7-2.9 (m, 1H), 2.88 (s, 3H), 3.0-3.6 (m, 8H), 3.93 (s, 2H), 4.13 (d, J=11.7, 2H), 4.26 (d, J=11.7, 2H), 4.34 (s, 2H), 7.2-7.3 (m, 5H), 7.51 (d, J=7.5, 1H), 7.74 (s, 1H), 8.37 (t, J=5.7, 1H), 9.95 (brs, 1H).

Example 18N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(3-hydroxypyrrolidin-1-yl)ethyl]glycinamide dihydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(3-hydroxypyrrolidin-1-yl)ethyl]glycinamide

Using the compound (453 mg, 0.837 mmol) of Example 17, step A, and 3-pyrrolidinol (0.5 ml), and according to the method of Example 17, step B, the title compound (426 mg, yield 93%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.7-1.9 (m, 1H), 2.0-2.3 (m, 3H), 2.42 (s, 3H), 2.5-2.7 (m, 2H), 2.62 (s, 3H), 2.95 (s, 3H), 2.95-3.15 (m, 2H), 3.3-3.5 (m, 2H), 3.6-3.8 (m, 2H), 4.0-4.4 (m, 7H), 7.1-7.3 (m, 5H), 7.69 (dd, J=1.5, 7.8, 1H), 7.94 (d, J=1.5, 1H), 8.90 (broad t, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(3-hydroxypyrrolidin-1-yl)ethyl]glycinamide dihydrochloride

Using the compound (419 mg, 0.765 mmol) obtained in step A and according to the method of Example 17, step C, the title compound (403 mg, yield 85%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.6-2.0 (m, 2H), 2.0-2.2 (m, 1H), 2.34 (s, 3H), 2.65 (s, 3H), 2.88 2.89 (2s, 3H), 2.9-3.6 (m, 8H), 3.93 3.94 (2s, 2H), 4.13 (d, J=11.7, 2H), 4.26 (d, J=11.7, 2H), 4.33 4.35 (2s, 2H), 7.19-7.30 (m, 5H), 7.51 (d, J=7.8, 1H), 7.75 (d, J=1.2, 1H), 8.33 (broad t, 1H), 10.13 10.58 (2brs, 1H).

Example 19N²-{2-[(4-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN-{2-[(4-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]glycine

Using the compound (471 mg, 1.54 mmol) of Reference Example 62, and the compound (431 mg, 2.13 mmol) of Reference Example 18, and according to the method of Example 1, step A, the title compound (442 mg, yield 63%) was obtained as a brown oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.38 (s, 3H), 2.63 (s, 3H), 3.06 (s, 3H), 3.94 (s, 2H), 4.2-4.4 (m, 6H), 6.92-7.02 (m, 2H), 7.22-7.32 (m, 2H), 7.75 (dd, J=1.5, 7.8, 1H), 7.92 (d, J=1.5, 1H), 13.2 (brs, 1H).

Step BN²-{2-[(4-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (436 mg, 0.961 mmol) obtained in step A, and the compound (278 mg, 1.48 mmol) of Reference Example 2, and according to the method of Example 1, step B, the title compound (503 mg, yield 84%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.05 (t, J=7.2, 3H), 1.44 (brs, 9H), 2.40 (s, 3H), 2.62 (s, 3H), 2.95 (s, 3H), 3.1-3.4 (m, 4H), 3.4-3.5 (m, 2H), 3.80 (s, 2H), 4.1-4.4 (m, 6H), 6.9-7.0 (m, 2H), 7.2-7.3 (m, 2H), 7.69 (d, J=7.2, 1H), 7.93 (d, J=1.5, 1H), 8.2-8.7 (broad, 1H).

Step CN²-{2-[(4-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (502 mg, 0.805 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (424 mg, yield 88%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.14 (t, J=7.2, 3H), 2.34 (s, 3H), 2.65 (s, 3H), 2.8-3.0 (m, 4H), 2.89 (s, 3H), 3.34-3.41 (m, 2H), 3.91 (s, 2H), 4.1-4.4 (m, 6H), 7.06-7.15 (m, 2H), 7.26-7.34 (m, 2H), 7.52 (dd, J=1.2, 7.8, 1H), 7.76 (d, J=1.2, 1H), 8.32 (t, J=5.7, 1H), 8.60 (brs, 2H).

Example 20N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide hydrochlorideStep AN²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

The compound (2.00 g, 6.55 mmol) of Reference Example 62 was dissolved in N,N-dimethylformamide (20 ml), WSC (1.27 g, 6.62 mmol) was added at room temperature, and the mixture was stirred at the same temperature for 1 hr. Then, the reaction mixture was stirred under ice-cooling, the compound (1.35 g, 6.66 mmol) of Reference Example 19 and N,N-diisopropylethylamine (1.15 ml, 6.76 mmol) were added, and the mixture was stirred for 2 hr under ice-cooling. Then, to the reaction mixture were added the compound (1.30 g, 6.90 mmol) of Reference Example 2, WSC (1.33 g, 6.94 mmol) and 1-hydroxybenzotriazole (940 mg, 6.96 mmol), and the mixture was stirred at room temperature for 4 hr. The reaction mixture was diluted with an ethyl acetate-hexane=1:1 mixed solvent, and the organic layer was washed with water, 10% aqueous citric acid solution, diluted aqueous sodium hydroxide solution and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-methanol) to give a pale-yellow amorphous solid (3.88 g). This was dissolved in diethyl ether (50 ml), and stood in a refrigerator overnight to allow precipitation of a solid, which was collected by filtration, washed with diethyl ether, and dried under reduced pressure to give the title compound (3.11 g, yield 76%) as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.05 (t, J=7.2, 3H), 1.44 (brs, 9H), 2.40 (s, 3H), 2.63 (s, 3H), 2.94 (s, 3H), 3.02-3.22 (m, 2H), 3.22-3.38 (m, 2H), 3.40-3.49 (m, 2H), 3.79 (s, 2H), 4.05-4.35 (m, 6H), 6.88-6.99 (m, 2H), 7.12-7.20 (m, 1H), 7.28 (d, J=8.1, 1H), 7.69 (dd, J=1.2, 8.1, 1H), 7.93 (d, J=1.2, 1H), 8.38, 8.64 (2broad, 1H).

Step BN²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

The compound (3.10 g, 4.97 mmol) obtained in step A was dissolved in dichloromethane (16 ml), trifluoroacetic acid (10 ml) was added at room temperature, and the mixture was stirred at the same temperature for 90 min. To the reaction mixture were added dichloromethane and aqueous ammonia to alkalify the aqueous layer and to extract the organic layer. The aqueous layer was extracted with dichloromethane again, the organic layer was mixed, and the mixture was washed with saturated brine, and dried over sodium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure to give a colorless amorphous solid (2.67 g). This was dissolved in ethyl acetate (30 ml), 4N hydrochloric acid-ethyl acetate solution (1.25 ml, 5 mmol) was added at room temperature, and the mixture was stirred at the same temperature to allow precipitation of a solid. This was collected by filtration, washed with ethyl acetate, and dried under reduced pressure to give a colorless solid (2.06 g). This was dissolved in ethanol (40 ml) with heating, and the mixture was gradually cooled by stirring to allow precipitation of a solid. This was collected by filtration, washed with ethanol (10 ml), and dried under reduced pressure to give the title compound (1.83 g, yield 66%) as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.14 (t, J=7.2, 3H), 2.33 (s, 3H), 2.65 (s, 3H), 2.8-3.0 (m, 4H), 2.88 (s, 3H), 3.3-3.4 (m, 2H), 3.92 (s, 2H), 4.0-4.3 (m, 4H), 4.33 (s, 2H), 7.0-7.2 (m, 2H), 7.27-7.33 (m, 2H), 7.52 (dd, J=1.2, 8.1, 1H), 7.75 (d, J=1.2, 1H), 8.32 (t, J=5.7, 1H), 8.57 (brs, 2H).

Example 21N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (845 mg, 1.46 mmol) obtained in Example 4, step B and according to the method of Reference Example 62, step A, the title compound (631 mg, yield 68%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.12 (d, J=6.6, 6H), 1.45 (brs, 9H), 2.41 (s, 3H), 2.62 (s, 3H), 2.93 (s, 3H), 3.1-3.3 (m, 2H), 3.35-3.50 (m, 2H), 3.80 (s, 2H), 4.0-4.3 (m, 7H), 6.8-7.0 (m, 2H), 7.1-7.2 (m, 1H), 7.25-7.33 (m, 1H), 7.69 (dd, J=1.2, 8.1, 1H), 7.94 (d, J=1.2, 1H), 8.2-8.8 (broad, 1H).

Step BN²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (627 mg, 0.983 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (560 mg, yield 93%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.18 (d, J=6.6, 6H), 2.34 (s, 3H), 2.65 (s, 3H), 2.8-3.0 (m, 2H), 2.88 (s, 3H), 3.1-3.3 (m, 1H), 3.35-3.42 (m, 2H), 3.92 (s, 2H), 4.0-4.3 (m, 4H), 4.34 (s, 2H), 7.0-7.2 (m, 2H), 7.26-7.32 (m, 2H), 7.52 (dd, J=1.2, 8.1, 1H), 7.75 (d, J=1.2, 1H), 8.34 (broad t, 1H), 8.64 (brs, 2H).

Example 22N²-{2-[(5-cyano-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-{2-[(5-cyano-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]glycine

Using the compound (225 mg, 0.737 mmol) of Reference Example 62 and the compound (195 mg, 0.930 mmol) of Reference Example 21, and according to the method of Example 4, step A, the title compound (302 mg, yield 89%) was obtained as a bistered amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.38 (s, 3H), 2.63 (s, 3H), 3.06 (s, 3H), 3.93 (s, 2H), 4.19-4.35 (m, 6H), 7.30 (d, J=8.1, 1H), 7.34 (d, J=7.8, 1H), 7.51 (s, 1H), 7.58 (d, J=8.1, 1H), 7.76 (dd, J=1.2, 7.8, 1H), 7.91 (d, J=1.2, 1H), 13.1 (brs, 1H).

Step BN²-{2-[(5-cyano-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (298 mg, 0.647 mmol) obtained in step A, and the compound (209 mg, 1.03 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (370 mg, yield 89%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.12 (d, J=6.8, 6H), 1.45 (s, 9H), 2.40 (s, 3H), 2.63 (s, 3H), 2.94 (s, 3H), 3.1-3.3 (m, 2H), 3.38-3.45 (m, 2H), 3.79 (s, 2H), 4.1-4.3 (m, 7H), 7.29-7.34 (m, 2H), 7.55 (s, 1H), 7.57 (dd, J=1.1, 7.6, 1H), 7.71 (dd, J=1.1, 7.7, 1H), 7.92 (d, J=1.4, 1H), 8.1-8.7 (broad, 1H).

Step CN²-{2-[(5-cyano-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (361 mg, 0.560 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (315 mg, yield 91%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.18 (d, J=6.6, 6H), 2.33 (s, 3H), 2.65 (s, 3H), 2.8-3.0 (m, 5H), 3.2-3.3 (m, 1H), 3.35-3.45 (m, 2H), 3.91-4.35 (m, 8H), 7.28 (d, J=7.8, 1H), 7.47-7.53 (m, 2H), 7.72-7.77 (m, 3H), 8.30-8.35 (m, 1H), 8.5-8.9 (broad, 2H).

Example 23N²-{2-[(5-methoxy-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-{2-[(5-methoxy-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]glycine

Using the compound (1.15 g, 3.77 mmol) of Reference Example 62 and the compound (1.23 g, 5.73 mmol) of Reference Example 20, and according to the method of Example 4, step A, the title compound (1.36 g, yield 77%) was obtained as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.38 (s, 3H), 2.63 (s, 3H), 3.05 (s, 3H), 3.79 (s, 3H), 3.94 (s, 2H), 4.0-4.3 (m, 4H), 4.31 (s, 2H), 6.75 (d, J=2.1, 1H), 6.81 (dd, J=2.1, 8.4, 1H), 7.11 (d, J=8.4, 1H), 7.29 (d, J=7.8, 1H), 7.75 (dd, J=1.2, 7.8, 1H), 7.92 (d, J=1.2, 1H), 13.5 (brs, 1H).

Step BN²-{2-[(5-methoxy-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (667 mg, 1.43 mmol) obtained in step A, and the compound (393 mg, 1.94 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (794 mg, yield 85%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.11 (d, J=6.8, 6H), 1.45 (brs, 9H), 2.40 (s, 3H), 2.62 (s, 3H), 2.93 (s, 3H), 3.0-3.2 (m, 2H), 3.37-3.45 (m, 2H), 3.79 (s, 3H), 3.81 (s, 2H), 4.0-4.3 (m, 7H), 6.73 (d, J=2.3, 1H), 6.80 (dd, J=2.3, 8.3, 1H), 7.09 (d, J=8.3, 1H), 7.27 (d, J=8.1, 1H), 7.69 (dd, J=1.2, 8.1, 1H), 7.94 (d, J=1.2, 1H), 8.2-8.7 (broad, 1H).

Step CN²-{2-[(5-methoxy-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (788 mg, 1.21 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (716 mg, yield 95%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.18 (d, J=6.6, 6H), 2.34 (s, 3H), 2.65 (s, 3H), 2.8-3.0 (m, 2H), 2.87 (s, 3H), 3.1-3.3 (m, 1H), 3.34-3.42 (m, 2H), 3.73 (s, 3H), 3.92 (s, 2H), 4.0-4.3 (m, 4H), 4.34 (s, 2H), 6.81 (dd, J=2.3, 8.3, 1H), 6.86 (d, J=2.3, 1H), 7.16 (d, J=8.3, 1H), 7.28 (d, J=8.0, 1H), 7.51 (dd, J=1.2, 8.0, 1H), 7.75 (d, J=1.2, 1H), 8.35 (t, J=5.7, 1H), 8.72 (brs, 2H).

Example 24N²-{2-[(5-methoxy-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[(5-methoxy-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (688 mg, 1.48 mmol) obtained in Example 23, step A, and the compound (423 mg, 2.25 mmol) of Reference Example 2, and according to the method of Example 1, step B, the title compound (816 mg, yield 87%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.04 (t, J=7.2, 3H), 1.44 (brs, 9H), 2.39 (s, 3H), 2.62 (s, 3H), 2.93 (s, 3H), 3.0-3.2 (m, 2H), 3.2-3.3 (m, 2H), 3.4-3.5 (m, 2H), 3.79 (s, 3H), 3.80 (s, 2H), 4.0-4.3 (m, 6H), 6.73 (d, J=2.1, 1H), 6.79 (dd, J=2.1, 8.3, 1H), 7.09 (d, J=8.3, 1H), 7.27 (d, J=8.0, 1H), 7.68 (dd, J=1.2, 8.0, 1H), 7.94 (d, J=1.2, 1H), 8.3-8.7 (broad, 1H).

Step BN²-{2-[(5-methoxy-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (810 mg, 1.27 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (744 mg, yield 96%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.2, 3H), 2.33 (s, 3H), 2.65 (s, 3H), 2.8-3.0 (m, 4H), 2.87 (s, 3H), 3.3-3.4 (m, 2H), 3.73 (s, 3H), 3.92 (s, 2H), 4.0-4.3 (m, 4H), 4.34 (s, 2H), 6.81 (dd, J=2.1, 8.1, 1H), 6.86 (d, J=2.1, 1H), 7.16 (d, J=8.1, 1H), 7.28 (d, J=7.8, 1H), 7.51 (d, J=7.8, 1H), 7.75 (s, 1H), 8.33 (t, J=5.7, 1H), 8.71 (brs, 2H).

The compounds of Examples 1-24 are shown below.

TABLE 7StructuralLC-MSExampleFormulaTMW(found)1 [Image Omitted]

535.51463 2 [Image Omitted]

521.48449 3 [Image Omitted]

565.53493 4 [Image Omitted]

553.50481 5 [Image Omitted]

535.51463 6 [Image Omitted]

512.09476 7 [Image Omitted]

496.06462 8 [Image Omitted]

528.09492 9 [Image Omitted]

514.06478 10 [Image Omitted]

516.05480 11 [Image Omitted]

532.50496 12 [Image Omitted]

512.09476 13 [Image Omitted]

512.09476 14 [Image Omitted]

580.57508 15 [Image Omitted]

592.56520 16 [Image Omitted]

578.53506 17 [Image Omitted]

634.60562 18 [Image Omitted]

620.57548 19 [Image Omitted]

596.52524 20 [Image Omitted]

560.06524 21 [Image Omitted]

610.55538 22 [Image Omitted]

617.57545 23 [Image Omitted]

622.59550 24 [Image Omitted]

608.56536

Example 25N²-{2-[2,3-dihydro-1H-inden-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochlorideStep AN-{2-[2,3-dihydro-1H-inden-2-yl(methyl)amino]-2-oxoethyl}-N-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]glycine

Using the compound (601 mg, 1.97 mmol) of Reference Example 62 and the compound of Reference Example 23 (576 mg, 3.14 mmol), and according to the method of Example 1, step A, the title compound (729 mg, yield 85%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.39 (s, 3H), 2.64 2.65 (2s, 3H), 2.76 2.90 (2s, 3H), 2.91-3.34 (m, 4H), 3.95 3.96 (2s, 2H), 4.02 4.17 (2s, 2H), 4.5-4.6 (m, 0.4H), 5.6-5.7 (m, 0.6H), 7.16-7.25 (m, 4H), 7.31 (d, J=8.0, 1H), 7.77 (d, J=8.0, 1H), 7.92 7.93 (2s, 1H), 13.9 (brs, 1H).

Step BN²-{2-[2,3-dihydro-1H-inden-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (360 mg, 0.829 mmol) obtained in step A, and the compound (253 mg, 1.25 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (459 mg, yield 89%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.11 (d, J=6.6, 6H), 1.45 (brs, 9H), 2.43 (s, 3H), 2.63 2.64 (2s, 3H), 2.74 2.78 (2s, 3H), 2.8-3.2 (m, 6H), 3.35-3.45 (m, 2H), 3.84 (s, 2H), 3.94 4.09 (2s, 2H), 4.1-4.4 (broad, 1H), 4.6-4.7 (m, 0.4H), 5.5-5.7 (m, 0.6H), 7.18 (broad, 4H), 7.29 (d, J=8.1, 1H), 7.71 (d, J=8.1, 1H), 7.92 7.94 (2s, 1H), 8.1-8.8 (broad, 1H).

Step CN²-{2-[2,3-dihydro-1H-inden-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochloride

Using the compound (455 mg, 0.735 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (362 mg, yield 89%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.19 (d, J=6.3, 6H), 2.36 (s, 3H), 2.66 (s, 3H), 2.68 2.77 (2s, 3H), 2.8-3.2 (m, 6H), 3.2-3.3 (m, 1H), 3.35-3.42 (m, 2H), 3.88 3.91 (2s, 2H), 4.10 4.27 (2s, 2H), 4.8-4.9 (m, 0.4H), 5.2-5.4 (m, 0.6H), 7.16 7.20 (2broad, 4H), 7.30 (d, J=8.0, 1H), 7.53 (d, J=8.0, 1H), 7.75 7.79 (2s, 1H), 8.42 (broad t, 1H), 8.69 (brs, 2H).

Example 26N²-{2-[2,3-dihydro-1H-inden-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide hydrochlorideStep AN²-{2-[2,3-dihydro-1H-inden-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (359 mg, 0.826 mmol) of Example 25, step A, and the compound (246 mg, 1.31 mmol) of Reference Example 2, and according to the method of Example 1, step B, the title compound (417 mg, yield 83%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.04 (t, J=7.1, 3H), 1.44 (brs, 9H), 2.42 (s, 3H), 2.63 2.64 (2s, 3H), 2.74 2.79 (2s, 3H), 2.8-3.3 (m, 8H), 3.4-3.5 (m, 2H), 3.84 (s, 2H), 3.94 4.09 (2s, 2H), 4.6-4.7 (m, 0.4H), 5.5-5.7 (m, 0.6H), 7.18 (broad, 4H), 7.29 (d, J=7.8, 1H), 7.71 (d, J=7.8, 1H), 7.91 7.93 (2s, 1H), 8.34 8.62 (2broad, 1H).

Step BN²-{2-[2,3-dihydro-1H-inden-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (414 mg, 0.685 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (328 mg, yield 88%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=7.2, 3H), 2.36 (s, 3H), 2.66 (s, 3H), 2.67 2.77 (2s, 3H), 2.8-3.2 (m, 8H), 3.34-3.41 (m, 2H), 3.88 3.91 (2s, 2H), 4.10 4.27 (2s, 2H), 4.8-4.9 (m, 0.4H), 5.2-5.4 (m, 0.6H), 7.16 7.20 (2broad, 4H), 7.30 (d, J=8.0, 1H), 7.53 (d, J=8.0, 1H), 7.75 7.79 (2s, 1H), 8.40 (broad t, 1H), 8.73 (brs, 2H).

Example 27N²-{2-[methyl(5-methyl-2,3-dihydro-1H-inden-2-yl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochloride

Using the compound (519 mg, 0.901 mmol) of Example 6, step B and according to the methods of Reference Example 62, step A, and Example 1, step C, the title compound (322 mg, yield 63%) was obtained as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.20 (d, J=6.1, 6H), 1.91 (s, 3H), 2.04-3.15 (m, 15H), 3.17-3.42 (m, 3H), 3.87-3.91 (m, 2H), 4.27 (s, 1.2H), 4.48 (s, 0.8H), 4.81-4.84 (m, 0.4H), 5.26-5.34 (m, 0.6H), 6.95 (d, J=7.4, 1H), 7.02 (s, 1H), 7.08 (d, J=7.5, 1H), 7.29 (d, J=7.9, 1H), 7.53 (d, J=7.7, 1H), 7.74-7.79 (m, 1H), 8.42-8.47 (m, 1H), 8.90 (brs, 2H).

Example 28N²-{2-[methyl(5-methyl-2,3-dihydro-1H-inden-2-yl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (519 mg, 0.924 mmol) of Example 7, step A and according to the methods of Reference Example 62, step A, and Example 1, step C, the title compound (309 mg, yield 60%) was obtained as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.13-1.20 (m, 3H), 1.91 (s, 3H), 2.26 (s, 3H), 2.36 (s, 3H), 2.52-3.10 (m, 11H), 3.33-3.41 (m, 2H), 3.87-3.92 (m, 2H), 4.26 (s, 1.2H), 4.48 (s, 0.8H), 4.81-4.85 (m, 0.4H), 5.27-5.33 (m, 0.6H), 6.95 (d, J=7.2, 1H), 7.02 (s, 1H), 7.08 (d, J=7.5, 1H), 7.30 (d, J=7.8, 1H), 7.53 (d, J=7.8, 1H), 7.75-7.79 (m, 1H), 8.39-8.42 (m, 1H), 8.82 (brs, 2H).

Example 29N²-{2-[(5-methoxy-2,3-dihydro-1H-inden-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochloride

Using the compound (610 mg, 1.03 mmol) of Example 8, step B and according to the methods of Reference Example 62, step A, and Example 1, step C, the title compound (357 mg, yield 59%) was obtained as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.07-1.21 (m, 6H), 2.36 (s, 3H), 2.64-3.17 (m, 12H), 3.20-3.45 (m, 3H), 3.71 (s, 3H), 3.87-3.91 (m, 2H), 4.11 (s, 1.2H), 4.27 (s, 0.8H), 4.85-4.89 (m, 0.4H), 5.28-5.36 (m, 0.6H), 6.71 (d, J=8.2, 1H), 6.80 (s, 1H), 7.10 (d, J=8.2, 1H), 7.29 (d, J=8.0, 1H), 7.51-7.55 (m, 1H), 7.74-7.79 (m, 1H), 8.44-8.47 (m, 1H), 8.95 (brs, 2H).

Example 30N²-{2-[(5-methoxy-2,3-dihydro-1H-inden-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (600 mg, 1.04 mmol) obtained in Example 9, step A and according to the methods of Reference Example 62, step A, and Example 1, step C, the title compound (406 mg, yield 68%) was obtained as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.13-1.20 (m, 3H), 2.35 (s, 3H), 2.64-3.15 (m, 14H), 3.34-3.40 (m, 2H), 3.71 (s, 3H), 3.87-3.91 (m, 2H), 4.26 (s, 1.2H), 4.48 (s, 0.8H), 4.81-4.85 (m, 0.4H), 5.27-5.34 (m, 0.6H), 6.72 (d, J=8.3, 1H), 6.80 (s, 1H), 7.10 (d, J=7.9, 1H), 7.30 (d, J=7.9, 1H), 7.51-7.55 (m, 1H), 7.74-7.79 (m, 1H), 8.40-8.42 (m, 1H), 8.76 (brs, 2H).

Example 31N²-{2-[(5-fluoro-2,3-dihydro-1H-inden-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochloride

Using the compound (700 mg, 1.21 mmol) of Example 10, step A and according to the methods of Reference Example 62, step A, and Example 1, step C, the title compound (531 mg, yield 77%) was obtained as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.19 (d, J=6.6, 6H), 2.36 (s, 3H), 2.66 (s, 3H), 2.67-2.78 (m, 3H), 2.85-3.27 (m, 6H), 3.28-3.34 (m, 1H), 3.35-3.47 (m, 2H), 3.87-3.91 (m, 2H), 4.11 (s, 1.2H), 4.27 (s, 0.8H), 4.86-4.93 (m, 0.4H), 5.28-5.35 (m, 0.6H), 6.96 (t, J=8.7, 1H), 7.04 (d, J=6.3, 1H), 7.20-7.24 (m, 1H), 7.30 (d, J=7.8, 1H), 7.52-7.56 (m, 1H), 7.73-7.79 (m, 1H), 8.41-8.44 (m, 1H), 8.80 (brs, 2H).

Example 32N²-{2-[(5-chloro-2,3-dihydro-1H-inden-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl][2-(isopropylamino)ethyl]glycinamide hydrochloride

Using the compound (1.00 g, 1.68 mmol) of Example 11, step A and according to the methods of Reference Example 62, step A, and Example 1, step C, the title compound (703 mg, yield 71%) was obtained as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.20 (d, J=6.4, 6H), 2.36 (s, 3H), 2.64-3.19 (m, 12H), 6.20-6.31 (m, 1H), 6.32-6.47 (m, 2H), 3.86-3.92 (m, 2H), 4.11 (s, 1.2H), 4.27 (s, 0.8H), 4.86-4.94 (m, 0.4H), 5.26-5.33 (m, 0.6H), 7.16-7.31 (m, 4H), 7.51-7.55 (m, 1H), 7.73-7.79 (m, 1H), 8.40-8.43 (m, 1H), 8.86 (brs, 2H).

Example 33N²-{2-[methyl(4-methyl-2,3-dihydro-1H-inden-2-yl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochloride

Using the compound (1.25 g, 2.17 mmol) of Example 12, step A and according to the methods of Reference Example 62, step A, and Example 1, step C, the title compound (608 mg, yield 49%) was obtained as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.20 (d, J=6.6, 6H), 2.18 (s, 3H), 2.37 (s, 3H), 2.66 (s, 3H), 2.67-3.18 (m, 9H), 3.18-3.23 (m, 1H), 3.24-3.48 (m, 2H), 3.87-3.92 (m, 2H), 4.11 (s, 1.2H), 4.29 (s, 0.8H), 4.83-4.88 (m, 0.4H), 5.28-5.35 (m, 0.6H), 6.94-7.08 (m, 3H), 7.30 (d, J=8.1, 1H), 7.53 (dd, J=1.5, 7.8, 1H), 7.74-7.80 (m, 1H), 8.31-8.45 (m, 1H), 8.91 (brs, 2H).

Example 34N²-{2-[(5,6-dimethoxy-2,3-dihydro-1H-inden-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochlorideStep AN-(5-cyano-2-methylphenyl)-N-{2-[(5,6-dimethoxy-2,3-dihydro-1H-inden-2-yl)(methyl)amino]-2-oxoethyl}glycine

Using the compound (1.00 g, 4.03 mmol) of Reference Example 61 and the compound (1.47 g, 6.05 mmol) of Reference Example 30, and according to the method of Example 4, step A, the title compound (966 mg, yield 55%) was obtained as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.33 (s, 3H), 2.64 2.75 (2s, 3H), 2.73-3.04 (m, 4H), 3.70 (s, 6H), 3.95 3.96 (2s, 2H), 4.09 4.24 (2s, 2H), 4.82-4.88 (m, 0.4H), 5.26-5.34 (m, 0.6H), 6.82 (s, 2H), 7.29-7.36 (m, 2H), 7.45-7.49 (m, 1H), 12.61 (brs, 1H).

Step BN²-(5-cyano-2-methylphenyl)-N²-{2-[(5,6-dimethoxy-2,3-dihydro-1H-inden-2-yl)(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (966 mg, 2.21 mmol) obtained in step A, and the compound (671 mg, 3.32 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (1.23 g, yield 90%) was obtained as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.12 (d, J=6.6, 6H), 1.44 (s, 9H), 2.42 (s, 3H), 2.73-3.45 (m, 11H), 3.75-4.21 (m, 5H), 3.86 (s, 6H), 4.59-4.66 (m, 0.4H), 5.52-5.61 (m, 0.6H), 6.74 (s, 2H), 7.23-7.34 (m, 2H), 7.49 (s, 1H), 7.78-8.59 (broad, 1H).

Step CN²-{2-[(5,6-dimethoxy-2,3-dihydro-1H-inden-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochloride

Using the compound (730 mg, 1.17 mmol) obtained in step B and according to the methods of Reference Example 62, step A, and Example 1, step C, the title compound (369 mg, yield 52%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.20 (d, J=6.5, 6H), 2.36 (s, 3H), 2.58-3.16 (m, 9H), 2.66 (s, 3H), 3.21-3.25 (m, 1H), 3.36-3.43 (m, 2H), 3.70 (s, 6H), 3.88 3.91 (2s, 2H), 4.11 4.27 (2s, 2H), 4.82-4.88 (m, 0.4H), 5.28-5.35 (m, 0.6H), 6.81 (s, 2H), 7.29 (d, J=7.9, 1H), 7.53 (d, J=7.8, 1H), 7.75-7.79 (m, 1H), 8.43-8.47 (m, 1H), 8.98 (brs, 2H).

Example 35N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N²-{2-[methyl(1,2,3,4-tetrahydronaphthalen-2-yl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochloride

Using the compound (700 mg, 1.22 mmol) of Example 13, step B and according to the methods of Reference Example 62, step A, and Example 1, step C, the title compound (387 mg, yield 52%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.19 (d, J=6.6, 6H), 1.64-1.98 (m, 2H), 2.32 2.37 (2s, 3H), 2.65 (s, 3H), 2.66-3.12 (m, 9H), 3.20-3.43 (m, 3H), 3.50-4.68 (m, 5H), 7.03-7.09 (m, 4H), 7.29 (t, J=6.9, 1H), 7.53 (d, J=7.5, 1H), 7.76 (d, J=11.4, 1H), 8.46 (t, J=5.4, 1H), 8.84 (brs, 2H).

Example 36N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N²-[2-{methyl[(3aR,7aS)-octahydro-2H-isoindol-2-yl]amino}-2-oxoethyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N-[2-{methyl[(3aR,7aS)-octahydro-2H-isoindol-2-yl]amino}-2-oxoethyl]glycine

Using the compound (689 mg, 2.26 mmol) of Reference Example 62 and the compound (436 mg, 2.83 mmol) of Reference Example 37, and according to the method of Example 4, step A, the title compound (844 mg, yield 85%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.2-1.7 (m, 8H), 2.0-2.2 (m, 2H), 2.36 (s, 3H), 2.65 2.66 (2s, 3H), 2.7-2.8 (m, 2H), 2.8-3.0 (m, 2H), 2.99 3.03 (2s, 3H), 3.93 3.96 (2s, 2H), 4.19 4.21 (2s, 2H), 7.30 (d, J=7.8, 1H), 7.74 (dd, J=1.8, 7.8, 1H), 7.94 (d, J=1.8, 1H), 13.7 (brs, 1H).

Step BN²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N²-[2-{methyl[(3aR,7aS)-octahydro-2H-isoindol-2-yl]amino}-2-oxoethyl]-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (410 mg, 0.929 mmol) obtained in step A, and the compound (284 mg, 1.40 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (553 mg, yield 95%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.10 (d, J=6.9, 6H), 1.2-1.8 (m, 8H), 1.46 (brs, 9H), 2.0-2.2 (m, 2H), 2.39 (s, 3H), 2.63 (s, 3H), 2.7-2.8 (m, 2H), 2.8-3.0 (m, 2H), 2.87 2.91 (2s, 3H), 3.0-3.2 (m, 2H), 3.3-3.5 (m, 2H), 3.79 3.82 (2s, 2H), 3.9-4.3 (broad, 1H), 4.16 4.17 (2s, 2H), 7.27 (d, J=7.8, 1H), 7.67 (d, J=7.8, 1H), 7.93 (s, 1H), 8.2-8.8 (broad, 1H).

Step CN²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N²-[2-{methyl[(3aR,7aS)-octahydro-2H-isoindol-2-yl]amino}-2-oxoethyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (540 mg, 0.863 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (438 mg, yield 85%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.18 (d, J=6.5, 6H), 1.2-1.6 (m, 8H), 2.0-2.2 (m, 2H), 2.33 (s, 3H), 2.6-2.7 (m, 2H), 2.64 (s, 3H), 2.79 2.82 (2s, 3H), 2.8-3.0 (m, 4H), 3.2-3.5 (m, 3H), 3.91 3.93 (2s, 2H), 4.24 4.27 (2s, 2H), 7.29 (d, J=7.8, 1H), 7.50 (d, J=7.8, 1H), 7.71 (s, 1H), 8.3-8.5 (m, 1H), 8.55 (brs, 2H).

Example 37N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N²-[2-{methyl[(3aR,7aS)-octahydro-2H-isoindol-2-yl]amino}-2-oxoethyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N²-[2-{methyl[(3aR,7aS)-octahydro-2H-isoindol-2-yl]amino}-2-oxoethyl]-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (429 mg, 0.972 mmol) obtained in Example 36, step A, and the compound (302 mg, 1.60 mmol) of Reference Example 2, and according to the method of Example 1, step B, the title compound (557 mg, yield 94%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.02 (t, J=7.2, 3H), 1.2-1.7 (m, 8H), 1.45 (brs, 9H), 2.0-2.2 (m, 2H), 2.38 (s, 3H), 2.63 (s, 3H), 2.7-2.8 (m, 2H), 2.8-3.0 (m, 2H), 2.88 2.91 (2s, 3H), 3.0-3.3 (m, 4H), 3.4-3.5 (m, 2H), 3.79 3.81 (2s, 2H), 4.15 4.17 (2s, 2H), 7.27 (d, J=7.5, 1H), 7.67 (d, J=7.5, 1H), 7.92 (s, 1H), 8.3-8.8 (broad, 1H).

Step BN²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N²-[2-{methyl[(3aR,7aS)-octahydro-2H-isoindol-2-yl]amino}-2-oxoethyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (553 mg, 0.904 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (429 mg, yield 81%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.2, 3H), 1.2-1.6 (m, 8H), 2.0-2.2 (m, 2H), 2.33 (s, 3H), 2.6-2.8 (m, 2H), 2.64 (s, 3H), 2.78 2.82 (2s, 3H), 2.8-3.0 (m, 6H), 3.34-3.41 (m, 2H), 3.91 3.93 (2s, 2H), 4.24 4.26 (2s, 2H), 7.28 (d, J=7.9, 1H), 7.50 (d, J=7.9, 1H), 7.71 (s, 1H), 8.3-8.5 (m, 1H), 8.62 (brs, 2H).

Example 38N²-{2-[3,4-dihydroisoquinolin-2(1H)-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-{2-[3,4-dihydroisoquinolin-2(1H)-yl(methyl)amino]-2-oxoethyl}-N-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]glycine

Using the compound (593 mg, 2.26 mmol) of Reference Example 62 and the compound (414 mg, 2.55 mmol) of Reference Example 42, and according to the method of Example 4, step A, the title compound (915 mg, yield>100%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.35 (s, 3H), 2.62 (s, 3H), 2.8-3.3 (m, 4H), 3.11 (s, 3H), 3.76 (d, J=14.1, 1H), 3.93 3.94 (2s, 2H), 4.17 (d, J=14.1, 1H), 4.23 4.26 (2s, 2H), 6.9-7.1 (m, 1H), 7.11-7.19 (m, 3H), 7.27 (d, J=7.8, 1H), 7.72 (dd, J=1.5, 7.8, 1H), 7.88 (d, J=1.5, 1H), 13.51 (brs, 1H).

Step BN²-{2-[3,4-dihydroisoquinolin-2(1H)-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (510 mg, 1.13 mmol) obtained in step A, and the compound (332 mg, 1.64 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (594 mg, yield 83%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.11 (d, J=6.8, 6H), 1.45 (brs, 9H), 2.38 (s, 3H), 2.62 (s, 3H), 2.7-2.9 (m, 1H), 2.9-3.3 (m, 5H), 2.98 (s, 3H), 3.3-3.5 (m, 2H), 3.69 (d, J=14.1, 1H), 3.80 (s, 2H), 3.9-4.3 (broad, 1H), 4.10 (d, J=14.1, 1H), 4.17 (d, J=17.5, 1H), 4.26 (d, J=17.5, 1H), 6.97-7.01 (m, 1H), 7.1-7.2 (m, 3H), 7.25 (d, J=7.8, 1H), 7.66 (dd, J=1.2, 7.8, 1H), 7.87 (d, J=1.2, 1H), 8.2-8.7 (broad, 1H).

Step CN²-{2-[3,4-dihydroisoquinolin-2(1H)-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (590 mg, 0.931 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (482 mg, yield 85%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.17 (d, J=6.4, 6H), 2.30 (s, 3H), 2.65 (s, 3H), 2.8-3.3 (m, 7H), 2.98 (s, 3H), 3.34-3.42 (m, 2H), 3.77 (d, J=14.4, 1H), 3.92 (s, 2H), 4.11 (d, J=14.4, 1H), 4.23 (d, J=17.7, 1H), 4.38 (d, J=17.7, 1H), 6.9-7.1 (m, 1H), 7.14-7.18 (m, 3H), 7.26 (d, J=7.8, 1H), 7.49 (dd, J=1.2, 7.8, 1H), 7.69 (d, J=1.2, 1H), 8.38 (t, J=5.7, 1H), 8.68 (brs, 2H).

Example 39N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N²-[2-{methyl[4-(methylsulfonyl)piperazin-1-yl]amino}-2-oxoethyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N²-[2-{methyl[4-(methylsulfonyl)piperazin-1-yl]amino}-2-oxoethyl]-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (531 mg, 1.74 mmol) of Reference Example 62, the compound (442 mg, 2.29 mmol) of Reference Example 48 and the compound (552 mg, 2.73 mmol) of Reference Example 3, and according to the methods of Example 4, step A, and Example 1, step B, the title compound (1.07 g, yield 92%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.13 (d, J=6.9, 6H), 1.46 (brs, 9H), 2.39 (s, 3H), 2.64 (s, 3H), 2.7-2.8 (m, 2H), 2.84 (s, 3H), 2.91 (s, 3H), 2.95-3.05 (m, 4H), 3.05-3.20 (m, 2H), 3.3-3.5 (m, 2H), 3.6-3.8 (m, 4H), 3.9-4.3 (broad, 1H), 4.22 (s, 2H), 7.28 (d, J=8.1, 1H), 7.69 (dd, J=1.2, 8.1, 1H), 7.87 (d, J=1.2, 1H), 8.2-8.8 (broad, 1H).

Step BN²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N²-[2-{methyl[4-(methylsulfonyl)piperazin-1-yl]amino}-2-oxoethyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (1.04 g, 1.56 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (951 mg, yield 96%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.19 (d, J=6.4, 6H), 2.33 (s, 3H), 2.64 (s, 3H), 2.7-3.0 (m, 8H), 2.83 (s, 3H), 2.91 (s, 3H), 3.1-3.3 (m, 1H), 3.3-3.4 (m, 2H), 3.4-3.5 (m, 2H), 3.93 (s, 2H), 4.30 (s, 2H), 7.29 (d, J=7.8, 1H), 7.50 (dd, J=1.1, 7.8, 1H), 7.68 (d, J=1.1, 1H), 8.42 (broad t, 1H), 8.81 (brs, 2H).

Example 40N²-{2-[(1-acetylpiperidin-4-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochlorideStep AN-[2-{[1-(tert-butoxycarbonyl)piperidin-4-yl](methyl)amino}-2-oxoethyl]-N-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]glycine

Using the compound (929 mg, 3.04 mmol) of Reference Example 62 and the compound (782 mg, 3.65 mmol) of Reference Example 46, and according to the method of Example 1, step A, the title compound (1.65 g, yield 100%) was obtained as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.46 (s, 9H), 1.56-1.67 (m, 4H), 2.37 (s, 3H), 2.65 (s, 3H), 2.80-2.96 (m, 5H), 3.95 (s, 2H), 4.02 (s, 2H), 4.23-4.24 (m, 2H), 4.69 (m, 1H), 7.30 (dd, J=3.0, 8.1, 1H), 7.76 (dd, J=1.5, 8.1, 1H), 7.92 (dd, J=1.5, 7.8, 1H).

Step BN²-[2-{[1-(tert-butoxycarbonyl)piperidin-4-yl](methyl)amino}-2-oxoethyl]-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-1(isopropyl)[(2-nitrophenyl)sulfonyl]amino}ethyl]glycinamide

Using the compound (744 mg, 1.48 mmol) obtained in step A, and the compound (469 mg, 1.63 mmol) of Reference Example 7, and according to the method of Example 1, step B, the title compound (1.04 g, yield 91%) was obtained as a yellow amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.15 (d, J=6.9, 6H), 1.45 (s, 9H), 1.53-1.60 (m, 4H), 2.43 (s, 3H), 2.63 (s, 3H), 2.77-2.79 (m, 5H), 3.35-3.37 (m, 2H), 3.49-3.51 (m, 2H), 3.87 (s, 2H), 3.99 (s, 2H), 4.05-4.16 (m, 3H), 4.60-4.62 (m, 1H), 7.29 (m, 1H), 7.58-7.69 (m, 4H), 7.89 (m, 1H), 7.99-8.02 (m, 1H), 8.50-8.52 (m, 1H).

Step CN²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N²-[2-{methyl(piperidin-4-yl)amino}-2-oxoethyl]-N¹-[2-{(isopropyl)[(2-nitrophenyl)sulfonyl]amino}ethyl]glycinamide hydrochloride

Using the compound (1.04 g, 1.35 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (950 mg, yield 100%) was obtained as a yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.00-1.04 (m, 6H), 1.60-1.91 (m, 4H), 2.50 (s, 3H), 2.62 (s, 3H), 2.79 (s, 3H), 2.97 (m, 2H), 3.15-3.37 (m, 6H), 3.78-4.13 (m, 5H), 4.48-4.52 (m, 1H), 7.26-7.30 (m, 1H), 7.49-7.52 (m, 1H), 7.72-7.76 (m, 1H), 7.81-7.92 (m, 2H), 7.95-8.04 (m, 2H), 8.24-8.30 (m, 1H), 8.43 (brs, 1H), 8.65 (brs, 1H).

Step DN²-{2-[(1-acetylpiperidin-4-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-1(isopropyl)[(2-nitrophenyl)sulfonyl]amino}ethyl]glycinamide

The compound (300 mg, 0.424 mmol) obtained in step C was dissolved in dichloromethane (3 ml), triethylamine (0.14 ml, 1.0 mmol) and acetyl chloride (0.042 ml, 0.59 mmol) were added under ice-cooling with stirring, and the mixture was stirred at room temperature for 5 hr. Water was added to the reaction mixture, and the mixture was extracted with dichloromethane. The organic layer was washed with diluted hydrochloric acid, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (methanol-dichloromethane) to give the title compound (266 mg, yield 88%) as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.16 (d, J=6.6, 6H), 1.54-1.67 (m, 4H), 2.10 (s, 3H), 2.43 (s, 3H), 2.5-2.6 (m, 1H), 2.64 (s, 3H), 2.77 (s, 3H), 3.1-3.2 (m, 1H), 3.37-3.40 (m, 2H), 3.48-3.52 (m, 2H), 3.87-3.89 (m, 3H), 4.00-4.14 (m, 3H), 4.67-4.75 (m, 2H), 7.26-7.30 (m, 1H), 7.58-7.61 (m, 1H), 7.67-7.70 (m, 3H), 7.89-7.92 (m, 1H), 8.00-8.03 (m, 1H), 8.52 (brs, 1H).

Step EN²-{2-[(1-acetylpiperidin-4-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide

The compound (260 mg, 0.365 mmol) obtained in step D was dissolved in acetonitrile (3 ml). Then, benzenethiol (0.057 ml, 0.547 mmol) and cesium carbonate (594 mg, 1.82 mmol) were added, and the mixture was stirred at room temperature for 10 hr. The reaction mixture was diluted with dichloromethane, and the organic layer was washed with diluted aqueous sodium hydroxide solution, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (NH silica gel use, methanol-dichloromethane) to give the title compound (161 mg, yield 84%) as a pale-yellow amorphous solid. This was directly used for the next step.

Step FN²-{2-[(1-acetylpiperidin-4-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochloride

The compound (161 mg, 0.303 mmol) obtained in step E was dissolved in ethyl acetate (2 ml), 4N hydrochloric acid-ethyl acetate solution (0.16 ml) was added at room temperature with stirring, and the mixture was stirred at the same temperature for 2.5 hr. To the reaction mixture was added diethyl ether (2 ml), the precipitated solid was collected by filtration, washed with diethyl ether, and dried under reduced pressure to give the title compound (164 mg, yield 96%) as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.18 (d, J=6.1, 6H), 1.45-1.62 (m, 4H), 1.99 (s, 3H), 2.34 (s, 3H), 2.65 (s, 3H), 2.77 (s, 3H), 2.90 (broad, 2H), 3.03-3.07 (m, 1H), 3.28-3.37 (m, 4H), 3.84-3.88 (m, 3H), 4.12 (d, J=11.7, 2H), 4.44-4.48 (m, 2H), 7.28-7.32 (m, 1H), 7.51 (m, 1H), 7.75 (d, J=13.1, 1H), 8.40 (broad, 3H).

Example 41N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N²-[2-{methyl[1-(methylsulfonyl)piperidin-4-yl]amino}-2-oxoethyl]-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochlorideStep AN²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N²-[2-{methyl[1-(methylsulfonyl)piperidin-4-yl]amino}-2-oxoethyl]-N¹-[2-{(isopropyl)[(2-nitrophenyl)sulfonyl]amino}ethyl]glycinamide

The compound (300 mg, 0.42 mmol) of Example 40, step C was dissolved in dichloromethane (3 ml), triethylamine (0.14 ml, 1.0 mmol) and methanesulfonylchloride (0.043 ml, 0.56 mmol) were added under ice-cooling with stirring, and the mixture was stirred at room temperature for 7 hr. The reaction mixture was diluted with dichloromethane, and the organic layer was washed with water and diluted hydrochloric acid, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (methanol-dichloromethane) to give the title compound (224 mg, yield 71%) as a yellow oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.15 (d, J=6.6, 6H), 1.73 (m, 4H), 2.43 (s, 3H), 2.64 (s, 3H), 2.79-2.81 (m, 8H), 3.38-3.50 (m, 4H), 3.87 (m, 4H), 4.02-4.11 (m, 3H), 7.26-7.30 (m, 1H), 7.62-7.70 (m, 4H), 7.89-7.99 (m, 2H), 8.59 (brs, 1H).

Step BN²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N²-[2-{methyl[1-(methylsulfonyl)piperidin-4-yl]amino}-2-oxoethyl]-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochloride

Using the compound (220 mg, 0.294 mmol) obtained in step A and according to the methods of Example 40, steps E and F, the title compound (133 mg, yield 76%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.18 (d, J=6.3, 6H), 1.51-1.76 (m, 4H), 2.34 (s, 3H), 2.65-2.87 (m, 13H), 3.26-3.38 (m, 3H), 3.58-3.63 (m, 2H), 3.85-3.89 (m, 2H), 4.08-4.17 (m, 2H), 4.33 (m, 1H), 7.28-7.32 (m, 1H), 7.51-7.54 (m, 1H), 7.75 (d, J=15.6, 1H), 8.38-8.43 (m, 1H), 8.56 (brs, 2H).

Example 42N²-[2-{[1-(methoxycarbonyl)piperidin-4-yl](methyl)amino}-2-oxoethyl]-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochlorideStep AN²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N²-[2-{methyl[1-(methoxycarbonyl)piperidin-4-yl]amino}-2-oxoethyl]-N¹-[2-1(isopropyl)[(2-nitrophenyl)sulfonyl]amino}ethyl]glycinamide

The compound (300 mg, 0.424 mmol) of Example 40, step C was dissolved in dichloromethane (3 ml), triethylamine (0.14 ml, 1.0 mmol) and methyl chloroformate (0.043 ml, 0.56 mmol) were added under ice-cooling with stirring, and the mixture was stirred at room temperature for 7 hr. The reaction mixture was diluted with dichloromethane, and the organic layer was washed with water and diluted hydrochloric acid, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (methanol-dichloromethane) to give the title compound (276 mg, yield 89%) as a yellow amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.15 (d, J=6.3, 6H), 1.56 (m, 4H), 2.43 (s, 3H), 2.63 (s, 3H), 2.77-2.84 (m, 5H), 3.36-3.51 (m, 4H), 3.69 (s, 3H), 3.87 (s, 2H), 3.99-4.21 (m, 5H), 4.62 (m, 1H), 7.26-7.29 (m, 1H), 7.58-7.61 (m, 1H), 7.64-7.70 (m, 3H), 7.89-7.92 (m, 1H), 7.99-8.02 (m, 1H), 8.50 (brs, 1H).

Step BN²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N²-[2-{[1-(methoxycarbonyl)piperidin-4-yl](methyl)amino}-2-oxoethyl]-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochloride

Using the compound (270 mg, 0.37 mmol) obtained in step A and according to the methods of Example 40, steps E and F, the title compound (165 mg, yield 77%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.18 (d, J=6.6, 6H), 1.45-1.59 (m, 4H), 2.34 (s, 3H), 2.65-2.66 (m, 4H), 2.77-2.90 (m, 6H), 3.23-3.38 (m, 3H), 3.58 (s, 3H), 3.83-3.88 (m, 2H), 4.02-4.16 (m, 4H), 4.38-4.40 (m, 1H), 7.28-7.32 (m, 1H), 7.51-7.53 (m, 1H), 7.75 (d, J=12.9, 1H), 8.39-8.47 (m, 3H).

Example 43N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2-methylphenyl)-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-(2-methylphenyl)glycine

Using the compound (500 mg, 2.24 mmol) of Reference Example 63 and the compound (620 mg, 3.36 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (650 mg, yield 82%) was obtained as a bistered amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.22 (s, 3H), 2.88 (s, 3H), 3.95-4.11 (m, 4H), 4.22-4.26 (m, 4H), 6.87-6.90 (m, 1H), 7.04-7.11 (m, 3H), 7.23-7.31 (m, 4H), 12.46 (brs, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2-methylphenyl)-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (650 mg, 1.84 mmol) obtained in step A, and the compound (558 mg, 2.76 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (870 mg, yield 88%) was obtained as a bistered oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.09 (d, J=6.9, 6H), 1.45 (s, 9H), 2.34 (s, 3H), 2.94 (s, 3H), 3.10 (brs, 2H), 3.33-3.41 (m, 2H), 3.83 (s, 2H), 4.05-4.24 (m, 7H), 6.97-7.02 (m, 1H), 7.10-7.28 (m, 7H), 8.01-8.45 (broad, 1H). % step C:

N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2-methylphenyl)-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (870 mg, 1.62 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (641 mg, yield 78%) was obtained as a pale-bistered amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.20 (d, J=6.5, 6H), 2.29 (s, 3H), 2.79-2.98 (m, 5H), 3.17-3.29 (m, 1H), 3.36-3.44 (m, 2H), 3.91 (s, 2H), 4.10 (d, J=11.4, 2H), 4.25 (d, J=11.7, 2H), 4.34 (s, 2H), 6.92 (t, J=7.2, 1H), 7.06-7.30 (m, 7H), 8.44 (t, J=5.5, 1H), 9.00 (brs, 2H).

Example 44N²-(3-chloro-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-(3-chloro-2-methylphenyl)-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound (382 mg, 1.48 mmol) of Reference Example 64 and the compound (426 mg, 2.31 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (386 mg, yield 67%) was obtained as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.28 (s, 3H), 3.05 (s, 3H), 3.89 (s, 2H), 4.16 (d, J=11.7, 2H), 4.25 (s, 2H), 4.27 (d, J=11.7, 2H), 7.0-7.1 (m, 1H), 7.17-7.29 (m, 6H), 13.3 (brs, 1H).

Step BN²-(3-chloro-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)isopropylamino]ethyl}glycinamide

Using the compound (382 mg, 0.985 mmol) obtained in step A, and the compound (284 mg, 1.41 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (485 mg, yield 86%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.09 (d, J=6.9, 6H), 1.44 (brs, 9H), 2.38 (s, 3H), 2.95 (s, 3H), 3.0-3.2 (m, 2H), 3.32-3.39 (m, 2H), 3.85 (s, 2H), 4.0-4.3 (broad, 1H), 4.09 (d, J=11.7, 2H), 4.14 (s, 2H), 4.23 (d, J=11.7, 2H), 7.02-7.13 (m, 2H), 7.19-7.28 (m, 5H), 7.8-8.1 (broad, 1H).

Step CN²-(3-chloro-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (482 mg, 0.842 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (406 mg, yield 88%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.19 (d, J=6.5, 6H), 2.30 (s, 3H), 2.8-3.0 (m, 2H), 2.87 (s, 3H), 3.1-3.3 (m, 1H), 3.3-3.5 (m, 2H), 3.87 (s, 2H), 4.10 (d, J=11.7, 2H), 4.24 (d, J=11.7, 2H), 4.26 (s, 2H), 7.05-7.15 (m, 3H), 7.26 (broad, 4H), 8.2-8.3 (m, 1H), 8.5-8.9 (broad, 2H).

Example 45N²-(5-chloro-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-(2-pyrrolidin-1-ylethyl)glycinamideStep AN-(5-chloro-2-methylphenyl)-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound (1.12 g, 4.35 mmol) of Reference Example 65 and the compound (843 mg, 4.56 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (1.59 g, yield 95%) was obtained as a bistered amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.26 (s, 3H), 3.06 (s, 3H), 3.89 (s, 2H), 4.16-4.31 (m, 6H), 7.02 (dd, J=2.1, 8.1, 1H), 7.10 (d, J=8.1, 1H), 7.21-7.29 (m, 5H).

Step BN²-(5-chloro-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-(2-pyrrolidin-1-ylethyl)glycinamide

Using the compound (300 mg, 0.77 mmol) obtained in step A, and 1-(2-aminoethyl)pyrrolidine (0.11 ml, 0.85 mmol), and according to the method of Example 1, step B, the title compound (275 mg, yield 74%) was obtained as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.72 (m, 4H), 2.30 (s, 3H), 2.46-2.57 (m, 6H), 2.95 (s, 3H), 3.35-3.41 (m, 2H), 3.83 (s, 2H), 4.11-4.27 (m, 6H), 6.95 (dd, J=2.1, 8.1, 1H), 7.07 (d, J=8.1, 1H), 7.21-7.29 (m, 5H), 8.08 (brs, 1H).

Example 46N²-(5-chloro-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(methylamino)ethyl]glycinamideStep AN²-(5-chloro-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl) (methyl)amino]ethyl}glycinamide

Using the compound (330 mg, 0.85 mmol) of Example 45, step A, the compound (197 mg, 0.94 mmol) of Reference Example 1 and triethylamine (0.13 ml, 0.94 mmol), and according to the method of Example 1, step B, the title compound (295 mg, yield 64%) was obtained as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.44 (s, 9H), 2.28 (s, 3H), 2.80 (s, 3H), 2.96 (s, 3H), 3.33 (m, 2H), 3.39-3.43 (m, 2H), 3.76 (s, 2H), 4.13-4.28 (m, 6H), 6.96 (d, J=8.1, 1H), 7.08 (d, J=8.4, 1H), 7.21-7.26 (m, 5H).

Step BN²-(5-chloro-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(methylamino)ethyl]glycinamide

The compound (294 mg, 0.54 mmol) obtained in step A was dissolved in dichloromethane (5.5 ml), 4N hydrochloric acid-ethyl acetate solution (1.35 ml) was added, and the mixture was stirred at room temperature for 8 hr. The aqueous layer was alkalified by addition of saturated aqueous sodium hydrogen carbonate, and the organic layer was extracted with dichloromethane, and dried over sodium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (NH silica gel use, methanol-dichloromethane) to give the title compound (179 mg, yield 75%) as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.30 (s, 3H), 2.37 (s, 3H), 2.68 (t, J=6.0, 2H), 2.98 (s, 3H), 3.40 (q, J=6.0, 2H), 3.79 (s, 2H), 4.13-4.28 (m, 6H), 6.97 (dd, J=1.8, 8.1, 1H), 7.09 (d, J=8.4, 1H), 7.21-7.29 (m, 5H), 8.35 (brs, 1H).

Example 47N²-(5-chloro-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamideStep AN²-(5-chloro-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (330 mg, 0.85 mmol) of Example 45, step A, and the compound (189 mg, 0.94 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (374 mg, yield 77%) was obtained as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.11 (d, J=6.6, 6H), 1.45 (s, 9H), 2.29 (s, 3H), 2.96 (s, 3H), 3.12 (m, 2H), 3.35-3.42 (m, 2H), 3.79 (s, 2H), 4.12-4.27 (m, 7H), 6.96 (d, J=9.3, 1H), 7.08 (d, J=8.1, 1H), 7.20-7.29 (m, 5H).

Step BN²-(5-chloro-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide

Using the compound (370 mg, 0.65 mmol) obtained in step A and according to the method of Example 46, step B, the title compound (241 mg, yield 79%) was obtained as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.00 (d, J=6.0, 6H), 2.30 (s, 3H), 2.69-2.80 (m, 3H), 2.97 (s, 3H), 3.39 (q, J=6.0, 2H), 3.79 (s, 2H), 4.13-4.28 (m, 6H), 6.97 (dd, J=2.1, 8.1, 1H), 7.08 (d, J=8.1, 1H), 7.21-7.29 (m, 5H), 8.39 (brs, 1H).

Example 48N²-(5-chloro-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-(2-aminoethyl)glycinamide dihydrochloride

Using the compound (400 mg, 1.03 mmol) of Example 45, step A, and tert-butyl (2-aminoethyl)carbamate (215 mg, 1.34 mmol), and according to the methods of Example 1, steps B and C, the title compound (372 mg, yield 72%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.22 (s, 3H), 2.77-2.84 (m, 2H), 2.89 (s, 3H), 3.28-3.35 (m, 2H), 3.86 (s, 2H), 4.11 (d, J=11.4, 2H), 4.26 (d, J=11.4, 2H), 4.28 (s, 2H), 6.92 (dd, J=2.1, 8.4, 1H), 7.09 (d, J=2.1, 1H), 7.11 (d, J=8.4, 1H), 7.2-7.3 (m, 4H), 7.89 (brs, 3H), 8.23 (t, J=5.7, 1H).

The compounds of Examples 25-48 are shown below.

TABLE 8StructuralLC-MSExampleFormulaTMW(found)25 [Image Omitted]

555.11519 26 [Image Omitted]

541.08505 27 [Image Omitted]

569.14533 28 [Image Omitted]

555.11519 29 [Image Omitted]

585.14549 30 [Image Omitted]

571.11535 31 [Image Omitted]

573.10537 32 [Image Omitted]

589.56553 33 [Image Omitted]

569.14533 34 [Image Omitted]

615.16579 35 [Image Omitted]

569.14533 36 [Image Omitted]

598.61526 37 [Image Omitted]

584.58512 38 [Image Omitted]

606.59534 39 [Image Omitted]

637.62565 40 [Image Omitted]

564.12528 41 [Image Omitted]

600.17564 42 [Image Omitted]

580.12544 43 [Image Omitted]

510.50438 44 [Image Omitted]

544.94472 45 [Image Omitted]

484.03484 46 [Image Omitted]

443.97444 47 [Image Omitted]

472.02472 48 [Image Omitted]

502.86430

Example 49N²-(5-chloro-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (400 mg, 1.03 mmol) of Example 45, step A, and the compound (252 mg, 1.34 mmol) of Reference Example 2, and according to the methods of Example 1, steps B and C, the title compound (487 mg, yield 89%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.2, 3H), 2.23 (s, 3H), 2.8-3.0 (m, 4H), 2.89 (s, 3H), 3.3-3.5 (m, 2H), 3.87 (s, 2H), 4.11 (d, J=11.7, 2H), 4.26 (d, J=11.7, 2H), 4.28 (s, 2H), 6.92 (dd, J=2.1, 8.1, 1H), 7.09 (d, J=2.1, 1H), 7.11 (d, J=8.1, 1H), 7.2-7.3 (m, 4H), 8.27 (t, J=5.7, 1H), 8.64 (brs, 2H).

Example 50N²-(5-chloro-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[3-(methylamino)propyl]glycinamide dihydrochlorideStep AN²-(5-chloro-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[3-{methyl[(2-nitrophenyl)sulfonyl]amino}propyl]glycinamide

Using the compound (400 mg, 1.03 mmol) of Example 45, step A, the compound (408 mg, 1.32 mmol) of Reference Example 5 and triethylamine (0.19 ml, 1.36 mmol), and according to the method of Example 1, step B, the title compound (629 mg) as a yellow oil. This was used for the next step as is.

Step BN²-(5-chloro-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[3-(methylamino)propyl]glycinamide dihydrochloride

The compound (629 mg) obtained in step A was dissolved in acetonitrile (20 ml). Then, benzenethiol (0.19 ml, 1.85 mmol) and cesium carbonate (1.00 g, 3.07 mmol) were added, and the mixture was stirred at room temperature for 3 hr. The reaction mixture was diluted with dichloromethane, washed with saturated brine, and dried over sodium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (NH silica gel, methanol-dichloromethane) to give a colorless amorphous solid (290 mg). This was dissolved in diethyl ether (6 ml), 4N hydrochloric acid-dioxane solution (0.5 ml, 2.0 mmol) was added, and the mixture was stirred at room temperature. The precipitated solid was collected by filtration, washed with diethyl ether, and dried under reduced pressure to give the title compound (307 mg, yield 56%) as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.6-1.8 (m, 2H), 2.23 (s, 3H), 2.45 (t, J=5.4, 3H), 2.6-2.8 (m, 2H), 2.90 (s, 3H), 3.0-3.2 (m, 2H), 3.83 (s, 2H), 4.12 (d, J=11.4, 2H), 4.26 (s, 2H), 4.27 (d, J=11.4, 2H), 6.93 (dd, J=2.1, 8.4, 1H), 7.09 (d, J=2.1, 1H), 7.12 (d, J=8.4, 1H), 7.2-7.3 (m, 4H), 8.20 (t, J=5.7, 1H), 8.61 (brs, 2H).

Example 51N²-(5-chloro-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(tert-butylamino) ethyl]glycinamide dihydrochloride

Using the compound (616 mg, 1.59 mmol) of Example 45, step A, and the compound (257 mg, 1.32 mmol) of Reference Example 16, and according to the methods of Example 1, step B, and Example 17, step C, the title compound (386 mg, yield 43%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.24 (s, 9H), 2.24 (s, 3H), 2.7-2.9 (m, 2H), 2.89 (s, 3H), 3.3-3.5 (m, 2H), 3.88 (s, 2H), 4.12 (d, J=11.7, 2H), 4.26 (d, J=11.7, 2H), 4.29 (s, 2H), 6.92 (dd, J=1.8, 8.1, 1H), 7.08 (d, J=1.8, 1H), 7.11 (d, J=8.1, 1H), 7.2-7.3 (m, 4H), 8.32 (broad t, 1H), 8.82 (brs, 2H).

Example 52N²-(5-chloro-2-methylphenyl)-N²-[2-{methyl[4-(methylsulfonyl)piperazin-1-yl]amino}-2-oxoethyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN²-(5-chloro-2-methylphenyl)-N²-[2-{methyl[4-(methylsulfonyl)piperazin-1-yl]amino}-2-oxoethyl]-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (357 mg, 1.39 mmol) of Reference Example 65, the compound (288 mg, 1.49 mmol) of Reference Example 48 and the compound (387 mg, 1.91 mmol) of Reference Example 3, and according to the methods of Example 4, step A, and Example 1, step B, the title compound (741 mg, yield 86%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.12 (d, J=6.9, 6H), 1.46 (brs, 9H), 2.27 (s, 3H), 2.6-2.8 (m, 2H), 2.84 (s, 3H), 2.89-3.03 (m, 4H), 2.93 (s, 3H), 3.0-3.2 (m, 2H), 3.35-3.43 (m, 2H), 3.7-3.9 (m, 4H), 3.9-4.4 (m, 3H), 6.97 (dd, J=2.1, 8.4, 1H), 7.09 (d, J=8.4, 1H), 7.17 (d, J=2.1, 1H), 7.8-8.4 (broad, 1H).

Step BN²-(5-chloro-2-methylphenyl)-N²-[2-{methyl[4-(methylsulfonyl)piperazin-1-yl]amino}-2-oxoethyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (735 mg, 1.19 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (675 mg, yield 96%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.20 (d, J=6.3, 6H), 2.22 (s, 3H), 2.7-3.0 (m, 8H), 2.84 (s, 3H), 2.92 (s, 3H), 3.1-3.3 (m, 1H), 3.34-3.42 (m, 2H), 3.5-3.6 (m, 2H), 3.87 (s, 2H), 4.22 (s, 2H), 6.91 (dd, J=2.1, 8.4, 1H), 7.06 (d, J=2.1, 1H), 7.12 (d, J=8.4, 1H), 8.36 (t, J=5.7, 1H), 8.78 (brs, 2H).

Example 53N²-(4-chloro-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-(4-chloro-2-methylphenyl)-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound (446 mg, 1.73 mmol) of Reference Example 66 and the compound (479 mg, 2.60 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (452 mg, yield 67%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.22 (s, 3H), 2.87 (s, 3H), 3.94 (s, 2H), 4.10 (d, J=11.4, 2H), 4.24 (d, J=11.4, 2H), 4.25 (s, 2H), 7.01-7.15 (m, 3H), 7.22-7.31 (m, 4H), 12.45 (brs, 1H).

Step BN²-(4-chloro-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (452 mg, 1.17 mmol) obtained in step A, and the compound (355 mg, 1.76 mmol) of Reference Example 3, and according to the methods of Example 1, steps B and C, the title compound (519 mg, yield 81%) was obtained as a pale-bistered amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.20 (d, J=6.3, 6H), 2.26 (s, 3H), 2.87 (brs, 5H), 3.17-3.27 (m, 1H), 3.39 (q, J=6.0, 2H), 3.85 (s, 2H), 4.10 (d, J=11.4, 2H), 4.22-4.28 (m, 4H), 7.07-7.18 (m, 3H), 7.23-7.32 (m, 4H), 8.33 (t, J=5.7, 1H), 8.92 (brs, 2H).

Example 54N²-(4-chloro-2-methylphenyl)-N²-{2-[2,3-dihydro-1H-inden-5-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochlorideStep AN-(4-chloro-2-methylphenyl)-N-{2-[2,3-dihydro-1H-inden-5-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound (500 mg, 1.94 mmol) of Reference Example 66, and the compound (535 mg, 2.91 mmol) of Reference Example 32, and according to the method of Example 4, step A, the title compound (532 mg, yield 71%) was obtained as a pale-bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.04 (t, J=7.5, 2H), 2.10 (s, 3H), 2.81-2.87 (m, 4H), 3.10 (s, 3H), 3.34 (s, 2H), 3.92 (s, 2H), 6.95-7.14 (m, 5H), 7.26 (d, J=7.8, 1H), 12.44 (brs, 1H).

Step BN²-(4-chloro-2-methylphenyl)-N²-{2-[2,3-dihydro-1H-inden-5-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochloride

Using the compound (532 mg, 1.37 mmol) obtained in step A, and the compound (416 mg, 2.06 mmol) of Reference Example 3, and according to the methods of Example 1, steps B and C, the title compound (493 mg, yield 71%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.21 (d, J=6.3, 6H), 2.07 (t, J=7.3, 2H), 2.13 (s, 3H), 2.78-2.94 (m, 6H), 3.10 (s, 3H), 3.21-3.27 (m, 1H), 3.35-3.40 (m, 2H), 3.68 (s, 2H), 3.82 (s, 2H), 6.97-7.04 (m, 3H), 7.09-7.16 (m, 2H), 7.27 (d, J=7.8, 1H), 8.30-8.34 (m, 1H), 8.78-8.93 (broad, 2H).

Example 55N²-(4-chloro-2-methylphenyl)-N²-{2-[(3,4-dichlorophenyl)(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochlorideStep AN-(4-chloro-2-methylphenyl)-N-{2-[(3,4-dichlorophenyl)(methyl)amino]-2-oxoethyl}glycine

Using the compound (500 mg, 1.94 mmol) of Reference Example 66 and the compound (559 mg, 2.91 mmol) of Reference Example 31, and according to the method of Example 1, step A, the title compound (545 mg, yield 68%) was obtained as a pale-bistered oil.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.96 (s, 3H), 2.98 (s, 3H), 3.16 (s, 2H), 3.70 (s, 2H), 6.82-7.00 (m, 3H), 7.18 (d, J=8.1, 1H), 7.49 (d, J=8.4, 2H), 12.29 (brs, 1H).

Step BN²-(4-chloro-2-methylphenyl)-N²-{2-[(3,4-dichlorophenyl)(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochloride

Using the compound (545 mg, 1.31 mmol) obtained in step A, and the compound (397 mg, 1.97 mmol) of Reference Example 3, and according to the methods of Example 1, steps B and C, the title compound (576 mg, yield 82%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.19 (d, J=6.5, 6H), 2.15 (s, 3H), 2.83-2.89 (m, 2H), 3.01-3.41 (m, 6H), 3.67-3.92 (m, 4H), 7.01-7.15 (m, 3H), 7.34 (d, J=7.8, 1H), 7.64-7.70 (m, 2H), 8.22-8.26 (m, 1H), 8.78 (brs, 2H).

Example 56N²-(5-acetyl-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-(5-acetyl-2-methylphenyl)-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound (567 mg, 2.14 mmol) of Reference Example 67 and the compound (518 mg, 2.81 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (692 mg, yield 82%) was obtained as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.38 (s, 3H), 2.55 (s, 3H), 3.06 (s, 3H), 3.93 (s, 2H), 4.18 (d, J=11.7, 2H), 4.29 (d, J=11.7, 2H), 4.31 (s, 2H), 7.19-7.29 (m, 5H), 7.62 (dd, J=1.5, 7.8, 1H), 7.81 (d, J=1.5, 1H), 13.5 (brs, 1H).

Step BN²-(5-acetyl-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (680 mg, 1.72 mmol) obtained in step A, and the compound (496 mg, 2.45 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (934 mg, yield 94%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.11 (d, J=6.9, 6H), 1.45 (brs, 9H), 2.41 (s, 3H), 2.55 (s, 3H), 2.94 (s, 3H), 3.0-3.2 (m, 2H), 3.36-3.44 (m, 2H), 3.82 (s, 2H), 3.9-4.3 (broad, 1H), 4.15 (d, J=11.7, 2H), 4.24 (d, J=11.7, 2H), 4.26 (s, 2H), 7.2-7.3 (m, 5H), 7.58 (dd, J=1.4, 7.8, 1H), 7.84 (d, J=1.4, 1H), 8.0-8.7 (broad, 1H).

Step CN²-(5-acetyl-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (933 mg, 1.61 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (866 mg, yield 97%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.19 (d, J=6.5, 6H), 2.34 (s, 3H), 2.51 (s, 3H), 2.8-3.0 (m, 2H), 2.88 (s, 3H), 3.1-3.3 (m, 1H), 3.34-3.42 (m, 2H), 3.90 (s, 2H), 4.12 (d, J=11.7, 2H), 4.26 (d, J=11.7, 2H), 4.33 (s, 2H), 7.2-7.3 (m, 5H), 7.51 (d, J=7.9, 1H), 7.66 (d, J=1.5, 1H), 8.37 (t, J=5.7, 1H), 8.80 (brs, 2H).

Example 57N²-(5-acetyl-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochlorideStep AN²-(5-acetyl-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (4.33 g, 10.95 mmol) of Example 56, step A, and the compound (2.78 g, 14.77 mmol) of Reference Example 2, and according to the method of Example 1, step B, the title compound (5.51 g, yield 89%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.05 (t, J=7.1, 3H), 1.43 (brs, 9H), 2.40 (s, 3H), 2.55 (s, 3H), 2.95 (s, 3H), 3.0-3.2 (m, 2H), 3.2-3.3 (m, 2H), 3.39-3.46 (m, 2H), 3.80 (s, 2H), 4.17 (d, J=11.7, 2H), 4.25 (d, J=11.7, 2H), 4.27 (s, 2H), 7.2-7.3 (m, 5H), 7.57 (dd, J=1.3, 7.6, 1H), 7.83 (d, J=1.3, 1H), 8.2-8.7 (broad, 1H).

Step BN²-(5-acetyl-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

The compound (5.45 g, 9.63 mmol) obtained in step A was dissolved in dichloromethane (25 ml), 4N hydrochloric acid-dioxane solution (25 ml) was added, and the mixture was stirred at room temperature for 100 min. To the reaction mixture were added dichloromethane and aqueous ammonia to extract the organic layer. Furthermore, the aqueous layer was extracted twice with dichloromethane, the organic layer was mixed and the mixture was dried over sodium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was dissolved in dichloromethane (10 ml), and 4N hydrochloric acid-ethyl acetate (2.4 ml, 9.6 mmol) was added. Then, diethyl ether (150 ml) was added to allow precipitation of a solid. This was collected by filtration, washed with diethyl ether, and dried under reduced pressure to give the title compound (4.23 g, yield 87%) as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.14 (t, J=7.2, 3H), 2.33 (s, 3H), 2.51 (s, 3H), 2.8-3.0 (m, 4H), 2.89 (s, 3H), 3.3-3.4 (m, 2H), 3.90 (s, 2H), 4.11 (d, J=11.7, 2H), 4.26 (d, J=11.7, 2H), 4.31 (s, 2H), 7.2-7.3 (m, 5H), 7.52 (dd, J=1.2, 7.8, 1H), 7.66 (d, J=1.2, 1H), 8.32 (t, J=5.7, 1H), 8.44 (brs, 2H).

Example 58N²-(5-acetyl-2-methylphenyl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-(5-acetyl-2-methylphenyl)-N-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}glycine

Using the compound (810 mg, 3.05 mmol) of Reference Example 67 and the compound (806 mg, 3.98 mmol) of Reference Example 19, and according to the method of Example 4, step A, the title compound (1.21 g, yield 96%) was obtained as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.38 (s, 3H), 2.55 (s, 3H), 3.06 (s, 3H), 3.94 (s, 2H), 4.08-4.26 (m, 4H), 4.30 (s, 2H), 6.9-7.0 (m, 2H), 7.14-7.20 (m, 1H), 7.25-7.29 (m, 1H), 7.62 (dd, J=1.5, 7.8, 1H), 7.81 (d, J=1.5, 1H), 13.4 (brs, 1H).

Step BN²-(5-acetyl-2-methylphenyl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (545 mg, 1.32 mmol) obtained in step A, and the compound (396 mg, 1.96 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (762 mg, yield 97%) was obtained as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.12 (d, J=6.8, 6H), 1.44 (brs, 9H), 2.41 (s, 3H), 2.55 (s, 3H), 2.94 (s, 3H), 3.0-3.2 (m, 2H), 3.36-3.44 (m, 2H), 3.81 (s, 2H), 3.9-4.3 (m, 5H), 4.25 (s, 2H), 6.9-7.0 (m, 2H), 7.1-7.3 (m, 2H), 7.57 (dd, J=1.5, 7.8, 1H), 7.83 (d, J=1.5, 1H), 8.0-8.7 (broad, 1H).

Step CN²-(5-acetyl-2-methylphenyl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (755 mg, 1.26 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (688 mg, yield 96%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.19 (d, J=6.6, 6H), 2.34 (s, 3H), 2.51 (s, 3H), 2.8-3.0 (m, 2H), 2.88 (s, 3H), 3.1-3.4 (m, 3H), 3.90 (s, 2H), 4.0-4.3 (m, 4H), 4.32 (s, 2H), 7.0-7.2 (m, 2H), 7.24-7.33 (m, 2H), 7.51 (dd, J=1.5, 7.8, 1H), 7.66 (d, J=1.5, 1H), 8.35 (broad t, 1H), 8.74 (brs, 2H).

Example 59N²-(5-acetyl-2-methylphenyl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-(5-acetyl-2-methylphenyl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (638 mg, 1.54 mmol) of Example 58, step A, and the compound (440 mg, 2.34 mmol) of Reference Example 2, and according to the method of Example 1, step B, the title compound (924 mg, yield>100%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.05 (t, J=7.1, 3H), 1.43 (brs, 9H), 2.40 (s, 3H), 2.55 (s, 3H), 2.94 (s, 3H), 3.0-3.2 (m, 2H), 3.25-3.35 (m, 2H), 3.39-3.47 (m, 2H), 3.79 (s, 2H), 4.08-4.22 (m, 4H), 4.26 (s, 2H), 6.9-7.0 (m, 2H), 7.1-7.3 (m, 2H), 7.57 (dd, J=1.5, 8.1, 1H), 7.83 (d, J=1.5, 1H), 8.1-8.7 (broad, 1H).

Step BN²-(5-acetyl-2-methylphenyl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (924 mg) obtained in step A and according to the method of Example 1, step C, the title compound (688 mg, yield 81%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=7.2, 3H), 2.33 (s, 3H), 2.51 (s, 3H), 2.8-3.0 (m, 4H), 2.88 (s, 3H), 3.35-3.42 (m, 2H), 3.90 (s, 2H), 4.0-4.3 (m, 4H), 4.32 (s, 2H), 7.0-7.2 (m, 2H), 7.24-7.33 (m, 2H), 7.51 (dd, J=1.2, 8.1, 1H), 7.66 (d, J=1.2, 1H), 8.34 (t, J=5.7, 1H), 8.81 (brs, 2H).

Example 60N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[5-(1-hydroxyethyl)-2-methylphenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[5-(1-hydroxyethyl)-2-methylphenyl]-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

The compound (421 mg, 0.744 mmol) of Example 57, step A was dissolved in an ethanol (4 ml)-dichloromethane (1 ml) mixed solvent. Thereto was added sodium borohydride (151 mg, 3.99 mmol), and the mixture was stirred at room temperature for 2 hr. To the reaction mixture was added 10% aqueous citric acid solution, and the reaction mixture was extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium hydrogen carbonate and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (methanol-dichloromethane) to give the title compound (431 mg, yield>100%) as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.01 (t, J=7.1, 3H), 1.41 (brs, 9H), 1.45 (d, J=6.6, 3H), 2.30 (s, 3H), 2.96 (s, 3H), 3.0-3.2 (m, 2H), 3.2-3.3 (m, 2H), 3.3-3.4 (m, 2H), 3.81 (s, 2H), 4.09 (d, J=11.7, 2H), 4.18 (s, 2H), 4.23 (d, J=11.7, 2H), 4.7-4.9 (m, 1H), 6.98-7.02 (m, 1H), 7.14 (d, J=7.8, 1H), 7.18-7.28 (m, 5H), 8.2-8.6 (broad, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[5-(1-hydroxyethyl)-2-methylphenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (420 mg, 0.74 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (281 mg, yield 70%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=7.2, 3H), 1.26 (d, J=6.6, 3H), 2.23 (s, 3H), 2.8-3.0 (m, 4H), 2.89 (s, 3H), 3.3-3.4 (m, 2H), 3.84 (s, 2H), 4.08 (d, J=11.7, 2H), 4.24 (d, J=11.7, 2H), 4.26 (s, 2H), 4.5-4.6 (m, 1H), 6.88 (dd, J=1.2, 7.8, 1H), 7.04 (d, J=7.8, 1H), 7.13 (d, J=1.2, 1H), 7.25 (broad, 4H), 8.42 (t, J=5.7, 1H), 8.66 (brs, 2H).

Example 61N²-(4-cyano-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-(4-cyano-2-methylphenyl)-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound (1.00 g, 4.03 mmol) of Reference Example 68 and the compound (1.12 g, 6.05 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (1.34 g, yield 88%) was obtained as a bistered amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.24 (s, 3H), 2.90 (s, 3H), 4.05 (s, 2H), 4.16 (d, 11.7, 2H), 4.27 (d, J=11.7, 2H), 4.38 (s, 2H), 6.95 (d, J=8.4, 1H), 7.22-7.30 (m, 4H), 7.45-7.50 (m, 2H), 12.65 (brs, 1H).

Step BN²-(4-cyano-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (670 mg, 1.77 mmol) obtained in step A, and the compound (537 mg, 2.66 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (957 mg, yield 96%) was obtained as a bistered amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.03 (d, J=5.4, 6H), 1.38 (s, 9H), 2.27 (s, 3H), 2.89-3.21 (m, 7H), 3.90 (s, 2H), 3.99-4.07 (m, 1H), 4.16 (d, J=11.7, 2H), 4.29 (d, J=11.7, 2H), 4.39 (s, 2H), 6.95 (d, J=8.1, 1H), 7.22-7.30 (m, 4H), 7.45-7.51 (m, 2H), 8.13-8.17 (m, 1H)

Step CN²-(4-cyano-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (200 mg, 0.36 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (171 mg, yield 89%) was obtained as a pale-bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.20 (d, J=6.5, 6H), 2.27 (s, 3H), 2.78-2.95 (m, 2H), 2.91 (s, 3H), 3.21-3.29 (m, 1H), 3.36-3.43 (m, 2H), 3.97 (s, 2H), 4.17 (d, J=11.7, 2H), 4.29 (d, J=11.7, 2H), 4.42 (s, 2H), 6.95 (d, J=8.3, 1H), 7.23-7.31 (m, 4H), 7.44-7.51 (m, 2H), 8.38 (t, J=5.6, 1H), 8.92 (brs, 2H).

Example 62N²-(4-cyano-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-(4-cyano-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (670 mg, 1.77 mmol) of Example 61, step A, and the compound (500 mg, 2.66 mmol) of Reference Example 2 (500 mg, 2.66 mmol), and according to the method of Example 1, step B, the title compound (902 mg, yield 93%) was obtained as a brown amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 0.91-1.02 (m, 3H), 1.37 (s, 9H), 2.26 (s, 3H), 2.91 (s, 3H), 3.02-3.24 (m, 6H), 3.89 (s, 2H), 4.16 (d, J=11.7, 2H), 4.28 (d, J=11.7, 2H), 4.39 (s, 2H), 6.94 (d, J=8.4, 1H), 7.22-7.31 (m, 4H), 7.44-7.50 (m, 2H), 8.11-8.20 (m, 1H).

Step BN²-(4-cyano-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycine amide 2 hydrochloride

Using the compound (200 mg, 0.36 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (181 mg, yield 96%) was obtained as a pale-brown solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=7.2, 3H), 2.27 (s, ³H), 2.78-2.93 (m, 4H), 3.35-3.41 (m, 2H), 3.97 (s, 2H), 4.17 (d, J=11.7, 2H), 4.29 (d, J=11.7, 2H), 4.42 (s, 2H), 6.95 (d, J=8.1, 1H), 7.23-7.31 (m, 4H), 7.44-7.50 (m, 2H), 8.34 (t, J=5.7, 1H), 8.83 (brs, 2H).

Example 63N²-(4-cyano-2-methylphenyl)-N²-{2-[2,3-dihydro-1H-inden-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycine amide hydrochlorideStep AN-(5-cyano-2-methylphenyl)-N-{2-[2,3-dihydro-1H-inden-2-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound of Reference Example 68 (1.00 g, 4.03 mmol) and the compound of Reference Example 23 (1.11 g, 6.05 mmol), and according to the method of Example 1, step A, the title compound (810 mg, yield 53%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.26 (s, 3H), 2.67-2.77 (m, 3H), 2.88-3.12 (m, 4H), 4.03 (s, 2H), 4.16 (s, 1.2H), 4.32 (s, 0.8H), 4.81-4.84 (m, 0.4H), 5.27-5.31 (m, 0.6H), 7.00 (t, J=8.6, 1H), 7.13-7.23 (m, 4H), 7.47-7.53 (m, 2H), 12.70 (brs, 1H).

Step BN²-(4-cyano-2-methylphenyl)-N²-{2-[2,3-dihydro-1H-inden-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycine amide

Using the compound (810 mg, 2.15 mmol) obtained in step A, and the compound of Reference Example 3 (652 mg, 3.23 mmol), and according to the method of Example 1, step B, the title compound (1.13 g, yield 94%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.09 (d, J=6.6, 6H), 1.42 (s, 9H), 2.35 (s, 3H), 2.75-2.96 (m, 5H), 2.98-3.38 (m, 6H), 3.89-4.20 (m, 1H), 3.95 (s, 2H), 4.02 (s, 1.2H), 4.16 (s, 0.8H), 4.58-4.65 (m, 0.4H), 5.52-5.62 (m, 0.6H), 7.12-7.27 (m, 5H), 7.38-7.42 (m, 2H), 7.80-8.15 (broad, 1H).

Step CN²-(4-cyano-2-methylphenyl)-N²-{2-[2,3-dihydro-1H-inden-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycine amide hydrochloride

Using the compound (500 mg, 0.89 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (374.7 mg, yield 85%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.21 (d, J=6.3, 6H), 2.28 (s, 3H), 2.69-2.78 (m, 3H), 2.80-3.45 (m, 9H), 3.95 (s, 2H), 4.20 (s, 1.2H), 4.37 (s, 0.8H), 4.76-4.83 (m, 0.4H), 5.29-5.36 (m, 0.6H), 6.98 (t, J=7.8, 1H), 7.14-7.25 (m, 4H), 7.49 (d, J=8.7, 1H), 7.52 (s, 1H), 8.45 (t, J=5.4, 1H), 8.88 (brs, 2H).

Example 64N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycine amide dihydrochloride

To ethanol (7.5 ml) were added the compound (757 mg, 1.35 mmol) obtained in Example 61, step B, hydroxylamine hydrochloride (131 mg, 1.89 mmol) and sodium acetate (155 mg, 1.35 mmol), and the mixture was heated under reflux for 7 hr. The reaction mixture was cooled to room temperature, and concentrated under reduced pressure. Water was added to the residue, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure to give an oil. To this was added N,N-dimethylacetamide dimethylacetal (2.0 ml), and the mixture was stirred at 100Â° C. for 6.5 hr. The reaction mixture was cooled to room temperature, water was added, and the mixture was extracted with diethyl ether. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solution was concentrated under reduced pressure, and the obtained oil was purified by silica gel column chromatography (methanol-chloroform) to give a colorless oil. Using this oil and according to the method of Example 1, step C, the title compound (338 mg, yield 41%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.19 (d, J=6.6, 6H), 2.33 (s, 3H), 2.63 (s, 3H), 2.79-2.99 (m, 2H), 2.91 (s, 3H), 3.16-3.32 (m, 1H), 3.34-3.45 (m, 2H), 3.96 (s, 2H), 4.15 (d, J=11.7, 2H), 4.28 (d, J=11.7, 2H), 4.39 (s, 2H), 7.09 (d, J=8.4, 1H), 7.22-7.31 (m, 4H), 7.64-7.71 (m, 2H), 8.36-8.39 (m, 1H), 8.91 (brs, 2H).

Example 65N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (702 mg, 1.28 mmol) of Example 62, step A and according to the method of Example 64, the title compound (236 mg, yield 32%) was obtained as a pale-bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=7.2, 3H), 2.32 (s, 3H), 2.63 (s, 3H), 2.80-2.99 (m, 4H), 2.91 (s, 3H), 3.36-3.47 (m, 2H), 3.96 (s, 2H), 4.15 (d, J=11.9, 2H), 4.28 (d, J=11.6, 2H), 4.39 (s, 2H), 7.09 (d, J=8.3, 1H), 7.24-7.32 (m, 4H), 7.67 (d, J=8.4, 1H), 7.71 (s, 1H), 8.34-8.38 (m, 1H), 8.77-9.00 (broad, 2H).

Example 66N²-{2-[2,3-dihydro-1H-inden-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochloride

Using the compound (630 mg, 1.12 mmol) of Example 63, step B and according to the method of Example 64, the title compound (350 mg, yield 56%) was obtained as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.15-1.22 (m, 6H), 2.28-2.35 (m, 3H), 2.63-2.79 (m, 6H), 2.80-3.49 (m, 9H), 3.90-3.94 (m, 2H), 4.16 (s, 1.2H), 4.32 (s, 0.8H), 4.83-4.87 (m, 0.4H), 5.31-5.37 (m, 0.6H), 7.09-7.24 (m, 5H), 7.66-7.70 (m, 1H), 7.73 (s, 1H), 8.43-8.45 (m, 1H), 8.79 (brs, 2H).

Example 67N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-[4-{(2-(tert-butoxycarbonyl)-2-methylhydrazino]carbonyl}-2-methylphenyl]-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound (2.50 g, 6.32 mmol) of Reference Example 70 and the compound (1.75 g, 9.47 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (3.42 g, yield>100%) was obtained as a gray amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.47 (brs, 9H), 2.13-2.26 (m, 3H), 3.03 (s, 3H), 3.18 (s, 3H), 3.95 (brs, 2H), 4.18-4.31 (m, 6H), 6.88-7.31 (m, 5H), 7.48-7.61 (m, 2H), 8.31-9.45 (broad, 1H).

Step BN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-{2-methyl-4-[(2-methylhydrazino)carbonyl]phenyl}glycine dihydrochloride

The compound (3.42 g) obtained in step A was dissolved in dichloromethane (18 ml). To this solution was added 4N hydrochloric acid-dioxane (9.8 ml, 39 mmol), and the mixture was stirred at room temperature for 3 hr. Diethyl ether was added to the reaction mixture, and the precipitated solid was collected by filtration, and dried under reduced pressure to give the title compound (3.06 g, yield 97%) as a colorless solid. This was directly used for the next step.

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-{2-methyl-4-[(2-methylhydrazino)carbonyl]phenyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (1.00 g, 2.01 mmol) obtained in step B, the compound (0.45 g, 2.22 mmol) of Reference Example 3 and triethylamine (0.60 ml, 4.21 mmol), and according to the method of Example 1, step B, the title compound (1.15 g, yield 94%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.08 1.14 (2d, J=6.8, 6H), 1.42 1.48 (2s, 9H), 2.36 (s, 3H), 2.70 2.88 (2s, 3H), 2.96 (s, 3H), 2.99-3.21 (m, 2H), 3.34 (q, J=6.8, 2H), 3.90 (s, 2H), 4.12-4.29 (m, 6H), 7.18-7.29 (m, 4H), 7.46-7.50 (m, 2H), 7.61 (s, 1H), 7.78 (brs, 1H), 8.01 (broad, 1H).

Step DN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-phenyl]-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

The compound (1.15 g, 1.88 mmol) obtained in step C was dissolved in tetrahydrofuran (33 ml), triphosgene (0.21 g, 0.63 mmol) and pyridine (0.76 ml, 9.42 mmol) were added under ice-cooling with stirring, and the mixture was stirred at room temperature for 30 min. The reaction mixture was concentrated, and the obtained oil was diluted with ethyl acetate, washed with 10% aqueous citric acid solution and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (methanol-dichloromethane) to give the title compound (1.06 g, yield 90%) as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.08 1.14 (2d, J=6.8, 6H), 1.42 1.48 (s, 9H), 2.37 (s, 3H), 2.98 (s, 3H), 3.04-3.11 (brs, 2H), 3.32-3.41 (m, 2H), 3.47 (s, 3H), 3.93 (s, 2H), 4.06-4.39 (m, 7H), 7.21-7.28 (m, 5H), 7.55-7.62 (m, 2H), 8.04-8.22 (broad, 1H).

Step EN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (1.06 g, 1.67 mmol) obtained in step D and according to the method of Example 1, step C, the title compound (795 mg, yield 78%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.19 (d, J=6.3, 6H), 2.31 (s, 3H), 2.90 (s, 5H), 3.23-3.32 (m, 1H), 3.37-3.42 (m, 5H), 3.95 (s, 2H), 4.16 (d, J=11.9, 2H), 4.28 (d, J=11.9, 2H), 4.39 (s, 2H), 7.05 (d, J=8.4, 1H), 7.27 (s, 4H), 7.46-7.51 (m, 2H), 8.34-8.39 (m, 1H), 8.88 (brs, 2H).

Example 68N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(4-methyl-5-oxo-1,3,4-oxadiazol-2-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-{2-methyl-4-[(2-methylhydrazino)carbonyl]phenyl}-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (1.00 g, 2.01 mmol) obtained in Example 67, step B, the compound (0.42 g, 2.23 mmol) of Reference Example 2 and triethylamine (0.60 ml, 4.21 mmol), and according to the method of Example 1, step B, the title compound (1.21 g, yield>100%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.00 (t, J=7.0, 3H), 1.41 (s, 9H), 2.35 (s, 3H), 2.69 2.88 (2s, 3H), 2.95 (s, 3H), 3.08 (q, J=7.0, 2H), 3.20 (brs, 2H), 3.33-3.40 (m, 2H), 3.88 (s, 2H), 4.10-4.29 (m, 6H), 7.17-7.29 (m, 5H), 7.49 (dd, J=1.5, 8.4, 1H), 7.61-7.71 (m, 1H), 7.94-8.2 (broad, 2H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (1.21 g) obtained in step A and according to the method of Example 67, step D, the title compound (880 mg, yield 73%) was obtained as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.00 (t, J=6.9, 3H), 1.40 (s, 9H), 2.36 (s, 3H), 2.98 (s, 3H), 3.06-3.14 (m, 2H), 3.21 (brs, 2H), 3.38 (q, J=6.0, 2H), 3.47 (s, 3H), 3.91 (s, 2H), 4.08-4.30 (m, 6H), 7.21-7.29 (m, 5H), 7.55-7.61 (m, 2H), 8.01 8.22 (2brs, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(4-methyl-5-oxo-1,3,4-oxadiazol-2-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (880 mg, 1.42 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (732 mg, yield 87%) was obtained as a colorless solid. ¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=6.9, 3H), 2.30 (s, 3H), 2.90 (m, 5H), 3.37 (m, 5H), 3.96 (s, 2H), 4.02-4.3 (m, 4H), 4.39 (s, 2H), 7.05 (d, J=8.4, 1H), 7.26-7.33 (m, 4H), 7.45-7.50 (m, 2H), 8.35 (brs, 1H), 8.93 (brs, 2H).

Example 69N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[4-(4-ethyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-2-methylphenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-[4-{[2-(tert-butoxycarbonyl)-2-ethylhydrazino]carbonyl}-2-methylphenyl]-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound (3.31 g, 8.08 mmol) of Reference Example 71 and the compound (2.30 g, 12.45 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (3.19 g, yield 73%) was obtained as a gray amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.14 (t, J=7.2, 3H), 1.46 (brs, 9H), 2.19 (brs, 3H), 3.03 (s, 3H), 3.59 (q, J=7.2, 2H), 3.95 (s, 2H), 4.19-4.32 (m, 6H), 6.94-7.14 (broad, 1H), 7.23-7.29 (m, 4H), 7.48-7.62 (m, 2H), 8.35 9.32 (2broad, 1H).

Step BN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-{4-[(2-ethylhydrazino)carbonyl]-2-methylphenyl}glycine dihydrochloride

Using the compound (3.19 g, 5.91 mmol) obtained by the method of step A and according to the method of Example 67, step B, the title compound (2.81 g, yield 93%) was obtained as a colorless solid.

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-{4-[(2-ethylhydrazino)carbonyl]-2-methylphenyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (1.00 g, 1.95 mmol) obtained in step B, the compound (0.43 g, 2.13 mmol) of Reference Example 3 and triethylamine (0.57 ml, 4.1 mmol), and according to the method of Example 1, step B, the title compound (1.36 g, yield>100%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.06-1.18 (m, 9H), 1.42 1.47 (2s, 9H), 2.35 (s, 3H), 2.87-3.03 (m, 5H), 3.09 (brs, 2H), 3.31-3.38 (m, 2H), 3.90 (s, 2H), 4.12-4.29 (m, 7H), 7.18-7.30 (m, 4H), 7.49-7.63 (m, 2H), 7.8-8.3 (broad, 2H).

Step DN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[4-(4-ethyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-2-methylphenyl]-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (1.36 g) obtained in step C and according to the method of Example 67, step D, the title compound (0.70 g, yield 55%) was obtained as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.08 (d, J=6.9, 6H), 1.32-1.43 (m, 12H), 2.37 (s, 3H), 2.98 (s, 3H), 3.10 (brs, 2H), 3.35 (q, J=6.9, 2H), 3.82 (q, J=7.2, 2H), 3.92 (s, 2H), 4.04-4.30 (m, 7H), 7.22-7.31 (m, 5H), 7.56-7.63 (m, 2H), 7.8-8.4 (broad, 1H).

Step EN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[4-(4-ethyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-2-methylphenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (0.70 g, 1.08 mmol) obtained in step D and according to the method of Example 1, step C, the title compound (515 mg, yield 77%) was obtained as a colorless solid. ¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.20 (d, 6H), 1.28 (t, J=7.0, 3H), 2.31 (s, 3H), 2.90 (m, 5H), 3.23-3.25 (m, 1H), 3.37-3.42 (m, 2H), 3.74 (q, J=7.0, 2H), 3.96 (s, 2H), 4.13-4.40 (m, 6H), 7.05 (d, J=8.3, 1H), 7.27 (m, 4H), 7.46-7.52 (m, 2H), 8.38 (brs, 1H), 8.95 (brs, 2H).

Example 70N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[4-(4-ethyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-2-methylphenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-{4-[(2-ethylhydrazino)carbonyl]-2-methylphenyl}-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (1.00 g, 1.95 mmol) of Example 69, step B, the compound (0.40 g, 2.13 mmol) of Reference Example 2 and triethylamine (0.57 ml, 4.09 mmol), and according to the method of Example 1, step B, the title compound (1.43 g, yield>100%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 0.96 (t, J=6.6, 3H), 1.09 (t, J=7.2, 3H), 1.38 1.43 (2s, 9H), 2.31 (s, 3H), 2.84-2.94 (m, 5H), 3.05 (q, J=6.9, 2H), 3.17 (brs, 2H), 3.32-3.43 (m, 2H), 3.85 (s, 2H), 4.09-4.26 (m, 6H), 7.13-7.27 (m, 5H), 7.46-7.59 (m, 2H), 7.97 (broad, 2H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[4-(4-ethyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-2-methylphenyl]-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (1.43 g) obtained in step A and according to the method of Example 67, step D, the title compound (0.98 g, yield 79%) was obtained as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.00 (t, J=6.9, 3H), 1.36-1.41 (m, 12H), 2.6 (s, 3H), 2.98 (s, 3H), 3.08 (q, J=6.6, 2H), 3.21 (brs, 2H), 3.34-3.40 (m, 2H), 3.82 (q, J=7.2, 2H), 3.91 (s, 2H), 4.08-4.31 (m, 6H), 7.21-7.29 (m, 5H), 7.57 (dd, J=1.8, 8.4, 2H), 8.03 8.25 (2brs, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[4-(4-ethyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-2-methylphenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (0.98 g, 1.54 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (0.69 g, yield 73%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=6.9, 3H), 1.27 (t, J=7.2, 3H), 2.31 (s, 3H), 2.8-3.0 (m, 7H), 3.38 (q, J=6.9, 2H), 3.74 (q, J=7.2, 2H), 3.95 (s, 2H), 4.13-4.40 (m, 6H), 7.04 (d, J=8.4, 1H), 7.20-7.32 (m, 4H), 7.46-7.51 (m, 2H), 8.34-8.39 (m, 1H), 8.95 (brs, 2H).

Example 71N²-(5-cyano-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(2R)-2-(hydroxymethyl)pyrrolidin-1-yl]ethyl}glycinamide dihydrochloride

Using the compound (911 mg, 2.41 mmol) of Example 1, step A, compound (718 mg, 4.98 mmol) of Reference Example 8, and according to the methods of Example 1, step B, Example 17, step C, the title compound (244 mg, yield 18%) was obtained as a pale-bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.61-2.16 (m, 6H), 2.34 (s, ³H), 2.88 (s, 3H), 2.89-3.10 (m, 2H), 3.25-3.58 (m, 4H), 3.59-3.77 (M, 2H), 3.90 (s, 2H), 4.00-4.15 (m, 1H), 4.14 (d, J=11.9, 2H), 4.26 (d, J=11.9, 2H), 4.30 (s, 2H), 7.24-7.32 (m, 6H), 7.45 (s, 1H), 8.26-8.30 (m, 1H), 9.83 (brs, 1H).

Example 72N²-(5-cyano-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(2,2,2-trifluoroethyl)amino]ethyl}glycinamide dihydrochloride

Using the compound (500 mg, 1.32 mmol) of Example 1, step A, and the compound (544 mg, 1.98 mmol) of Reference Example 14, and according to the method of Example 1, step B, a brown oil was obtained. This was dissolved in a methanol (5 ml)-water (1 ml) mixed solvent, then potassium carbonate (300 mg, 2.17 mmol) was added, and the mixture was stirred at room temperature overnight. The reaction mixture was diluted with water, and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (methanol-chloroform) to give the title compound (salt free) as an oil. Using this oil and according to the method of Example 17, step C, the title compound (269 mg, yield 35%) was obtained as a pale-bistered amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.33 (s, 3H), 2.89 (s, 3H), 3.04-3.09 (m, 2H), 3.42-3.47 (m, 2H), 3.90 (s, 2H), 4.03-4.16 (m, 4H), 4.26 (d, J=12.6, 2H), 4.30 (s, 2H), 7.25-7.31 (m, 6H), 7.44 (s, 1H), 8.30-8.34 (m, 1H), 9.25-10.48 (broad, 2H).

The compounds of Examples 49-72 are shown below.

TABLE 9StructuralLC-MSExampleFormulaTMW(found)49 [Image Omitted]

530.92458 50 [Image Omitted]

530.92458 51 [Image Omitted]

558.97486 52 [Image Omitted]

590.01517 53 [Image Omitted]

544.94472 54 [Image Omitted]

507.50471 55 [Image Omitted]

536.32499 56 [Image Omitted]

552.54480 57 [Image Omitted]

502.05466 58 [Image Omitted]

570.53498 59 [Image Omitted]

556.50484 60 [Image Omitted]

540.53486 61 [Image Omitted]

535.51463 62 [Image Omitted]

521.48449 63 [Image Omitted]

498.06462 64 [Image Omitted]

592.56520 65 [Image Omitted]

578.53506 66 [Image Omitted]

555.11519 67 [Image Omitted]

608.56536 68 [Image Omitted]

594.53522 69 [Image Omitted]

622.59550 70 [Image Omitted]

608.56536 71 [Image Omitted]

577.55505 72 [Image Omitted]

575.45503

Example 73N²-(5-cyano-2-methylphenyl)-N²-{2-[2,3-dihydro-1H-inden-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(2,2,2-trifluoroethyl)amino]ethyl}glycinamide hydrochloride % step A:N-(5-cyano-2-methylphenyl)-N-{2-[2,3-dihydro-1H-inden-2-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound (1.00 g, 4.03 mmol) of Reference Example 61 and the compound (1.11 g, 6.05 mmol) of Reference Example 23, and according to the method of Example 4, step A, the title compound (820 mg, yield 54%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.33 (s, 3H), 2.66 (s, 1.2H), 2.76 (s, 1.8H), 2.79-3.17 (m, 4H), 3.95 (s, 2H), 4.09 (s, 1.2H), 4.24 (s, 0.8H), 4.83-4.99 (m, 0.4H), 5.24-5.31 (m, 0.6H), 7.13-7.24 (m, 4H), 7.29-7.36 (m, 2H), 7.48 (d, J=12.0, 1H), 12.60 (brs, 1H).

Step BN²-(5-cyano-2-methylphenyl)-N²-{2-[2,3-dihydro-1H-inden-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(2,2,2-trifluoroethyl)amino]ethyl}glycinamide hydrochloride

Using the compound (500 mg, 1.32 mmol) obtained in step A and the compound (544 mg, 1.98 mmol) of Reference Example 14, and according to the method of Example 72, the title compound (293 mg, yield 41%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.35 (s, 3H), 2.68 (s, 1.2H), 2.76 (s, 1.8H), 2.79-3.17 (m, 6H), 3.41-3.48 (m, 2H), 3.86-3.88 (m, 2H), 4.04-4.27 (m, 4H), 4.78-4.88 (m, 0.4H), 5.27-5.35 (m, 0.6H), 7.12-7.24 (m, 4H), 7.31-7.35 (m, 2H), 7.48 (d, J=10.2, 1H), 8.41-8.45 (m, 1H), 9.55-10.80 (broad, 2H).

Example 74N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-(5-cyano-2-methylphenyl)-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine tert-butyl ester

The compound (2.06 g, 5.44 mmol) of Example 1, step A, 4-dimethylaminopyridine (1.40 g, 11.5 mmol) and WSC (1.46 g, 7.62 mmol) were dissolved in dichloromethane (22 ml), tert-butanol (1.0 ml, 10 mmol) was added at room temperature, and the mixture was stirred at the same temperature overnight. The reaction mixture was diluted with an ethyl acetate-hexane=1:1 mixed solvent, and the organic layer was washed with 10% aqueous citric acid solution, water, diluted aqueous sodium hydroxide solution and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (1.76 g, yield 74%) as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.41 (s, 9H), 2.37 (s, 3H), 2.95 (s, 3H), 4.00 (s, 2H), 4.15 (d, J=11.4, 2H), 4.26 (d, J=11.4, 2H), 4.36 (s, 2H), 7.19-7.29 (m, 6H), 7.44 (s, 1H).

Step BN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-[2-methyl-5-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)phenyl]glycine tert-butyl ester

To an ethanol (20 ml)-water (5 ml) solution were added the compound (584 mg, 1.34 mmol) obtained in step A, hydroxylamine hydrochloride (775 mg, 11.2 mmol) and sodium acetate (956 mg, 11.7 mmol), and the mixture was heated under reflux for 3 hr. The reaction mixture was cooled, and diluted with ethyl acetate and water to extract the organic layer. The organic layer washed with saturated aqueous sodium hydrogen carbonate and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure to give a colorless oil. This oil was dissolved in pyridine (10 ml), ethyl chloroformate (0.17 ml, 1.8 mmol) was added under ice-cooling, and the mixture was stirred at room temperature for 30 min and stirred with heating at 130Â° C. for 90 min. The reaction mixture was cooled, diluted with 10% aqueous citric acid solution, and the organic layer was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (474 mg, yield 71%) as a pale-yellow amorphous solid

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.35 (s, 9H), 2.39 (s, 3H), 2.98 (s, 3H), 4.06 (s, 2H), 4.23 (d, J=13.5, 2H), 4.29 (d, J=13.5, 2H), 4.46 (s, 2H), 7.19-7.30 (m, 6H), 7.56 (d, J=1.2, 1H), 10.53 (brs, 1H).

Step CN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-[2-methyl-5-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)phenyl]glycine

The compound (449 mg, 0.910 mmol) obtained in step B was dissolved in dichloromethane (4 ml), trifluoroacetic acid (4 ml) was added under ice-cooling and the mixture was stirred at room temperature for 3 hr. The reaction mixture was concentrated under reduced pressure, and the obtained oil was purified by silica gel column chromatography (methanol-chloroform) to give the title compound (407 mg, yield>100%) as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.35 (s, 3H), 3.06 (s, 3H), 4.05 (s, 2H), 4.20 (d, J=11.7, 2H), 4.30 (d, J=11.7, 2H), 4.35 (s, 2H), 7.19-7.31 (m, 5H), 7.50 (dd, J=1.5, 7.8, 1H), 7.59 (d, J=1.5, 1H), 11.07 (brs, 1H).

Step DN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (397 mg, 0.908 mmol) obtained in step C, and the compound (232 mg, 1.15 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (275 mg, yield 49%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.15 (broad, 6H), 1.37 (brs, 9H), 2.41 (s, 3H), 2.95 (s, 3H), 3.1-3.5 (m, 4H), 3.9-4.2 (broad, 1H), 3.95 (s, 2H), 4.14 (d, J=11.7, 2H), 4.24 (d, J=11.7, 2H), 4.26 (s, 2H), 7.19-7.29 (m, 5H), 7.56 (d, J=7.5, 1H), 7.80 (brs, 1H), 8.63 (brs, 1H), 11.50 (brs, 1H).

Step EN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (269 mg, 0.433 mmol) obtained in step D and according to the method of Example 1, step C, the title compound (242 mg, yield 94%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.19 (d, J=6.6, 6H), 2.34 (s, 3H), 2.8-3.0 (m, 2H), 2.88 (s, 3H), 3.1-3.3 (m, 1H), 3.34-3.42 (m, 2H), 3.92 (s, 2H), 4.12 (d, J=11.7, 2H), 4.26 (d, J=11.7, 2H), 4.33 (s, 2H), 7.22-7.36 (m, 6H), 7.59 (s, 1H), 8.33 (broad t, 1H), 8.79 (brs, 2H), 12.97 (s, 1H).

Example 75N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(4-methyl-5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-[2-methyl-5-(4-methyl-5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)phenyl]glycine tert-butyl ester

The compound (680 mg, 1.38 mmol) of Example 74, step B was dissolved in N,N-dimethylformamide (10 ml) and the mixture was stirred under ice-cooling. Then, 60% sodium hydride (74 mg, 1.85 mmol) was added, and the mixture was stirred at room temperature for 10 min. After ice-cooling again, methyl iodide (0.5 ml) was added with stirring, and the mixture was stirred under ice-cooling for 40 min. The reaction mixture was diluted with 10% citric acid, and extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium hydrogen carbonate and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (678 mg, yield 97%) as a pale-yellow amorphous solid

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.40 (s, 9H), 2.40 (s, 3H), 2.94 (s, 3H), 3.31 (s, 3H), 4.05 (s, 2H), 4.15 (d, J=11.7, 2H), 4.26 (d, J=11.7, 2H), 4.38 (s, 2H), 7.15-7.31 (m, 6H), 7.43 (d, J=1.5, 1H).

Step BN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-[2-methyl-5-(4-methyl-5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)phenyl]glycine

Using the compound (666 mg, 1.31 mmol) obtained in step A and according to the method of Example 74, step C, the title compound (582 mg, yield 98%) was obtained as a pale-yellow amorphous solid

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.38 (s, 3H), 3.08 (s, 3H), 3.30 (s, 3H), 3.98 (s, 2H), 4.20 (d, J=11.5, 2H), 4.31 (d, J=11.5, 2H), 4.36 (s, 2H), 7.2-7.3 (m, 5H), 7.36 (d, J=7.8, 1H), 7.44 (d, J=1.5, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(4-methyl-5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (576 mg, 1.28 mmol) obtained in step B, and the compound (387 mg, 1.91 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (691 mg, yield 85%) was obtained as a pale-yellow amorphous solid

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.10 (d, J=6.9, 6H), 1.42 (brs, 9H), 2.42 (s, 3H), 2.96 (s, 3H), 3.0-3.2 (m, 2H), 3.3-3.4 (m, 2H), 3.32 (s, 3H), 3.89 (s, 2H), 3.9-4.3 (broad, 1H), 4.15 (d, J=11.4, 2H), 4.26 (s, 2H), 4.27 (d, J=11.4, 2H), 7.2-7.3 (m, 5H), 7.33 (d, J=7.8, 1H), 7.47 (d, J=1.2, 1H), 7.9-8.5 (broad, 1H).

Step DN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(4-methyl-5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (685 mg, 1.08 mmol) obtained in step C and according to the method of Example 1, step C, the title compound (578 mg, yield 88%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.18 (d, J=6.3, 6H), 2.35 (s, 3H), 2.8-3.0 (m, 2H), 2.89 (s, 3H), 3.19 (s, 3H), 3.2-3.5 (m, 3H), 3.92 (s, 2H), 4.12 (d, J=11.7, 2H), 4.26 (d, J=11.7, 2H), 4.33 (s, 2H), 7.22 (dd, J=1.2, 7.8, 1H), 7.26 (broad, 4H), 7.34 (d, J=7.8, 1H), 7.39 (d, J=1.2, 1H), 8.30 (t, J=5.7, 1H), 8.56 (brs, 2H).

Example 76N²-(5-carboxy-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN²-(5-tert-butoxycarbonyl-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound (2.42 g, 7.48 mmol) of Reference Example 72 and the compound (2.07 g, 11.2 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (3.89 g, yield>100%) was obtained as a gray amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.55 (s, 9H), 2.35 (s, 3H), 3.04 (s, 3H), 3.94 (s, 2H), 4.15-4.31 (m, 6H), 7.17-7.28 (m, 5H), 7.64 (dd, J=1.62, 7.82, 1H), 7.84 (d, J=1.23, 1H).

Step BN²-(5-tert-butoxycarbonyl-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-{(isopropyl)[(2-nitrophenyl)sulfonyl]amino}ethyl]glycinamide

Using the compound (3.89 g) obtained in step A, and the compound (3.82 g, 13.3 mmol) of Reference Example 7, and according to the method of Example 1, step B, the title compound (4.01 g, yield 74%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.18 (d, J=6.8, 6H), 1.56 (s, 9H), 2.40 (s, 3H), 2.95 (s, 3H), 3.36-3.39 (m, 2H), 3.48-3.52 (m, 2H), 3.79 (s, 2H), 4.08-4.23 (m, 5H), 4.30 (s, 2H), 7.18-7.28 (m, 5H), 7.58-7.69 (m, 4H), 7.85 (d, J=1.3, 1H), 8.00 (d, J=9.1, 1H), 8.75 (m, 1H).

Step CN²-(5-tert-butoxycarbonyl-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide

Using the compound (0.80 g, 1.11 mmol) obtained in step B and according to the method of Example 40, step E, the title compound (0.55 g, yield 92%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.01 (d, J=6.8, 6H), 1.56 (s, 9H), 2.40 (s, 3H), 2.72-2.79 (m, 3H), 2.95 (s, 3H), 3.39-3.42 (m, 2H), 3.79 (s, 2H), 4.12-4.24 (m, 6H), 7.19-7.31 (m, 5H), 7.60-7.63 (m, 1H), 7.85 (s, 1H), 8.52 (s, 1H).

Step DN²-(5-carboxy-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide

The compound (0.30 g, 0.56 mmol) obtained in step C was dissolved in dichloromethane (10 ml), trifluoroacetic acid (1.36 ml) was added, and the mixture was stirred at room temperature overnight. The reaction mixture was concentrated under reduced pressure, water was added, and the mixture was extracted with dichloromethane. The organic layer was dried over anhydrous magnesium sulfate, and the insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (methanol-dichloromethane) to give the title compound (0.32 g) as a colorless amorphous solid. This was directly used for the next step.

Step EN²-(5-carboxy-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (0.32 g) obtained in step D and according to the method of Example 17, step C, the title compound (0.25 g, yield from step D 81%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.19 (d, J=6.5, 6H), 2.32 (s, 3H), 2.87 (m, 5H), 3.21-3.26 (m, 1H), 3.38 (q, J=7.1, 2H), 3.89 (s, 2H), 4.10-4.34 (m, 6H), 7.20-7.26 (m, 5H), 7.46 (d, J=7.6, 1H), 7.70 (s, 1H), 8.35-8.40 (m, 1H), 8.91 (brs, 2H).

Example 77N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-{2-methyl-5-[(methylamino)carbonyl]phenyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN²-(5-carboxy-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-{(isopropyl)[(2-nitrophenyl)sulfonyl]amino}ethyl]glycinamide

Using the compound (3.18 g, 4.4 mmol) of Example 76, step B and according to the method of Reference Example 61, step D, the title compound (3.17 g, yield>100%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.11-1.20 (m, 6H), 2.38 2.41 (2s, 3H), 2.93 2.97 (2s, 3H), 3.35-3.40 (m, 2H), 3.49-3.54 (m, 2H), 3.90 (s, 2H), 4.09-4.36 (m, 7H), 7.19-7.27 (m, 5H), 7.58-7.71 (m, 4H), 7.95-7.99 (m, 2H), 8.96 (m, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-{2-methyl-5-[(methylamino)carbonyl]phenyl}-N¹-[2-{(isopropyl)[(2-nitrophenyl)sulfonyl]amino}ethyl]glycinamide

The compound (0.70 g, 1.05 mmol) obtained in step A was dissolved in dichloromethane (10 ml). Under ice-cooling with stirring, triethylamine (0.20 ml, 1.43 mmol) and isobutyl chloroformate (0.20 ml, 1.52 mmol) were added, and the mixture was stirred at room temperature for 3 hr. Then, under ice-cooling with stirring, 40% methylamine-methanol solution (0.45% g) was added, and the mixture was stirred at room temperature for 2 hr. The reaction mixture was diluted with dichloromethane, washed with saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (NH silica gel use, methanol-dichloromethane) to give the title compound (0.70 g, yield 98%) as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.15 (d, J=6.7, 6H), 2.37 (s, 3H), 2.94 (s, 6H), 3.29-3.35 (m, 2H), 3.43-3.51 (m, 2H), 3.84 (s, 2H), 4.02-4.28 (m, 7H), 6.42 (brs, 1H), 7.18-7.28 (m, 5H), 7.44 (d, J=7.8, 1H), 7.57-7.69 (m, 4H), 7.95-7.99 (m, 1H), 8.57-8.60 (m, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-{2-methyl-5-[(methylamino)carbonyl]phenyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (0.70 g, 1.03 mmol) obtained in step B and according to the method of Example 50, step B, the title compound (0.45 g, yield 77%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.15 (d, J=6.6, 6H), 2.30 (s, ³H), 2.74 (s, 3H), 2.8-3.0 (m, 5H), 3.20-3.28 (m, 1H), 3.34-3.42 (m, 2H), 3.92 (s, 2H), 4.11 (d, J=11.7, 2H), 4.25 (d, J=11.7, 2H), 4.32 (s, 2H), 7.15-7.39 (m, 6H), 7.65 (s, 1H), 8.36-8.41 (m, 2H), 8.89 (brs, 2H).

Example 78N²-[5-(aminocarbonyl)-2-methylphenyl]-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN²-[5-(aminocarbonyl)-2-methylphenyl]-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-{(isopropyl) [(2-nitrophenyl)sulfonyl]amino}ethyl]glycinamide

Using the compound (0.70 g, 1.05 mmol) of Example 77, step A, and a 7N ammonia-methanol solution (0.8 ml), and according to the method of Example 77, step B, the title compound (0.70 g, yield 100%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.14 (d, J=6.3, 6H), 2.38 (s, 3H), 2.95 (s, 3H), 3.29-3.34 (m, 2H), 3.44-3.48 (m, 2H), 3.87 (s, 2H), 4.01-4.29 (m, 7H), 6.00 6.60 (2brs, 2H), 7.20-7.28 (m, 6H), 7.45-7.49 (m, 1H), 7.57-7.59 (m, 1H), 7.64-7.68 (m, 1H), 7.77 (s, 1H), 7.95-7.97 (m, 1H), 8.62-8.64 (m, 1H).

Step BN²-[5-(aminocarbonyl)-2-methylphenyl]-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide

Using the compound (0.70 g, 1.05 mmol) obtained in step A and according to the method of Example 46, step B, the title compound (0.45 g, yield 89%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 0.98 (d, J=6.3, 6H), 2.37 (s, 3H), 2.65-2.78 (m, 3H), 2.95 (s, 3H), 3.33-3.40 (m, 2H), 3.87 (s, 2H), 4.12-4.25 (m, 6H), 6.21 (broad, 1H), 6.81 (broad, 1H), 7.18-7.29 (m, 5H), 7.48 (dd, J=0.9, 7.5, 1H), 7.78 (d, J=1.5, 1H), 8.40-8.45 (m, 1H).

Step CN²-[5-(aminocarbonyl)-2-methylphenyl]-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (0.40 g, 0.83 mmol) obtained in step B and according to the method of Example 17, step C, the title compound (0.46 g, yield>100%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.19 (d, J=6.3, 6H), 2.31 (s, ³H), 2.8-3.0 (m, 5H), 3.21-3.26 (m, 1H), 3.34-3.42 (m, 2H), 3.90 (s, 2H), 4.10-4.33 (m, 6H), 7.14-7.26 (m, 5H), 7.41 (d, J=7.5, 1H), 7.67 (s, 1H), 8.37-8.40 (m, 1H), 8.90 (brs, 2H).

Example 79N²-[5-(aminocarbonyl)-2-methylphenyl]-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamideStep AN-[5-(aminocarbonyl)-2-methylphenyl]-N-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}glycine

Using the compound (1.18 g, 4.43 mmol) of Reference Example 73 and the compound (1.12 g, 5.53 mmol) of Reference Example 19, and according to the method of Example 4, step A, the title compound (1.22 g, yield 66%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.27 (s, 3H), 2.87 (s, 3H), 3.99 (s, 2H), 4.0-4.3 (m, 4H), 4.27 (s, 2H), 7.0-7.2 (m, 4H), 7.27-7.32 (m, 1H), 7.39 (d, J=7.8, 1H), 7.61 (s, 1H), 7.83 (brs, 1H), 12.44 (brs, 1H).

Step BN²-[5-(aminocarbonyl)-2-methylphenyl]-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (1.21 g, 2.92 mmol) obtained in step A and the compound (808 mg, 3.99 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (1.70 g, yield 97%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.12 (d, J=6.6, 6H), 1.42 (brs, 9H), 2.38 (s, 3H), 2.94 (s, 3H), 3.0-3.3 (m, 2H), 3.35-3.44 (m, 2H), 3.83 (s, 2H), 4.0-4.3 (m, 5H), 4.23 (s, 2H), 5.4-5.7 (broad, 0.6H), 6.0-6.7 (broad, 0.4H), 6.9-7.0 (m, 2H), 7.1-7.3 (m, 3H), 7.4-7.5 (m, 1H), 7.75 (brs, 1H), 8.2-8.7 (broad, 1H).

Step CN²-[5-(aminocarbonyl)-2-methylphenyl]-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide

Using the compound (466 mg, 778 mmol) obtained in step B and according to the method of Example 46, step B, the title compound (377 mg, yield 97%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 0.99 (d, J=6.3, 6H), 2.39 (s, 3H), 2.6-2.8 (m, 3H), 2.95 (s, 3H), 3.35-3.42 (m, 2H), 3.83 (s, 2H), 4.0-4.3 (m, 4H), 4.24 (s, 2H), 5.3-6.5 (broad, 2H), 6.9-7.0 (m, 2H), 7.14-7.26 (m, 2H), 7.45 (dd, J=1.5, 7.8, 1H), 7.71 (d, J=1.5, 1H), 8.42 (broad t, 1H).

Example 80N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino}-2-oxoethyl]-N²-[2-methyl-5-(5-methyl-1H-1,2,4-triazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide trihydrochlorideStep AN²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1H-1,2,4-triazol-3-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

The compound (612 mg, 1.02 mmol) of Example 79, step B was dissolved in N,N-dimethylacetamide dimethylacetal (3 ml), and the mixture was stirred at 110Â° C. for 40 min. The reaction mixture was concentrated under reduced pressure, and the obtained residue was dissolved in acetic acid (2 ml). Then, hydrazine monohydrate (0.04 ml) was added, and the mixture was stirred with heating at 110Â° C. for 10 min. The reaction mixture was cooled to room temperature, diluted with an ethyl acetate-hexane=1:1 mixed solvent, washed with diluted aqueous sodium hydroxide solution and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure to give a solid. This was washed with diethyl ether, and dried under reduced pressure to give the title compound (536 mg, yield 79%) as a pale-pink solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.0-1.2 (broad d, 6H), 1.44 (brs, 9H), 2.36 (s, 3H), 2.47 (s, 3H), 2.99 (s, 3H), 3.0-3.3 (m, 2H), 3.38-3.45 (m, 2H), 3.85 (s, 2H), 3.9-4.3 (m, 7H), 6.8-7.0 (m, 2H), 7.10-7.15 (m, 1H), 7.25 (d, J=7.8, 1H), 7.72 (dd, J=1.2, 7.8, 1H), 7.92 (brs, 1H), 8.4-8.9 (broad, 1H).

Step BN²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1H-1,2,4-triazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide trihydrochloride

Using the compound (527 mg, 0.828 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (528 mg, yield 99%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.19 (d, J=6.6, 6H), 2.33 (s, 3H), 2.53 (s, 3H), 2.8-3.0 (m, 2H), 2.87 (s, 3H), 3.1-3.3 (m, 1H), 3.36-3.43 (m, 2H), 3.93 (s, 2H), 4.0-4.3 (m, 4H), 4.35 (s, 2H), 7.0-7.2 (m, 2H), 7.26-7.33 (m, 2H), 7.57 (dd, J=1.2, 8.1, 1H), 7.84 (d, J=1.2, 1H), 8.36 (t, J=5.7, 1H), 8.83 (brs, 2H).

Example 81N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(1H-1,2,4-triazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide trihydrochlorideStep AN-[5-(aminocarbonyl)-2-methylphenyl]-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound (1.00 g, 3.76 mmol) of Reference Example 73 and the compound (763 mg, 4.13 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (1.11 g, yield 83%) was obtained as a pale-bistered amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.36 (s, 3H), 3.06 (s, 3H), 3.93 (s, 2H), 4.17-4.31 (m, 6H), 7.20-7.29 (m, 5H), 7.46 (dd, J=1.5, 7.8, 1H), 7.70 (d, J=1.5, 1H).

Step BN-[5-(aminocarbonyl)-2-methylphenyl]-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine tert-butyl ester

Using the compound (1.11 g, 2.80 mmol) obtained in step A and according to the method of Example 74, step A, the title compound (917 mg, yield 72%) as a pale-yellow amorphous solid

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.39 (s, 9H), 2.37 (s, 3H), 2.93 (s, 3H), 4.04 (s, 2H), 4.13 (d, J=11.4, 2H), 4.23 (d, J=11.4, 2H), 4.37 (s, 2H), 7.19-7.29 (m, 5H), 7.39 (dd, J=1.8, 7.8, 1H), 7.65 (d, J=1.8, 1H).

Step CN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-[2-methyl-5-(1H-1,2,4-triazol-3-yl)phenyl]glycine

Using the compound (350 mg, 0.77 mmol) obtained in step B, and N,N-dimethylformamide dimethylacetal (2.5 ml), and according to the methods of Example 80, step A, Example 74, step C, the title compound (162 mg, yield 50%) was obtained as a pale-bistered amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.35 (s, 3H), 3.04 (s, 3H), 3.98 (s, 2H), 4.17 (d, J=12.0, 2H), 4.27 (d, J=12.0, 2H), 4.33 (s, 2H), 7.18-7.29 (m, 5H), 7.72 (dd, J=1.2, 7.5, 1H), 7.90 (d, J=1.2, 1H), 8.24 (s, 1H).

Step DN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(1H-1,2,4-triazol-3-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (160 mg, 0.38 mmol) obtained in step C, and the compound (92 mg, 0.46 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (96 mg, yield 42%) was obtained as a pale-yellow amorphous solid

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.11-1.25 (m, 6H), 1.43 (s, 9H), 2.36 (s, 3H), 2.95 (s, 3H), 3.09-3.44 (m, 4H), 3.86 (s, 2H), 4.09-4.24 (m, 7H), 7.18-7.30 (m, 5H), 7.78 (d, J=7.2, 1H), 8.04 (m, 1H), 8.79 (brs, 1H).

Step EN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(1H-1,2,4-triazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide trihydrochloride

Using the compound (95 mg, 0.16 mmol) obtained in step D and according to the method of Example 1, step C, the title compound (86 mg, yield 89%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, CD₃OD); Î´(ppm) 1.31 (d, J=6.6, 6H), 2.46 (s, 3H), 2.99 (s, 3H), 3.13 (m, 2H), 3.50-3.52 (m, 2H), 4.06-4.13 (m, 4H), 4.29 (d, J=11.7, 2H), 4.44 (s, 2H), 7.21 (m, 4H), 7.44 (d, J=7.8, 1H), 7.63 (d, J=7.8, 1H), 7.92 (s, 1H), 9.23 (s, 1H).

Example 82N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1H-1,2,4-triazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide trihydrochlorideStep AN²-[5-(aminocarbonyl)-2-methylphenyl]-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (0.35 g, 0.883 mmol) of Example 81, step A, and the compound (267 mg, 1.32 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (0.36 g, yield 71%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.11 (d, J=6.6, 6H), 1.42 (brs, 9H), 2.38 (s, 3H), 2.94 (s, 3H), 3.17 (brs, 2H), 3.38 (q, J=6.6, 2H), 3.83 (s, 2H), 3.9-4.3 (m, 7H), 5.55-6.60 (broad, 2H), 7.19-7.28 (m, 5H), 7.48-7.51 (m, 1H), 7.74 (s, 1H), 8.39-8.44 (broad, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1H-1,2,4-triazol-3-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (0.36 g, 0.62 mmol) obtained in step A and according to the method of Example 80, step A, the title compound (0.46 g, yield>100%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.09 (d, J=6.5, 6H), 1.44 (s, 9H), 2.36 (s, 3H), 2.44 (s, 3H), 3.00 (s, 3H), 3.16 (brs, 2H), 3.38-3.50 (m, 2H), 3.86 (s, 2H), 4.00-4.30 (m, 7H), 7.15-7.29 (m, 5H), 7.71 (d, J=8.0, 1H), 7.95 (s, 1H), 8.53-8.69 (broad, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1H-1,2,4-triazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide trihydrochloride

Using the compound (0.46 g) obtained in step B and according to the method of Example 1, step C, the title compound (0.28 g, yield 72%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.21 (d, J=5.7, 6H), 2.36 (s, 3H), 2.65 (s, 3H), 2.87 (m, 5H), 3.24-3.57 (m, 3H), 3.97 (s, 2H), 4.14-4.28 (m, 4H), 4.39 (s, 2H), 7.26-7.35 (m, 5H), 7.66-7.69 (m, 1H), 7.91 (s, 1H), 8.40 (brs, 1H), 9.09 (brs, 2H).

Example 83N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(1,2,4-oxadiazol-5-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamideStep AN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-[2-methyl-5-(1,2,4-oxadiazol-5-yl)phenyl]glycine tert-butyl ester

The compound (400 mg, 0.88 mmol) of Example 81, step B, was dissolved in N,N-dimethylformamide dimethylacetal (2.5 ml), and the mixture was stirred at 110Â° C. for 1 hr. The reaction mixture was concentrated and the obtained residue was dissolved in 1,4-dioxane (1.5 ml). Then, acetic acid (1.5 ml), hydroxylamine hydrochloride (95 mg, 1.33 mmol) and 2N aqueous sodium hydroxide solution (0.7 ml, 1.4 mmol) were added, and the mixture was stirred at 90Â° C. for 30 min. The reaction mixture was concentrated under reduced pressure, diluted with water, and extracted with dichloromethane. The organic layer was dried over anhydrous magnesium sulfate, the insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-dichloromethane) to give the title compound (219 mg, yield 52%) as a pale-yellow amorphous solid

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.42 (s, 9H), 2.42 (s, 3H), 2.95 (s, 3H), 4.07 (s, 2H), 4.16 (d, J=11.4, 2H), 4.26 (d, J=11.4, 2H), 4.42 (s, 2H), 7.20-7.30 (m, 5H), 7.71 (dd, J=1.5, 8.1, 1H), 7.93 (d, J=1.5, 1H), 8.43 (s, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(1,2,4-oxadiazol-5-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (210 mg, 0.44 mmol) obtained in step A and the compound (92 mg, 0.45 mmol) of Reference Example 3, and according to the methods of Example 74, step C, and Example 1, step B, the title compound (196 mg, yield 75%) was obtained as a pale-yellow amorphous solid

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.11 (d, J=6.6, 6H), 1.44 (s, 9H), 2.44 (s, 3H), 3.96 (s, 3H), 3.18 (brm, 2H), 3.37-3.44 (m, 2H), 3.86 (s, 2H), 4.13-4.30 (m, 7H), 7.20-7.28 (m, 4H), 7.33 (d, J=7.8, 1H), 7.77 (d, J=7.8, 1H), 8.02 (d, J=1.5, 1H), 8.43 (s, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(1,2,4-oxadiazol-5-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide

Using the compound (190 mg, 0.31 mmol) obtained in step B and according to the method of Example 46, step B, the title compound (59 mg, yield 37%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.01 (d, J=6.3, 6H), 2.42 (s, 3H), 2.71-2.79 (m, 3H), 2.96 (s, 3H), 3.36-3.42 (m, 2H), 4.08-4.26 (m, 8H), 7.04 (brs, 1H), 7.18-7.29 (m, 4H), 7.61 (d, J=7.5, 1H), 8.00 (s, 1H), 8.38-8.40 (m, 1H), 8.47 (s, 1H).

Example 84N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(3-methyl-1,2,4-oxadiazol-5-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamideStep AN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-[2-methyl-5-(3-methyl-1,2,4-oxadiazol-5-yl)phenyl]glycine tert-butyl ester

Using the compound (500 mg, 1.11 mmol) of Example 81, step B, and N,N-dimethylacetamide dimethylacetal (2.5 ml), and according to the method of Example 83, step A, the title compound (406 mg, yield 75%) was obtained as a pale-bistered amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.42 (s, 9H), 2.40 (s, 3H), 2.45 (s, 3H), 2.94 (s, 3H), 4.07 (s, 2H), 4.15 (d, J=11.7, 2H), 4.25 (d, J=11.7, 2H), 4.41 (s, 2H), 7.19-7.28 (m, 5H), 7.66 (dd, J=1.5, 7.8, 1H), 7.89 (d, J=1.5, 1H).

Step BN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-[2-methyl-5-(3-methyl-1,2,4-oxadiazol-5-yl)phenyl]glycine

Using the compound (500 mg, 1.11 mmol) obtained in step A and according to the method of Example 74, step C, the title compound (310 mg, yield 88%) was obtained as a pale-bistered amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.40 (s, 3H), 2.45 (s, 3H), 3.07 (s, 3H), 3.96 (s, 2H), 4.19 (d, J=11.4, 2H), 4.30 (d, J=11.4, 2H), 4.33 (s, 2H), 7.20-7.29 (m, 4H), 7.34 (d, J=8.1, 1H), 7.78 (dd, J=1.5, 8.1, 1H), 7.96 (d, J=1.2, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(3-methyl-1,2,4-oxadiazol-5-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (310 mg, 0.71 mmol) obtained in step B, and the compound (158 mg, 0.78 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (373 mg, yield 84%) was obtained as a pale-yellow amorphous solid

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.11 (d, J=6.6, 6H), 1.45 (s, 9H), 2.43 (s, 3H), 2.45 (s, 3H), 2.95 (s, 3H), 3.18 (broad, 2H), 3.37-3.44 (m, 2H), 3.84 (s, 2H), 4.11-4.29 (m, 7H), 7.20-7.28 (m, 4H), 7.31 (d, J=8.1, 1H), 7.73 (d, J=8.1, 1H), 7.98 (d, J=1.2, 1H).

Step DN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(3-methyl-1,2,4-oxadiazol-5-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide

Using the compound (370 mg, 0.60 mmol) obtained in step C and according to the method of Example 46, step B, the title compound (247 mg, yield 80%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.02 (d, J=6.3, 6H), 2.44 (s, 6H), 2.72-2.80 (m, 3H), 2.96 (s, 3H), 3.39-3.45 (m, 2H), 3.83 (s, 2H), 4.17 (d, J=11.4, 2H), 4.25 (d, J=11.4, 2H), 4.30 (s, 2H), 7.20-7.28 (m, 4H), 7.32 (d, J=8.1, 1H), 7.73 (d, J=8.1, 1H), 7.99 (s, 1H), 8.49 (brs, 1H).

Example 85N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(3-methyl-1,2,4-oxadiazol-5-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-[5-(aminocarbonyl)-2-methylphenyl]-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (483 mg, 1.22 mmol) of Example 81, step A, and the compound (258 mg, 1.37 mmol) of Reference Example 2, and according to the method of Example 1, step B, the title compound (559 mg, yield 81%) was obtained as a pale-bistered amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.05 (t, J=7.2, 3H), 1.36 (s, 9H), 2.36 (s, 3H), 2.95 (s, 3H), 3.17 (q, J=7.2, 2H), 3.32-3.42 (m, 4H), 3.80 (s, 2H), 4.12-4.26 (m, 6H), 7.20-7.28 (m, 5H), 7.53 (m, 1H), 7.78 (m, 1H), 8.55 (brs, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(3-methyl-1,2,4-oxadiazol-5-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (550 mg, 0.97 mmol) obtained in step A and according to the method of Example 84, step A, the title compound (477 mg, yield 81%) was obtained as a yellow amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.05 (t, J=7.2, 3H), 1.43 (s, 9H), 2.42 (s, 3H), 2.45 (s, 3H), 2.95 (s, 3H), 3.17 (broad, 2H), 3.29-3.31 (m, 2H), 3.40-3.47 (m, 2H), 3.82 (s, 2H), 4.13-4.29 (m, 6H), 7.19-7.28 (m, 4H), 7.31 (d, J=8.1, 1H), 7.72 (d, J=6.5, 1H), 7.97 (s, 1H) 8.28-8.56 (brs, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(3-methyl-1,2,4-oxadiazol-5-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (470 mg, 0.78 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (316 mg, yield 91%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.14 (t, J=7.2, 3H), 2.36 (s, ³H), 2.41 (s, 3H), 2.89-2.91 (m, 7H), 3.25-3.39 (m, 2H), 3.95 (s, 2H), 4.13 (d, J=11.4, 2H), 4.27 (d, J=11.4, 2H), 4.35 (s, 2H), 7.26 (m, 4H), 7.35 (d, J=8.1, 1H), 7.61 (d, J=7.8, 1H), 7.82 (d, J=1.2, 1H), 8.29 (t, J=5.4, 1H) 8.47 (brs, 2H).

Example 86N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(3-methyl-1,2,4-oxadiazol-5-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(3-methyl-1,2,4-oxadiazol-5-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (618 mg, 1.03 mmol) of Example 79, step B and according to the method of Example 84, step A, the title compound (492 mg, yield 75%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.12 (d, J=6.9, 6H), 1.45 (brs, 9H), 2.43 (s, 3H), 2.45 (s, 3H), 2.95 (s, 3H), 3.0-3.3 (m, 2H), 3.37-3.45 (m, 2H), 3.83 (s, 2H), 3.9-4.3 (m, 5H), 4.28 (s, 2H), 6.9-7.0 (m, 2H), 7.13-7.18 (m, 1H), 7.31 (d, J=7.8, 1H), 7.73 (dd, J=1.5, 7.8, 1H), 7.97 (d, J=1.5, 1H), 8.0-8.6 (broad, 1H).

Step BN²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(3-methyl-1,2,4-oxadiazol-5-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (491 mg, 0.77 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (426 mg, yield 91%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₅); Î´(ppm) 1.18 (d, J=6.6, 6H), 2.37 (s, 3H), 2.41 (s, 3H), 2.8-3.0 (m, 2H), 2.88 (s, 3H), 3.1-3.3 (m, 1H), 3.35-3.42 (m, 2H), 3.94 (s, 2H), 4.0-4.3 (m, 4H), 4.35 (s, 2H), 7.04-7.16 (m, 2H), 7.27-7.33 (m, 1H), 7.35 (d, J=7.8, 1H), 7.60 (d, J=7.8, 1H), 7.81 (s, 1H), 8.33 (broad t, 1H), 8.73 (brs, 2H).

Example 87N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(3-methyl-1,2,4-oxadiazol-5-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-[5-(aminocarbonyl)-2-methylphenyl]-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (683 mg, 1.65 mmol) of Example 79, step A, and the compound (500 mg, 2.66 mmol) of Reference Example 2, and according to the method of Example 1, step B, the title compound (558 mg, yield 58%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.06 (t, J=7.1, 3H), 1.38 (brs, 9H), 2.37 (s, 3H), 2.94 (s, 3H), 3.18 (q, J=7.1, 2H), 3.2-3.4 (m, 2H), 3.39-3.46 (m, 2H), 3.80 (s, 2H), 4.0-4.2 (m, 4H), 4.22 (s, 2H), 5.2-6.8 (broad, 2H), 6.9-7.0 (m, 2H), 7.1-7.3 (m, 2H), 7.50 (brs, 1H), 7.76 (brs, 1H), 8.4-8.7 (broad, 1H).

Step BN²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(3-methyl-1,2,4-oxadiazol-5-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (550 mg, 0.941 mmol) obtained in step A and according to the method of Example 84, step A, the title compound (521 mg, yield 89%) was obtained as a pale-orange oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.05 (t, J=7.1, 3H), 1.43 (brs, 9H), 2.42 (s, 3H), 2.45 (s, 3H), 2.95 (s, 3H), 3.15-3.25 (m, 2H), 3.25-3.35 (m, 2H), 3.4-3.5 (m, 2H), 3.82 (s, 2H), 4.05-4.25 (m, 4H), 4.29 (s, 2H), 6.9-7.0 (m, 2H), 7.13-7.18 (m, 1H), 7.31 (d, J=7.8, 1H), 7.73 (dd, J=1.2, 7.8, 1H), 7.96 (d, J=1.2, 1H), 8.1-8.7 (broad, 1H).

Step CN²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(3-methyl-1,2,4-oxadiazol-5-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (520 mg, 0.834 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (370 mg, yield 74%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.14 (t, J=7.2, 3H), 2.36 (s, 3H), 2.41 (s, 3H), 2.8-3.0 (m, 4H), 2.88 (s, 3H), 3.33-3.40 (m, 2H), 3.94 (s, 2H), 4.0-4.3 (m, 4H), 4.35 (s, 2H), 7.04-7.16 (m, 2H), 7.27-7.33 (m, 1H), 7.35 (d, J=8.1, 1H), 7.60 (d, J=8.1, 1H), 7.82 (s, 1H), 8.30 (broad, 1H), 8.4-8.8 (broad, 2H).

Example 88N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-[5-{[2-(tert-butoxycarbonyl)-2-methylhydrazino]carbonyl}-2-methylphenyl]-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound (2.44 g, 6.17 mmol) of Reference Example 74 and the compound (1.71 g, 9.26 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (2.78 g, yield 68%) was obtained as a gray amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.46 (brs, 9H), 2.26-2.32 (brs, 3H), 3.04 (s, 3H), 3.20 (s, 3H), 3.90 (s, 2H), 4.18-4.31 (m, 6H), 7.21-7.30 (m, 5H), 7.39-7.42 (m, 1H), 7.70 (brs, 1H).

Step BN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-{2-methyl-5-[(2-methylhydrazino)carbonyl]phenyl}glycine dihydrochloride

Using the compound (2.32 g, 4.41 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (1.81 g, yield 81%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.31 (s, 3H), 2.49 (s, 3H), 2.87 (s, 3H), 4.03 (s, 2H), 4.11-4.31 (m, 5H), 7.25-7.28 (m, 5H), 7.45-7.48 (m, 1H), 7.65 (s, 1H), 11.89 (s, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-{2-methyl-5-[(2-methylhydrazino) carbonyl]phenyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (351 mg, 0.70 mmol) obtained in step B, the compound (157 mg, 0.78 mmol) of Reference Example 3, and triethylamine (0.21 ml, 1.5 mmol), and according to the method of Example 1, step B, the title compound (440 mg, yield>100%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.11 (d, J=6.6, 6H), 1.41 1.47 (2s, 9H), 2.37 (s, 3H), 2.71 (s, 3H), 2.95 (s, 3H), 3.11-3.18 (m, 2H), 3.33-3.42 (m, 2H), 3.83 (s, 2H), 4.08-4.29 (m, 7H), 7.19-7.28 (m, 5H), 7.42-7.46 (m, 1H), 7.67 (m, 1H), 8.01-8.35 (broad, 2H).

Step DN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (440 mg) obtained in step C and according to the method of Example 67, step D, the title compound (440 mg, yield 99%) was obtained as a pale-yellow amorphous solid

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.11 (d, J=6.9, 6H), 1.44 1.48 (2s, 9H), 2.39 (s, 3H), 2.95 (s, 3H), 3.17 (brs, 2H), 3.34-3.44 (m, 2H), 3.47 (s, 3H), 3.82 (brs, 2H), 4.08-4.28 (m, 7H), 7.20-7.29 (m, 5H), 7.42-7.45 (m, 1H), 7.69 (s, 1H).

Step EN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (440 mg, 0.69 mmol) obtained in step D and according to the method of Example 1, step C, the title compound (340 mg, yield 81%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.19 (d, J=6.6, 6H), 2.33 (s, 3H), 2.87-2.95 (m, 5H), 3.22-3.31 (m, 1H), 3.34-3.46 (m, 5H), 3.92 (s, 2H), 4.10-4.35 (m, 6H), 7.23-7.33 (m, 6H), 7.52 (s, 1H), 8.34-8.39 (m, 1H), 8.90 (brs, 2H).

Example 89N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-{2-methyl-5-[(2-methylhydrazino)carbonyl]phenyl}-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (1.00 g, 2.01 mmol) of Example 88, step B, the compound (0.42 g, 2.23 mmol) of Reference Example 2 and triethylamine (0.60 ml, 4.21 mmol), and according to the method of Example 1, step B, the title compound (0.70 g, yield 59%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.05 (t, J=7.2, 3H), 1.38 (brs, 9H), 2.35 (s, 3H), 2.70 (s, 3H), 2.95 (s, 3H), 3.17 (q, J=7.0, 2H), 3.30 (brs, 2H), 3.35-3.45 (m, 2H), 3.80 (s, 2H), 4.08-4.26 (m, 6H), 7.20-7.30 (m, 5H), 7.46-7.49 (m, 1H), 7.70 (s, 1H), 8.49 (broad, 2H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (0.70 g, 1.18 mmol) obtained in step A and according to the method of Example 67, step D, the title compound (0.70 g, yield 96%) was obtained as a pale-yellow amorphous solid

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.04 (t, J=7.2, 3H), 1.43 (s, 9H), 2.38 (s, 3H), 2.96 (s, 3H), 3.15-3.36 (m, 4H), 3.39-3.47 (m, 5H), 3.81 (s, 2H), 4.08-4.50. (m, 6H), 7.14-7.30 (m, 5H), 7.43 (d, J=8.4, 1H), 7.69 (d, J=1.2, 1H), 8.25 8.54 (2brs, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (0.70 g, 1.13 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (0.51 g, yield 89%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=7.1, 3H), 2.50 (s, 3H), 2.87 (m, 7H), 3.35-3.39 (m, 5H), 3.92 (s, 2H), 4.10-4.34 (m, 6H), 7.26-7.32 (m, 6H), 7.52 (s, 1H), 8.32-8.37 (m, 1H), 8.91 (brs, 2H).

Example 90N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-{2-methyl-5-[(2-methylhydrazino)carbonyl]phenyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (0.54 g, 0.91 mmol) of Example 89, step A and according to the method of Example 1, step C, the title compound (0.45 g, yield 86%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.18 (t, J=7.2, 3H), 2.34 (s, 3H), 2.88 (m, 8H), 3.35-3.42 (m, 4H), 3.95 (s, 2H), 4.15 (d, J=12.0, 2H), 4.26 (d, J=12.0, 2H), 4.35 (s, 2H), 7.26 (m, 5H), 7.48-7.51 (m, 1H), 7.71 (s, 1H), 8.35 (m, 1H), 9.03 (brs, 2H), 12.04 (s, 1H).

Example 91N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[5-(4-ethyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-2-methylphenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-[5-{[2-(tert-butoxycarbonyl)-2-ethylhydrazino]carbonyl}-2-methylphenyl]-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound (2.25 g, 5.50 mmol) of Reference Example 75 and the compound (1.53 g, 8.29 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (2.41 g, yield 81%) was obtained as a gray amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.14 (t, J=7.2, 3H), 1.45 (brs, 9H), 2.22 (brs, 3H), 3.03 (s, 3H), 3.58 (q, J=7.1, 2H), 3.88 (s, 2H), 4.19-4.30 (m, 6H), 7.14-7.34 (m, 6H), 7.73 (s, 1H), 9.25 (brs, 1H).

Step BN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-{5-[(2-ethylhydrazino)carbonyl]-2-methylphenyl}glycine dihydrochloride

Using the compound (1.00 g, 1.85 mmol) obtained by the method of step A and according to the method of Example 1, step C, the title compound (0.89 g, yield>100%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.25 (t, J=7.2, 3H), 2.31 (s, 3H), 2.87 (s, 3H), 3.27 (q, J=7.2, 2H), 4.03 (s, 2H), 4.11-4.32 (m, 6H), 7.25-7.28 (m, 5H), 7.48 (d, J=7.5, 1H), 7.66 (s, 1H), 11.85 (s, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-{5-[(2-ethylhydrazino) carbonyl]-2-methylphenyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (0.50 g, 1.14 mmol) obtained in step B, the compound (0.36 g, 1.78 mmol) of Reference Example 3 and triethylamine (0.40 ml, 2.39 mmol), and according to the method of Example 1, step B, the title compound (0.60 g, yield 85%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.12 (d, J=6.8, 6H), 1.15-1.29 (m, 3H), 1.46 (s, 9H), 2.21 (s, 3H), 2.92 2.94 (2s, 3H), 3.23-3.40 (m, 6H), 3.64 (m, 1H), 3.78-3.80 (m, 2H), 4.08-4.22 (m, 6H), 7.13-7.29 (m, 6H), 7.68-7.75 (m, 1H).

Step DN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[5-(4-ethyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-2-methylphenyl]-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (0.60 g, 0.96 mmol) obtained in step C and according to the method of Example 67, step the title compound (0.18 g, yield 24%) was obtained as a pale-yellow amorphous solid

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.12 (d, J=6.8, 6H), 1.36-1.48 (m, 12H), 2.40 (s, 3H), 2.95 (s, 3H), 3.19 (brs, 2H), 3.36-3.42 (m, 2H), 3.78-3.87 (m, 4H), 4.08-4.27 (m, 6H), 7.20-7.29 (m, 5H), 7.42-7.46 (m, 1H), 7.70 (d, J=1.6, 1H).

Step EN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[5-(4-ethyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-2-methylphenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (0.18 g, 0.28 mmol) obtained in step D and according to the method of Example 1, step C, the title compound (0.21 g, yield>100%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.18-1.33 (m, 9H), 2.33 (s, 3H), 2.88 (m, 5H), 3.24-3.40 (m, 3H), 3.73-3.82 (m, 2H), 3.92 (s, 2H), 4.13 (d, J=11.7, 2H), 4.26 (d, J=11.7, 2H), 4.35 (s, 2H), 7.26-7.33 (m, 6H), 7.51 (s, 1H), 8.35-8.37 (m, 1H), 8.8 (brs, 2H).

Example 92N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[5-(4-ethyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-2-methylphenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-{5-[(2-ethylhydrazino)carbonyl]-2-methylphenyl}-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (0.85 g, 1.66 mmol) obtained in Example 91, step B, the compound (0.34 g, 1.81 mmol) of Reference Example 2, and triethylamine (0.50 ml, 3.49 mmol), and according to the method of Example 1, step B, the title compound (0.84 g, yield 83%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.04 (t, J=6.9, 3H), 1.13 (t, J=6.9, 3H), 1.36 (s, 3H), 2.35 (s, 3H), 2.95 (m, 5H), 3.15-3.44 (m, 6H), 3.97 (s, 2H), 4.11-4.26 (m, 6H), 7.20-7.29 (m, 5H), 7.45 (brs, 1H), 7.68 (brs, 1H), 8.49-8.61 (broad, 2H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[5-(4-ethyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-2-methylphenyl]-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (0.84 g, 1.38 mmol) obtained in step A and according to the method of Example 67, step D, the title compound (0.69 g, yield 79%) was obtained as a pale-yellow amorphous solid

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.05 (t, J=7.1, 3H), 1.37-1.44 (m, 12H), 2.39 (s, 3H), 2.96 (s, 3H), 3.16-3.19 (m, 2H), 3.28-3.31 (m, 2H), 3.43 (q, J=6.3, 2H), 3.79-3.87 (m, 4H), 4.08-4.28 (m, 6H), 7.20-7.30 (m, 5H), 7.42-7.46 (d, J=8.3, 1H), 7.69 (d, J=1.1, 1H), 8.25 8.52 (2broad, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[5-(4-ethyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-2-methylphenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (0.69 g, 1.09 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (0.48 g, yield 73%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=7.1, 3H), 1.29 (t, J=7.2, 3H), 2.33 (s, 3H), 2.88 (m, 7H), 3.37-3.42 (m, 2H), 3.77 (q, J=7.2, 2H), 3.92 (s, 2H), 4.05-4.29 (m, 4H), 4.35 (s, 2H), 7.26-7.34 (m, 6H), 7.51 (s, 1H), 8.33-8.37 (m, 1H), 8.93 (brs, 2H).

Example 93N²-[5-(acetylamino)-2-methylphenyl]-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-[5-(tert-butoxycarbonylamino)-2-methylphenyl]-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound (1.00 g, 2.73 mmol) of Reference Example 76 and the compound of Reference Example 17 (555 mg, 3.00 mmol), and according to the method of Example 1, step A, the title compound (1.13 g, yield 88%) was obtained as a pale-bistered amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.49 (s, 9H), 2.24 (s, 3H), 3.05 (s, 3H), 3.90 (s, 2H), 4.11-4.29 (m, 6H), 6.40 (brs, 1H), 7.01-7.09 (m, 2H), 7.20-7.23 (m, 3H), 7.23-7.28 (m, 2H).

Step BN²-[5-(tert-butoxycarbonylamino)-2-methylphenyl]-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(isopropyl) [(2-nitrophenyl)sulfonyl]amino}ethyl]glycinamide

Using the compound (1.13 g, 2.41 mmol) obtained in step A and the compound (762 mg, 2.65 mmol) of Reference Example 7, and according to the method of Example 1, step B, the title compound (774 mg, yield 44%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.16 (d, J=6.6, 6H), 1.49 (s, 9H), 2.27 (s, 3H), 2.96 (s, 3H), 3.29-3.33 (m, 2H), 3.44-3.50 (m, 2H), 3.80 (s, 2H), 4.08-4.26 (m, 7H), 6.44 (brs, 1H), 7.05-7.14 (m, 2H), 7.19-7.23 (m, 5H), 7.56-7.59 (m, 1H), 7.65-7.68 (m, 2H), 7.98-8.01 (m, 1H), 8.56-8.59 (m, 1H).

Step CN²-[5-amino-2-methylphenyl]-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-{(isopropyl) [(2-nitrophenyl)sulfonyl]amino}ethyl]glycinamide

To a dichloromethane (10 ml)-ethyl acetate (5 ml) mixed solvent was added the compound (774 mg, 1.05 mmol) obtained in step B, 4N hydrochloric acid-ethyl acetate solution (2.6 ml, 10 mmol) was added at room temperature, and the mixture was stirred at the same temperature for 6.5 hr. The reaction mixture was concentrated under reduced pressure, diluted with dichloromethane, and the organic layer was washed with saturated aqueous sodium hydrogen carbonate, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure to give the title compound (662 mg, yield 99%) as a yellow amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.16 (d, J=6.9, 6H), 2.21 (s, 3H), 2.96 (s, 3H), 3.27-3.32 (m, 2H), 3.42-3.49 (m, 2H), 3.53 (brs, 2H), 3.80 (s, 2H), 4.10-4.25 (m, 7H), 6.35 (dd, J=2.4, 8.1, 1H), 6.65 (d, J=2.4, 1H), 6.78 (d, J=8.1, 1H), 7.20-7.26 (m, 4H), 7.58-7.59 (m, 1H), 7.65-7.68 (m, 2H), 7.99-8.02 (m, 1H), 8.51-8.53 (m, 1H).

Step DN²-[5-acetylamino-2-methylphenyl]-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-{(isopropyl)[(2-nitrophenyl)sulfonyl]amino}ethyl]glycinamide

Using the compound (220 mg, 0.35 mmol) obtained in step C and according to the method of Example 40, step D, the title compound (220 mg, yield 94%) was obtained as a yellow amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.13 (d, J=6.6, 6H), 2.13 (s, ³H), 2.28 (s, 3H), 2.96 (s, 3H), 3.32 (t, J=6.9, 2H), 3.45-3.52 (m, 2H), 3.82 (s, 2H), 4.07-4.25 (m, 7H), 7.11 (d, J=8.4, 1H), 7.18-7.25 (m, 4H), 7.35 (s, 1H), 7.45 (m, 1H), 7.60 (m, 1H), 7.66-7.69 (m, 2H), 7.96 (m, 1H), 8.70 (brt, J=6.0, 1H).

Step EN²-[5-acetylamino-2-methylphenyl]-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (220 mg, 0.32 mmol) obtained in step D and according to the methods of Example 40, steps E and F, the title compound (154 mg, yield 84%) was obtained as a yellow solid.

¹H-NMR (300 MHz, CD₃OD); Î´(ppm) 1.31 (d, J=6.6, 6H), 2.08 (s, ³H), 2.30 (s, 3H), 2.98 (s, 3H), 3.12 (t, J=6.0, 2H), 3.35-3.38 (m, 1H), 3.50-3.54 (m, 2H), 3.93 (s, 2H), 4.08 (d, J=11.4, 2H), 4.18 (d, J=13.2, 2H), 4.29 (s, 2H), 7.09-7.15 (m, 2H), 7.22-7.24 (m, 4H), 7.59 (s, 1H).

Example 94N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-{2-methyl-5-[(methylsulfonyl)amino]phenyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN²-[2-methyl-5-(methylsulfonylamino)phenyl]-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-{(isopropyl)[(2-nitrophenyl)sulfonyl]amino}ethyl]glycinamide

Using the compound (220 mg, 0.35 mmol) obtained in Example 93, step C and according to the method of Example 41, step A, the title compound (224 mg, yield 91%) was obtained as a yellow amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.14 (d, J=6.9, 6H), 2.30 (s, 3H), 2.97 (s, 3H), 2.98 (s, 3H), 3.32 (t, J=6.9, 2H), 3.40-3.48 (m, 2H), 3.86 (s, 2H), 4.06-4.28 (m, 7H), 6.49 (s, 1H), 6.89-6.92 (m, 1H), 7.07-7.13 (m, 2H), 7.20-7.24 (m, 4H), 7.59-7.61 (m, 1H), 7.66-7.69 (m, 2H), 7.98-8.02 (m, 1H), 8.46-8.48 (m, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-{2-methyl-5-[(methylsulfonyl)amino]phenyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (220 mg, 0.31 mmol) obtained in step A and according to the methods of Example 40, steps E and F, the title compound (115 mg, yield 62%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.18 (d, J=6.0, 6H), 2.19 (s, 3H), 2.90-2.91 (m, 8H), 3.25-3.36 (m, 3H), 3.85 (s, 2H), 4.11 (d, J=11.7, 2H), 4.26-4.29 (m, 4H), 6.70 (d, J=9.9, 1H), 7.03 (d, J=8.1, 1H), 7.26 (m, 4H), 8.30 (brs, 3H), 9.51 (s, 1H).

Example 95N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-{5-[(methoxycarbonyl)amino]-2-methylphenyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-{5-[(methoxycarbonyl)amino]-2-methylphenyl}-N¹-[2-{(isopropyl)[(2-nitrophenyl)sulfonyl]amino}ethyl]glycinamide

Using the compound (220 mg, 0.35 mmol) of Example 93, step C and according to the method of Example 42, step A, the title compound (191 mg, yield 80%) was obtained as a yellow amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.15 (d, J=6.9, 6H), 2.28 (s, 3H), 2.96 (s, 3H), 3.29-3.33 (m, 2H), 3.43-3.50 (m, 2H), 3.74 (s, 3H), 3.81 (s, 2H), 4.05-4.25 (m, 7H), 6.58 (s, 1H), 7.07-7.10 (m, 1H), 7.19-7.23 (m, 5H), 7.56-7.59 (m, 1H), 7.65-7.68 (m, 2H), 7.98-8.01 (m, 1H), 8.55 (m, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-{5-[(methoxycarbonyl)amino]-2-methylphenyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (190 mg, 0.27 mmol) obtained in step A and according to the methods of Example 40, steps E and F, the title compound (133 mg, yield 83%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.19 (d, J=6.6, 6H), 2.18 (s, 3H), 2.89 (brm, 5H), 3.26-3.28 (m, 1H), 3.36-3.42 (m, 2H), 3.63 (s, 3H), 3.81 (s, 2H), 4.09-4.27 (m, 6H), 6.99 (m, 2H), 7.24-7.29 (m, 5H), 8.37 (broad t, J=5.7, 1H), 8.61 (brs, 2H), 9.44 (s, 1H).

Example 96N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[5-(ethoxycarbonyl)-2-methylphenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-[5-(ethoxycarbonyl)-2-methylphenyl]glycine

Using the compound (0.52 g, 1.76 mmol) of Reference Example 77 and the compound (0.50 g, 2.71 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (0.58 g, yield 77%) was obtained as a gray amorphous solid.

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[5-(ethoxycarbonyl)-2-methylphenyl]-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (0.29 g, 0.68 mmol) obtained in step A and the compound (214 mg, 1.06 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (0.20 g, yield 49%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.12 (d, J=6.8, 6H), 1.36 (t, J=7.1, 3H), 1.45 (s, 9H), 2.40 (s, 3H), 2.95 (s, 3H), 3.17 (brs, 2H), 3.40 (q, J=7.8, 2H), 3.81 (s, 2H), 4.08-4.25 (m, 7H), 4.34 (q, J=7.3, 2H), 7.19-7.29 (m, 5H), 7.67 (d, J=7.7, 1H), 7.90 (s, 1H), 8.33-8.55 (broad, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[5-(ethoxycarbonyl)-2-methylphenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (0.20 g, 0.33 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (0.15 g, yield 81%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.19 (d, J=6.3, 6H), 1.30 (t, J=6.9, 3H), 2.33 (s, 3H), 2.88 (s, 3H), 3.22-3.27 (m, 1H), 3.38-3.40 (m, 2H), 3.56-3.62 (m, 2H), 3.90 (s, 2H), 4.10-4.34 (m, 8H), 7.22-7.26 (m, 5H), 7.46-7.50 (d, J=7.8, 1H), 7.67 (s, 1H), 8.35 (s, 1H), 8.82 (brs, 2H).

The compounds of Examples 73-96 are shown below.

TABLE 10StructuralLC-MSExampleFormulaTMW(found)73 [Image Omitted]

638.00502 74 [Image Omitted]

594.53522 75 [Image Omitted]

608.56536 76 [Image Omitted]

554.51482 77 [Image Omitted]

567.55495 78 [Image Omitted]

552.52481 79 [Image Omitted]

498.59499 80 [Image Omitted]

646.03537 81 [Image Omitted]

614.01505 82 [Image Omitted]

628.04519 83 [Image Omitted]

505.61NT 84 [Image Omitted]

519.64520 85 [Image Omitted]

578.53506 86 [Image Omitted]

610.55538 87 [Image Omitted]

596.52524 88 [Image Omitted]

608.56536 89 [Image Omitted]

594.53522 90 [Image Omitted]

568.54496 91 [Image Omitted]

622.59550 92 [Image Omitted]

608.56536 93 [Image Omitted]

567.55495 94 [Image Omitted]

603.61531 95 [Image Omitted]

583.55511 96 [Image Omitted]

582.56510

Example 97N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[5-(ethoxycarbonyl)-2-methylphenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[5-(ethoxycarbonyl)-2-methylphenyl]-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (0.29 g, 0.68 mmol) of Example 96, step A, and the compound (0.20 g, 1.06 mmol) of Reference Example 2, and according to the method of Example 1, step B, the title compound (0.22 g, yield 54%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.05 (t, J=7.2, 3H), 1.36 (t, J=7.5, 3H), 1.43 (s, 9H), 2.39 (s, 3H), 2.95 (s, 3H), 3.16-3.19 (m, 2H), 3.28-3.31 (m, 2H), 3.44 (q, J=6.6, 2H), 3.79 (s, 2H), 4.07-4.26 (m, 6H), 4.34 (q, J=6.9, 2H), 7.19-7.30 (m, 5H), 7.66 (d, J=8.1, 1H), 7.89 (d, J=0.9, 1H), 8.34-8.60 (broad, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[5-(ethoxycarbonyl)-2-methylphenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (0.22 g, 0.37 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (0.17 g, yield 82%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=6.9, 3H), 1.30 (t, J=7.2, 3H), 2.32 (s, 3H), 2.88 (s, 3H), 3.37-3.40 (m, 2H), 3.56-3.79 (m, 4H), 3.90 (s, 2H), 4.10-4.33 (m, 8H), 7.22-7.27 (m, 5H), 7.46-7.50 (m, 1H), 7.68 (s, 1H), 8.34 (m, 1H), 8.84 (brs, 2H).

Example 98N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,3-oxazol-2-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-[2-methyl-5-(5-methyl-1,3-oxazol-2-yl)phenyl]glycine

Using the compound (0.78 g, 2.56 mmol) of Reference Example 78 and the compound (0.71 g, 3.84 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (0.82 g, yield 74%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.36 (s, 3H), 2.37 (s, 3H), 3.04 (s, 3H), 3.95 (s, 2H), 4.15-4.32 (m, 6H), 6.79 (s, 1H), 7.18-7.28 (m, 5H), 7.64-7.68 (m, 1H), 7.85 (s, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,3-oxazol-2-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (0.82 g, 1.89 mmol) obtained in step A and the compound (592 mg, 2.93 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (0.93 g, yield 79%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.10-1.16 (m, 6H), 1.47 (s, 9H), 2.36 (s, 3H), 2.39 (s, 3H), 2.94 (s, 3H), 3.17 (brs, 2H), 3.28-3.45 (m, 2H), 3.85 (s, 2H), 4.11-4.28 (m, 7H), 6.78 (s, 1H), 7.17-7.32 (m, 5H), 7.64 (d, J=7.8, 1H), 7.89 (s, 1H), 8.30-8.59 (broad, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,3-oxazol-2-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (0.93 g, 1.50 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (0.87 g, yield 98%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.19 (d, J=6.5, 6H), 2.32 (s, 3H), 2.38 (s, 3H), 2.88-2.94 (m, 5H), 3.20-3.25 (m, 1H), 3.35-3.45 (m, 2H), 3.93 (s, 2H), 4.14 (d, J=11.7, 2H), 4.27 (d, J=11.7, 2H), 4.37 (s, 2H), 6.96 (s, 1H), 7.04-7.30 (m, 5H), 7.45 (dd, J=1.1, 7.6, 1H), 7.68 (d, J=1.1, 1H), 8.3-8.44 (m, 1H), 9.02 (broad, 2H).

Example 99N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,3-thiazol-2-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-[2-methyl-5-(5-methyl-1,3-thiazol-2-yl)phenyl]glycine

Using the compound (0.50 g, 1.56 mmol) of Reference Example 80 and the compound (0.43 g, 2.33 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (0.40 g, yield 57%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.34 (s, 3H), 2.47 (s, 3H), 3.03 (s, 3H), 3.96 (s, 2H), 4.16 (d, J=11.7, 2H), 4.26 (d, J=11.7, 2H), 4.32 (s, 2H), 7.12-7.27 (m, 5H), 7.44-7.52 (m, 2H), 7.78 (s, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,3-thiazol-2-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (0.40 g, 0.89 mmol) obtained in step A and the compound (0.28 g, 1.38 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (0.56 g, yield 99%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.11 (d, J=6.6, 6H), 1.47 (s, 9H), 2.38 (s, 3H), 2.48 (s, 3H), 2.94 (s, 3H), 3.15-3.18 (brs, 2H), 3.28-3.45 (m, 2H), 3.83 (s, 2H), 3.9-4.3 (broad, 1H), 4.14 (d, J=12.0, 2H), 4.22 (d, J=12.0, 2H), 4.28 (s, 2H), 6.90-7.30 (m, 5H), 7.43-7.52 (m, 2H), 7.81 (s, 1H), 8.35-8.66 (broad, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,3-thiazol-2-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (0.56 g, 0.88 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (0.41 g, yield 72%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.18 (d, J=6.3, 6H), 2.31 (s, 3H), 2.50 (s, 3H), 2.88 (m, 5H), 3.19-3.42 (m, 3H), 3.93 (s, 2H), 4.14 (d, J=11.7, 2H), 4.26 (d, J=11.7, 2H), 4.38 (s, 2H), 7.19-7.27 (m, 5H), 7.36-7.39 (m, 1H), 7.62 (d, J=16.5, 2H), 8.41-8.46 (m, 1H), 9.02 (brs, 2H).

Example 100N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(4-methyl-1,3-thiazol-2-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-[2-methyl-5-(4-methyl-1,3-thiazol-2-yl)phenyl]glycine

Using the compound (0.86 g, 2.68 mmol) of Reference Example 79 and the compound (0.75 g, 4.06 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (0.87 g, yield 72%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.34 (s, 3H), 2.45 (s, 3H), 3.03 (s, 3H), 3.97 (s, 2H), 4.14-4.28 (m, 4H), 4.33 (s, 2H), 6.82 (s, 1H), 7.17-7.28 (m, 5H), 7.53-7.57 (m, 1H), 7.82 (s, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(4-methyl-1,3-thiazol-2-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (0.87 g, 1.93 mmol) obtained in step A and the compound (0.60 g, 2.97 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (0.95 g, yield 78%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.11 (d, J=6.8, 6H), 1.45 (s, 9H), 2.38 (s, 3H), 2.47 (s, 3H), 2.94 (s, 3H), 3.17 (brs, 2H), 3.38-3.45 (m 2H), 3.83 (s, 2H), 3.9-4.3 (m, 7H), 6.82 (s, 1H), 7.17-7.29 (m, 5H), 7.51-7.54 (m, 1H), 7.84 (s, 1H), 8.35-8.66 (broad, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(4-methyl-1,3-thiazol-2-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (0.95 g, 1.50 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (0.85 g, yield 94%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.19 (d J=6.3, 6H), 2.32 (s, 3H), 2.44 (s, 3H), 2.88 (m, 5H), 3.20-3.23 (m, 1H), 3.34-3.42 (m, 2H), 3.95 (s, 2H), 4.16 (d, J=11.7, 2H), 4.27 (d, J=11.7, 2H), 4.39 (s, 2H), 7.21-7.33 (m, 6H), 7.42-7.45 (m, 1H), 7.68 (s, 1H), 8.44 (m, 1H), 9.07 (brs, 2H).

Example 101N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(4-methyl-1,3-thiazol-2-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(4-methyl-1,3-thiazol-2-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (0.50 g, 1.11 mmol) of Example 100, step A, and the compound (0.33 g, 1.75 mmol) of Reference Example 2, and according to the method of Example 1, step B, the title compound (0.56 g, yield 81%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.04 (t, J=6.9, 3H), 1.44 (s, 9H), 2.37 (s, 3H), 2.46 (s, 3H), 2.94 (s, 3H), 3.17 (brs, 2H), 3.27-3.32 (m, 2H), 3.41-3.48 (m, 2H), 3.82 (s, 2H), 4.16 (d, J=12.3, 2H), 4.23 (d, J=12.3, 2H), 4.29 (s, 2H), 6.82 (s, 1H), 7.12-7.30 (m, 5H), 7.50-7.53 (m, 1H), 7.76-7.88 (m, 1H), 8.41-8.66 (broad, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(4-methyl-1,3-thiazol-2-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (0.50 g, 0.81 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (0.44 g, yield 92%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=6.9, 3H), 2.32 (s, 3H), 2.44 (s, 3H), 2.88 (m, 7H), 3.34-3.42 (m, 2H), 3.96 (s, 2H), 4.16 (d, J=12.3, 2H), 4.27 (d, J=12.3, 2H), 4.39 (s, 2H), 7.14-7.45 (m, 7H), 7.69 (s, 1H), 8.42 (m, 1H), 9.07 (brs, 2H).

Example 102N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[5-(4-ethyl-1,3-thiazol-2-yl)-2-methylphenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-[5-(4-ethyl-1,3-thiazol-2-yl)-2-methylphenyl]glycine

Using the compound (0.91 g, 2.72 mmol) of Reference Example 81 and the compound (0.75 g, 4.06 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (0.73 g, yield 58%) was obtained as a colorless amorphous solid.

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[5-(4-ethyl-1,3-thiazol-2-yl)-2-methylphenyl]-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (0.73 g, 1.57 mmol) obtained in step A and the compound (0.46 g, 2.44 mmol) of Reference Example 2, and according to the method of Example 1, step B, the title compound (0.60 g, yield 60%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.04 (t, J=7.0, 3H), 1.32 (t, J=7.5, 3H), 1.44 (s, 9H), 2.37 (s, 3H), 2.83 (q, J=7.0, 2H), 2.94 (s, 3H), 3.17 (brs, 2H), 3.27-3.32 (m, 2H), 3.41-3.48 (m, 2H), 3.83 (s, 2H), 4.07-4.29 (m, 6H), 6.82 (s, 1H), 7.16-7.29 (m, 5H), 7.52 (dd, J=1.3, 7.9, 1H), 7.84 (d, J=1.3, 1H), 8.25-8.75 (broad, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[5-(4-ethyl-1,3-thiazol-2-yl)-2-methylphenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (0.60 g, 0.95 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (0.50 g, yield 88%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=7.2, 3H), 1.27 (t, J=7.5, 3H), 2.31 (s, 3H), 2.79 (q, J=7.8, 2H), 2.88 (s, 7H), 3.34-3.44 (m, 2H), 3.95 (s, 2H), 4.16 (d, J=11.7, 2H), 4.28 (d, J=11.7, 2H), 4.39 (s, 2H), 7.20-7.33 (m, 5H), 7.42-7.46 (dd, J=1.2, 7.5, 1H), 7.67 (s, 1H), 8.40-8.44 (m, 1H), 9.04 (brs, 2H).

Example 103N²-[5-(4-tert-butyl-1,3-thiazol-2-yl)-2-methylphenyl]-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-[5-(4-tert-butyl-1,3-thiazol-2-yl)-2-methylphenyl]-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound (0.91 g, 2.51 mmol) of Reference Example 82 and the compound (0.70 g, 3.79 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (0.60 g, yield 48%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.36 (s, 9H), 2.33 (s, 3H), 3.03 (s, 3H), 4.01 (s, 2H), 4.17 (d, J=11.7, 2H), 4.27 (d, J=11.7, 2H), 4.34 (s, 2H), 6.83 (s, 1H), 7.17-7.27 (m, 5H), 7.57 (dd, J=1.5, 7.9, 1H), 7.78 (d, J=1.5, 1H).

Step BN²-[5-(4-tert-butyl-1,3-thiazol-2-yl)-2-methylphenyl]-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (0.60 g, 1.22 mmol) obtained in step A and the compound (0.38 g, 1.88 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (0.69 g, yield 84%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.12 (d, J=6.7, 6H), 1.83 (s, 9H), 1.45 (s, 9H), 2.38 (s, 3H), 2.94 (s, 3H), 3.19 (brs, 2H), 3.40-3.44 (m, 2H), 3.85 (s, 2H), 4.09-4.27 (m, 7H), 6.83 (s, 1H), 7.17-7.31 (m, 5H), 7.54-7.57 (m, 1H), 7.82 (s, 1H), 8.61 (broad, 1H).

Step CN²-[5-(4-tert-butyl-1,3-thiazol-2-yl)-2-methylphenyl]-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (0.62 g, 0.92 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (0.44 g, yield 74%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.19 (d, J=6.3, 6H), 1.35 (s, 9H), 2.31 (s, 3H), 2.90 (m, 5H), 3.18-3.25 (m, 1H), 3.34-3.43 (m, 2H), 3.95 (s, 2H), 4.17 (d, J=11.7, 2H), 4.29 (d, J=11.7, 2H), 4.40 (s, 2H), 7.12-7.26 (m, 6H), 7.39-7.42 (m, 1H), 7.58 (s, 1H), 8.42-8.47 (m, 1H), 9.00 (brs, 2H).

Example 104N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,3,4-oxadiazol-2-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-[2-methyl-5-(5-methyl-1,3,4-oxadiazol-2-yl)phenyl]glycine

Using the compound (0.25 g, 0.82 mmol) of Reference Example 83 and the compound (0.23 g, 1.25 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (0.10 g, yield 28%) was obtained as a bistered amorphous solid.

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (0.10 g, 0.23 mmol) obtained in step A and the compound (70 mg, 0.35 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (33 mg, yield 24%) was obtained as a pale-yellow amorphous solid

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.10 (d, J=6.9, 6H), 1.44 (s, 9H), 2.41 (s, 3H), 2.59 (s, 3H), 2.88 (s, 3H), 3.16-3.19 (brs, 2H), 3.36-3.42 (m, 2H), 3.87 (s, 2H), 3.9-4.3 (m, 7H), 7.20-7.30 (m, 6H), 7.66-7.70 (m, 1H), 7.87 (s, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,3,4-oxadiazol-2-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (33 mg, 0.053 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (15.8 mg, yield 50%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.17 (d, J=6.6, 6H), 2.34 (s, 3H), 2.57 (s, 3H), 2.88 (m, 5H), 3.23-3.30 (m, 1H), 3.37-3.42 (m, 2H), 3.94 (s, 2H), 4.10-4.36 (m, 6H), 7.26-7.32 (m, 5H), 7.46-7.50 (m, 1H), 7.69 (s, 1H), 8.33-8.37 (m, 1H), 8.69 (brs, 2H).

Example 105N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,3,4-thiadiazol-2-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-[2-methyl-5-(5-methyl-1,3,4-thiadiazol-2-yl)phenyl]glycine

Using the compound (0.23 g, 0.72 mmol) of Reference Example 84 and the compound (0.20 g, 1.08 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (0.28 g, yield 87%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.36 (s, 3H), 1.77 (s, 3H), 3.04 (s, 3H), 3.97 (s, 2H), 4.18 (d, J=11.7, 2H), 4.28 (d, J=11.7, 2H), 4.35 (s, 2H), 7.18-7.28 (m, 5H), 7.50-7.54 (m, 1H), 7.81 (s, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,3,4-thiadiazol-2-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (0.28 g, 0.62 mmol) obtained in step A and the compound (0.20 g, 0.99 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (0.50 g) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.11 (d, J=6.9, 6H), 1.44 (s, 9H), 2.40 (s, 3H), 2.78 (s, 3H), 2.94 (s, 3H), 3.16-3.46 (m, 4H), 3.84 (s, 2H), 4.0-4.4.3 (m, 7H), 7.19-7.30 (m, 5H), 7.45-7.55 (m, 1H), 7.80 (s, 1H), 8.20-8.60 (broad, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,3,4-thiadiazol-2-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (0.50 g) obtained in step B and according to the method of Example 1, step C, the title compound (0.28 g, yield 74%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.19 1.24 (2d, J=6.4, 6H), 2.33 (s, 3H), 2.76 (s, 3H), 2.89 (m, 5H), 3.23-3.44 (m, 3H), 3.94 (s, 2H), 4.14 (d, J=11.7, 2H), 4.27 (d, J=11.7, 2H), 4.37 (s, 2H), 7.23-7.29 (m, 5H), 7.40 (dd, J=1.3, 7.7, 1H), 7.65 (d, J=1.3, 1H), 8.40-8.44 (m, 1H), 8.97 (brs, 2H).

Example 106N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,3,4-thiadiazol-2-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,3,4-thiadiazol-2-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (0.94 g, 2.08 mmol) of Example 105, step A, and the compound (0.61 g, 3.24 mmol) of Reference Example 2, and according to the method of Example 1, step B, the title compound (0.87 g, yield 67%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.04 (t, J=7.2, 3H), 1.43 (s, 9H), 2.39 (s, 3H), 2.79 (s, 3H), 2.95 (s, 3H), 3.01-3.30 (m, 4H), 3.39-3.46 (m, 2H), 3.83 (s, 2H), 4.08-4.29 (m, 6H), 7.17-7.30 (m, 5H), 7.51-7.54 (m, 1H), 7.81 (s, 1H), 8.30-8.57 (broad, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,3,4-thiadiazol-2-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (0.87 g, 1.40 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (0.78 g, yield 94%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.1, 3H), 2.32 (s, 3H), 2.76 (s, 3H), 2.892 (m, 7H), 3.37-3.41 (m, 2H), 3.94 (s, 2H), 4.14 (d, J=11.6, 2H), 4.27 (d, J=11.6, 2H), 4.37 (s, 2H), 7.26-7.30 (m, 5H), 7.39-7.42 (m, 1H), 7.65 (s, 1H), 8.38-8.42 (m, 1H), 8.96 (m, 2H).

Example 107N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-[2-methyl-5-(5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)phenyl]glycine

Using the compound (0.94 g, 3.06 mmol) of Reference Example 85 and the compound (0.85 g, 4.60 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (0.31 g, yield 23%) was obtained as a colorless amorphous solid.

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (0.31 g, 0.71 mmol) obtained in step A and the compound (0.23 g, 1.13 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (70 mg, yield 16%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.11 (d, J=6.8, 6H), 1.44 (s, 9H), 2.39 (s, 3H), 2.95 (s, 3H), 3.18 (brs, 2H), 3.37-3.49 (m, 2H), 3.90 (s, 2H), 3.8-4.3 (m, 7H), 7.19-7.27 (m, 5H), 7.41 (d, J=7.8, 1H), 7.72 (d, J=1.1, 1H), 8.23-8.46 (broad, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (70 mg, 0.11 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (53 mg, yield 79%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.17 (d, J=6.6, 6H), 2.32 (s, 3H), 2.88 (m, 5H), 3.25-3.57 (m, 3H), 3.91 (s, 2H), 4.10-4.34 (m, 6H), 7.26 (m, 6H), 7.51 (s, 1H), 8.33 (m, 1H), 8.64 (brs, 2H).

Example 108N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2,6-dimethylphenyl)-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-(2,6-dimethylphenyl)glycine

Using the compound (1.00 g, 4.21 mmol) of Reference Example 87 and the compound (1.17 g, 6.32 mmol) of Reference Example 17, and according to the method of Example 4, step A, the title compound (1.21 g, yield 78%) was obtained as a pale-gray amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.31 (s, 6H), 2.92 (s, 3H), 3.82 (s, 2H), 4.03 (d, J=11.7, 2H), 4.18-4.24 (m, 4H), 6.89-6.98 (m, 3H), 7.23 (s, 4H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2,6-dimethylphenyl)-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (600 mg, 1.63 mmol) obtained in step A and the compound (495 mg, 2.45 mmol) of Reference Example 3, and according to the methods of Example 1, step B, and Example 1, step C, the title compound (284 mg, yield 33%) was obtained as a pale-bistered amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.24 (d, J=6.6, 6H), 2.33 (s, 6H), 2.97 (s, 3H), 2.97-3.04 (m, 2H), 3.23-3.51 (m, 3H), 3.69 (s, 2H), 3.94 (d, J=11.7, 2H), 4.18 (d, J=11.7, 2H), 4.24 (s, 2H), 6.91-7.01 (m, 3H), 7.23 (s, 4H), 8.67-9.00 (broad, 2H), 9.17 (t, J=5.6, 1H).

Example 109N²-(4-bromo-2,6-dimethylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-(4-bromo-2,6-dimethylphenyl)-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound (2.00 g, 6.33 mmol) of Reference Example 88 and the compound (1.75 g, 9.50 mmol) of Reference Example 17, and according to the method of Example 4, step A, the title compound (2.02 g, yield 71%) was obtained as a bistered amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.32 (s, 6H), 2.90 (s, 3H), 3.81 (s, 2H), 3.99-4.07 (m, 2H), 4.20 (s, 2H), 4.21 (d, J=11.4, 2H), 7.16 (s, 2H), 7.24 (s, 4H), 11.8-13.0 (broad, 1H).

Step BN²-(4-bromo-2,6-dimethylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (2.02 g, 4.53 mmol) obtained in step A and the compound (1.37 g, 6.80 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (2.35 g, yield 82%) was obtained as a pale-bistered amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.16 (d, J=6.6, 6H), 1.43 (s, 9H), 2.35 (s, 6H), 2.94 (s, 3H), 3.17-3.32 (m, 2H), 3.40-3.49 (m, 2H), 3.69 (s, 2H), 3.94 (d, J=11.7, 2H), 4.15 (s, 2H), 4.16 (d, J=9.3, 2H), 4.16-4.38 (m, 1H), 7.14-7.33 (m, 6H), 9.21-9.68 (broad, 1H).

Step CN-(4-bromo-2,6-dimethylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (500 mg, 0.79 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (365 mg, yield 77%) was obtained as a pale-bistered amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.23 (d, J=6.6, 6H), 2.33 (s, 6H), 2.89 (s, 3H), 2.89-3.02 (m, 2H), 3.23-3.60 (m, 3H), 3.68 (s, 2H), 3.97 (d, J=11.7, 2H), 4.19 (d, J=11.7, 2H), 4.21 (s, 2H), 7.18 (s, 2H), 7.24 (s, 4H), 8.70 (brs, 2H), 8.95 (t, J=5.7, 1H).

Example 110N²-(4-cyano-2,6-dimethylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN²-(4-cyano-2,6-dimethylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (1.00 g, 1.59 mmol) of Example 109, step B and according to the method of Reference Example 112, step D, the title compound (550 mg, yield 60%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.03 (d, J=6.0, 6H), 1.39 (s, 9H), 2.40 (s, 6H), 2.87 (s, 3H), 2.88-3.24 (m, 4H), 3.70 (s, 2H), 3.8-4.1 (broad, 1H), 4.03 (d, J=11.4, 2H), 4.21 (d, J=11.7, 2H), 4.24 (s, 2H), 7.25 (s, 4H), 7.43 (s, 2H), 8.37-8.43 (m, 1H).

Step BN²-(4-cyano-2,6-dimethylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (550 mg, 0.95 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (55.2 mg, yield 11%) was obtained as a pale-bistered amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.21 (d, J=6.3, 6H), 2.41 (s, 6H), 2.79-3.01 (m, 2H), 2.87 (s, 3H), 3.17-3.42 (m, 3H), 3.78 (s, 2H), 4.03 (d, J=12.0, 2H), 4.21 (d, J=12.3, 2H), 4.26 (s, 2H), 7.25 (s, 4H), 7.43 (s, 2H), 8.53-8.56 (m, 1H), 8.79 (brs, 2H).

Example 111N²-(4-bromo-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-(4-bromo-2-methylphenyl)-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound (6.60 g, 21.8 mmol) of Reference Example 86 and the compound (6.00 g, 32.7 mmol) of Reference Example 17, and according to the method of Example 4, step A, the title compound (9.00 g, yield 95%) was obtained as a bistered oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.22 (s, 3H), 2.87 (s, 3H), 3.94 (s, 2H), 4.10 (d, J=11.7. 2H), 4.24 (d, J=11.7, 2H), 4.25 (s, 2H), 7.01 (d, J=8.7, 1H), 7.19-7.32 (m, 6H), 12.47 (brs, 1H).

Step BN²-(4-bromo-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (4.50 g, 10.41 mmol) obtained in step A and the compound (3.16 g, 15.62 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (5.88 g, yield 92%) was obtained as a bistered amorphous solid.

35 ¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.02 (d, J=6.6, 6H), 1.38 (s, 9H), 2.25 (s, 3H), 2.87 (s, 3H), 2.89-3.00 (m, 2H), 3.05-3.20 (m, 2H), 3.77 (s, 2H), 3.95-4.19 (m, 1H), 4.09 (d, J=11.7, 2H), 4.23 (s, 2H), 4.25 (d, J=11.4, 2H), 7.04 (d, J=8.7, 1H), 7.16-7.29 (m, 6H), 8.01-8.08 (m, 1H).

Step CN²-(4-bromo-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (500 mg, 0.81 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (380 mg, yield 80%) was obtained as a pale-gray amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.20 (d, J=6.6, 6H), 2.26 (s, 3H), 2.80-2.95 (m, 2H), 2.87 (s, 3H), 3.18-3.28 (m, 1H), 3.34-3.42 (m, 2H), 3.85 (s, 2H), 4.10 (d, J=11.7, 2H), 4.25 (d, J=12.0, 2H), 4.27 (s, 2H). 7.04 (d, J=8.4, 1H), 7.21-7.29 (m, 6H), 8.32 (t, J=5.7, 1H), 8.90 (brs, 2H).

Example 112N²-(4-bromo-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-(4-bromo-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (4.50 g, 10.41 mmol) of Example 111, step A, and the compound (2.94 g, 15.62 mmol) of Reference Example 2, and according to the method of Example 1, step B, the title compound (5.43 g, yield 87%) was obtained as a bistered amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 0.95 (t, J=7.0, 3H), 1.36 (s, 9H), 2.24 (s, 3H), 2.87 (s, 3H), 3.01-3.19 (m, 6H), 3.76 (s, 2H), 4.0-4.3 (broad, 1H), 4.09 (d, J=11.6, 2H), 4.22 (s, 2H), 4.24 (d, J=11.6, 2H), 7.03 (d, J=8.5, 1H), 7.19-7.31 (m, 6H), 8.00-8.05 (m, 1H).

Step BN²-(4-bromo-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (500 mg, 0.83 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (422 mg, yield 88%) was obtained as a pale-gray amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.14-1.20 (m, 3H), 2.25 (s, 3H), 2.83-2.92 (m, 4H), 2.87 (s, 3H), 3.33-3.40 (m, 2H), 3.85 (s, 2H), 4.10 (d, J=11.6, 2H), 4.25 (d, J=11.6, 2H), 4.27 (s, 2H), 7.04 (d, J=8.6, 1H), 7.19-7.30 (m, 6H), 8.29-8.34 (m, 1H), 8.92 (brs, 2H).

Example 113N²-(5-bromo-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-(5-bromo-2-methylphenyl)-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound (2.34 g, 7.75 mmol) of Reference Example 89, and the compound (2.00 g, 10.9 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (2.91 g, yield 87%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.25 (s, 3H), 3.06 (s, 3H), 3.70 (s, 2H), 4.18 (d, J=11.7, 2H), 4.27 (s, 2H), 4.29 (d, J=11.7, 2H), 7.04 (d, J=8.1, 1H), 7.15-7.30 (m, 5H), 7.35 (d, J=2.1, 1H), 13.49 (brs, 1H).

Step BN²-(5-bromo-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (2.91 g, 6.73 mmol) obtained in step A and the compound (1.97 g, 9.74 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (3.60 g, yield 87%) was obtained as a pale-yellow amorphous solid

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.11 (d, J=6.6, 6H), 1.45 (brs, 9H), 2.28 (s, 3H), 2.95 (s, 3H), 3.0-3.2 (m, 2H), 3.35-3.43 (m, 2H), 3.78 (s, 2H), 3.9-4.3 (broad, 1H), 4.14 (d, J=11.7, 2H), 4.20 (s, 2H), 4.25 (d, J=11.7, 2H), 7.01 (d, J=8.1, 1H), 7.11 (dd, J=1.2, 8.1, 1H), 7.2-7.3 (m, 4H), 7.37 (d, J=1.2, 1H), 7.9-8.6 (broad, 1H).

Step CN²-(5-bromo-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (415 mg, 0.673 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (382 mg, yield 96%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.19 (d, J=6.6, 6H), 2.22 (s, 3H), 2.8-3.0 (m, 2H), 2.89 (s, 3H), 3.1-3.3 (m, 1H), 3.34-3.42 (m, 2H), 3.86 (s, 2H), 4.12 (d, J=11.6, 2H), 4.26 (d, J=11.6, 2H), 4.28 (s, 2H), 7.06 (broad, 2H), 7.2-7.3 (m, 5H), 8.30 (t, J=5.7, 1H), 8.70 (brs, 2H).

Example 114N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(4-methylbiphenyl-3-yl)-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(4-methylbiphenyl-3-yl)-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

To an ethanol (15 ml)-toluene (15 ml) mixed solvent were added the compound (493 mg, 0.800 mmol) of Example 113, step B, phenylboronic acid (153 mg, 1.26 mmol), tetrakistriphenylphosphinepalladium(0) (124 mg, 0.09 mmol) and sodium carbonate (300 mg, 2.83 mmol), and the mixture was heated under reflux for 23 hr. The reaction mixture was diluted with ethyl acetate, washed with water, diluted aqueous sodium hydroxide solution and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure, and the obtained oil was purified by silica gel column chromatography (ethyl acetate-dichloromethane) to give the title compound (337 mg, yield 69%) as a pale-yellow amorphous solid

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.09 (d, J=6.9, 6H), 1.45 (brs, 9H), 2.38 (s, 3H), 2.95 (s, 3H), 3.0-3.2 (m, 2H), 3.35-3.43 (m, 2H), 3.88 (s, 2H), 3.9-4.3 (broad, 1H), 4.07 (d, J=11.4, 2H), 4.21 (d, J=11.4, 2H), 4.23 (s, 2H), 7.1-7.7 (m, 12H), 8.0-8.6 (broad, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(4-methylbiphenyl-3-yl)-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (337 mg, 0.549 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (275 mg, yield 85%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.16 (d, J=6.4, 6H), 2.31 (s, 3H), 2.8-3.0 (m, 2H), 2.89 (s, 3H), 3.1-3.3 (m, 1H), 3.35-3.40 (m, 2H), 3.95 (s, 2H), 4.09 (d, J=11.7, 2H), 4.25 (d, J=11.7, 2H), 4.32 (s, 2H), 7.19 (broad, 2H), 7.25 (broad, 4H), 7.3-7.5 (m, 4H), 7.55-7.59 (m, 2H), 8.36 (t, J=5.7, 1H), 8.62 (brs, 2H).

Example 115N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(4â€²-fluoro-4-methylbiphenyl-3-yl)-N¹-[2-[(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(4â€²-fluoro-4-methylbiphenyl-3-yl)-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (488 mg, 0.791 mmol) of Example 113, step B, and 4-fluorophenylboronic acid (171 mg, 1.22 mmol), and according to the method of Example 114, step A, the title compound (406 mg, yield 81%) was obtained as a pale-yellow amorphous solid

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.08 (d, J=6.9, 6H), 1.44 (brs, 9H), 2.37 (s, 3H), 2.95 (s, 3H), 3.0-3.2 (m, 2H), 3.34-3.42 (m, 2H), 3.88 (s, 2H), 3.9-4.3 (broad, 1H), 4.07 (d, J=11.4, 2H), 4.22 (d, J=11.4, 2H), 4.22 (s, 2H), 7.04-7.11 (m, 2H), 7.16-7.27 (m, 3H), 7.4-7.7 (m, 6H), 7.9-8.5 (broad, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(4â€²-fluoro-4-methylbiphenyl-3-yl)-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (394 mg, 0.624 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (314 mg, yield 83%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.16 (d, J=6.5, 6H), 2.30 (s, ³H), 2.8-3.0 (m, 2H), 2.88 (s, 3H), 3.1-3.3 (m, 1H), 3.3-3.5 (m, 2H), 3.94 (s, 2H), 4.09 (d, J=11.7, 2H), 4.25 (d, J=11.7, 2H), 4.31 (s, 2H), 7.1-7.4 (m, 9H), 7.57-7.63 (m, 2H), 8.34 (t, J=5.7, 1H), 8.62 (brs, 2H).

Example 116N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2â€²-fluoro-4-methylbiphenyl-3-yl)-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (500 mg, 0.81 mmol) of Example 113, step B, and 2-fluorophenylboronic acid (181 mg, 1.30 mmol), and according to the methods of Example 114, step A, and Example 1, step C, the title compound (419 mg, yield 86%) was obtained as a pale-bistered amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.18 (d, J=6.3, 6H), 2.33 (s, 3H), 2.88 (brs, 5H), 3.15-3.24 (m, 1H), 3.41 (q, J=6.0, 2H), 3.94 (s, 2H), 4.09 (d, J=12.6, 2H), 4.25 (d, J=12.0, 2H), 4.34 (s, 2H), 7.10 (d, J=7.5, 1H), 7.19-7.32 (m, 8H), 7.36-7.50 (m, 2H), 8.34-8.43 (m, 1H), 8.89 (brs, 2H).

Example 117N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3â€²-fluoro-4-methylbiphenyl-3-yl)-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (500 mg, 0.81 mmol) of Example 113, step B, and 3-fluorophenylboronic acid (181 mg, 1.30 mmol), and according to the methods of Example 114, step A, and Example 1, step C, the title compound (288 mg, yield 59%) was obtained as a pale-bistered amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.17 (d, J=6.6, 6H), 2.32 (s, 3H), 2.78-2.91 (m, 5H), 3.18-3.24 (m, 1H), 3.37-3.44 (m, 2H), 3.98 (s, 2H), 4.10 (d, J=11.7, 2H), 4.25 (d, J=11.7, 2H), 4.36 (s, 2H), 7.14-7.28 (m, 7H), 7.39-7.60 (m, 4H), 8.33-8.43 (m, 1H), 8.87 (brs, 2H).

Example 118N²-(4â€²-cyano-4-methylbiphenyl-3-yl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN²-(4â€²-cyano-4-methylbiphenyl-3-yl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (483 mg, 0.783 mmol) of Example 113, step B, and 4-cyanophenylboronic acid (193 mg, 1.31 mmol), and according to the method of Example 114, step A, the title compound (399 mg, yield 80%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.08 (d, J=6.6, 6H), 1.43 (brs, 9H), 2.39 (s, 3H), 2.96 (s, 3H), 3.0-3.2 (m, 2H), 3.33-3.41 (m, 2H), 3.8-4.2 (broad, 1H), 3.91 (s, 2H), 4.08 (d, J=11.4, 2H), 4.23 (s, 2H), 4.23 (d, J=11.4, 2H), 7.1-7.3 (m, 6H), 7.50 (brs, 1H), 7.62 (d, J=8.4, 2H), 7.68 (d, J=8.4, 2H), 7.9-8.4 (broad, 1H).

Step BN²-(4â€²-cyano-4-methylbiphenyl-3-yl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (398 mg, 0.623 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (337 mg, yield 88%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.16 (d, J=6.4, 2H), 2.32 (s, 3H), 2.8-3.0 (m, 2H), 2.88 (s, 3H), 3.1-3.3 (m, 1H), 3.3-3.5 (m, 2H), 3.96 (s, 2H), 4.09 (d, J=11.7, 2H), 4.25 (d, J=11.7, 2H), 4.32 (s, 2H), 7.2-7.3 (m, 6H), 7.47 (s, 1H), 7.79 (d, J=8.3, 2H), 7.91 (d, J=8.3, 2H), 8.33 (t, J=5.7, 1H), 8.62 (brs, 2H).

Example 119N²-(4â€²-chloro-4-methylbiphenyl-3-yl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN²-(4â€²-chloro-4-methylbiphenyl-3-yl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (467 mg, 0.76 mmol) of Example 113, step B, and 4-chlorophenylboronic acid (187 mg, 1.19 mmol), and according to the method of Example 114, step A, the title compound (490 mg, yield 100%) was obtained as a bistered oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.08 (d, J=6.9, 6H), 1.44 (s, 9H), 2.37 (s, 3H), 2.95 (s, 3H), 3.11 (brs, 2H), 3.34-3.42 (m, 2H), 3.89 (brs, 2H), 4.04-4.25 (m, 7H), 7.17-7.69 (m, 11H), 7.99-8.64 (broad, 1H).

Step BN²-(4â€²-chloro-4-methylbiphenyl-3-yl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (490 mg, 0.76 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (265 mg, yield 56%) was obtained as a pale-yellow amorphous solid

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.17 (d, J=6.3, 6H), 2.32 (s, 3H), 2.80-2.97 (m, 5H), 3.21 (brs, 1H), 3.35-3.43 (m, 2H), 3.98 (s, 2H), 4.10 (d, J=11.4, 2H), 4.25 (d, J=12.0, 2H), 4.36 (s, 2H), 7.21 (s, 2H), 7.25 (s, 4H), 7.42 (s, 1H), 7.50 (d, J=7.2, 2H), 7.61 (d, J=8.7, 2H), 8.42 (brs, 1H), 8.93 (brs, 2H).

Example 120N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(3-thienyl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (500 mg, 0.81 mmol) of Example 113, step B, and 3-thienylboronic acid (166 mg, 1.30 mmol), and according to the methods of Example 114, step A, and Example 1, step C, the title compound (196 mg, yield 41%) was obtained as a pale-bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.17 (d, J=6.3, 6H), 2.29 (s, 3H), 2.78-2.95 (m, 5H), 3.15-3.24 (m, 1H), 3.26-3.43 (m, 2H), 3.95 (s, 2H), 4.10 (d, J=11.7, 2H), 4.26 (d, J=11.7, 2H), 4.33 (s, 2H), 7.15 (d, J=7.8, 1H), 7.25 (s, 5H), 7.45 (d, J=3.6, 2H), 7.62 (s, 1H), 7.73 (s, 1H), 8.41 (brs, 1H), 8.72 (brs, 2H).

The compounds of Examples 97-120 are shown below.

TABLE 11StructuralLC-MSExampleFormulaTMW(found)97 [Image Omitted]

568.54496 98 [Image Omitted]

591.57519 99 [Image Omitted]

644.10535 100 [Image Omitted]

607.64535 101 [Image Omitted]

593.61521 102 [Image Omitted]

607.64535 103 [Image Omitted]

649.72577 104 [Image Omitted]

592.56520 105 [Image Omitted]

608.63536 106 [Image Omitted]

594.60522 107 [Image Omitted]

594.53522 108 [Image Omitted]

524.53452 109 [Image Omitted]

601.16530 110 [Image Omitted]

549.54477 111 [Image Omitted]

589.40516 112 [Image Omitted]

575.37502 113 [Image Omitted]

589.40516 114 [Image Omitted]

586.60514 115 [Image Omitted]

604.59532 116 [Image Omitted]

604.59532 117 [Image Omitted]

604.59532 118 [Image Omitted]

611.60539 119 [Image Omitted]

621.04548 120 [Image Omitted]

592.62520

Example 121N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(2-thienyl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

To toluene (15 ml) were added the compound (350 mg, 0.57% mmol) of Example 113, step B, 2-(tri-n-butylstanyl)thiophene (319 mg, 0.86 mmol) and bis(triphenylphosphine)palladium(II)dichloride (40 mg, 0.06 mmol), and the mixture was heated under reflux for 11 hr. After cooling to room temperature, the reaction mixture was diluted with water, and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the obtained solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (methanol-chloroform) to give a bistered oil. Using this, the method of Example 1, step C, was performed to give the title compound (217 mg, yield 65%) as a pale-bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.16 (d, J=6.4, 6H), 2.28 (s, 3H), 2.89-2.91 (m, 5H), 3.19-3.24 (m, 1H), 3.38-3.45 (m, 2H), 3.94 (s, 2H), 4.13 (d, J=11.6, 2H), 4.27 (d, J=11.6, 2H), 4.36 (s, 2H), 7.05-7.29 (m, 7H), 7.35-7.39 (m, 2H), 7.49 (d, J=5.1, 1H), 8.43 (brs, 1H), 8.95 (brs, 2H).

Example 122N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[5-(2-furyl)-2-methylphenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (350 mg, 0.57 mmol) of Example 113, step B, and 2-(tri-n-butylstanyl)furan (305 mg, 0.86 mmol), and according to the method of Example 121, the title compound (193 mg, yield 58%) was obtained as a pale-bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.15-1.21 (m, 6H), 2.29 (s, 3H), 2.79-2.98 (m, 5H), 3.12-3.24 (m, 1H), 3.35-3.47 (m, 2H), 3.93 (s, 2H), 4.12 (d, J=11.7, 2H), 4.26 (d, J=11.7, 2H), 4.35 (s, 2H), 6.57 (dd, J=2.1, 3.3, 1H), 6.81 (d, J=3.3, 1H), 7.05-7.30 (m, 6H), 7.46 (s, 1H), 7.71 (d, J=1.2, 1H), 8.41 (t, J=5.4, 1H), 8.92 (brs, 2H).

Example 123N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(1H-pyrazol-4-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide trihydrochloride

Using the compound (500 mg, 0.81 mmol) of Example 113, step B, and tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole-1-carboxylate (381 mg, 1.30 mmol), and according to the methods of Example 114, step A, and Example 1, step C, the title compound (138 mg, yield 28%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.15-1.20 (m, 6H), 2.31 (s, 3H), 2.79-2.96 (m, 5H), 3.16-3.23 (m, 1H), 3.38-3.48 (m, 2H), 4.02 (s, 2H), 4.12 (d, J=11.7, 2H), 4.25 (d, J=11.7, 2H), 4.44 (s, 2H), 6.08 (brs, 2H), 7.13 (d, J=7.8, 1H), 7.19-7.32 (m, 5H), 7.49 (s, 1H), 8.12 (s, 2H), 8.55 (t, J=5.6, 1H), 8.97 (brs, 2H).

Example 124N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(1-methyl-1H-pyrazol-4-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide trihydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(1-methyl-1H-pyrazol-4-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (500 mg, 0.81 mmol) of Example 113, step B, and 1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (270 mg, 1.30 mmol), and according to the method of Example 114, step A, the title compound (276 mg, yield 55%) was obtained as a pale-yellow amorphous solid

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.01 (d, J=6.2, 6H), 1.37 (s, 9H), 2.24 (s, 3H), 2.82-3.01 (m, 5H), 3.13-3.22 (m, 2H), 3.81 (s, 2H), 3.84 (s, 3H), 3.99-4.11 (m, 3H), 4.22-4.27 (m, 4H), 7.08 (s, 2H), 7.24-7.30 (m, 5H), 7.71 (s, 1H), 7.98 (s, 1H), 8.19 (s, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(1-methyl-1H-pyrazol-4-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide trihydrochloride

Using the compound (276 mg, 0.45 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (283 mg, yield 100%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.18 (d, J=6.1, 6H), 2.30 (s, 3H), 2.81-2.89 (m, 5H), 3.16-3.24 (m, 1H), 3.39-3.46 (m, 2H), 3.85 (s, 3H), 4.02 (s, 2H), 4.12 (d, J=11.7, 2H), 4.25 (d, J=11.7, 2H), 4.42 (s, 2H), 5.21-5.84 (broad, 1H), 7.09-7.17 (m, 2H), 7.26 (s, 4H), 7.42 (s, 1H), 7.78 (s, 1H), 8.06 (s, 1H), 8.54 (brs, 1H), 8.98 (brs, 2H).

Example 125N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2-methyl-5-pyridin-4-ylphenyl)-N¹-[2-(isopropylamino)ethyl]glycinamide trihydrochloride

Using the compound (1.12 g, 1.81 mmol) of Example 113, step B, and 4-(tri-n-butylstanyl)pyridine (1.00 g, 2.72 mmol), and according to the method of Example 121, the title compound (22.2 mg, yield 2%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.19 (d, J=6.9, 6H), 2.39 (s, 3H), 2.81-2.89 (m, 5H), 3.17-3.31 (m, 1H), 3.32-3.50 (m, 2H), 3.60-4.39 (m, 8H), 7.01-7.75 (m, 7H), 8.32-8.39 (m, 3H), 8.81-9.04 (m, 5H).

Example 126N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2-methyl-5-pyridin-2-ylphenyl)-N¹-[2-(isopropylamino)ethyl]glycinamide trihydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2-methyl-5-pyridin-2-ylphenyl)-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

To toluene (15 ml) were added the compound (350 mg, 0.57 mmol) of Example 113, step B, 2-(tri-n-butylstanyl)pyridine (315 mg, 0.86 mmol), and bis(triphenylphosphine)palladium(II)dichloride (40 mg, 0.06 mmol), and the mixture was heated under reflux for 11 hr. After cooling to room temperature, the reaction mixture was diluted with water and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (methanol-chloroform) to give the title compound (298 mg, yield 85%) as a pale-yellow amorphous solid

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 0.97-1.01 (m, 6H), 1.36 (s, 9H), 2.31 (s, 3H), 2.81-3.12 (m, 5H), 3.15 (brs, 2H), 3.85 (s, 2H), 3.87-4.06 (m, 1H), 4.13 (d, J=11.9, 2H), 4.25 (d, J=11.9, 2H), 4.32 (s, 2H), 7.15-7.33 (m, 6H), 7.52-7.60 (m, 1H), 7.80-7.89 (m, 3H), 8.22 (brs, 1H), 8.62 (brs, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2-methyl-5-pyridin-2-ylphenyl)-N¹-[2-(isopropylamino)ethyl]glycinamide trihydrochloride

Using the compound (298 mg, 0.48 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (207 mg, yield 69%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.19 (d, J=6.6, 6H), 2.38 (s, 3H), 2.76-2.97 (m, 5H), 3.18-3.29 (m, 1H), 3.38-3.45 (m, 2H), 4.02 (s, 2H), 4.15 (d, J=11.7, 2H), 4.25 (d, J=11.7, 2H), 4.39 (s, 2H), 7.22-7.29 (s, 4H), 7.35 (d, J=8.4, 1H), 7.54-7.62 (m, 2H), 7.78-7.86 (m, 2H), 8.19-8.27 (m, 1H), 8.35-8.42 (m, 2H), 8.78-8.82 (m, 1H), 8.92 (brs, 2H).

Example 127N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2-methyl-5-pyridin-3-ylphenyl)-N¹-[2-(isopropylamino)ethyl]glycinamide trihydrochlorideStep AN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-(2-methyl-5-pyridin-3-ylphenyl)glycine

Using the compound (740 mg, 2.46 mmol) of Reference Example 93 and the compound (692 mg, 3.75 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (968 mg, yield 91%) was obtained as a pale-yellow amorphous solid

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.36 (s, 3H), 3.06 (s, 3H), 3.97 (s, 2H), 4.17 (d, J=11.7, 2H), 4.29 (d, J=11.7, 2H), 4.33 (s, 2H), 7.19-7.38 (m, 7H), 7.44 (s, 1H), 7.81-7.85 (m, 1H), 8.56-8.58 (m, 1H), 8.78 (d, J=2.0, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2-methyl-5-pyridin-3-ylphenyl)-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (963 mg, 2.24 mmol) obtained in step A and the compound (696 mg, 3.44 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (1.23 g, yield 89%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.09 (d, J=6.6, 6H), 1.44 (brs, 9H), 2.39 (s, 3H), 2.96 (s, 3H), 3.0-3.2 (m, 2H), 3.34-3.42 (m, 2H), 3.8-4.3 (broad, 1H), 3.90 (s, 2H), 4.09 (d, J=11.7, 2H), 4.23 (d, J=11.7, 2H), 4.24 (s, 2H), 7.17-7.35 (m, 7H), 7.47 (d, J=1.2, 1H), 7.8-7.9 (m, 1H), 7.9-8.5 (broad, 1H), 8.56 (dd, J=1.2, 4.5, 1H), 8.79 (d, J=2.1, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2-methyl-5-pyridin-3-ylphenyl)-N¹-[2-(isopropylamino)ethyl]glycinamide trihydrochloride

Using the compound (1.21 g, 1.97 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (1.32 g, yield>100%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.19 (d, J=6.5, 6H), 2.36 (s, 3H), 2.8-3.0 (m, 2H), 2.88 (s, 3H), 3.1-3.3 (m, 1H), 3.3-3.5 (m, 2H), 4.00 (s, 2H), 4.11 (d, J=11.7, 2H), 4.25 (d, J=11.7, 2H), 4.35 (s, 2H), 7.25 (broad, 4H), 7.31 (d, J=8.0, 1H), 7.40 (d, J=8.0, 1H), 7.60 (s, 1H), 8.0-8.1 (m, 1H), 8.38 (t, J=5.4, 1H), 8.7-8.8 (m, 1H), 8.83 (d, J=5.4, 1H), 8.92 (brs, 2H), 9.16 (s, 1H).

Example 128N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2-methyl-5-pyrimidin-2-ylphenyl)-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-(2-methyl-5-pyrimidin-2-ylphenyl)glycine

Using the compound (857 mg, 2.84 mmol) of Reference Example 90 and the compound (790 mg, 4.28 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (783 mg, yield 64%) was obtained as a gray amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.40 (s, 3H), 3.06 (s, 3H), 3.98 (s, 2H), 4.17 (d, J=11.7, 2H), 4.27 (d, J=11.7, 2H), 4.35 (s, 2H), 7.14-7.28 (m, 5H), 7.31 (d, J=7.8, 1H), 8.14 (dd, J=1.5, 7.8, 1H), 8.35 (d, J=1.5, 1H), 8.76 (d, J=4.8, 2H), 13.5 (brs, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2-methyl-5-pyrimidin-2-ylphenyl)-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (777 mg, 1.80 mmol) obtained in step A and the compound (626 mg, 3.09 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (1.01 g, yield 91%) was obtained as a pale-yellow amorphous solid

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.11 (d, J=6.8, 6H), 1.46 (brs, 9H), 2.42 (s, 3H), 2.94 (s, 3H), 3.0-3.3 (m, 2H), 3.38-3.46 (m, 2H), 3.85 (s, 2H), 3.9-4.4 (broad, 1H), 4.15 (d, J=11.7, 2H), 4.22 (d, J=11.7, 2H), 4.31 (s, 2H), 7.13-7.27 (m, 5H), 7.30 (d, J=7.8, 1H), 8.09 (dd, J=1.4, 7.8, 1H), 8.3-8.8 (broad, 1H), 8.40 (d, J=1.4, 1H), 8.74 (d, J=5.2, 2H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2-methyl-5-pyrimidin-2-ylphenyl)-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (985 mg, 1.60 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (910 mg, yield 97%) was obtained as a yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.17 (d, J=6.4, 6H), 2.35 (s, 3H), 2.8-3.0 (m, 2H), 2.88 (s, 3H), 3.1-3.3 (m, 1H), 3.3-3.5 (m, 2H), 3.93 (s, 2H), 4.14 (d, J=11.7, 2H), 4.27 (d, J=11.7, 2H), 4.38 (s, 2H), 7.2-7.3 (m, 5H), 7.39-7.43 (m, 1H), 7.95 (dd, J=1.2, 8.2, 1H), 8.22 (d, J=1.2, 1H), 8.42 (t, J=5.7, 1H), 8.74 (brs, 2H), 8.88 (d, J=4.6, 2H).

Example 129N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2-methyl-5-pyrimidin-2-ylphenyl)-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2-methyl-5-pyrimidin-2-ylphenyl)-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (563 mg, 1.31 mmol) of Example 128, step A, and the compound (346 mg, 1.84 mmol) of Reference Example 2, and according to the method of Example 1, step B, the title compound (615 mg, yield 78%) was obtained as a gray amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.03 (t, J=6.9, 3H), 1.45 (brs, 9H), 2.41 (s, 3H), 2.95 (s, 3H), 3.0-3.3 (m, 4H), 3.41-3.48 (m, 2H), 3.84 (s, 2H), 4.16 (d, J=11.7, 2H), 4.23 (d, J=11.7, 2H), 4.31 (s, 2H), 7.13-7.31 (m, 6H), 8.08 (d, J=8.7, 1H), 8.3-8.7 (broad, 1H), 8.39 (d, J=1.2, 1H), 8.75 (d, J=5.1, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2-methyl-5-pyrimidin-2-ylphenyl)-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (612 mg, 1.02 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (579 mg, yield 99%) was obtained as a yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.14 (t, J=7.3, 3H), 2.34 (s, 3H), 2.8-3.0 (m, 4H), 2.88 (s, 3H), 3.34-3.42 (m, 2H), 3.93 (s, 2H), 4.14 (d, J=11.7, 2H), 4.26 (d, J=11.7, 2H), 4.38 (s, 2H), 7.0-7.3 (m, 5H), 7.39-7.43 (m, 1H), 7.94 (d, J=8.0, 1H), 8.23 (s, 1H), 8.41 (t, J=5.7, 1H), 8.76 (brs, 2H), 8.88 (d, J=4.6, 2H).

Example 130N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2-methyl-5-pyrimidin-4-ylphenyl)-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-(2-methyl-5-pyrimidin-4-ylphenyl)glycine

Using the compound (378 mg, 1.25 mmol) of Reference Example 91 and the compound (394 mg, 2.13 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (388 mg, yield 72%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.39 (s, 3H), 3.07 (s, 3H), 3.98 (s, 2H), 4.18 (d, J=11.7, 2H), 4.29 (d, J=11.7, 2H), 4.35 (s, 2H), 7.2-7.3 (m, 4H), 7.33 (d, J=8.1, 1H), 7.66 (dd, J=1.5, 5.4, 1H), 7.75 (dd, J=1.5, 8.1, 1H), 8.03 (d, J=1.5, 1H), 8.74 (d, J=5.4, 1H), 9.21 (d, J=1.5, 1H), 13.6 (brs, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2-methyl-5-pyrimidin-4-ylphenyl)-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (370 mg, 0.857 mmol) obtained in step A and the compound (286 mg, 1.41 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (440 mg, yield 83%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.10 (d, J=6.8, 6H), 1.45 (brs, 9H), 2.42 (s, 3H), 2.95 (s, 3H), 3.0-3.2 (m, 2H), 3.36-3.44 (m, 2H), 3.88 (s, 2H), 3.9-4.3 (broad, 1H), 4.15 (d, J=11.7, 2H), 4.24 (d, J=11.7, 2H), 4.30 (s, 2H), 7.17-7.28 (m, 4H), 7.31 (d, J=7.8, 1H), 7.66-7.73 (m, 2H), 8.06 (d, J=1.5, 1H), 8.1-8.6 (broad, 1H), 8.72 (d, J=5.3, 1H), 9.20 (d, J=1.5, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2-methyl-5-pyrimidin-4-ylphenyl)-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (437 mg, 0.710 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (422 mg, yield 100%) was obtained as an orange solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.17 (d, J=6.6, 6H), 2.36 (s, 3H), 2.8-3.0 (m, 2H), 2.88 (s, 3H), 3.1-3.3 (m, 1H), 3.3-3.5 (m, 2H), 3.96 (s, 2H), 4.14 (d, J=11.7, 2H), 4.27 (d, J=11.7, 2H), 4.38 (s, 2H), 7.2-7.3 (m, 4H), 7.30 (d, J=8.1, 1H), 7.74 (dd, J=1.5, 8.1, 1H), 8.03 (s, 1H), 8.04 (d, J=5.4, 1H), 8.42 (t, J=5.7, 1H), 8.7-9.0 (broad, 2H), 8.84 (d, J=5.4, 1H), 9.24 (s, 1H).

Example 131N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2-methyl-5-pyrimidin-5-ylphenyl)-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-(2-methyl-5-pyrimidin-5-ylphenyl)glycine

Using the compound (270 mg, 0.896 mmol) of Reference Example 92, and the compound (259 mg, 1.40 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (310 mg, yield 80%) was obtained as a gray solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.30 (s, 3H), 2.88 (s, 3H), 4.06 (s, 2H), 4.13 (d, J=11.7, 2H), 4.26 (d, J=11.7, 2H), 4.33 (s, 2H), 7.22-7.33 (m, 5H), 7.43 (d, J=1.2, 1H), 8.32 (s, 1H), 9.04 (s, 2H), 9.16 (s, 1H), 12.51 (brs, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2-methyl-5-pyrimidin-5-ylphenyl)-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (303 mg, 0.702 mmol) obtained in step A and the compound (244 mg, 1.21 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (313 mg, yield 72%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.09 (d, J=6.8, 6H), 1.43 (brs, 9H), 2.41 (s, 3H), 2.96 (s, 3H), 3.0-3.2 (m, 2H), 3.34-3.41 (m, 2H), 3.9-4.3 (broad, 1H), 3.92 (s, 2H), 4.10 (d, J=11.4, 2H), 4.25 (d, J=11.4, 2H), 4.25 (s, 2H), 7.18-7.33 (m, 6H), 7.48 (d, J=1.2, 1H), 7.8-8.6 (broad, 1H), 8.89 (s, 2H), 9.18 (s, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2-methyl-5-pyrimidin-5-ylphenyl)-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (311 mg, 0.505 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (278 mg, yield 100%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.18 (d, J=6.4, 6H), 2.34 (s, 3H), 2.8-3.0 (m, 2H), 2.88 (s, 3H), 3.1-3.3 (m, 1H), 3.3-3.5 (m, 2H), 3.97 (s, 2H), 4.11 (d, J=11.7, 2H), 4.25 (d, J=11.7, 2H), 4.35 (s, 2H), 7.24-7.33 (m, 5H), 7.34 (d, J=8.0, 1H), 7.52 (d, J=1.0, 1H), 8.40 (t, J=5.7, 1H), 8.84 (brs, 2H), 9.07 (s, 2H), 9.17 (s, 1H).

Example 132N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2-methyl-5-pyrazin-2-ylphenyl)-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2-methyl-5-pyrazin-2-ylphenyl)-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (789 mg, 1.28 mmol) of Example 113, step B, and 2-(tri-n-butylstanyl)pyrazine (715 mg, 1.94 mmol), and according to the method of Example 126, step A, the title compound (162 mg, yield 21%) was obtained as a yellow amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.10 (d, J=6.6, 6H), 1.45 (brs, 9H), 2.42 (s, 3H), 2.95 (s, 3H), 3.0-3.2 (m, 2H), 3.36-3.44 (m, 2H), 3.89 (s, 2H), 3.9-4.3 (broad, 1H), 4.13 (d, J=11.7, 2H), 4.24 (d, J=11.7, 2H), 4.28 (s, 2H), 7.17-7.28 (m, 4H), 7.31 (d, J=8.1, 1H), 7.62 (dd, J=1.2, 8.1, 1H), 7.99 (d, J=1.2, 1H), 8.0-8.7 (broad, 1H), 8.47 (d, J=2.1, 1H), 8.57 (dd, J=1.2, 2.1, 1H), 8.98 (d, J=1.2, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2-methyl-5-pyrazin-2-ylphenyl)-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (160 mg, 0.260 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (121 mg, yield 79%) was obtained as a bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.17 (d, J=6.4, 6H), 2.34 (s, 3H), 2.8-3.0 (m, 2H), 2.88 (s, 3H), 3.1-3.3 (m, 1H), 3.3-3.5 (m, 2H), 3.95 (s, 2H), 4.13 (d, J=11.7, 2H), 4.26 (d, J=11.7, 2H), 4.37 (s, 2H), 7.25-7.30 (m, 5H), 7.67 (d, J=7.8, 1H), 7.92 (s, 1H), 8.41 (broad t, 1H), 8.58 (d, J=2.4, 1H), 8.70 (dd, J=1.4, 2.4, 1H), 8.73 (brs, 2H), 9.16 (s, 1H).

Example 133N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(4â€²-fluoro-3-methylbiphenyl-4-yl)-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (500 mg, 0.81 mmol) of Example 111, step B, and 4-fluorophenylboronic acid (181 mg, 1.30 mmol), and according to the method of Example 114, step A, Example 1, step C, the title compound (227 mg, yield 46%) was obtained as a pale-bistered amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.19 (d, J=6.5, 6H), 2.35 (s, 3H), 2.84-2.95 (m, 2H), 2.90 (s, 3H), 3.16-3.28 (m, 1H), 3.38-3.45 (m, 2H), 3.93 (s, 2H), 4.13 (d, J=11.5, 2H), 4.27 (d, J=11.7, 2H), 4.36 (s, 2H), 7.16-7.28 (m, 7H), 7.33-7.41 (m, 2H), 7.59-7.66 (m, 2H), 8.40-8.44 (m, 1H), 8.95 (brs, 2H).

Example 134N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(4â€²-fluoro-3-methylbiphenyl-4-yl)-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (500 mg, 0.83 mmol) of Example 112, step A, and 4-fluorophenylboronic acid (181 mg, 1.30 mmol), and according to the methods of Example 114, step A, and Example 1, step C, the title compound (262.5 mg, yield 54%) was obtained as a pale-bistered amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=7.2, 3H), 2.34 (s, 3H), 2.80-2.99 (m, 4H), 2.90 (s, 3H), 3.36-3.43 (m, 2H), 3.92 (s, 2H), 4.13 (d, J=11.7, 2H), 4.27 (d, J=11.7, 2H), 4.35 (s, 2H), 7.15-7.28 (m, 7H), 7.33-7.41 (m, 2H), 7.60-7.68 (m, 2H), 8.36-8.41 (m, 1H), 8.88 (brs, 2H).

Example 135N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(1-methyl-1H-pyrazol-4-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide trihydrochloride

Using the compound (1.00 g, 1.62 mmol) of Example 111, step B, and 1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (540 mg, 2.59 mmol), and according to the methods of Example 114, step A, and Example 1, step C, the title compound (197 mg, yield 19%) was obtained as a pale-bistered amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.19 (d, J=6.6, 6H), 2.33 (s, 3H), 2.76-2.94 (m, 2H), 2.89 (s, 3H), 3.18-3.29 (m, 1H), 3.37-3.50 (m, 2H), 3.85 (s, 3H), 3.94 (s, 2H), 4.11 (d, J=11.7, 2H), 4.25 (d, J=11.7, 2H), 4.39 (s, 2H), 7.17-7.35 (m, 7H), 7.79 (s, 1H), 8.05 (s, 1H), 8.47-8.52 (m, 1H), 8.99 (brs, 2H).

Example 136N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(1-methyl-1H-pyrazol-4-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide trihydrochloride

Using the compound (1.00 g, 1.66 mmol) of Example 112, step A, and 1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (540 mg, 2.59 mmol), and according to the methods of Example 114, step A, and Example 1, step C, the title compound (233 mg, yield 23%) was obtained as a pale-bistered amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.12-1.20 (m, 3H), 2.31 (s, 3H), 2.79-3.00 (m, 4H), 2.89 (s, 3H), 3.34-3.42 (m, 2H), 3.84 (s, 3H), 3.90 (s, 2H), 4.10 (d, J=11.6, 2H), 4.25 (d, J=11.7, 2H), 4.34 (s, 2H), 7.16 (d, J=8.2, 1H), 7.21-7.29 (m, 5H), 7.33 (s, 1H), 7.77 (s, 1H), 8.03 (s, 1H), 8.41-8.46 (m, 1H), 8.89 (brs, 2H).

Example 137N²-(5-cyano-2-ethylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-(5-cyano-2-ethylphenyl)-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound (1.98 g, 7.55 mmol) of Reference Example 94, and the compound (2.11 g, 11.4 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (2.42 g, yield 82%) was obtained as a pale-purple amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.24 (t, J=7.5, 3H), 2.74 (q, J=7.5, 2H), 3.07 (s, 3H), 3.91 (s, 2H), 4.17 (d, J=11.7, 2H), 4.28 (s, 2H), 4.30 (d, J=11.7, 2H), 7.2-7.3 (m, 4H), 7.33 (d, J=7.8, 1H), 7.41 (dd, J=1.5, 7.8, 1H), 7.52 (d, J=1.5, 1H), 13.4 (brs, 1H).

Step BN²-(5-cyano-2-ethylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (1.14 g, 2.91 mmol) obtained in step A and the compound (906 mg, 4.48 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (1.41 g, yield 84%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.12 (d, J=6.8, 6H), 1.26 (t, J=7.5, 3H), 1.44 (brs, 9H), 2.78 (q, J=7.5, 2H), 2.95 (s, 3H), 3.0-3.2 (m, 2H), 3.35-3.43 (m, 2H), 3.81 (s, 2H), 3.9-4.4 (broad, 1H), 4.12 (d, J=11.7, 2H), 4.21 (s, 2H), 4.25 (d, J=11.7, 2H), 7.2-7.4 (m, 6H), 7.57 (s, 1H), 7.8-8.5 (broad, 1H).

Step CN²-(5-cyano-2-ethylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (476 mg, 0.825 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (422 mg, yield 93%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.1-1.3 (m, 9H), 2.73 (q, J=7.5, 2H), 2.8-3.0 (m, 2H), 2.87 (s, 3H), 3.1-3.3 (m, 1H), 3.3-3.5 (m, 2H), 3.88 (s, 2H), 4.09 (d, J=11.7, 2H), 4.25 (d, J=11.7, 2H), 4.28 (s, 2H), 7.26 (broad, 4H), 7.36 (d, J=7.8, 1H), 7.41 (d, J=7.8, 1H), 7.58 (s, 1H), 8.29 (broad t, 1H), 8.72 (brs, 2H).

Example 138N²-(5-cyano-2-ethylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-(5-cyano-2-ethylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-Nâ€²-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (1.20 g, 3.06 mmol) of Example 137, step A, and the compound (954 mg, 5.07 mmol) of Reference Example 2, and according to the method of Example 1, step B, the title compound (1.52 g, yield 88%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.06 (t, J=7.2, 3H), 1.26 (t, J=7.5, 3H), 1.42 (brs, 9H), 2.77 (q, J=7.5, 2H), 2.96 (s, 3H), 3.0-3.3 (m, 4H), 3.38-3.45 (m, 2H), 3.79 (s, 2H), 4.13 (d, J=11.7, 2H), 4.21 (s, 2H), 4.25 (d, J=11.7, 2H), 7.19-7.37 (m, 6H), 7.57 (d, J=1.0, 1H), 8.0-8.5 (broad, 1H).

Step BN²-(5-cyano-2-ethylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (520 mg, 0.924 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (443 mg, yield 90%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=6.9, 3H), 1.18 (t, J=7.5, 3H), 2.75 (q, J=7.5, 2H), 2.8-3.0 (m, 4H), 2.87 (s, 3H), 3.33-3.40 (m, 2H), 3.86 (s, 2H), 4.09 (d, J=11.7, 2H), 4.24 (d, J=11.7, 2H), 4.28 (s, 2H), 7.26 (broad, 4H), 7.36 (d, J=7.8, 1H), 7.41 (d, J=7.8, 1H), 7.58 (s, 1H), 8.27 (t, J=5.7, 1H), 8.76 (brs, 2H).

Example 139N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-ethyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl](isopropylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-ethyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (922 mg, 1.60 mmol) of Example 137, step B and according to the method of Reference Example 62, step A, the title compound (677 mg, yield 67%) was obtained as a pale-yellow amorphous solid

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.12 (d, J=6.9, 6H), 1.27 (t, J=7.5, 3H), 1.47 (brs, 9H), 2.62 (s, 3H), 2.82 (q, J=7.5, 2H), 2.94 (s, 3H), 3.0-3.2 (m, 2H), 3.3-3.5 (m, 2H), 3.79 (s, 2H), 3.9-4.4 (broad, 1H), 4.08 (d, J=11.7, 2H), 4.20 (d, J=11.7, 2H), 4.24 (s, 2H), 7.16-7.28 (m, 4H), 7.33 (d, J=8.1, 1H), 7.78 (dd, J=1.2, 8.1, 1H), 7.98 (d, J=1.2, 1H), 8.2-8.7 (broad, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-ethyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (669 mg, 1.06 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (588 mg, yield 91%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.17-1.23 (m, 9H), 2.65 (s, 3H), 2.73 (q, J=7.5, 2H), 2.8-3.0 (m, 2H), 2.87 (s, 3H), 3.1-3.3 (m, 1H), 3.34-3.42 (m, 2H), 3.89 (s, 2H), 4.07 (d, J=11.7, 2H), 4.24 (d, J=11.7, 2H), 4.32 (s, 2H), 7.25 (broad, 4H), 7.35 (d, J=7.8, 1H), 7.62 (dd, J=1.2, 7.8, 1H), 7.86 (d, J=1.2, 1H), 8.36 (t, J=5.7, 1H), 8.65 (brs, 2H).

Example 140N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-ethyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-ethyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (994 mg, 1.77 mmol) of Example 138, step A and according to the method of Reference Example 62, step A, the title compound (744 mg, yield 68%) was obtained as a pale-yellow amorphous solid

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.06 (t, J=6.9, 3H), 1.27 (t, J=7.5, 3H), 1.45 (brs, 9H), 2.62 (s, 3H), 2.80 (q, J=7.5, 2H), 2.94 (s, 3H), 3.0-3.4 (m, 4H), 3.4-3.5 (m, 2H), 3.78 (s, 2H), 4.09 (d, J=11.4, 2H), 4.20 (d, J=11.4, 2H), 4.24 (s, 2H), 7.16-7.27 (m, 4H), 7.33 (d, J=7.8, 1H), 7.77 (dd, J=1.2, 7.8, 1H), 7.98 (d, J=1.2, 1H), 8.3-8.7 (broad, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-ethyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (739 mg, 1.19 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (679 mg, yield 96%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.3, 3H), 1.20 (t, J=7.5, 3H), 2.65 (s, 3H), 2.73 (q, J=7.5, 2H), 2.8-3.0 (m, 4H), 2.87 (s, 3H), 3.3-3.4 (m, 2H), 3.89 (s, 2H), 4.07 (d, J=11.7, 2H), 4.24 (d, J=11.7, 2H), 4.32 (s, 2H), 7.25 (broad, 4H), 7.35 (d, J=8.1, 1H), 7.61 (d, J=8.1, 1H), 7.86 (s, 1H), 8.34 (t, J=5.7, 1H), 8.67 (brs, 2H).

Example 141N²-(2-benzylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-(2-pyrrolidin-1-ylethyl)glycinamideStep AN-(2-benzylphenyl)-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound (1.00 g, 3.34 mmol) of Reference Example 95, and the compound (1.23 g, 6.66 mmol of Reference Example 17), and according to the method of Example 1, step A, the title compound (1.57 g, yield>100%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.89 (s, 3H), 3.71-3.76 (m, 2H), 3.88 (s, 2H), 3.92 (s, 2H), 3.98-4.02 (m, 2H), 4.07 (s, 2H), 7.08-7.32 (m, 13H).

Step BN²-(2-benzylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-(2-pyrrolidin-1-ylethyl)glycinamide

Using the compound (0.50 g, 1.16 mmol) obtained in step A and 1-(2-aminoethyl)pyrrolidine (0.21 ml, 1.61 mmol), and according to the method of Example 1, step B, the title compound (0.43 g, yield 70%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.65-1.70 (m, 4H), 2.39-2.48 (m, 6H), 2.87 (s, 3H), 3.30 (q, J=5.7, 2H), 3.66-3.71 (m, 2H), 3.86 (s, 2H), 3.96 (s, 2H), 3.99-4.04 (m, 2H), 4.16 (s, 2H), 7.11-7.36 (m, 13H), 7.88 (brs, 1H).

Example 142N²-(2-benzylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(methylamino)ethyl]glycinamide dihydrochlorideStep AN²-(2-benzylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(methyl)amino]ethyl}glycinamide

Using the compound (0.50 g, 1.16 mmol) of Example 141, step A, the compound (0.39 g, 1.85 mmol) of Reference Example 1 and triethylamine (0.26 ml, 1.89 mmol), and according to the method of Example 1, step B, the title compound (0.50 g, yield 73%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.44 (s, 9H), 2.72 (s, 3H), 2.83 (s, 3H), 3.19-3.27 (m, 4H), 3.70-3.82 (m, 2H), 4.01-4.15 (m, 6H), 7.05-7.36 (m, 13H), 7.99-8.14 (broad, 1H).

Step BN²-(2-benzylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(methylamino)ethyl]glycinamide dihydrochloride

Using the compound (0.50 g, 0.85 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (0.39 g, yield 82%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.49 (s, 3H), 2.84-2.90 (m, 5H), 3.30-3.37 (m, 2H), 3.74-3.79 (m, 2H), 3.86 (s, 2H), 4.08-4.14 (m, 6H), 6.96-7.32 (m, 13H), 8.24-8.29 (m, 1H), 8.81 (broad, 2H).

Example 143N²-(2-chlorophenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-(2-chlorophenyl)-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound (546 mg, 2.24 mmol) of Reference Example 96 and the compound (620 mg, 3.36 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (710 mg, yield 85%) was obtained as a bistered amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 3.04 (s, 3H), 4.00 (s, 2H), 4.20 (d, J=11.7, 2H), 4.28 (d, J=11.7, 2H), 4.38 (s, 2H), 7.04-7.10 (m, 1H), 7.20-7.29 (m, 5H), 7.33-7.39 (m, 2H).

Step BN²-(2-chlorophenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (710 mg, 1.90 mmol) obtained in step A and the compound (577 mg, 2.85 mmol) of Reference Example 3, and according to the methods of Example 1, steps B and C, the title compound (278 mg, yield 28%) was obtained as a pale-bistered amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.20 (d, J=6.5, 6H), 2.84-3.04 (m, 5H), 3.23-3.36 (m, 1H), 3.41 (q, J=6.0, 2H), 3.96 (s, 2H), 4.14 (d, J=11.7, 2H), 4.28 (d, J=11.7, 2H), 4.34 (s, 2H), 6.79-6.99 (m, 1H), 7.17-7.38 (m, 7H), 8.34 (t, J=5.6, 1H), 8.92 (brs, 2H).

Example 144N²-(3-chlorophenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-(2-pyrrolidin-1-ylethyl)glycinamideStep AN-(3-chlorophenyl)-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound (1.00 g, 4.10 mmol) of Reference Example 97 and the compound (834 mg, 4.52 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (896 mg, yield 58%) was obtained as a bistered amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 3.10 (s, 3H), 4.14 (s, 2H), 4.41 (s, 4H), 4.61 (s, 2H), 6.45 (d, J=8.3, 1H), 6.50 (s, 1H), 6.81 (d, J=8.3, 1H), 7.18 (t, J=8.1, 1H), 7.30-7.31 (m, 4H).

Step BN²-(3-chlorophenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-(2-pyrrolidin-1-ylethyl)glycinamide

Using the compound (143 mg, 0.35 mmol) obtained in step A and 1-(2-aminoethyl)pyrrolidine (0.05 ml, 0.39 mmol), and according to the method of Example 1, step B, the title compound (115 mg, yield 65%) was obtained as a pale-yellow amorphous solid

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.68 (m, 4H), 2.44 (m, 4H), 2.52-2.54 (m, 2H), 3.04 (s, 3H), 3.38-3.42 (m, 2H), 3.98 (s, 2H), 4.34 (d, J=12.0, 2H), 4.40 (d, J=12.0, 2H), 4.52 (s, 2H), 6.38-6.42 (m, 1H), 6.48 (m, 1H), 6.74 (d, J=6.3, 1H), 7.12 (t, J=8.1, 1H), 7.29 (broad, 4H), 8.94 (brs, 1H).

The compounds of Examples 121-144 are shown below.

TABLE 12StructuralLC-MSExampleFormulaTMW(found)121 [Image Omitted]

592.62520 122 [Image Omitted]

576.56504 123 [Image Omitted]

613.02504 124 [Image Omitted]

627.05518 125 [Image Omitted]

624.04515 126 [Image Omitted]

624.04515 127 [Image Omitted]

624.04515 128 [Image Omitted]

588.57516 129 [Image Omitted]

574.54502 130 [Image Omitted]

588.57516 131 [Image Omitted]

588.57516 132 [Image Omitted]

588.57516 133 [Image Omitted]

604.59532 134 [Image Omitted]

590.56518 135 [Image Omitted]

627.05518 136 [Image Omitted]

613.02504 137 [Image Omitted]

549.54477 138 [Image Omitted]

535.51463 139 [Image Omitted]

606.59534 140 [Image Omitted]

592.56520 141 [Image Omitted]

525.68526 142 [Image Omitted]

558.54486 143 [Image Omitted]

530.92458 144 [Image Omitted]

470.01470

Example 145N²-(2,5-dichlorophenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-(2-pyrrolidin-1-ylethyl)glycinamideStep AN-(2,5-dichlorophenyl)-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound (470 mg, 1.69 mmol) of Reference Example 98 and the compound (343 mg, 1.86 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (896 mg, yield 87%) was obtained as a bistered amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 3.05 (s, 3H), 4.01 (s, 2H), 4.22 (d, J=11.7, 2H), 4.30 (d, J=11.7, 2H), 4.39 (s, 2H), 7.01-7.04 (m, 1H), 7.21-7.25 (m, 3H), 7.26-7.30 (m, 3H).

Step BN²-(2,5-dichlorophenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-(2-pyrrolidin-1-ylethyl)glycinamide

Using the compound (253 mg, 0.68 mmol) obtained in step A and 1-(2-aminoethyl)pyrrolidine (0.09 ml, 0.74 mmol), and according to the method of Example 1, step B, the title compound (217 mg, yield 68%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.68 (m, 4H), 2.42 (m, 4H), 2.52 (m, 2H), 2.94 (s, 3H), 3.36-3.40 (m, 2H), 3.98 (s, 2H), 4.17 (d, J=11.4, 2H), 4.26 (d, J=11.4, 2H), 4.32 (s, 2H), 6.96 (dd, J=2.4, 8.4, 1H), 7.19-7.33 (m, 5H), 7.41 (d, J=2.4, 1H), 7.83 (brs, 1H).

Example 146N²-(2,5-dichlorophenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(methylamino)ethyl]glycinamide dihydrochlorideStep AN²-(2,5-dichlorophenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(methyl)amino]ethyl}glycinamide

Using the compound (262 mg, 0.64 mmol) of Example 145, step A, the compound (162 mg, 0.77 mmol) of Reference Example 1 and triethylamine (0.11 ml, 0.77 mmol), and according to the method of Example 1, step B, the title compound (225 mg, yield 62%) was obtained as a pale-yellow amorphous solid

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.38 (s, 9H), 2.76 (s, 3H), 2.93 (s, 3H), 3.25 (m, 2H), 3.35-3.39 (m, 2H), 3.93 (s, 2H), 4.19-4.29 (m, 6H), 6.89-6.96 (m, 1H), 7.22-7.24 (m, 5H), 7.37 (d, J=2.3, 1H).

Step BN²-(2,5-dichlorophenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(methylamino)ethyl]glycinamide dihydrochloride

Using the compound (220 mg, 0.39 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (167 mg, yield 80%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.54-2.55 (m, 3H), 2.90-2.97 (m, 5H), 3.38-3.41 (m, 2H), 3.98 (s, 2H), 4.15 (d, J=11.7, 2H), 4.29 (d, J=11.7, 2H), 4.45 (s, 2H), 6.99 (dd, J=2.3, 8.4, 1H), 7.15 (d, J=2.3, 1H), 7.24-7.31 (m, 4H), 7.36 (d, J=8.3, 1H), 8.27 (t, J=5.7, 1H), 8.59 (brs, 2H).

Example 147N²-(2,5-dichlorophenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN²-(2,5-dichlorophenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (261 mg, 0.64 mmol) of Example 145, step A, and the compound (155 mg, 0.77 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (264 mg, yield 70%) was obtained as a pale-yellow amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.06 (d, J=6.7, 6H), 1.40 (s, 9H), 2.93-3.16 (m, 5H), 3.34-3.38 (m, 2H), 3.95 (s, 2H), 4.14-4.29 (m, 7H), 6.94-6.97 (m, 1H), 7.17-7.22 (m, 5H), 7.38-7.39 (m, 1H), 7.90 (brs, 1H).

Step BN²-(2,5-dichlorophenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (264 mg, 0.44 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (195 mg, yield 79%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.19 (d, J=6.3, 6H), 2.91 (m, 5H), 3.35-3.39 (m, 3H), 3.98 (s, 2H), 4.15 (d, J=11.7, 2H), 4.29 (d, J=11.7, 2H), 4.45 (s, 2H), 7.00 (dd, J=2.4, 8.4, 1H), 7.16 (d, J=2.4, 1H), 7.24-7.30 (m, 4H), 7.36 (d, J=8.4, 1H), 8.26 (t, J=6.0, 1H), 8.46 (brs, 2H).

Example 148N²-(2,4-dichlorophenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-(2,4-dichlorophenyl)-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound (480 mg, 1.73 mmol) of Reference Example 99 and the compound (479 mg, 2.60 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (573 mg, yield 81%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.87 (s, 3H), 4.08 (s, 2H), 4.14 (d, J=11.7, 2H), 4.26 (d, J=11.7, 2H), 4.42 (s, 2H), 7.12 (d, J=8.7, 1H), 7.22-7.30 (m, 5H), 7.42 (d, J=2.4, 1H), 12.53 (brs, 1H).

Step BN²-(2,4-dichlorophenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using a mixture of the compound (573 mg, 1.40 mmol) obtained in step A and the compound (425 mg, 2.10 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (641 mg, yield 75%) was obtained as a bistered amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.08 (d, J=6.6, 6H), 1.42 (s, 9H), 2.93 (s, 3H), 2.99-3.21 (m, 2H), 3.31-3.39 (m, 2H), 3.9-4.3 (broad, 1H), 3.97 (s, 2H), 4.15 (d, J=11.4, 2H), 4.24 (d, J=11.4, 2H), 4.28 (s, 2H), 7.16-7.29 (m, 5H), 7.35 (d, J=2.4, 1H), 7.40 (d, J=8.7, 1H), 7.83 (brs, 1H).

Step CN²-(2,4-dichlorophenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (641 mg, 1.06 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (258 mg, yield 43%) was obtained as a pale-bistered amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.20 (d, J=6.6, 6H), 2.89 (brs, 5H), 3.21-3.29 (m, 3H), 3.96 (s, 2H), 4.14 (d, J=11.7, 2H), 4.28 (d, J=11.7, 2H), 4.43 (s, 2H), 7.16 (d, J=9.0, 1H), 7.21-7.27 (m, 5H), 7.45 (d, J=2.4, 1H), 8.30 (t, J=5.1, 1H), 8.81 (brs, 2H).

Example 149N²-(2-chloro-5-cyanophenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-(2-chloro-5-cyanophenyl)-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound (460 mg, 1.71 mmol) of Reference Example 100 and the compound (440 mg, 2.38 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (564 mg, yield 83%) was obtained as a gray amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.88 (s, 3H), 4.13 (s, 2H), 4.17 (d, J=11.7, 2H), 4.27 (d, J=11.7, 2H), 4.48 (s, 2H), 7.23-7.31 (m, 4H), 7.36 (dd, J=1.5, 8.1, 1H), 7.52 (d, J=1.5, 1H), 7.54 (d, J=8.1, 1H), 12.60 (brs, 1H).

Step BN²-(2-chloro-5-cyanophenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (558 mg, 1.40 mmol) obtained in step A and the compound (388 mg, 1.92 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (744 mg, yield 91%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.09 (d, J=6.9, 6H), 1.41 (brs, 9H), 2.96 (s, 3H), 3.0-3.2 (m, 2H), 3.34-3.41 (m, 2H), 3.9-4.4 (broad, 1H), 4.00 (s, 2H), 4.19 (d, J=11.7, 2H), 4.28 (d, J=11.7, 2H), 4.35 (s, 2H), 7.2-7.3 (m, 5H), 7.44 (d, J=8.1, 1H), 7.64 (s, 1H), 7.7-8.0 (broad, 1H).

Step CN²-(2-chloro-5-cyanophenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (726 mg, 1.25 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (610 mg, yield 88%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.19 (d, J=6.6, 6H), 2.8-3.0 (m, 2H), 2.90 (s, 3H), 3.1-3.3 (m, 1H), 3.35-3.42 (m, 2H), 4.02 (s, 2H), 4.17 (d, J=11.7, 2H), 4.29 (d, J=11.7, 2H), 4.48 (s, 2H), 7.23-7.31 (m, 4H), 7.37 (d, J=8.1, 1H), 7.54 (s, 1H), 7.55 (d, J=8.1, 1H), 8.30 (broad t, 1H), 8.67 (brs, 2H).

Example 150N²-[2-chloro-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN²-[2-chloro-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (616 mg, 1.06 mmol) of Example 149, step B and according to the method of, Reference Example 62, step A, the title compound (577 mg, yield 85%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.08 (d, J=6.9, 6H), 1.43 (brs, 9H), 2.64 (s, 3H), 2.94 (s, 3H), 3.0-3.2 (m, 2H), 3.34-3.42 (m, 2H), 3.9-4.4 (broad, 1H), 4.03 (s, 2H), 4.20 (d, J=12.0, 2H), 4.26 (d, J=12.0, 2H), 4.36 (s, 2H), 7.2-7.3 (m, 4H), 7.45 (d, J=8.1, 1H), 7.69 (dd, J=1.5, 8.1, 1H), 7.7-8.2 (broad, 1H), 8.10 (d, J=1.5, 1H).

Step BN²-[2-chloro-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (569 mg, 0.889 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (486 mg, yield 89%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.17 (d, J=6.6, 6H), 2.67 (s, 3H), 2.8-3.0 (m, 2H), 2.91 (s, 3H), 3.2-3.4 (m, 3H), 4.04 (s, 2H), 4.16 (d, J=11.7, 2H), 4.31 (d, J=11.7, 2H), 4.51 (s, 2H), 7.2-7.3 (m, 4H), 7.54 (s, 2H), 7.78 (s, 1H), 8.2-8.4 (m, 3H).

Example 151N²-[2-chloro-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-(2-chloro-5-cyanophenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (460 mg, 1.15 mmol) of Example 149, step A, and the compound (362 mg, 1.92 mmol) of Reference Example 2, and according to the method of Example 1, step B, the title compound (624 mg, yield 95%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.03 (t, J=7.2, 3H), 1.39 (brs, 9H), 2.96 (s, 3H), 3.0-3.3 (m, 4H), 3.36-3.44 (m, 2H), 3.98 (s, 2H), 4.19 (d, J=11.7, 2H), 4.28 (d, J=11.7, 2H), 4.35 (s, 2H), 7.2-7.3 (m, 5H), 7.44 (d, J=8.1, 1H), 7.63 (d, J=1.5, 1H), 7.7-8.0 (broad, 1H).

Step BN²-[2-chloro-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (623 mg, 1.09 mmol) obtained in step A and according to the method of Reference Example 62, step A, the title compound (555 mg, yield 81%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.01 (t, J=7.2, 3H), 1.41 (brs, 9H), 2.64 (s, 3H), 2.94 (s, 3H), 3.0-3.3 (m, 4H), 3.37-3.44 (m, 2H), 4.02 (s, 2H), 4.21 (d, J=11.7, 2H), 4.26 (d, J=11.7, 2H), 4.36 (s, 2H), 7.2-7.3 (m, 4H), 7.45 (d, J=8.1, 1H), 7.68 (dd, J=1.5, 8.1, 1H), 7.8-8.3 (broad, 1H), 8.09 (d, J=1.5, 1H).

Step CN²-[2-chloro-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (552 mg, 0.882 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (478 mg, yield 90%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.14 (t, J=7.5, 3H), 2.67 (s, 3H), 2.8-3.0 (m, 4H), 2.90 (s, 3H), 3.2-3.4 (m, 2H), 4.04 (s, 2H), 4.16 (d, J=11.7, 2H), 4.30 (d, J=11.7, 2H), 4.51 (s, 2H), 7.23-7.31 (m, 4H), 7.54 (s, 2H), 7.78 (s, 1H), 8.33 (broad t, 1H), 8.52 (brs, 2H).

Example 152N²-{5-(tert-butoxycarbonyl)-2-chlorophenyl}-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamideStep AN-{5-(tert-butoxycarbonyl)-2-chlorophenyl}-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound (1.00 g, 2.91 mmol) of Reference Example 101 and the compound (0.81 g, 4.39 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (1.47 g, yield>100%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.57 (s, 9H), 3.04 (s, 3H), 4.08 (s, 2H), 4.22 (d, J=11.7, 2H), 4.29 (d, J=11.7, 2H), 4.44 (s, 2H), 7.19-7.29 (m, 4H), 7.39 (d, J=8.4, 1H), 7.62 (dd, J=1.8, 8.3, 1H), 7.90 (d, J=2.1, 1H).

Step BN²-{5-(tert-butoxycarbonyl)-2-chlorophenyl}-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-{(isopropyl) [(2-nitrophenyl)sulfonyl]amino}ethyl]glycinamide

Using the compound (1.47 g) obtained in step A and the compound (1.38 g, 4.80 mmol) of Reference Example 7, and according to the method of Example 1, step B, the title compound (2.00 g, yield 87%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.16 (d, J=6.6, 6H), 1.57 (s, 9H), 2.95 (s, 3H), 3.32-3.37 (m, 2H), 3.44-3.49 (m, 2H), 3.98 (s, 2H), 4.0-4.2 (m, 1H), 4.2-4.4 (m, 4H), 4.41 (s, 2H), 7.22-7.28 (m, 4H), 7.38 (d, J=8.1, 1H), 7.57-7.68 (m, 4H), 7.94-8.00 (m, 2H), 8.31 (m, 1H).

Step CN²-{5-(tert-butoxycarbonyl)-2-chlorophenyl}-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide

Using the compound (0.50 g, 0.67 mmol) obtained in step B and according to the method of Example 50, step B, the title compound (0.32 g, yield 85%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 0.98 (d, J=6.2, 6H), 1.57 (s, 9H), 2.67-2.75 (m, 3H), 2.95 (s, 3H), 3.35-3.42 (m, 2H), 3.97 (s, 2H), 4.19 (d, J=11.7, 2H), 4.26 (d, J=11.7, 2H), 4.33 (s, 2H), 7.20-7.29 (m, 4H), 7.39 (d, J=8.3, 1H), 7.60 (dd, J=1.8, 8.3, 1H), 7.95 (d, J=1.8, 1H), 8.19 (m, 1H).

Example 153N²-{2-chloro-5-[(methylamino)carbonyl]phenyl}-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamideStep AN²-(5-carboxy-2-chlorophenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-{(isopropyl)[(2-nitrophenyl)sulfonyl]amino}ethyl]glycinamide

Using the compound (1.00 g, 1.35 mmol) of Example 152, step B and according to the method of Reference Example 61, step D, the title compound (1.06 g, yield>100%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.14 (d, J=6.9, 6H), 2.98 (s, 3H), 3.32-3.37 (m, 2H), 3.47-3.54 (m, 2H), 4.02-4.12 (m, 3H), 4.21-4.29 (m, 4H), 4.45 (s, 2H), 7.21 (s, 4H), 7.42 (d, J=8.4, 1H), 7.53-7.71 (m, 4H), 7.94-7.98 (m, 1H), 8.12 (s, 1H), 8.52-8.55 (m, 1H), 10.10 (broad, 1H).

Step BN²-{2-chloro-5-[(methylamino)carbonyl]phenyl}-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-{(isopropyl)[(2-nitrophenyl)sulfonyl]amino}ethyl]glycinamide

Using the compound (0.35 g, 0.51 mmol) obtained in step A and according to the method of Example 77, step B, the title compound (0.37 g, yield>100%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.13 (d, J=6.7, 6H), 2.92 (s, 3H), 2.93 (s, 3H), 3.28-3.34 (m, 2H), 3.41-3.49 (m, 2H), 3.99-4.10 (m, 3H), 4.17-4.27 (m, 4H), 4.39 (s, 2H), 6.88-6.91 (m, 1H), 7.21-7.23 (m, 4H), 7.35-7.47 (m, 2H), 7.57-7.59 (m, 1H), 7.64-7.68 (m, 2H), 7.80-7.81 (m, 1H), 7.93-7.95 (m, 1H), 8.37 (m, 1H).

Step CN²-{2-chloro-5-[(methylamino)carbonyl]phenyl}-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide

Using the compound (0.37 g) obtained in step B and according to the method of Example 50, step B, the title compound (0.16 g, yield 61%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 0.95 (d, J=6.5, 6H), 2.63-2.74 (m, 3H), 2.92 (s, 3H), 2.94 (s, 3H), 3.34 (q, J=5.9, 2H), 4.00 (s, 2H), 4.19 (d, J=11.8, 2H), 4.25 (d, J=11.8, 2H), 4.34 (s, 2H), 7.20-7.28 (m, 5H), 7.36-7.39 (m, 1H), 7.48-7.51 (m, 1H), 7.79 (s, 1H), 8.18 (m, 1H).

Example 154N²-[5-(aminocarbonyl)-2-chlorophenyl]-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamideStep AN²-[5-(aminocarbonyl)-2-chlorophenyl]-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-{(isopropyl)[(2-nitrophenyl)sulfonyl]amino}ethyl]glycinamide

Using the compound (0.35 g, 0.51 mmol) of Example 153, step A and according to the method of Example 78, step A, the title compound (0.37 g, yield>100%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.12 (d, J=6.9, 6H), 2.94 (s, 3H), 3.29-3.34 (m, 2H), 3.42-3.49 (m, 2H), 4.00-4.10 (m, 3H), 4.18-4.27 (m, 4H), 4.40 (s, 2H), 6.42 (brs, 1H), 6.97 (brs, 1H), 7.20-7.23 (m, 4H), 7.39 (d, J=8.4, 1H), 7.49-7.68 (m, 4H), 7.93-7.97 (m, 2H), 8.36 (m, 1H).

Step BN²-[5-(aminocarbonyl)-2-chlorophenyl]-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide

Using the compound (0.37 g) obtained in step B and according to the method of Example 50, step B, the title compound (0.18 g, yield 71%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 0.96 (d, J=6.2, 6H), 2.64-2.76 (m, 3H), 2.96 (s, 3H), 3.22-3.39 (m, 2H), 4.06 (s, 2H), 4.19 (d, J=12.3, 2H), 4.26 (d, J=12.3, 2H), 4.34 (s, 2H), 6.41 (brs, 1H), 7.00 (brs, 1H), 7.20-7.28 (m, 4H), 7.39-7.55 (m, 2H), 7.91 (s, 1H), 8.16-8.19 (m, 1H).

Example 155N²-(5-chloro-2-fluorophenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-(5-chloro-2-fluorophenyl)-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound (453 mg, 1.73 mmol) of Reference Example 102 and the compound (479 mg, 2.60 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (543 mg, yield 80%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.92 (s, 3H), 4.07 (s, 2H), 4.20 (d, J=11.7, 2H), 4.31 (d, J=11.7, 2H), 4.47 (s, 2H), 6.65-6.76 (m, 2H), 7.06 (dd, J=8.7, 14.1, 1H), 7.23-7.32 (m, 4H), 12.73 (brs, 1H).

Step BN²-(5-chloro-2-fluorophenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (543 mg, 1.39 mmol) obtained in step A and the compound (422 mg, 2.09 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (815 mg, yield 99%) was obtained as a bistered amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.12 (d, J=6.3, 6H), 1.42 (s, 9H), 3.00 (s, 3H), 3.06-3.18 (m, 2H), 3.33-3.42 (m, 2H), 3.95 (s, 2H), 4.0-4.3 (m, 1H), 4.25 (d, J=11.7, 2H), 4.33 (d, J=11.7, 2H), 4.50 (s, 2H), 6.69-6.75 (m, 2H), 6.85-6.93 (m, 1H), 7.22-7.29 (m, 4H).

Step CN²-(5-chloro-2-fluorophenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (815 mg, 1.38 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (395 mg, yield 52%) was obtained as a pale-bistered amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.19 (d, J=6.3, 6H), 2.90 (t, J=6.3, 2H), 2.94 (s, 3H), 3.21-3.31 (m, 1H), 3.34-3.47 (m, 2H), 3.95 (s, 2H), 4.21 (d, J=11.4, 2H), 4.33 (d, J=11.4, 2H), 4.57 (s, 2H), 6.62 (dd, J=2.4, 8.1, 1H), 6.70-6.75 (m, 1H), 7.07 (dd, J=8.4, 14.1, 1H), 7.24-7.33 (m, 4H), 8.66 (t, J=5.7, 1H), 8.87 (brs, 2H).

Example 156N²-(5-cyano-2-fluorophenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamideStep AN-(5-cyano-2-fluorophenyl)-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound (2.04 g, 8.09 mmol) of Reference Example 103 and the compound (2.30 g, 12.5 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (1.46 g, yield 47%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.92 (s, 3H), 4.09 4.10 (2s, 2H), 4.22 (d, J=12.0, 2H), 4.30 (d, J=12.0, 2H), 4.49 (s, 2H), 7.12-7.32 (m, 7H), 12.71 (brs, 1H).

Step BN²-(5-cyano-2-fluorophenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (716 mg, 1.87 mmol) obtained in step A and the compound (588 mg, 2.91 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (1.11 g, yield>100%) was obtained as a pale-yellow amorphous solid

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.11 (d, J=6.9, 6H), 1.41 1.43 (2brs, 9H), 3.0-3.2 (m, 2H), 3.02 (s, 3H), 3.34-3.41 (m, 2H), 3.9-4.4 (broad, 1H), 3.98 3.99 (2s, 2H), 4.26 (d, J=11.7, 2H), 4.34 (d, J=11.7, 2H), 4.53 (s, 2H), 6.9-7.1 (m, 3H), 7.23-7.31 (m, 4H), 8.3-8.9 (broad, 1H).

Step CN²-(5-cyano-2-fluorophenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide

Using the compound (450 mg, 0.794 mmol) obtained in step B and according to the method of Example 46, step B, the title compound (276 mg, yield 75%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 0.98 (d, J=6.3, 6H), 2.66-2.76 (m, 3H), 3.03 (s, 3H), 3.34-3.41 (m, 2H), 4.00 (s, 2H), 4.26 (d, J=11.7, 2H), 4.35 (d, J=11.7, 2H), 4.56 4.57 (2s, 2H), 6.95-7.11 (m, 3H), 7.24-7.32 (m, 4H), 8.74 (broad t, 1H).

Example 157N²-(5-cyano-2-fluorophenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamideStep AN²-(5-cyano-2-fluorophenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (747 mg, 1.95 mmol) of Example 156, step A, and the compound (635 mg, 3.37 mmol) of Reference Example 2, and according to the method of Example 1, step B, the title compound (1.11 g, yield>100%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm 1.05 (t, J=7.2, 3H), 1.39 1.42 (2brs, 9H), 3.02 (s, 3H), 3.15 (q, J=7.2, 2H), 3.2-3.3 (m, 2H), 3.3-3.5 (m, 2H), 3.98 (s, 2H), 4.26 (d, J=11.7, 2H), 4.34 (d, J=11.7, 2H), 4.53 (s, 2H), 6.9-7.1 (m, 3H), 7.23-7.31 (m, 4H), 8.3-8.8 (broad, 1H).

Step BN²-(5-cyano-2-fluorophenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide

Using the compound (456 mg, 0.825 mmol) obtained in step A and according to the method of Example 46, step B, the title compound (280 mg, yield 75%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.03 (t, J=7.1, 3H), 2.54-2.62 (m, 2H), 2.71 (t, J=6.0, 2H), 3.03 (s, 3H), 3.35-3.42 (m, 2H), 4.00 (s, 2H), 4.26 (d, J=11.7, 2H), 4.35 (d, J=11.7, 2H), 4.56 4.57 (2s, 2H), 6.9-7.1 (m, 3H), 7.26-7.32 (m, 4H), 8.73 (broad t, 1H).

Example 158N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-fluoro-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-fluoro-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (653 mg, 1.15 mmol) of Example 156, step B and according to the method of Reference Example 62, step A, the title compound (523 mg, yield 73%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.09 (d, J=6.6, 6H), 1.42 (brs, 9H), 2.63 (s, 3H), 3.00 (s, 3H), 3.0-3.2 (m, 2H), 3.34-3.42 (m, 2H), 3.8-4.3 (broad, 1H), 4.04 (s, 2H), 4.33 (brs, 4H), 4.56 (s, 2H), 7.07 (dd, J=8.7, 13.8, 1H), 7.23-7.31 (m, 4H), 7.46-7.53 (m, 2H), 8.4-9.0 (broad, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-fluoro-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (521 mg, 0.835 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (453 mg, yield 91%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.17 (d, J=6.3, 6H), 2.66 (s, ³H), 2.8-3.0 (m, 2H), 2.96 (s, 3H), 3.1-3.3 (m, 1H), 3.3-3.5 (m, 2H), 4.02 (s, 2H), 4.25 (d, J=11.7, 2H), 4.36 (d, J=11.7, 2H), 4.64 (s, 2H), 7.19-7.38 (m, 7H), 8.4-8.9 (broad, 2H), 8.74 (t, J=5.7, 1H).

Example 159N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-fluoro-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-fluoro-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (653 mg, 1.18 mmol) of Example 157, step A and according to the method of Reference Example 62, step A, the title compound (524 mg, yield 73%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.01 (t, J=7.2, 3H), 1.41 (brs, 9H), 2.63 (s, 3H), 3.0-3.3 (m, 4H), 3.01 (s, 3H), 3.37-3.45 (m, 2H), 4.02 4.03 (2s, 2H), 4.33 (brs, 4H), 4.55 (s, 2H), 7.07 (dd, J=8.4, 13.8, 1H), 7.25-7.31 (m, 4H), 7.46-7.52 (m, 2H), 8.4-9.0 (broad, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-fluoro-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (520 mg, 0.853 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (462 mg, yield 93%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.14 (t, J=7.2, 3H), 2.66 (s, 3H), 2.8-3.0 (m, 4H), 2.96 (s, 3H), 3.35-3.42 (m, 2H), 4.02 (s, 2H), 4.25 (d, J=11.7, 2H), 4.36 (d, J=11.7, 2H), 4.65 (s, 2H), 7.18-7.39 (m, 7H), 8.5-8.8 (broad, 2H), 8.74 (t, J=5.7, 1H).

Example 160N²-biphenyl-3-yl-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-biphenyl-3-yl-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound (1.00 g, 3.51 mmol) of Reference Example 104 and the compound (0.97 g, 5.25 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (1.40 g, yield 96%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 3.08 (s, 3H), 4.20 (s, 2H), 4.38-4.45 (m, 4H), 4.67 (s, 2H), 6.53 (dd, J=2.4, 8.3, 1H), 6.73 (s, 1H), 7.04 (d, J=7.5, 1H), 7.25-7.56 (m, 10H).

Step BN²-biphenyl-3-yl-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (0.35 g, 0.84 mmol) obtained in step A and the compound (264 mg, 1.31 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (0.60 g, yield>100%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.05 (d, J=6.9, 6H), 1.41 (s, 9H), 3.02 (s, 3H), 3.0-3.2 (m, 2H), 3.32-3.40 (m, 2H), 4.04 (s, 2H), 4.29-4.38 (m, 5H), 4.57 (s, 2H), 6.52 (m, 1H), 6.70-6.72 (m, 1H), 6.97-7.01 (m, 1H), 7.23-7.44 (m, 8H), 7.52-7.56 (m, 2H), 9.40 (broad, 1H).

Step CN²-biphenyl-3-yl-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (0.60 g) obtained in step B and according to the method of Example 1, step C, the title compound (0.41 g, yield 85%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.15 (d, J=6.5, 6H), 2.86-2.89 (m, 2H), 2.97 (s, 3H), 3.20-3.25 (m, 1H), 3.34-3.42 (m, 2H), 4.06 (s, 2H), 4.31-4.41 (m, 4H), 4.72 (s, 2H), 6.48 (m, 1H), 6.63 (s, 1H), 6.93-6.96 (m, 1H), 7.24-7.58 (m, 10H), 8.85 (brs, 2H), 9.08-9.12 (m, 1H).

Example 161N²-biphenyl-2-yl-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(methylamino)ethyl]glycinamide dihydrochlorideStep AN-biphenyl-2-yl-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound (0.72 g, 2.52 mmol) of Reference Example 105 and the compound (0.77 g, 4.17 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (0.93 g, yield 89%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.82 (s, 3H), 3.79 (s, 2H), 3.86-3.90 (m, 2H), 4.00-4.04 (m, 2H), 4.12 (s, 2H), 7.00-7.05 (m, 1H), 7.13-7.36 (m, 12H).

Step BN²-biphenyl-2-yl-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(methyl)amino]ethyl}glycinamide

Using the compound (0.45 g, 1.08 mmol) obtained in step A, the compound (0.35 g, 1.66 mmol) of Reference Example 1, and triethylamine (0.25 ml, 1.8 mmol), and according to the method of Example 1, step B, the title compound (0.60 g, yield 97%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.44 (brs, 9H), 2.74 (brs, 3H), 2.82 (s, 3H), 3.24-3.34 (m, 4H), 3.72 (s, 2H), 3.85-4.12 (m, 6H), 7.02-7.04 (m, 1H), 7.15-7.43 (m, 12H), 7.85-8.11 (broad, 1H).

Step CN²-biphenyl-2-yl-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(methylamino)ethyl]glycinamide dihydrochloride

Using the compound (0.60 g, 1.05 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (0.45 g, yield 79%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.50 (s, 3H), 2.76 (s, 3H), 2.86-2.91 (m, 2H), 3.28-3.35 (m, 2H), 3.79-3.84 (m, 4H), 4.03-4.12 (m, 4H), 6.96-6.99 (m, 1H), 7.06-7.27 (m, 8H), 7.36 (t, J=7.2 2H), 7.58-7.62 (m, 2H), 8.18-8.21 (m, 1H), 8.95 (brs, 2H).

Example 162N²-biphenyl-2-yl-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN²-biphenyl-2-yl-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (0.45 g, 1.08 mmol) of Example 161, step A, and the compound (0.34 g, 1.68 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (0.65 g, yield 100%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.08 (d, J=6.9, 6H), 1.46 (s, 9H), 2.80 (s, 3H), 3.07 (brs, 2H), 3.27-3.35 (m, 2H), 3.72 (s, 2H), 3.83-3.88 (m, 2H), 4.01-4.12 (m, 4H), 4.1-4.3 (broad, 1H), 7.01 (m, 1H), 7.14-7.30 (m, 8H), 7.39-7.47 (m, 4H), 8.03 (broad, 1H).

Step BN²-biphenyl-2-yl-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (0.65 g, 1.08 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (0.59 g, yield 95%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.19 (d, J=6.4, 6H), 2.77 (s, 3H), 2.84-2.87 (brs, 2H), 3.21-3.40 (m, 3H), 3.79-3.84 (m, 4H), 4.04-4.13 (m, 4H), 6.93-6.99 (m, 1H), 7.06-7.27 (m, 8H), 7.30-7.39 (m, 2H), 7.59-7.63 (m, 2H), 8.23-8.28 (m, 1H), 8.99 (brs, 2H).

Example 163N²-(4-cyanobiphenyl-2-yl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-(4-cyanobiphenyl-2-yl)-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound (305 mg, 0.983 mmol) of Reference Example 106 and the compound (267 mg, 1.45 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (321 mg, yield 74%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.92 (s, 3H), 3.76 (s, 2H), 3.98 (d, J=11.7, 2H), 4.12 (d, J=11.7, 2H), 4.21 (s, 2H), 7.1-7.5 (m, 12H).

Step BN²-(4-cyanobiphenyl-2-yl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (295 mg, 0.670 mmol) obtained in step A and the compound (247 mg, 1.22 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (289 mg, yield 69%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.11 (d, J=6.8, 6H), 1.46 (brs, 9H), 2.86 (s, 3H), 2.9-3.2 (m, 2H), 3.26-3.33 (m, 2H), 3.69 (s, 2H), 3.8-4.3 (broad, 1H), 3.94 (d, J=11.7, 2H), 4.13 (s, 2H), 4.15 (d, J=11.7, 2H), 7.1-7.6 (m, 12H), 7.6-8.0 (broad, 1H).

Step CN²-(4-cyanobiphenyl-2-yl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (282 mg, 0.451 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (264 mg, yield 98%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.19 (d, J=6.3, 2H), 2.77 (s, 3H), 2.8-3.0 (m, 2H), 3.1-3.4 (m, 3H), 3.82 (d, J=11.7, 2H), 3.86 (s, 2H), 4.04 (s, 2H), 4.10 (d, J=11.7, 2H), 7.23 (broad, 4H), 7.25-7.43 (m, 5H), 7.46 (s, 1H), 7.68 (d, J=7.5, 2H), 8.21 (t, J=5.7, 1H), 8.66 (brs, 2H). H

Example 164N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-1-naphthyl-N¹-[2-(isopropylamino)ethyl]glycinamideStep AN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-1-naphthylglycine

Using the compound (1.00 g, 3.86 mmol) of Reference Example 107 and the compound (927 mg, 5.02 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (1.35 g, yield 90%) was obtained as a pale-bistered amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 3.07 (s, 3H), 4.08 (d, J=11.6, 2H), 4.10 (s, 2H), 4.24 (d, J=11.2, 2H), 4.43 (s, 2H), 7.10-7.25 (m, 4H), 7.30-7.55 (m, 4H), 7.66 (d, J=7.7, 1H), 7.86 (d, J=7.3, 1H), 8.04 (d, J=8.7, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-1-naphthyl-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (600 mg, 1.54 mmol) obtained in step A and the compound (469 mg, 2.32 mmol) of Reference Example 17, and according to the method of Example 1, step B, the title compound (797 mg, yield 90%) was obtained as a pale-bistered amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 0.99 (d, J=6.3, 6H), 1.38 (s, 9H), 2.70-3.20 (m, 5H), 3.20-3.40 (m, 2H), 3.95-4.25 (m, 7H), 4.33 (s, 2H), 7.10-7.25 (m, 4H), 7.35-7.60 (m, 5H), 7.83 (d, J=7.5, 1H), 8.00 (broad t, 1H), 8.20 (d, J=7.8, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-1-naphthyl-N¹-[2-(isopropylamino)ethyl]glycinamide

Using the compound (797 mg, 1.39 mmol) obtained in step B and according to the method of Example 46, step B, the title compound (627 mg, yield 95%) was obtained as a bistered oil.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 0.79 (d, J=6.3, 6H), 2.45-2.55 (m, 3H), 3.00 (s, 3H), 3.30 (q, J=5.8, 2H), 4.03 (d, J=11.0, 2H), 4.04 (s, 2H), 4.21 (d, J=11.2, 2H), 4.32 (s, 2H), 7.10-7.25 (m, 4H), 7.35-7.60 (m, 5H), 7.80-7.85 (m, 1H), 8.10 (broad t, 1H), 8.19 (d, J=7.1, 1H).

Example 165N²-(4-chloro-1-naphthyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-(4-chloro-1-naphthyl)-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound (500 mg, 1.70 mmol) of Reference Example 108 and the compound (408 mg, 2.21 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (730 mg, yield>100%) was obtained as a yellow amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 3.07 (s, 3H), 4.07 (d, J=11.4, 2H), 4.08 (s, 2H), 4.23 (d, J=11.4, 2H), 4.41 (s, 2H), 7.10-7.25 (m, 4H), 7.40 (d, J=7.8, 1H), 7.48 (d, J=8.1, 1H), 7.60-7.70 (m, 2H), 8.05-8.10 (m, 1H), 8.25-8.30 (m, 1H).

Step BN²-(4-chloro-1-naphthyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (730 mg) obtained in step A and the compound (516 mg, 2.55 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (850 mg, yield 82%) was obtained as a yellow amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.01 (d, J=4.8, 6H), 1.38 (s, 9H), 2.70-3.20 (m, 5H), 3.20-3.40 (m, 2H), 4.00-4.20 (m, 7H), 4.32 (s, 2H), 7.10-7.25 (m, 4H), 7.35 (d, J=7.8, 1H), 7.47 (d, J=8.1, 1H), 7.50-7.65 (m, 2H), 7.95 (broad t, 1H), 8.25-8.30 (m, 2H).

Step CN²-(4-chloro-1-naphthyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (850 mg, 1.40 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (731 mg, yield 90%) was obtained as a bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.18 (d, J=6.3, 6H), 2.80-2.90 (m, 2H), 2.88 (s, 3H), 3.20-3.30 (m, 1H), 3.37-3.44 (m, 2H), 4.01 (d, J=11.7, 2H), 4.06 (s, 2H), 4.21 (d, J=11.7, 2H), 4.46 (s, 2H), 7.30 (d, J=8.1, 1H), 7.54-7.70 (m, 3H), 8.13 (d, J=7.8, 1H), 8.36 (d, J=8.1, 1H), 8.42 (broad t, 1H), 9.05 (brs, 2H).

Example 166N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3-methoxy-2-naphthyl)-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-(3-methoxy-2-naphthyl)glycine

Using the compound (480 mg, 1.66 mmol) of Reference Example 109 and the compound (435 mg, 2.36 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (555 mg, yield 80%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 3.05 (s, 3H), 3.92 (s, 3H), 4.06 (s, 2H), 4.26 (d, J=11.7, 2H), 4.33 (d, J=11.7, 2H), 4.52 (s, 2H), 7.12 (s, 1H), 7.2-7.4 (m, 7H), 7.6-7.7 (m, 2H), 13.2 (brs, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3-methoxy-2-naphthyl)-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (546 mg, 1.30 mmol) obtained in step A and the compound (344 mg, 1.70 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (694 mg, yield 88%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.05 (d, J=6.6, 6H), 1.42 (brs, 9H), 2.97 (s, 3H), 3.0-3.2 (m, 2H), 3.32-3.40 (m, 2H), 3.9-4.4 (broad, 1H), 3.91 (s, 3H), 4.01 (s, 2H), 4.19 (d, J=11.7, 2H), 4.30 (d, J=11.7, 2H), 4.40 (s, 2H), 7.09 (s, 1H), 7.22-7.33 (m, 6H), 7.36 (s, 1H), 7.62-7.67 (m, 2H), 8.2-8.7 (broad, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3-methoxy-2-naphthyl)-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (686 mg, 1.14 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (624 mg, yield 95%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.16 (d, J=6.3, 6H), 2.8-3.0 (m, 2H), 2.95 (s, 3H), 3.1-3.3 (m, 1H), 3.3-3.5 (m, 2H), 3.84 (s, 3H), 3.98 (s, 2H), 4.23 (d, J=11.7, 2H), 4.36 (d, J=11.7, 2H), 4.55 (s, 2H), 7.00 (s, 1H), 7.23-7.34 (m, 7H), 7.6-7.7 (m, 2H), 8.59 (t, J=5.7, 1H), 8.74 (brs, 2H).

Example 167N²-(3-methoxy-2-naphthyl)-N²-[2-{methyl[4-(methylsulfonyl)piperazin-1-yl]amino}-2-oxoethyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN²-(3-methoxy-2-naphthyl)-N²-[2-{methyl[4-(methylsulfonyl)piperazin-1-yl]amino}-2-oxoethyl]-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (379 mg, 1.31 mmol) of Reference Example 109, the compound (253 mg, 1.31 mmol) of Reference Example 48 and compound (359 mg, 1.77 mmol) of Reference Example 3, and according to the methods of Example 4, step A, and Example 1, step B, the title compound (425 mg, yield 50%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.06 (broad d, 6H), 1.42 (brs, 9H), 2.7-2.9 (m, 2H), 2.81 (s, 3H), 2.9-3.2 (m, 6H), 2.96 (s, 3H), 3.3-3.4 (m, 2H), 3.7-3.9 (m, 2H), 3.9-4.3 (broad, 1H), 3.92 (s, 3H), 4.00 (s, 2H), 4.30 (s, 2H), 7.11 (s, 1H), 7.28-7.32 (m, 3H), 7.6-7.7 (m, 2H), 7.9-8.4 (broad, 1H).

Step BN²-(3-methoxy-2-naphthyl)-N²-[2-{methyl[4-(methylsulfonyl)piperazin-1-yl]amino}-2-oxoethyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (420 mg, 0.647 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (371 mg, yield 92%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.18 (d, J=6.5, 6H), 2.8-3.0 (m, 14H), 3.1-3.3 (m, 1H), 3.3-3.5 (m, 2H), 3.5-3.6 (m, 2H), 3.83 (s, 3H), 3.98 (s, 2H), 4.53 (s, 2H), 7.01 (s, 1H), 7.2-7.3 (m, 3H), 7.5-7.7 (m, 2H), 8.62 (t, J=5.7, 1H), 8.86 (brs, 2H).

Example 168N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(5,6,7,8-tetrahydronaphthalen-1-yl)-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-(5,6,7,8-tetrahydronaphthalen-1-yl)glycine

Using the compound (500 mg, 1.90 mmol) of Reference Example 110 and the compound (456 mg, 2.47 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (660 mg, yield 88%) was obtained as a pale-yellow amorphous solid

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.70-1.85 (m, 4H), 2.65-2.80 (m, 4H), 3.04 (s, 3H), 3.85 (s, 2H), 4.15 (d, J=11.6, 2H), 4.23 (s, 2H), 4.26 (d, J=11.6, 2H), 6.91 (d, J=7.2, 1H), 7.03 (d, J=7.8, 1H), 7.09 (d, J=8.1, 1H), 7.15-7.25 (m, 4H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(5,6,7,8-tetrahydronaphthalen-1-yl) [(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (660 mg, 1.68 mmol) obtained in step A and the compound (509 mg, 2.52 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (672 mg, yield 69%) was obtained as a yellow amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.10 (d, J=6.6, 6H), 1.39 (s, 9H), 1.65-1.85 (m, 4H), 2.65-2.80 (m, 4H), 2.94 (s, 3H), 3.00-3.20 (m, 2H), 3.33-3.41 (m, 2H), 3.78 (s, 2H), 4.04 (d, J=11.7, 2H), 4.13 (s, 2H), 4.20 (d, J=11.7, 2H), 4.20-4.30 (m, 1H), 6.85 (d, J=7.2, 1H), 7.04 (t, J=7.5, 1H), 7.12 (d, J=7.5, 1H), 7.20-7.35 (m, 4H), 8.30 (brs, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(5,6,7,8-tetrahydronaphthalen-1-yl)-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (650 mg, 1.13 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (628 mg, yield 100%) was obtained as a pale-gray solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.04 (d, J=6.1, 6H), 1.60-1.70 (m, 4H), 2.65-2.75 (m, 4H), 2.80-2.90 (m, 2H), 2.87 (s, 3H), 3.20-3.30 (m, 1H), 3.39 (q, J=6.0, 2H), 3.87 (s, 2H), 4.01 (d, J=11.6, 2H), 4.21 (d, J=11.6, 2H), 4.27 (s, 2H), 6.79 (d, J=6.9, 1H), 6.95-7.10 (m, 2H), 7.25 (brs, 4H), 8.38 (t, J=5.6, 1H), 8.88 (brs, 2H).

The compounds of Examples 145-168 are shown below.

TABLE 13StructuralLC-MSExampleFormulaTMW(found)145 [Image Omitted]

504.45504 146 [Image Omitted]

537.31464 147 [Image Omitted]

565.36492 148 [Image Omitted]

565.36492 149 [Image Omitted]

555.93483 150 [Image Omitted]

612.98540 151 [Image Omitted]

598.95526 152 [Image Omitted]

558.11558 153 [Image Omitted]

515.05515 154 [Image Omitted]

501.02501 155 [Image Omitted]

548.91476 156 [Image Omitted]

466.55467 157 [Image Omitted]

452.52453 158 [Image Omitted]

596.52524 159 [Image Omitted]

582.50510 160 [Image Omitted]

572.57500 161 [Image Omitted]

544.52472 162 [Image Omitted]

572.57500 163 [Image Omitted]

597.58525 164 [Image Omitted]

473.61474 165 [Image Omitted]

580.98508 166 [Image Omitted]

576.56504 167 [Image Omitted]

621.62549 168 [Image Omitted]

550.56478

Example 169N²-(2,3-dihydro-1H-inden-4-yl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-(2,3-dihydro-1H-inden-4-yl)-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound (500 mg, 2.01 mmol) of Reference Example 111 and the compound (483 mg, 2.61 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (680 mg, yield 89%) was obtained as a pale-yellow amorphous solid

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.04 (quintet, J=7.5, 2H), 2.87 (t, J=7.5, 2H), 2.90 (t, J=7.5, 2H), 3.07 (s, 3H), 4.04 (s, 2H), 4.23 (d, J=11.7, 2H), 4.33 (d, J=11.7, 2H), 4.58 (s, 2H), 6.73 (d, J=7.8, 1H), 6.88 (d, J=7.2, 1H), 7.05 (d, J=7.7, 1H), 7.20-7.35 (m, 4H).

Step BN²-(2,3-dihydro-1H-inden-4-yl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (680 mg, 1.79 mmol) obtained in step A and the compound (544 mg, 2.69 mmol) of Reference Example 3, and according to the method of Example 1, step B, Example 1, step C, the title compound (777 mg, yield 81%) was obtained as a pale-bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.19 (d, J=6.5, 6H), 1.91 (quintet, J=7.1, 2H), 2.76 (t, J=7.3, 2H), 2.80-2.90 (m, 4H), 2.93 (s, 3H), 3.20-3.30 (m, 1H), 3.38-3.45 (m, 2H), 3.95 (s, 2H), 4.18 (d, J=11.6, 2H), 4.31 (d, J=11.6, 2H), 4.47 (s, 2H), 6.47 (d, J=8.1, 1H), 6.72 (d, J=7.3, 1H), 6.96 (t, J=7.7, 1H), 7.25-7.35 (m, 4H), 8.58 (t, J=5.7, 1H), 8.92 (brs, 2H).

Example 170N²-(5-cyano-2,3-dihydro-1-benzofuran-7-yl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-(5-cyano-2,3-dihydro-1-benzofuran-7-yl)-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound (938 mg, 3.40 mmol) of Reference Example 112 and the compound (942 mg, 5.10 mmol) of Reference Example 17, and according to the method of Example 4, step A, the title compound (1.05 g, yield 76%) was obtained as a pale-bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.91 (s, 3H), 3.13 (t, J=8.7, 2H), 4.12 (s, 2H), 4.18 (d, J=11.7, 2H), 4.30 (d, J=11.7, 2H), 4.51-4.59 (m, 2H), 4.52 (s, 2H), 6.71 (d, J=1.0, 1H), 7.08 (s, 1H), 7.22-7.32 (m, 4H), 12.66 (brs, 1H).

Step BN²-(5-cyano-2,3-dihydro-1-benzofuran-7-yl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (500 mg, 1.23 mmol) obtained in step A and the compound (373 mg, 1.85 mmol) of Reference Example 3, and according to the method of Example 1, step C, the title compound (726 mg, yield 100%) was obtained as a bistered solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.13 (d, J=6.0, 6H), 1.42 (brs, 9H), 3.00 (s, 3H), 3.01-3.25 (m, 2H), 3.18 (t, J=8.9, 2H), 3.34-3.41 (m, 2H), 3.60-3.69 (m, 1H), 3.99 (s, 2H), 4.25 (d, J=11.7, 2H), 4.34 (d, J=11.7, 2H), 4.53 (s, 2H), 4.57 (t, J=9.0, 2H), 6.68 (d, J=1.0, 1H), 6.99 (s, 1H), 7.22-7.32 (m, 4H), 8.21-8.84 (broad, 1H).

Step CN²-(5-cyano-2,3-dihydro-1-benzofuran-7-yl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (225 mg, 0.38 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (200 mg, yield 94%) was obtained as a bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.20 (d, J=6.3, 6H), 2.86-2.94 (m, 2H), 2.93 (s, 3H), 3.15 (t, J=8.7, 2H), 3.20-3.35 (m, 1H), 3.36-3.48 (m, 2H), 3.97 (s, 2H), 4.20 (d, J=11.7, 2H), 4.32 (d, J=11.7, 2H), 4.55 (t, J=8.7, 2H), 4.63 (s, 2H), 6.64 (s, 1H), 7.09 (s, 1H), 7.23-7.34 (m, 4H), 8.68 (t, J=5.7, 1H), 8.92 (brs, 2H).

Example 171N²-(5-cyano-2,3-dihydro-1-benzofuran-7-yl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-(5-cyano-2,3-dihydro-1-benzofuran-7-yl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (550 mg, 1.35 mmol) of Example 170, step A, and the compound (382 mg, 2.03 mmol) of Reference Example 2, and according to the method of Example 1, step B, the title compound (693 mg, yield 89%) was obtained as a pale-bistered solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.05 (t, J=7.0, 3H), 1.41 (s, 9H), 3.00 (s, 3H), 3.11-3.28 (m, 6H), 3.35-3.41 (m, 2H), 3.99 (s, 2H), 4.26 (d, J=11.7, 2H), 4.34 (d, J=11.7, 2H), 4.53 (s, 2H), 4.57 (t, J=8.9, 2H), 6.67 (s, 1H), 6.99 (s, 1H), 7.22-7.32 (m, 4H), 8.40-8.89 (broad, 1H).

Step BN²-(5-cyano-2,3-dihydro-1-benzofuran-7-yl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (192 mg, 0.33 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (170 mg, yield 94%) was obtained as a bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.17 (t, J=7.2, 3H), 2.79-3.00 (m, 4H), 2.92 (s, 3H), 3.14 (t, J=8.7, 2H), 3.34-3.47 (m, 2H), 3.97 (s, 2H), 4.20 (d, J=11.7, 2H), 4.32 (d, J=11.6, 2H), 4.55 (t, J=8.7, 2H), 4.65 (s, 2H), 6.63 (d, J=1.0, 1H), 7.09 (s, 1H), 7.23-7.33 (m, 4H), 8.68 (t, J=5.7, 1H), 8.96 (brs, 2H).

Example 172N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[5-(5-methyl-1,2,4-oxadiazol-3-yl)-2,3-dihydro-1-benzofuran-7-yl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (500 mg, 0.85 mmol) of Example 170, step B and according to the methods of Reference Example 62, step A, and Example 1, step C, the title compound (266 mg, yield 51%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.16 (d, J=6.5, 6H), 2.63 (s, 3H), 2.80-2.93 (m, 2H), 2.94 (s, 3H), 3.14-3.28 (m, 1H), 3.18 (t, J=9.1, 2H), 3.34-3.40 (m, 2H), 4.00 (s, 2H), 4.23 (d, J=11.8, 2H), 4.35 (d, J=11.8, 2H), 4.54 (t, J=8.6, 2H), 4.68 (s, 2H), 6.97 (d, J=1.1, 1H), 7.24-7.35 (m, 5H), 8.64 (brs, 2H), 8.80-8.85 (m, 1H).

Example 173N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[5-(5-methyl-1,2,4-oxadiazol-3-yl)-2,3-dihydro-1-benzofuran-7-yl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (500 mg, 0.87 mmol) of Example 171, step A and according to the methods of Reference Example 62, step A, and Example 1, step C, the title compound (191 mg, yield 36%) was obtained as a pale-bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.14 (t, J=6.9, 3H), 2.63 (s, 3H), 2.79-3.00 (m, 4H), 2.94 (s, 3H), 3.18 (t, J=8.7, 2H), 3.33-3.41 (m, 2H), 4.00 (s, 2H), 4.24 (d, J=11.7, 2H), 4.36 (d, J=11.7, 2H), 4.54 (t, J=8.7, 2H), 4.69 (s, 2H), 6.98 (s, 1H), 7.24-7.35 (m, 5H), 8.61-8.85 (m, 3H).

Example 174N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(1,7-dimethyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-yl)-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-(1,7-dimethyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-yl)glycine

Using the compound (1.05 g, 3.43 mmol) of Reference Example 113 and the compound (950 mg, 5.15 mmol) of Reference Example 17, and according to the method of Example 4, step A, the title compound (1.20 g, yield 80%) was obtained as a bistered amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.24 (s, 3H), 2.41-2.52 (m, 2H), 2.69-2.78 (m, 2H), 2.88 (s, 3H), 3.20 (s, 3H), 3.92 (s, 2H), 4.09 (d, J=11.7, 2H), 4.21 (s, 2H), 4.24 (d, J=11.7, 2H), 6.85 (s, 1H), 7.02 (s, 1H), 7.21-7.30 (m, 4H), 12.49 (brs, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(1,7-dimethyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-yl)-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (600 mg, 1.37 mmol) obtained in step A and the compound (417 mg, 2.06 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (723 mg, yield 85%) was obtained as a bistered amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.03 (d, J=6.6, 6H), 1.38 (s, 9H), 2.71 (s, 3H), 2.43-2.50 (m, 2H), 2.70-2.78 (m, 2H), 2.88 (s, 3H), 2.96-3.10 (m, 2H), 3.12-3.21 (m, 2H), 3.20 (s, 3H), 3.71 (s, 2H), 4.06 (d, J=11.7, 2H), 4.17 (s, 2H), 4.24 (d, J=11.7, 2H), 6.86 (s, 1H), 7.07 (s, 1H), 7.20-7.29 (m, 4H), 8.18-8.23 (m, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(1,7-dimethyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-yl)-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (723 mg, 1.17 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (610 mg, yield 88%) was obtained as a pale-bistered amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.21 (d, J=6.6, 6H), 2.32 (s, 3H), 2.44-2.51 (m, 2H), 2.72-2.79 (m, 2H), 2.79-2.95 (m, 2H), 2.88 (s, 3H), 3.16-3.28 (m, 1H), 3.21 (s, 3H), 3.34-3.35 (m, 2H), 3.88 (s, 2H), 4.10 (d, J=11.7, 2H), 4.24 (d, J=11.7, 2H), 4.32 (s, 2H), 6.88 (s, 1H), 7.16 (s, 1H), 7.21-7.30 (m, 4H), 8.48-8.54 (m, 1H), 9.02 (brs, 2H).

Example 175N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(1,7-dimethyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-yl)-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(1,7-dimethyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-yl)-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (600 mg, 1.37 mmol) of Example 174, step A, and the compound (387 mg, 2.06 mmol) of Reference Example 2, and according to the method of Example 1, step B, the title compound (741 mg, yield 89%) was obtained as a bistered amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 0.96 (t, J=6.8, 3H), 1.36 (s, 9H), 2.26 (s, 3H), 2.42-2.51 (m, 2H), 2.69-2.78 (m, 2H), 2.87 (s, 3H), 3.01-3.28 (m, 6H), 3.20 (s, 3H), 3.71 (s, 2H), 4.06 (d, J=11.7, 2H), 4.16 (s, 2H), 4.24 (d, J=11.7, 2H), 6.85 (s, 1H), 7.07 (s, 1H), 7.19-7.30 (m, 4H), 8.14-8.19 (m, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(1,7-dimethyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-yl)-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (741 mg, 1.22 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (610 mg, yield 86%) was obtained as a pale-bistered amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.18 (t, J=7.2, 3H), 2.32 (s, 3H), 2.44-2.51 (m, 2H), 2.72-2.80 (m, 2H), 2.84-3.00 (m, 4H), 2.88 (s, 3H), 3.21 (s, 3H), 3.35-3.42 (m, 2H), 3.89 (s, 2H), 4.10 (d, J=11.7, 2H), 4.25 (d, J=11.7, 2H), 4.34 (s, 2H), 6.88 (s, 1H), 7.17 (s, 1H), 7.21-7.30 (m, 4H), 8.52 (t, J=5.7, 1H), 9.04 (brs, 2H).

Example 176N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(1-ethyl-7-methyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-yl)-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochlorideStep AN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-(1-ethyl-7-methyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-yl)glycine

Using the compound (1.00 g, 3.12 mmol) of Reference Example 114 and the compound (864 mg, 4.68 mmol) of Reference Example 17, and according to the method of Example 4, step A, the title compound (1.14 g, yield 81%) was obtained as a pale-bistered amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.11 (t, J=6.9, 3H), 2.25 (s, 3H), 2.42-2.53 (m, 2H), 2.68-2.74 (m, 2H), 2.88 (s, 3H), 3.81-3.90 (m, 2H), 3.92 (s, 2H), 4.09 (d, J=11.7, 2H), 4.21 (s, 2H), 4.24 (d, J=12.0, 2H), 6.87 (s, 1H), 7.01 (s, 1H), 7.21-7.32 (m, 4H), 12.21-12.80 (broad, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(1-ethyl-7-methyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-yl)-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (570 mg, 1.27 mmol) obtained in step A and the compound (385 mg, 1.91 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (724 mg, yield 90%) was obtained as a pale-yellow amorphous solid

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.02 (d, J=6.0, 6H), 1.10 (t, J=6.9, 3H), 1.38 (s, 9H), 2.27 (s, 3H), 2.41-2.48 (m, 2H), 2.68-2.75 (m, 2H), 2.70 (s, 3H), 2.70-3.08 (m, 2H), 3.12-3.19 (m, 2H), 3.72 (s, 2H), 3.81-3.88 (m, 2H), 4.00-4.10 (m, 3H), 4.24 (d, J=11.7, 2H), 6.89 (s, 1H), 7.06 (s, 1H), 7.22-7.29 (m, 4H), 8.17-8.21 (m, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(1-ethyl-7-methyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-yl)-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochloride

Using the compound (724 mg, 1.14 mmol) obtained in step B and according to the method of Example 57, step B, the title compound (633 mg, yield 99%) was obtained as a pale-bistered amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.11 (t, J=6.9, 3H), 1.19 (d, J=6.6, 6H), 2.28 (s, 3H), 2.42-2.50 (m, 2H), 2.72-2.75 (m, 2H), 2.87-2.95 (m, 2H), 2.88 (s, 3H), 3.20-3.45 (m, 3H), 3.79 (s, 2H), 3.80-3.90 (m, 2H), 4.07 (d, J=11.7, 2H), 4.20 (s, 2H), 4.24 (d, J=11.7, 2H), 6.88 (s, 1H), 7.06 (s, 1H), 7.25 (s, 4H), 8.41 (t, J=5.7, 1H), 8.75 (brs, 2H).

Example 177N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(1-ethyl-7-methyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-yl)-N¹-[2-(ethylamino)ethyl]glycinamide hydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(1-ethyl-7-methyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-yl)-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (570 mg, 1.27 mmol) of Example 176, step A, and the compound (359 mg, 1.91 mmol) of Reference Example 2, and according to the method of Example 1, step B, the title compound (680 mg, yield 86%) was obtained as a bistered amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 0.95 (t, J=5.8, 3H), 1.10 (t, J=7.1, 3H), 1.36 (s, 9H), 2.27 (s, 3H), 2.41-2.50 (m, 2H), 2.69-2.73 (m, 2H), 2.88 (s, 3H), 3.00-3.25 (m, 6H), 3.17 (s, 2H), 3.81-3.89 (m, 2H), 4.07 (d, J=11.7, 2H), 4.16 (s, 2H), 4.24 (d, J=11.7, 2H), 6.88 (s, 1H), 7.06 (s, 1H), 7.21-7.29 (m, 4H), 8.15-8.19 (m, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(1-ethyl-7-methyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-yl)-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (680 mg, 1.10 mmol) obtained in step A and according to the method of Example 57, step B, the title compound (602 mg, yield 100%) was obtained as a pale-bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.08-1.20 (m, 6H), 2.28 (s, 3H), 2.41-2.50 (m, 2H), 2.69-2.76 (m, 2H), 2.84-2.93 (m, 2H), 2.88 (s, 3H), 3.21-3.42 (m, 2H), 3.79 (s, 2H), 3.81-3.87 (m, 2H), 4.07 (d, J=11.7, 2H), 4.20 (s, 2H), 4.24 (d, J=11.7, 2H), 6.88 (s, 1H), 7.06 (s, 1H), 7.21-7.30 (m, 4H), 8.40 (t, J=6.0, 1H), 8.72 (brs, 2H).

Example 178N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-phenyl-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochlorideStep AN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-phenylglycine

Using N-phenyliminodiacetic acid (1.00 g, 4.78 mmol) and the compound (1.32 g, 7.17 mmol) of Reference Example 17, and according to the method of Example 4, step A, the title compound (990 mg, yield 61%) was obtained as a pale-gray solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.97 (s, 3H), 4.11 (s, 2H), 4.31 (d, J=12.0, 2H), 4.37 (d, J=12.0, 2H), 4.56 (s, 2H), 6.48 (d, J=8.4, 2H), 6.67 (t, J=7.2, 1H), 7.13-7.21 (m, 2H), 7.24-7.35 (m, 4H), 13.14 (brs, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-phenyl-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (495 mg, 1.46 mmol) obtained in step A and the compound (443 mg, 2.19 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (744 mg, yield 97%) was obtained as a bistered amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.01 (d, J=6.0, 6H), 1.37 (s, 9H), 2.88-3.02 (m, 2H), 2.97 (s, 3H), 3.00-3.15 (m, 2H), 3.91 (s, 2H), 3.98-4.08 (m, 1H), 4.31 (d, J=11.7, 2H), 4.38 (d, J=11.7, 2H), 4.59 (s, 2H), 6.41 (d, J=8.4, 2H), 6.66 (t, J=7.2, 1H), 7.17 (t, J=7.8, 2H), 7.24-7.35 (m, 4H), 8.95-9.03 (broad, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-phenyl-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochloride

Using the compound (744 mg, 1.42 mmol) obtained in step B and according to the method of Example 57, step B, the title compound (421 mg, yield 64%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.18 (d, J=6.3, 6H), 2.87 (t, J=6.3, 2H), 2.97 (s, 3H), 3.16-3.40 (m, 3H), 3.97 (s, 2H), 4.29-4.41 (m, 4H), 4.63 (s, 2H), 6.44 (d, J=8.4, 2H), 6.67 (t, J=7.5, 1H), 7.17 (t, J=7.8, 2H), 7.24-7.35 (m, 4H), 8.72 (brs, 2H), 9.05 (t, J=5.4, 1H).

Example 179N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-phenyl-N¹-[2-(ethylamino)ethyl]glycinamide hydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-phenyl-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (495 mg, 1.46 mmol) of Example 178, step A, and the compound (412.0 mg, 2.19 mmol) of Reference Example 2, and according to the method of Example 1, step B, the title compound (724 mg, yield 97%) was obtained as a pale-bistered amorphous solid.

35 ¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 0.91 (t, J=7.2, 3H), 1.36 (s, 9H), 2.88-3.24 (m, 6H), 2.98 (s, 3H), 3.91 (s, 2H), 4.31 (d, J=12.0, 2H), 4.37 (d, J=12.0, 2H), 4.59 (s, 2H), 6.39 (d, J=8.4, 2H), 6.66 (t, J=7.2, 1H), 7.16 (t, J=8.1, 2H), 7.24-7.35 (m, 4H), 8.93-9.05 (broad, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-phenyl-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (724 mg, 1.42 mmol) obtained in step A and according to the method of Example 57, step B, the title compound (464 mg, yield 73%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.14 (t, J=7.2, 3H), 2.82-2.96 (m, 4H), 2.97 (s, 3H), 3.31-3.38 (m, 2H), 3.97 (s, 2H), 4.29-4.42 (m, 4H), 4.64 (s, 2H), 6.43 (d, J=8.2, 2H), 6.67 (t, J=7.2, 1H), 7.17 (t, J=7.7, 2H), 7.24-7.36 (m, 4H), 8.70 (brs, 2H), 9.07 (t, J=5.5, 1H).

Example 180N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3,6-dimethyl-1,2-benzisoxazol-5-yl)-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-(3,6-dimethyl-1,2-benzisoxazol-5-yl)glycine

Using the compound (958 mg, 3.44 mmol) of Reference Example 116 and the compound (983 mg, 5.32 mmol) of Reference Example 17, and according to the method of Example 4, step A, the title compound (1.00 g, yield 71%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.42 (s, 3H), 2.47 (s, 3H), 2.86 (s, 3H), 3.99 (s, 2H), 4.09 (d, J=11.7, 2H), 4.23 (d, J=11.7, 2H), 4.27 (s, 2H), 7.25 (broad, 4H), 7.46 (s, 1H), 7.60 (s, 1H), 12.44 (brs, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3,6-dimethyl-1,2-benzisoxazol-5-yl)-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (0.50 g, 1.22 mmol) obtained in step A and the compound (0.38 g, 1.88 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (0.88 g, yield>100%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.10 (d, J=6.8, 6H), 1.44-1.49 (brs, 9H), 2.49 (s, 6H), 2.96 (s, 3H), 3.16 (brs, 2H), 3.29-3.44 (m, 2H), 3.87 (s, 2H), 4.03-4.25 (m, 7H), 7.17-7.28 (m, 4H), 7.34 (s, 1H), 7.59 (s, 1H), 8.1-8.5 (broad, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3,6-dimethyl-1,2-benzisoxazol-5-yl)-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (0.88 g) obtained in step B and according to the method of Example 1, step C, the title compound (0.74 g, yield 93%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.18 (d, J=6.3, 6H), 2.45 (s, 3H), 2.47 (s, 3H), 2.8-3.0 (m, 5H), 3.20-3.42 (m, 3H), 3.87 (s, 2H), 4.08 (d, J=11.7, 2H), 4.23 (d, J=11.7, 2H), 4.30 (s, 2H), 7.25 (broad, 4H), 7.47 (s, 1H), 7.67 (s, 1H), 8.42 (t, J=5.7, 1H), 8.92 (brs, 2H).

Example 181N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3,6-dimethyl-1,2-benzisoxazol-5-yl)-N¹-[2-(ethylamino)ethyl]glycinamide hydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3,6-dimethyl-1,2-benzisoxazol-5-yl)-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (1.26 g, 3.08 mmol) of Example 180, step A, and the compound (843 mg, 4.48 mmol) of Reference Example 2, and according to the method of Example 1, step B, the title compound (1.30 g, yield 73%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.03 (t, J=7.2, 3H), 1.42 (brs, 9H), 2.49 (s, 3H), 2.51 (s, 3H), 2.95 (s, 3H), 3.0-3.2 (m, 2H), 3.2-3.3 (m, 2H), 3.38-3.45 (m, 2H), 3.85 (s, 2H), 4.05 (d, J=11.4, 2H), 4.18 (s, 2H), 4.22 (d, J=11.4, 2H), 7.17-7.28 (m, 4H), 7.36 (s, 1H), 7.58 (s, 1H), 8.1-8.5 (broad, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3,6-dimethyl-1,2-benzisoxazol-5-yl)-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (1.26 g, 2.18 mmol) obtained in step A and according to the method of Example 57, step B, the title compound (839 mg, yield 75%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.14 (t, J=7.2, 3H), 2.45 (s, 3H), 2.47 (s, 3H), 2.8-3.0 (m, 4H), 2.87 (s, 3H), 3.0-3.4 (m, 2H), 3.86 (s, 2H), 4.07 (d, J=11.7, 2H), 4.23 (d, J=11.7, 2H), 4.27 (s, 2H), 7.25 (broad, 4H), 7.48 (s, 1H), 7.66 (s, 1H), 8.36 (t, J=5.7, 1H), 8.58 (brs, 2H).

Example 182N²-(3,6-dimethyl-1,2-benzisoxazol-5-yl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-(3,6-dimethyl-1,2-benzisoxazol-5-yl)-N-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}glycine

Using the compound (893 mg, 3.21 mmol) of Reference Example 116 and the compound (743 mg, 3.67 mmol) of Reference Example 19, and according to the method of Example 4, step A, the title compound (1.21 g, yield 88%) was obtained as a pale-yellow amorphous solid

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.42 (s, 3H), 2.47 (s, 3H), 2.86 (s, 3H), 3.99 (s, 2H), 4.0-4.2 (m, 4H), 4.26 (s, 2H), 7.03-7.15 (m, 2H), 7.26-7.31 (m, 1H), 7.46 (s, 1H), 7.60 (s, 1H), 12.42 (brs, 1H).

Step BN²-(3,6-dimethyl-1,2-benzisoxazol-5-yl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (580 mg, 1.36 mmol) obtained in step A and the compound (390 mg, 1.93 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (746 mg, yield 90%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.10 (d, J=6.6, 6H), 1.44 (brs, 9H), 2.50 (s, 3H), 2.51 (s, 3H), 2.94 (s, 3H), 3.0-3.2 (m, 2H), 3.35-3.43 (m, 2H), 3.88 (s, 2H), 3.9-4.3 (m, 5H), 4.16 (s, 2H), 6.89-6.99 (m, 2H), 7.11-7.16 (m, 1H), 7.36 (s, 1H), 7.58 (s, 1H), 7.9-8.5 (broad, 1H).

Step CN²-(3,6-dimethyl-1,2-benzisoxazol-5-yl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (730 mg, 1.20 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (696 mg, yield 99%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.18 (d, J=6.6, 6H), 2.45 (s, 3H), 2.47 (s, 3H), 2.8-3.0 (m, 2H), 2.86 (s, 3H), 3.1-3.3 (m, 1H), 3.34-3.57 (m, 2H), 3.86 (s, 2H), 4.0-4.3 (m, 4H), 4.27 (s, 2H), 7.03-7.15 (m, 2H), 7.26-7.31 (m, 1H), 7.48 (s, 1H), 7.66 (s, 1H), 8.38 (t, J=5.7, 1H), 8.73 (brs, 2H).

Example 183N²-(3,6-dimethyl-1,2-benzisoxazol-5-yl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-(3,6-dimethyl-1,2-benzisoxazol-5-yl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (585 mg, 1.37 mmol) of Example 182, step A, and the compound (371 mg, 1.97 mmol) of Reference Example 2, and according to the method of Example 1, step B, the title compound (677 mg, yield 83%) was obtained as a colorless solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.03 (t, J=7.2, 3H), 1.42 (brs, 9H), 2.49 (s, 3H), 2.51 (s, 3H), 2.94 (s, 3H), 3.0-3.2 (m, 2H), 3.2-3.3 (m, 2H), 3.38-3.45 (m, 2H), 3.86 (s, 2H), 3.9-4.3 (m, 4H), 4.16 (s, 2H), 6.88-6.99 (m, 2H), 7.11-7.16 (m, 1H), 7.36 (s, 1H), 7.58 (s, 1H), 8.0-8.5 (broad, 1H).

Step BN²-(3,6-dimethyl-1,2-benzisoxazol-5-yl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (655 mg, 1.10 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (636 mg, yield>100%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.2, 3H), 2.45 (s, 3H), 2.47 (s, 3H), 2.8-3.0 (m, 4H), 2.86 (s, 3H), 3.34-3.42 (m, 2H), 3.86 (s, 2H), 4.0-4.3 (m, 4H), 4.27 (s, 2H), 7.03-7.16 (m, 2H), 7.26-7.31 (m, 1H), 7.48 (s, 1H), 7.66 (s, 1H), 8.37 (t, J=5.7, 1H), 8.74 (brs, 2H).

Example 184N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3,5-dimethyl-1,2-benzisoxazol-6-yl)-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-(3,5-dimethyl-1,2-benzisoxazol-6-yl)glycine

Using the compound (690 mg, 2.48 mmol) of Reference Example 117 and the compound (724 mg, 3.92 mmol) of Reference Example 17, and according to the method of Example 4, step A, the title compound (662 mg, yield 65%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.40 (s, 3H), 2.51 (s, 3H), 3.08 (s, 3H), 4.02 (s, 2H), 4.19 (d, J=11.7, 2H), 4.31 (d, J=11.7, 2H), 4.38 (s, 2H), 7.2-7.3 (m, 4H), 7.36 (s, 1H), 7.40 (s, 1H), 13.3 (brs, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3,5-dimethyl-1,2-benzisoxazol-6-yl)-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (308 mg, 0.754 mmol) obtained in step A and the compound (274 mg, 1.35 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (434 mg, yield 97%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.09 (d, J=6.8, 6H), 1.43 (brs, 9H), 2.43 (s, 3H), 2.50 (s, 3H), 2.96 (s, 3H), 3.0-3.2 (m, 2H), 3.33-3.41 (m, 2H), 3.88 (s, 2H), 3.9-4.4 (broad, 1H), 4.17 (d, J=11.7, 2H), 4.28 (d, J=11.7, 2H), 4.30 (s, 2H), 7.2-7.3 (m, 5H), 7.37 (s, 1H), 7.8-8.4 (broad, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3,5-dimethyl-1,2-benzisoxazol-6-yl)-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (432 mg, 0.729 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (392 mg, yield 95%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.18 (d, J=6.5, 6H), 2.36 (s, 3H), 2.45 (s, 3H), 2.8-3.0 (m, 2H), 2.89 (s, 3H), 3.1-3.3 (m, 1H), 3.34-3.42 (m, 2H), 3.96 (s, 2H), 4.14 (d, J=11.7, 2H), 4.27 (d, J=11.7, 2H), 4.39 (s, 2H), 7.2-7.3 (m, 4H), 7.22 (s, 1H), 7.52 (s, 1H), 8.32 (t, J=5.7, 1H), 8.74 (brs, 2H).

Example 185N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3,5-dimethyl-1,2-benzisoxazol-6-yl)-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3,5-dimethyl-1,2-benzisoxazol-6-yl)-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (322 mg, 0.788 mmol) of Example 184, step A, and the compound (260 mg, 1.38 mmol) of Reference Example 2, and according to the method of Example 1, step B, the title compound (433 mg, yield 95%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.00 (t, J=7.1, 3H), 1.42 (brs, 9H), 2.42 (s, 3H), 2.50 (s, 3H), 2.97 (s, 3H), 3.11 (q, J=7.1, 2H), 3.2-3.3 (m, 2H), 3.36-3.44 (m, 2H), 3.86 (s, 2H), 4.18 (d, J=11.7, 2H), 4.28 (d, J=11.7, 2H), 4.30 (s, 2H), 7.2-7.3 (s, 4H), 7.36 (s, 1H), 7.37 (s, 1H), 7.9-8.4 (broad, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3,5-dimethyl-1,2-benzisoxazol-6-yl)-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (428 mg, 0.740 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (372 mg, yield 91%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.14 (t, J=7.0, 3H), 2.36 (s, 3H), 2.45 (s, 3H), 2.8-3.0 (m, 4H), 2.90 (s, 3H), 3.3-3.5 (m, 2H), 3.96 (s, 2H), 4.14 (d, J=11.7, 2H), 4.27 (d, J=11.7, 2H), 4.38 (s, 2H), 7.2-7.3 (m, 4H), 7.22 (s, 1H), 7.52 (s, 1H), 8.29 (broad t, 1H), 8.67 (brs, 2H).

Example 186N²-(3,5-dimethyl-1,2-benzisoxazol-6-yl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochlorideStep AN-(3,5-dimethyl-1,2-benzisoxazol-6-yl)-N-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}glycine

Using the compound (2.10 g, 7.60 mmol) of Reference Example 117, and the compound (2.30 g, 11.40 mmol) of Reference Example 19, and according to the method of Example 4, step A, the title compound (850 mg, yield 26%) was obtained as a bistered solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.33 (s, 3H), 2.45 (s, 3H), 2.88 (s, 3H), 4.05 (s, 2H), 4.06-4.29 (m, 4H), 4.36 (s, 2H), 7.02-7.17 (m, 2H), 7.19 (s, 1H), 7.30 (dd, J=5.4, 8.4, 1H), 7.51 (s, 1H), 12.52 (brs, 1H).

Step BN²-(3,5-dimethyl-1,2-benzisoxazol-6-yl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochloride

Using the compound (425 mg, 1.00 mmol) obtained in step A and the compound (303 mg, 1.50 mmol) of Reference Example 3, and according to the methods of Example 1, step B, and Example 251, step B, the title compound (479 mg, yield 88%) was obtained as a pale-bistered amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.06 (d, J=6.7, 6H), 2.36 (s, 3H), 2.45 (s, 3H), 2.77 (t, J=5.9, 2H), 2.98 (s, 3H), 3.00-3.18 (m, 1H), 3.20-3.43 (m, 2H), 3.94 (s, 2H), 4.08-4.31 (m, 4H), 4.36 (s, 2H), 7.03-7.18 (m, 2H), 7.22 (s, 1H), 7.30 (dd, J=5.2, 8.2, 1H), 7.52 (s, 1H), 7.6-8.4 (broad, 2H), 8.22 (t, J=5.5, 1H).

Example 187N²-(3,5-dimethyl-1,2-benzisoxazol-6-yl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (425 mg, 1.00 mmol) of Example 186, step A, and the compound (282 mg, 1.50 mmol) of Reference Example 2, and according to the methods of Example 1, step B, and Example 57, step B, the title compound (472 mg, yield 89%) was obtained as a pale-bistered amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.11 (t, J=7.0, 3H), 2.35 (s, 3H), 2.45 (s, 3H), 2.78-2.88 (m, 4H), 2.89 (s, 3H), 3.16-3.50 (m, 2H), 3.95 (s, 2H), 4.00-4.33 (m, 4H), 4.37 (s, 2H), 7.04-7.18 (m, 2H), 7.22 (s, 1H), 7.27-7.33 (m, 1H), 7.52 (s, 1H), 7.61-8.80 (broad, 2H), 8.22-8.26 (m, 1H).

Example 188N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(6-methyl-1,3-benzodioxol-5-yl)-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-(6-methyl-1,3-benzodioxol-5-yl)glycine

Using the compound (5.14 g, 19.23 mmol) of Reference Example 118 and the compound (5.33 g, 28.86 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (5.52 g, yield 72%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.21 (s, 3H), 3.03 (s, 3H), 3.79 (s, 2H), 4.15 (d, J=11.6, 2H), 4.21 (s, 2H), 4.27 (d, J=11.6, 2H), 5.87 (s, 2H), 6.61 (s, 1H), 6.79 (s, 1H), 7.19-7.28 (m, 4H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(6-methyl-1,3-benzodioxol-5-yl)-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (1.00 g, 2.52 mmol) obtained in step A and the compound (789 mg, 3.90 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (1.28 g, yield 88%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.12 (d, J=6.8, 6H), 1.46 (s, 9H), 2.26 (s, 3H), 2.94 (s, 3H), 3.17 (brs, 2H), 3.36-3.43 (m, 2H), 3.72 (s, 2H), 4.05-4.29 (m, 7H), 5.87 (s, 2H), 6.62 (s, 1H), 6.88 (s, 1H), 7.19-7.31 (m, 4H), 8.30-8.58 (broad, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(6-methyl-1,3-benzodioxol-5-yl)-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (1.28 g, 2.20 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (1.06 g, yield 87%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.22 (d, J=5.9, 6H), 2.21 (s, 3H), 2.87 (m, 5H), 3.26-3.40 (m, 3H), 3.78 (s, 2H), 4.04-4.26 (m, 6H), 5.91 (s, 2H), 6.71 (s, 1H), 6.94 (s, 1H), 7.25 (m, 4H), 8.43 (brs, 1H), 8.84 (brs, 2H).

Example 189N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(6-methyl-1,3-benzodioxol-5-yl)-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(6-methyl-1,3-benzodioxol-5-yl)-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (1.00 g, 2.52 mmol) of Example 188, step A, and the compound (0.73 g, 3.88 mmol) of Reference Example 2, and according to the method of Example 1, step B, the title compound (1.32 g, yield 92%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.06 (t, J=6.9, 3H), 1.44 (s, 9H), 2.26 (s, 3H), 2.95 (s, 3H), 3.19-3.31 (m, 4H), 3.42 (q, J=6.3, 2H), 3.71 (s, 2H), 4.06-4.25 (m, 6H), 5.85 (s, 2H), 6.61 (s, 1H), 6.88 (s, 1H), 7.18-7.32 (m, 4H), 8.39-8.65 (broad, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(6-methyl-1,3-benzodioxol-5-yl)-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (1.32 g, 2.33 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (1.17 g, yield 93%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.17 (t, J=7.2, 3H), 2.21 (s, 3H), 2.80-2.91 (m, 7H), 3.34-3.42 (m, 2H), 3.79 (s, 2H), 4.08-4.25 (m, 6H), 5.91 (s, 2H), 6.71 (s, 1H), 6.95 (s, 1H), 7.25 (m, 4H), 8.42-8.47 (m, 1H), 8.88 (brs, 2H).

Example 190N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3,6-dimethyl-1,3-benzoxazol-2(3H)-on-5-yl)-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochlorideStep AN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-(3,6-dimethyl-1,3-benzoxazol-2(3H)-on-5-yl)glycine

Using the compound (1.00 g, 3.40 mmol) of Reference Example 119, and the compound (942 mg, 5.10 mmol) of Reference Example 17, and according to the method of Example 4, step A, the title compound (1.04 g, yield 72%) was obtained as a pale-purple solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.28 (s, 3H), 2.87 (s, 3H), 3.27 (s, 3H), 3.96 (s, 2H), 4.09 (d, J=8.7, 2H), 4.23 (s, 2H), 4.24 (d, J=8.7, 2H), 7.11 (s, 1H), 7.12 (s, 1H), 7.22-7.29 (m, 4H), 12.48 (brs, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3,6-dimethyl-1,3-benzoxazol-2(3H)-on-5-yl)-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochloride

Using the compound (520 mg, 1.23 mmol) obtained in step A and the compound (373 mg, 1.85 mmol) of Reference Example 3, and according to the methods of Example 1, step B, and Example 57, step B, the title compound (534 mg, yield 80%) was obtained as a pale-bistered amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.14 (d, J=6.2, 6H), 2.31 (s, 3H), 2.81-2.89 (m, 2H), 2.87 (s, 3H), 3.08-3.20 (m, 1H), 3.26 (s, 3H), 3.31-3.37 (m, 2H), 3.81 (s, 2H), 4.02 (d, J=11.8, 2H), 4.21-4.26 (m, 2H), 4.22 (s, 2H), 7.12 (s, 1H), 7.19 (s, 1H), 7.22-7.26 (m, 4H), 7.75-8.62 (broad, 2H), 8.34 (brs, 1H).

Example 191N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3,6-dimethyl-1,3-benzoxazol-2(3H)-on-5-yl)-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (520 mg, 1.23 mmol) of Example 190, step A, and the compound (347 mg, 1.85 mmol) of Reference Example 2, and according to the methods of Example 1, step B, and Example 57, step B, the title compound (518 mg, yield 79%) was obtained as a pale-bistered amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.2, 3H), 2.31 (s, 3H), 2.85-2.93 (m, 4H), 2.87 (s, 3H), 3.26 (s, 3H), 3.31-3.41 (m, 2H), 3.81 (s, 2H), 4.05 (d, J=11.4, 2H), 4.22 (s, 2H), 4.23 (d, J=11.4, 2H), 7.12 (s, 1H), 7.18 (s, 1H), 7.21-7.25 (m, 4H), 8.37 (t, J=5.9, 1H), 8.62 (brs, 2H).

Example 192N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3,5-dimethyl-1,3-benzoxazol-2(3H)-on-6-yl)-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochlorideStep AN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-(3,5-dimethyl-1,3-benzoxazole-2(3H)-on-6-yl)glycine

Using the compound (678 mg, 2.30 mmol) of Reference Example 120 and the compound (637 mg, 3.45 mmol) of Reference Example 17, and according to the method of Example 4, step A, the title compound (463 mg, yield 47%) was obtained as a pale-purple solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.30 (s, 3H), 2.86 (s, 3H), 3.28 (s, 3H), 3.92 (s, 2H), 4.09 (d, J=11.7, 2H), 4.22 (s, 2H), 4.23 (d, J=11.7, 2H), 7.01 (s, 1H), 7.21 (s, 1H), 7.24-7.29 (m, 4H), 12.45 (brs, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3,5-dimethyl-1,3-benzoxazol-2(3H)-on-6-yl)-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochloride

Using the compound (231 mg, 0.54 mmol) obtained in step A and), and the compound (164 mg, 0.81 mmol) of Reference Example 3, and according to the methods of Example 1, step B, and Example 57, step B, the title compound (229 mg, yield 78%) was obtained as a pale-bistered amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.20 (d, J=6.4, 6H), 2.33 (s, 3H), 2.85-2.93 (m, 2H), 2.86 (s, 3H), 3.18-3.29 (m, 1H), 3.28 (s, 3H), 3.31-3.42 (m, 2H), 3.81 (s, 2H), 4.07 (d, J=11.6, 2H), 4.23 (s, 2H), 4.23 (d, J=11.6, 2H), 7.02 (s, 1H), 7.22-7.26 (m, 4H), 7.28 (s, 1H), 8.37 (t, J=5.5, 1H), 8.85 (brs, 2H).

The compounds of Examples 169-192 are shown below.

TABLE 14StructuralLC-MSExampleFormulaTMW(found)169 [Image Omitted]

536.54464 170 [Image Omitted]

563.52491 171 [Image Omitted]

549.49477 172 [Image Omitted]

620.57548 173 [Image Omitted]

606.54534 174 [Image Omitted]

593.59521 175 [Image Omitted]

579.56507 176 [Image Omitted]

571.15535 177 [Image Omitted]

557.13521 178 [Image Omitted]

460.01424 179 [Image Omitted]

445.99410 180 [Image Omitted]

565.53493 181 [Image Omitted]

515.05479 182 [Image Omitted]

583.53511 183 [Image Omitted]

569.50497 184 [Image Omitted]

565.53493 185 [Image Omitted]

551.51479 186 [Image Omitted]

547.06511 187 [Image Omitted]

533.04497 188 [Image Omitted]

554.51482 189 [Image Omitted]

540.48468 190 [Image Omitted]

545.07509 191 [Image Omitted]

531.05495 192 [Image Omitted]

545.07509

Example 193N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3,5-dimethyl-1,3-benzooxazol-2(3H)-on-6-yl)-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (231 mg, 0.54 mmol) of Example 192, step A, and the compound (152 mg, 0.81 mmol) of Reference Example 2, and according to the methods of Example 1, step B, and Example 57, step B, the title compound (228 mg, yield 80%) was obtained as a pale-bistered amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.06-1.17 (m, 3H), 2.33 (s, 3H), 2.82-2.91 (m, 4H), 2.86 (s, 3H), 3.28 (s, 3H), 3.28-3.42 (m, 2H), 3.79 (s, 2H), 4.07 (d, J=11.5, 2H), 4.21 (s, 2H), 4.23 (d, J=11.5, 2H), 7.03 (s, 1H), 7.25-7.26 (s, 4H), 7.27 (s, 1H), 8.32 (t, J=5.7, 1H), 8.48 (brs, 2H).

Example 194N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3-methoxy-8-oxo-5,6,7,8-tetrahydronaphthalen-2-yl)-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-(3-methoxy-8-oxo-5,6,7,8-tetrahydronaphthalen-2-yl)glycine

Using the compound (0.70 g, 2.28 mmol) of Reference Example 115 and the compound (0.63 g, 3.41 mmol) of Reference Example 17, and according to the method of Example 1, step A, the title compound (0.92 g, yield 92%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 2.09 (quintet, J=6.3, 2H), 2.57 (t, J=6.3, 2H), 2.87 (t, J=6.3, 2H), 3.02 (s, 3H), 3.85 (s, 3H), 3.97 (s, 2H), 4.30-4.40 (m, 4H), 4.52 (s, 2H), 6.65 (s, 1H), 7.28 (s, 4H), 7.56 (s, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3-methoxy-8-oxo-5,6,7,8-tetrahydronaphthalen-2-yl)-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (0.44 g, 1.01 mmol) obtained in step A and the compound (0.32 g, 1.58 mmol) of Reference Example 3 and according to the method of Example 1, step B, the title compound (0.76 g, yield>100%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.14 (d, J=6.8, 6H), 1.46 (brs, 9H), 2.04-2.12 (m, 2H), 2.56 (t, J=6.0, 2H), 2.86 (t, J=6.0, 2H), 2.96 (s, 3H), 3.19 (brs, 2H), 3.38-3.46 (m, 2H), 3.85 (s, 5H), 4.0-4.2 (broad, 1H), 4.31-4.40 (m, 6H), 6.64 (s, 1H), 7.29 (s, 4H), 7.55 (s, 1H), 8.32-8.63 (broad, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3-methoxy-8-oxo-5,6,7,8-tetrahydronaphthalen-2-yl)-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (0.76 g) obtained in step B and according to the method of Example 1, step C, the title compound (0.67 g, yield>100%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.19 (d, J=6.4, 6H), 1.98 (t, J=5.5, 2H), 2.45-2.51 (m, 2H), 2.83 (t, J=5.1, 2H), 2.9-3.0 (m, 5H), 3.25-3.30 (m, 1H), 3.34-3.41 (m, 2H), 3.79 (s, 3H), 3.84 (s, 2H), 4.19 (d, J=11.7, 2H), 4.33 (d, J=11.7, 2H), 4.42 (s, 2H), 6.83 (s, 1H), 7.23-7.33 (m, 5H), 8.54 (t, J=5.6, 1H), 8.71 (brs, 2H).

Example 195N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3-methoxy-8-oxo-5,6,7,8-tetrahydronaphthalen-2-yl)-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3-methoxy-8-oxo-5,6,7,8-tetrahydronaphthalen-2-yl)-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (0.44 g, 1.01 mmol) of Example 194, step A, and the compound (0.29 g, 1.54 mmol) of Reference Example 2, and according to the method of Example 1, step B, the title compound (0.74 g, yield>100%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.07 (t, J=6.9, 3H), 1.43 (brs, 9H), 2.04-2.12 (m, 2H), 2.56 (t, J=6.0, 2H), 2.86 (t, J=6.0, 2H), 2.96 (s, 3H), 3.21-3.31 (m, 4H), 3.43 (q, J=6.2, 2H), 3.84 (brs, 5H), 4.35-4.39 (m, 6H), 6.63 (s, 1H), 7.27 (s, 4H), 7.54 (s, 1H), 8.39-8.65 (broad, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3-methoxy-8-oxo-5,6,7,8-tetrahydronaphthalen-2-yl)-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (0.74 g, 1.22 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (0.57 g, yield 97%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=7.1, 3H), 1.98 (t, J=5.4, 2H), 2.46-2.51 (m, 2H), 2.83 (t, J=5.2, 2H), 2.91 (brs, 7H), 3.38 (q, J=6.8, 2H), 3.79 (s, 3H), 3.84 (s, 2H), 4.19 (d, J=11.7, 2H), 4.33 (d, J=11.7, 2H), 4.43 (s, 2H), 6.83 (s, 1H), 7.23-7.33 (m, 5H), 8.53 (t, J=5.6, 1H), 8.69 (brs, 2H).

Example 196N²-{2-[4,6-dihydro-5H-thieno[2,3-c]pyrrol-5-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochlorideStep AN-{2-[4,6-dihydro-5H-thieno[2,3-c]pyrrol-5-yl(methyl)amino]-2-oxoethyl}-N-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]glycine

Using the compound (490 mg, 1.61 mmol) of Reference Example 62 and the compound (409 mg, 2.14 mmol) of Reference Example 59, and according to the method of Example 4, step A, the title compound (655 mg, yield 92%) was obtained as a pale-pink amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.31 (s, 3H), 2.65 (s, 3H), 2.87 (s, 3H), 4.04 (s, 2H), 4.10 (s, 2H), 4.23 (s, 2H), 4.35 (s, 2H), 6.94 (d, J=4.5, 1H), 7.28 (d, J=7.8, 1H), 7.48-7.53 (m, 2H), 7.74 (d, J=1.5, 1H), 12.48 (s, 1H).

Step BN²-{2-[4,6-dihydro-5H-thieno[2,3-c]pyrrol-5-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(isopropyl)amino]ethyl}glycinamide

Using the compound (276 mg, 0.625 mmol) obtained in step A and the compound (177 mg, 0.875 mmol) of Reference Example 3, and according to the method of Example 1, step B, the title compound (329 mg, yield 84%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.12 (d, J=6.9, 6H), 1.46 (brs, 9H), 2.41 (s, 3H), 2.63 (s, 3H), 2.95 (s, 3H), 3.1-3.3 (m, 2H), 3.3-3.5 (m, 2H), 3.83 (s, 2H), 4.0-4.4 (m, 7H), 6.83 (d, J=5.1, 1H), 7.2-7.3 (m, 2H), 7.69 (d, J=8.1, 1H), 7.96 (d, J=1.5, 1H), 8.2-8.8 (broad, 1H).

Step CN²-{2-[4,6-dihydro-5H-thieno[2,3-c]pyrrol-5-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (325 mg, 0.519 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (309 mg, yield 99%) was obtained as a gray solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.18 (d, J=6.3, 6H), 2.35 (s, 3H), 2.65 (s, 3H), 2.8-3.0 (m, 2H), 2.87 (s, 3H), 3.1-3.3 (m, 1H), 3.34-3.42 (m, 2H), 3.93 (s, 2H), 4.10 (s, 2H), 4.24 (s, 2H), 4.37 (s, 2H), 6.95 (d, J=5.1, 1H), 7.29 (d, J=7.8, 1H), 7.48-7.54 (m, 2H), 7.76 (d, J=1.5, 1H), 8.34 (t, J=5.7, 1H), 8.68 (brs, 2H).

Example 197N²-{2-[4,6-dihydro-5H-thieno[2,3-c]pyrrol-5-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[4,6-dihydro-5H-thieno[2,3-c]pyrrol-5-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (367 mg, 0.831 mmol) of Example 196, step A, and the compound (245 mg, 1.30 mmol) of Reference Example 2, and according to the method of Example 1, step B, the title compound (423 mg, yield 83%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.04 (t, J=7.2, 3H), 1.44 (brs, 9H), 2.40 (s, 3H), 2.63 (s, 3H), 2.95 (s, 3H), 3.0-3.5 (m, 6H), 3.82 (s, 2H), 4.0-4.4 (m, 6H), 6.83 (d, J=4.8, 1H), 7.2-7.3 (m, 2H), 7.69 (d, J=7.8, 1H), 7.95 (d, J=1.5, 1H), 8.2-8.8 (broad, 1H).

Step BN²-{2-[4,6-dihydro-5H-thieno[2,3-c]pyrrol-5-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (418 mg, 0.683 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (376 mg, yield 94%) was obtained as a gray solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=7.2, 3H), 2.35 (s, 3H), 2.65 (s, 3H), 2.8-3.0 (m, 4H), 2.87 (s, 3H), 3.3-3.5 (m, 2H), 3.93 (s, 2H), 4.10 (s, 2H), 4.24 (s, 2H), 4.38 (s, 2H), 6.95 (d, J=5.1, 1H), 7.28 (d, J=8.1, 1H), 7.48-7.53 (m, 2H), 7.76 (s, 1H), 8.35 (t, J=5.7, 1H), 8.85 (brs, 2H).

Example 198N²-{2-[4,6-dihydro-5H-thieno[2,3-c]pyrrol-5-yl(methyl)amino]-2-oxoethyl}-N²-(3,6-dimethyl-1,2-benzisoxazol-5-yl)-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN-{2-[4,6-dihydro-5H-thieno[2,3-c]pyrrol-5-yl(methyl)amino]-2-oxoethyl}-N-(3,6-dimethyl-1,2-benzisoxazol-5-yl)glycine

Using the compound (147 mg, 0.528 mmol) of Reference Example 116 and the compound (130 mg, 0.682 mmol) of Reference Example 59, and according to the method of Example 4, step A, the title compound (196 mg, yield 90%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.44 (s, 3H), 2.48 (s, 3H), 2.85 (s, 3H), 4.00 (s, 2H), 4.07 (s, 2H), 4.21 (s, 2H), 4.30 (s, 2H), 6.94 (d, J=5.1, 1H), 7.47 (s, 1H), 7.49 (d, J=5.1, 1H), 7.62 (s, 1H), 12.45 (s, 1H).

Step BN²-{2-[4,6-dihydro-5H-thieno[2,3-c]pyrrol-5-yl(methyl)amino]-2-oxoethyl}-N²-(3,6-dimethyl-1,2-benzisoxazol-5-yl)-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (195 mg, 0.470 mmol) obtained in step A and the compound (132 mg, 0.701 mmol) of Reference Example 2, and according to the method of Example 1, step B, the title compound (254 mg, yield 92%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.03 (t, J=7.2, 3H), 1.42 (brs, 9H), 2.50 (s, 3H), 2.53 (s, 3H), 2.95 (s, 3H), 3.0-3.3 (m, 4H), 3.38-3.45 (m, 2H), 3.88 (s, 2H), 4.06 (s, 2H), 4.18 (s, 2H), 4.20 (s, 2H), 6.83 (d, J=5.1, 1H), 7.28 (d, J=5.1, 1H), 7.36 (s, 1H), 7.59 (s, 1H), 8.0-8.7 (broad, 1H).

Step CN²-{2-[4,6-dihydro-5H-thieno[2,3-c]pyrrol-5-yl(methyl)amino]-2-oxoethyl}-N²-(3,6-dimethyl-1,2-benzisoxazol-5-yl)-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (248 mg, 0.424 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (219 mg, yield 93%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.14 (t, J=7.2, 3H), 2.46 (s, 3H), 2.48 (s, 3H), 2.8-3.0 (m, 4H), 2.86 (s, 3H), 3.3-3.4 (m, 2H), 3.86 (s, 2H), 4.07 (s, 2H), 4.20 (s, 2H), 4.30 (s, 2H), 6.94 (d, J=5.1, 1H), 7.49 (s, 1H), 7.49 (d, J=5.1, 1H), 7.67 (s, 1H), 8.35 (t, J=5.7, 1H), 8.58 (brs, 2H).

Example 199N²-{2-[methyl(5-methyl-1,3-dihydro-2H-isoindol-2-yl)amino]-2-oxoethyl}-N²-[2-methyl-4-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[methyl(5-methyl-1,3-dihydro-2H-isoindol-2-yl)amino]-2-oxoethyl}-N²-[2-methyl-4-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (305 mg, 1.00 mmol) of Reference Example 69, the compound (209 mg, 1.05 mmol) of Reference Example 60 and the compound (192 mg, 1.02 mmol) of Reference Example 2, and according to the methods of Example 4, step A, and Example 1, step B, the title compound (386 mg, yield 63%) was obtained as a brown oil.

Step BN²-{2-[methyl(5-methyl-1,3-dihydro-2H-isoindol-2-yl)amino]-2-oxoethyl}-N²-[2-methyl-4-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (386 mg, 0.623 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (330 mg, yield 89%) was obtained as a brown amorphous solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=7.2, 3H), 2.29 (s, 3H), 2.32 (s, 3H), 2.63 (s, 3H), 2.86-2.92 (m, 4H), 2.89 (s, 3H), 3.36-3.41 (m, 2H), 3.95 (s, 2H), 4.09-4.12 (m, 2H), 4.20-4.25 (m, 2H), 4.38 (s, 2H), 7.05-7.10 (s, 3H), 7.14-7.16 (m, 1H), 7.66-7.68 (m, 1H), 7.71 (s, 1H), 8.35 (t, J=5.8, 1H), 8.84 (brs, 1H).

Example 200N²-{2-[2,3-dihydro-1H-inden-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide hydrochlorideStep AN²-{2-[2,3-dihydro-1H-inden-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (305 mg, 1.00 mmol) of Reference Example 69, the compound (193 mg, 1.05 mmol) of Reference Example 23 and the compound (192 mg, 1.02 mmol) of Reference Example 2, and according to the methods of Example 4, step A, and Example 1, step B, the title compound (383 mg, yield 63%) was obtained as a brown oil.

Step BN²-{2-[2,3-dihydro-1H-inden-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (383 mg, 0.633 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (325 mg, yield 89%) was obtained as a colorless amorphous solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.07-1.23 (m, 3H), 2.34 (s, 3H), 2.63 (s, 3H), 2.70 2.78 (2s, 3H), 2.91-3.16 (m, 8H), 3.38-3.39 (m, 2H), 3.91 3.93 (2s, 2H), 4.16 4.32 (2s, 2H), 4.84 4.87 (m, 0.4H), 5.32 5.35 (m, 0.6H), 7.11-7.23 (m, 5H), 7.68 (d, J=8.3, 1H), 7.74 (s, 1H), 8.42-8.43 (m, 1H), 8.73 (brs, 2H).

Example 201N²-{2-[2,3-dihydro-1H-inden-2-yl(methyl)amino]-2-oxoethyl}-N²-(3,5-dimethyl-1,2-benzisoxazol-6-yl)-N¹-[2-(ethylamino)ethyl]glycinamide hydrochlorideStep AN²-{2-[2,3-dihydro-1H-inden-2-yl(methyl)amino]-2-oxoethyl}-N²-(3,5-dimethyl-1,2-benzisoxazol-6-yl)-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (278 mg, 1.00 mmol) of Reference Example 117, the compound (193 mg, 1.05 mmol) of Reference Example 23 and the compound (192 mg, 1.02 mmol) of Reference Example 2, and according to the methods of Example 4, step A, and Example 1, step B, the title compound (404 mg, yield 70%) was obtained as a brown oil.

Step BN²-{2-[2,3-dihydro-1H-inden-2-yl(methyl)amino]-2-oxoethyl}-N²-(3,5-dimethyl-1,2-benzisoxazol-6-yl)-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (404 mg, 0.699 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (310 mg, yield 86%) was obtained as a pale-yellow amorphous solid

¹H-NMR (400 MHz, DMSO-d₆; Î´(ppm) 1.14 (t, J=7.2, 3H), 2.38 (s, 3H), 2.46 (s, 3H), 2.67 2.79 (2s, 3H), 2.87-3.14 (m, 8H), 3.36-3.40 (m, 2H), 3.90 3.93 (2s, 2H), 4.17 4.33 (2s, 2H), 4.90-4.96 (m, 0.4H), 5.27-5.35 (m, 0.6H), 7.13-7.25 (m, 4H), 7.29 (s, 1H), 7.54 (s, 1H), 8.41-8.42 (m, 1H), 8.86 (brs, 2H).

Example 202N²-{2-[2,3-dihydro-1H-inden-2-yl(methyl)amino]-2-oxoethyl}-N²-(3,6-dimethyl-1,2-benzisoxazol-5-yl)-N¹-[2-(ethylamino)ethyl]glycinamide hydrochlorideStep AN²-{2-[2,3-dihydro-1H-inden-2-yl(methyl)amino]-2-oxoethyl}-N²-(3,6-dimethyl-1,2-benzisoxazol-5-yl)-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (278 mg, 1.00 mmol) of Reference Example 116, the compound (193 mg, 1.05 mmol) of Reference Example 23 and the compound (192 mg, 1.02 mmol) of Reference Example 2, and according to the methods of Example 4, step A, and Example 1, step B, the title compound (329 mg, yield 57%) was obtained as a brown oil.

Step BN²-{2-[2,3-dihydro-1H-inden-2-yl(methyl)amino]-2-oxoethyl}-N²-(3,6-dimethyl-1,2-benzisoxazol-5-yl)-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (329 mg, 0.569 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (186 mg, yield 63%) was obtained as a brown amorphous solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.14-1.21 (m, 3H), 2.48 (s, 3H), 2.49 (s, 3H), 2.66 2.75 (2s, 3H), 2.83-3.08 (m, 8H), 3.36-3.40 (m, 2H), 3.81 3.84 (2s, 2H), 4.07 4.25 (2s, 2H), 4.88-4.92 (m, 0.4H), 5.27-5.31 (m, 0.6H), 7.13-7.20 (m, 4H), 7.50 (s, 1H), 7.69 7.72 (2s, 1H), 8.50-8.52 (m, 1H), 8.92 (brs, 2H).

Example 203N²-{2-[methyl(5-methyl-1,3-dihydro-2H-isoindol-2-yl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[methyl(5-methyl-1,3-dihydro-2H-isoindol-2-yl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (305 mg, 1.00 mmol) of Reference Example 62, the compound (209 mg, 1.05 mmol) of Reference Example 60 and the compound (157 mg, 0.836 mmol) of Reference Example 2, and according to the methods of Example 4, step A, and Example 1, step B, the title compound (338 mg, yield 57%) was obtained as a brown oil.

Step BN²-{2-[methyl(5-methyl-1,3-dihydro-2H-isoindol-2-yl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (338 mg, 0.545 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (264 mg, yield 82%) was obtained as a brown amorphous solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.2, 3H), 2.30 (s, 3H), 2.33 (s, 3H), 2.65 (s, 3H), 2.86 (s, 3H), 2.89-2.90 (m, 4H), 3.36-3.41 (m, 2H), 3.93 (s, 2H), 4.07 4.10 (2s, 2H), 4.19-4.35 (m, 4H), 7.05-7.08 (m, 2H), 7.15 (d, J=7.6, 1H), 7.28 (d, J=7.8, 1H), 7.51 (dd, J=8.0, 1.1, 1H), 7.75 (d, J=1.6, 1H), 8.37 (t, J=5.8, 1H), 8.89 (brs, 2H).

Example 204N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

The compound (2.00 g, 6.55 mmol) of Reference Example 69 was dissolved in N,N-dimethylformamide (22 ml), WSC (1.27 g, 6.62 mmol) was added at room temperature, and the mixture was stirred at the same temperature for 30 min. Then, the reaction mixture was stirred under ice-cooling, and the compound (1.34 g, 6.61 mmol) of Reference Example 19 and N,N-diisopropylethylamine (1.12 ml, 6.59 mmol) were added. The mixture was stirred at room temperature for 2 hr. Then, the compound (1.35 g, 7.17 mmol) of Reference Example 2, WSC (1.38 g, 7.20 mmol) and 1-hydroxybenzotriazole (974 mg, 7.21 mmol) were added to the reaction mixture, and the mixture was stirred at room temperature for 2 hr. The reaction mixture was diluted with ethyl acetate, and the organic layer was washed with water, 10% aqueous citric acid solution, diluted aqueous sodium hydroxide solution and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-methanol) to give the title compound (3.62 g, yield 89%) as a pale-yellow amorphous solid

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 0.94 (brs, 3H), 1.36 (s, 9H), 2.31 (s, 3H), 2.63 (s, 3H), 2.90 (s, 3H), 3.02-3.18 (m, 6H), 3.87 (s, 2H), 4.11-4.29 (m, 4H), 4.34 (s, 2H), 7.05-7.10 (m, 2H), 7.15 (dd, J=8.0, 1.9, 1H), 7.29-7.32 (m, 1H), 7.67 (dd, J=8.5, 1.7, 1H), 7.71 (d, J=1.7, 1H), 8.11 (brs, 1H).

Step BN²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

The compound (3.62 g, 5.80 mmol) obtained in step A was dissolved in dichloromethane (12 ml), 4N hydrochloric acid-dioxane solution (12 ml) was added, and the mixture was stirred at room temperature for 2 hr. The reaction mixture was diluted with chloroform, and the organic layer was washed with 1N aqueous sodium hydroxide solution, and dried over sodium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was dissolved in diethyl ether (58 ml), and 4N hydrochloric acid-ethyl acetate (3.14 ml, 12.6 mmol) was added to allow precipitation of a solid. This was collected by filtration, washed with diethyl ether, and dried under reduced pressure to give the title compound (2.96 g, yield 86%) as a pale-yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.14 (t, J=7.2, 3H), 2.32 (s, 3H), 2.63 (s, 3H), 2.88-2.90 (m, 4H), 2.90 (s, 3H), 3.35-3.41 (m, 2H), 3.95 (s, 3H), 4.11-4.29 (m, 4H), 4.36 (s, 2H), 7.06-7.11 (m, 2H), 7.15 (dd, J=8.8, 2.0, 1H), 7.29-7.32 (m, 1H), 7.67 (dd, J=8.4, 2.1, 1H), 7.72 (d, J=1.9, 1H), 8.30 (t, J=5.9, 1H), 8.59 (brs, 2H).

Example 205N²-{2-[(4-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[(4-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (416 mg, 1.36 mmol) of Reference Example 69, the compound (280 mg, 1.38 mmol) of Reference Example 18 and the compound (282 mg, 1.47 mmol) of Reference Example 2, and according to the method of Example 204, step A, the title compound (763 mg, yield 90%) was obtained as a pale-yellow amorphous solid

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.00 (t, J=7.1, 3H), 1.41 (brs, 9H), 2.38 (s, 3H), 2.64 (s, 3H), 2.97 (s, 3H), 3.0-3.3 (m, 4H), 3.37-3.42 (m, 2H), 3.91 (s, 2H), 4.15-4.32 (m, 4H), 4.26 (s, 2H), 6.93-7.02 (m, 2H), 7.21-7.32 (m, 2H), 7.81 (dd, J=2.0, 8.4, 1H), 7.86 (s, 1H), 8.02 8.22 (2broad, 1H).

Step BN²-{2-[(4-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

The compound (753 mg, 1.21 mmol) obtained in step A was dissolved in dichloromethane (2 ml), trifluoroacetic acid (2 ml) was added at room temperature, and the mixture was stirred at the same temperature for 1 hr. To the reaction mixture was added aqueous ammonia, and the organic layer was extracted twice with dichloromethane. The organic layer was dried over sodium sulfate, the insoluble material was filtered off, and the solution was concentrated under reduced pressure to give a pale-yellow oil. This oil was dissolved in ethyl acetate (2 ml), and 4N hydrochloric acid-ethyl acetate solution (0.75 ml, 3.0 mmol) was added at room temperature. Then, diethyl ether (20 ml) was added to allow precipitation of a solid. This was filtered, washed with diethyl ether, and dried under reduced pressure to give the title compound (655 mg, yield 91%) as a pale-yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.2, 3H), 2.33 (s, 3H), 2.63 (s, 3H), 2.8-3.0 (m, 4H), 2.92 (s, 3H), 3.35-3.41 (m, 2H), 3.95 (s, 2H), 4.20-4.34 (m, 4H), 4.39 (s, 2H), 7.07-7.15 (m, 3H), 7.29-7.35 (m, 1H), 7.67 (dd, J=2.0, 8.4, 1H), 7.71 (d, J=2.0, 1H), 8.31 (t, J=5.7, 1H), 8.71 (brs, 2H).

Example 206N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(3-methylisoxazol-5-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (194 mg, 0.638 mmol) of Reference Example 122, the compound (119 mg, 0.644 mmol) of Reference Example 17 and the compound (132 mg, 0.701 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 1, step C, the title compound (220 mg, yield 60%) was obtained as a brown solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.1, 3H), 2.25 (s, 3H), 2.31 (s, 3H), 2.86-2.88 (m, 4H), 2.90 (s, 3H), 3.36-3.40 (m, 2H), 3.94 (s, 2H), 4.13 4.16 (2s, 2H), 4.26 4.29 (2s, 2H), 4.36 (s, 2H), 6.67 (s, 1H), 7.07 (d, J=8.4, 1H), 7.24-7.29 (m, 4H), 7.50 (dd, J=8.5, 2.0, 1H), 7.55 (d, J=1.6, 1H), 8.32 (t, J=5.8, 1H), 8.75 (brs, 2H).

Example 207N²-{2-[(4-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(3-methylisoxazol-5-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (194 mg, 0.638 mmol) of Reference Example 122, the compound (131 mg, 0.646 mmol) of Reference Example 19 and the compound (132 mg, 0.701 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 1, step C, the title compound (212 mg, yield 56%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.3, 3H), 2.25 (s, 3H), 2.31 (s, 3H), 2.86-2.90 (m, 4H), 2.92 (s, 3H), 3.36-3.40 (m, 2H), 3.93 (s, 2H), 4.11-4.29 (m, 4H), 4.35 (s, 2H), 6.67 (s, 1H), 7.06-7.11 (m, 2H), 7.15 (dd, J=8.8, 1.9, 1H), 7.29-7.32 (m, 1H), 7.50 (dd, J=8.4, 1.9, 1H), 7.55 (d, J=1.9, 1H), 8.32 (t, J=5.8, 1H), 8.77 (brs, 2H).

Example 208N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(3-methylisoxazol-5-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (153 mg, 0.504 mmol) of Reference Example 123, the compound (94 mg, 0.51 mmol) of Reference Example 17 and the compound (104 mg, 0.55 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 1, step C, the title compound (187 mg, yield 64%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.3, 3H), 2.27 (s, 3H), 2.32 (s, 3H), 2.86-2.88 (m, 4H), 2.90 (s, 3H), 3.36-3.40 (m, 2H), 3.93 (s, 2H), 4.11 4.13 (2s, 2H), 4.24 4.27 (2s, 2H), 4.33 (s, 2H), 6.75 (s, 1H), 7.24-7.29 (m, 5H), 7.34 (dd, J=7.8, 1.1, 1H), 7.55 (d, J=1.0, 1H), 8.35 (t, J=5.8, 1H), 8.79 (brs, 2H).

Example 209N²-{2-[(4-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(3-methylisoxazol-5-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (153 mg, 0.504 mmol) of Reference Example 123, the compound (103 mg, 0.508 mmol) of Reference Example 19 and the compound (104 mg, 0.55 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 1, step C, the title compound (164 mg, yield 55%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.2, 3H), 2.27 (s, 3H), 2.32 (s, 3H), 2.84-2.90 (m, 4H), 2.88 (s, 3H), 3.36-3.41 (m, 2H), 3.93 (s, 2H), 4.03-4.27 (m, 4H), 4.33 (s, 2H), 6.75 (s, 1H), 7.05-7.15 (m, 2H), 7.24-7.36 (m, 3H), 7.55 (d, J=1.0, 1H), 8.35 (t, J=5.8, 1H), 8.85 (brs, 2H).

Example 210N²-(4-acetyl-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (531 mg, 2.00 mmol) of Reference Example 124, the compound (384 mg, 2.08 mmol) of Reference Example 17 and the compound (522 mg, 2.77 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 1, step C, the title compound (768 mg, yield 71%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=7.2, 3H), 2.30 (s, 3H), 2.47 (s, 3H), 2.8-3.0 (m, 4H), 2.91 (s, 3H), 3.35-3.41 (m, 2H), 3.98 (s, 2H), 4.17 (d, J=11.5, 2H), 4.29 (d, J=11.5, 2H), 4.42 (s, 2H), 6.93 (d, J=8.4, 1H), 7.2-7.3 (m, 4H), 7.64-7.68 (m, 2H), 8.35 (t, J=5.8, 1H), 8.81 (brs, 2H).

Example 211N²-(4-acetyl-2-methylphenyl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (265 mg, 1.00 mmol) of Reference Example 124, the compound (205 mg, 1.01 mmol) of Reference Example 19 and the compound (207 mg, 1.10 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 1, step C, the title compound (459 mg, yield 82%) was obtained as a pale-pink solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.2, 3H), 2.30 (s, ³H), 2.47 (s, 3H), 2.88-2.93 (m, 4H), 2.91 (s, 3H), 3.97 (s, 2H), 4.12-4.31 (m, 4H), 4.40 (s, 2H), 6.63 (d, J=8.5, 1H), 7.06-7.11 (m, 1H), 7.15-7.27 (m, 1H), 7.29-7.33 (m, 1H), 7.64-7.68 (m, 2H), 8.32 (t, J=5.8, 1H), 8.59 (brs, 2H).

Example 212N²-(4-acetyl-2-methylphenyl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (265 mg, 1.00 mmol) of Reference Example 124, the compound (205 mg, 1.01 mmol) of Reference Example 19 and the compound (222 mg, 1.10 mmol) of Reference Example 3, and according to the methods of Example 204, step A, and Example 1, step C, the title compound (334 mg, yield 58%) was obtained as a brown solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.19 (d, J=6.6, 6H), 2.30 (s, 3H), 2.47 (s, 3H), 2.88-2.91 (m, 5H), 3.22-3.28 (m, 1H), 3.37-3.41 (m, 2H), 3.97 (s, 2H), 4.13-4.31 (s, 4H), 4.41 (s, 2H), 6.92 (d, J=8.3, 1H), 7.06-7.11 (m, 1H), 7.16 (dd, J=9.0, 1.9, 1H), 7.29-7.33 (m, 1H), 7.64-7.67 (m, 2H), 7.36 (t, J=5.7, 1H), 8.77 (brs, 2H).

Example 213N²-(4-acetyl-2-methylphenyl)-N²-{2-[(4-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (297 mg, 1.12 mmol) of Reference Example 124, the compound (234 mg, 1.15 mmol) of Reference Example 18 and the compound (228 mg, 1.21 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 1, step C, the title compound (497 mg, yield 80%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.2, 3H), 2.30 (s, 3H), 2.47 (s, 3H), 2.8-3.0 (m, 4H), 2.93 (s, 3H), 3.35-3.41 (m, 2H), 3.97 (s, 2H), 4.21-4.35 (m, 4H), 4.43 (s, 2H), 6.93 (d, J=8.4, 1H), 7.07-7.16 (m, 2H), 7.29-7.36 (m, 1H), 7.64-7.68 (m, 2H), 8.34 (t, J=5.8, 1H), 8.76 (brs, 2H).

Example 214N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(6-methyl-3-oxo-2,3-dihydro-1H-inden-5-yl)-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-(6-methyl-3-oxo-2,3-dihydro-1H-inden-5-yl)glycine

The compound (297 mg, 1.07 mmol) of Reference Example 126 was dissolved in N,N-dimethylformamide (5 ml), WSC (213 mg, 1.11 mmol) was added at room temperature, and the mixture was stirred at the same temperature for 2 hr. Then, the reaction mixture was stirred under ice-cooling, the compound (211 mg, 1.14 mmol) of Reference Example 17 and N,N-diisopropylethylamine (0.31 ml, 1.8 mmol) were added, and the mixture was stirred at room temperature for 4 hr. To the reaction mixture was added diluted hydrochloric acid, and the precipitated solid was filtered, washed with water, and dried under reduced pressure to give the title compound (343 mg, yield 79%) as a pale-yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 2.34 (s, 3H), 2.55-2.59 (m, 2H), 2.86 (s, 3H), 2.94-2.98 (m, 2H), 3.98 (s, 2H), 4.11 (d, J=11.6, 2H), 4.24 (d, J=11.6, 2H), 4.29 (s, 2H), 7.2-7.3 (m, 4H), 7.32-7.34 (m, 2H), 12.44 (brs, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(6-methyl-3-oxo-2,3-dihydro-1H-inden-5-yl)-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (337 mg, 0.827 mmol) obtained in step A and the compound (224 mg, 1.19 mmol) of Reference Example 2, and according to the method of Example 1, step B, the title compound (388 mg, yield 81%) was obtained as a pale-yellow amorphous solid

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.06 (t, J=7.1, 3H), 1.44 (brs, 9H), 2.44 (s, 3H), 2.64-2.68 (m, 2H), 2.93 (s, 3H), 3.01-3.05 (m, 2H), 3.10-3.25 (m, 2H), 3.25-3.40 (m, 2H), 3.41-3.47 (m, 2H), 3.71 (s, 2H), 4.20 (d, J=11.6, 2H), 4.25 (d, J=11.6, 2H), 4.27 (s, 2H), 7.22-7.30 (m, 5H), 7.60 (s, 1H), 8.31 8.60 (2brs, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(6-methyl-3-oxo-2,3-dihydro-1H-inden-5-yl)-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (382 mg, 0.661 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (356 mg, yield 98%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.2, 3H), 2.37 (s, 3H), 2.56-2.60 (m, 2H), 2.8-3.0 (m, 6H), 2.87 (s, 3H), 3.32-3.40 (m, 2H), 3.87 (s, 2H), 4.10 (d, J=11.5, 2H), 4.25 (d, J=11.5, 2H), 4.29 (s, 2H), 7.2-7.3 (m, 4H), 7.33 (s, 1H), 7.37 (s, 1H), 8.28 (t, J=5.9, 1H), 8.67 (brs, 2H).

Example 215N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-(6-methyl-3-oxo-2,3-dihydro-1H-inden-5-yl)-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N-(6-methyl-3-oxo-2,3-dihydro-1H-inden-5-yl)glycine

Using the compound (281 mg, 1.01 mmol) of Reference Example 126 and the compound (211 mg, 1.04 mmol) of Reference Example 19, and according to the method of Example 214, step A, the title compound (362 mg, yield 84%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 2.34 (s, 3H), 2.55-2.59 (m, 2H), 2.85 (s, 3H), 2.95-2.99 (m, 2H), 3.98 (s, 2H), 4.06-4.26 (m, 4H), 4.28 (s, 2H), 7.04-7.10 (m, 1H), 7.12-7.16 (m, 1H), 7.27-7.32 (m, 1H), 7.32-7.33 (m, 2H), 12.44 (brs, 1H).

Step BN²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-(6-methyl-3-oxo-2,3-dihydro-1H-inden-5-yl)[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (362 mg, 0.851 mmol) obtained in step A and the compound (231 mg, 1.23 mmol) of Reference Example 2, and according to the method of Example 1, step B, the title compound (445 mg, yield 88%) was obtained as a pale-yellow amorphous solid

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.07 (t, J=7.1, 3H), 1.44 (brs, 9H), 2.44 (s, 3H), 2.64-2.68 (m, 2H), 2.93 (s, 3H), 3.01-3.05 (m, 2H), 3.10-3.25 (m, 2H), 3.25-3.40 (m, 2H), 3.41-3.47 (m, 2H), 3.70 (s, 2H), 4.16-4.23 (m, 4H), 4.26 (s, 2H), 6.93-7.00 (m, 2H), 7.16-7.21 (m, 1H), 7.30 (s, 1H), 7.59 (s, 1H), 8.29 8.59 (2brs, 1H).

Step CN²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-(6-methyl-3-oxo-2,3-dihydro-1H-inden-5-yl)-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (442 mg, 0.742 mmol) obtained in step B and according to the method of Example 1, step C, the title compound (409 mg, yield 97%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.2, 3H), 2.37 (s, 3H), 2.56-2.60 (m, 2H), 2.8-2.9 (m, 4H), 2.86 (s, 3H), 2.95-2.99 (m, 2H), 3.32-3.40 (m, 2H), 3.87 (s, 2H), 4.05-4.27 (m, 4H), 4.28 (s, 2H), 7.05-7.11 (m, 1H), 7.13-7.16 (m, 1H), 7.28-7.32 (m, 1H), 7.33 (s, 1H), 7.37 (s, 1H), 8.28 (brs, 1H), 8.72 (brs, 2H).

Example 216N²-{2-[(4-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-(6-methyl-3-oxo-2,3-dihydro-1H-inden-5-yl)-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (308 mg, 1.11 mmol) of Reference Example 126, the compound (232 mg, 1.14 mmol) of Reference Example 18 and the compound (230 mg, 1.22 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 1, step C, the title compound (512 mg, yield 81%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.2, 3H), 2.37 (s, 3H), 2.56-2.60 (m, 2H), 2.80-2.95 (m, 4H), 2.88 (s, 3H), 2.95-2.99 (m, 2H), 3.33-3.40 (m, 2H), 3.87 (s, 2H), 4.1-4.4 (m, 4H), 4.30 (s, 2H), 7.07-7.15 (m, 2H), 7.29-7.35 (m, 1H), 7.33 (s, 1H), 7.38 (s, 1H), 8.29 (t, J=5.8, 1H), 8.76 (brs, 2H).

The compounds of Examples 193-216 are shown below.

TABLE 15StructuralLC-MSExampleFormulaTMW(found)193 [Image Omitted]

531.05495 194 [Image Omitted]

594.57522 195 [Image Omitted]

580.55508 196 [Image Omitted]

598.59526 197 [Image Omitted]

584.56512 198 [Image Omitted]

557.54485 199 [Image Omitted]

592.56520 200 [Image Omitted]

541.08505 201 [Image Omitted]

514.06478 202 [Image Omitted]

514.06478 203 [Image Omitted]

592.56520 204 [Image Omitted]

596.52524 205 [Image Omitted]

596.52524 206 [Image Omitted]

577.55505 207 [Image Omitted]

595.54523 208 [Image Omitted]

577.55505 209 [Image Omitted]

595.54523 210 [Image Omitted]

538.51466 211 [Image Omitted]

556.50484 212 [Image Omitted]

570.53498 213 [Image Omitted]

556.50484 214 [Image Omitted]

550.52478 215 [Image Omitted]

568.51496 216 [Image Omitted]

568.51496

Example 217N²-{2-[2,3-dihydro-1H-inden-2-yl(methyl)amino]-2-oxoethyl}-N²-(6-methyl-3-oxo-2,3-dihydro-1H-inden-5-yl)-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (354 mg, 1.28 mmol) of Reference Example 126, the compound (240 mg, 1.31 mmol) of Reference Example 23 and the compound (296 mg, 1.57 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 1, step C, the title compound (220 mg, yield 33%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=7.2, 3H), 2.39 (s, 3H), 2.57-2.60 (m, 2H), 2.65 2.75 (2s, 3H), 2.84-3.12 (m, 10H), 3.33-3.38 (m, 2H), 3.80 3.84 (2s, 2H), 4.06 4.22 (2s, 2H), 4.84-4.91 5.25-5.34 (2m, 1H), 7.12-7.22 (m, 4H), 7.35 (s, 1H), 7.40 7.43 (2s, 1H), 8.35-8.39 (m, 1H), 8.73 (brs, 2H).

Example 218N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(6-methyl-3-oxo-2,3-dihydro-1H-inden-5-yl)-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (277 mg, 0.999 mmol) of Reference Example 126, the compound (187 mg, 1.01 mmol) of Reference Example 17 and the compound (223 mg, 1.10 mmol) of Reference Example 3, and according to the methods of Example 204, step A, and Example 1, step C, the title compound (295 mg, yield 52%) was obtained as a brown solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.19 (t, J=6.5, 6H), 2.38 (s, 3H), 2.56-2.59 (m, 2H), 2.86-2.88 (m, 5H), 2.96-2.98 (m, 2H), 3.20-3.27 (m, 1H), 3.36-3.39 (m, 2H), 3.88 (s, 2H), 4.09-4.30 (m, 6H), 7.24-7.29 (m, 4H), 7.33 (s, 1H), 7.37 (s, 1H), 8.33 (t, J=5.7, 1H), 8.86 (brs, 2H).

Example 219N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-(6-methyl-3-oxo-2,3-dihydro-1H-inden-5-yl)-N¹-[2-(isopropylamino)ethyl]glycinamide dihydrochloride

Using the compound (277 mg, 0.999 mmol) of Reference Example 126, the compound (205 mg, 1.01 mmol) of Reference Example 19 and the compound (223 mg, 1.10 mmol) of Reference Example 3, and according to the methods of Example 204, step A, and Example 1, step C, the title compound (415 mg, yield 71%) was obtained as a brown solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.19 (d, J=6.6, 6H), 2.37 (s, 3H), 2.56-2.59 (m, 2H), 2.86-2.88 (m, 5H), 2.96-2.98 (m, 2H), 3.20-3.27 (m, 1H), 3.36-3.39 (m, 2H), 3.88 (s, 2H), 4.06-4.26 (m, 4H), 4.29 (s, 2H), 7.05-7.10 (m, 1H), 7.15 (dd, J=8.8, 1.9, 1H), 7.28-7.32 (m, 1H), 7.33 (s, 1H), 7.36 (s, 1H), 8.32 (t, J=5.8, 1H), 8.87 (brs, 2H).

Example 220N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(6-methyl-1-oxo-2,3-dihydro-1H-inden-5-yl)-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (261 mg, 0.941 mmol) of Reference Example 125, the compound (176 mg, 1.01 mmol) of Reference Example 17 and the compound (195 mg, 1.10 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 1, step C, the title compound (94 mg, yield 18%) was obtained as a pale-pink solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.16 (d, J=7.3, 3H), 2.29 (s, 3H), 2.49-2.54 (m, 2H), 2.89-2.92 (m, 9H), 3.38-3.40 (m, 2H), 3.99 (s, 2H), 4.15 4.18 (2s, 2H), 4.28 4.31 (2s, 2H), 4.43 (s, 2H), 6.97 (s, 1H), 7.24-7.30 (m, 4H), 7.34 (s, 1H), 8.36 (t, J=5.7, 1H), 8.85 (brs, 2H).

Example 221N²-{2-[(4-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-(6-methyl-1-oxo-2,3-dihydro-1H-inden-5-yl)-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (261 mg, 0.941 mmol) of Reference Example 125, the compound (193 mg, 1.01 mmol) of Reference Example 18 and the compound (195 mg, 1.10 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 1, step C, the title compound (98 mg, yield 18%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=7.2, 3H), 2.29 (s, 3H), 2.49-2.54 (m, 2H), 2.90-2.96 (m, 6H), 2.93 (s, 3H), 3.37-3.41 (m, 2H), 3.98 (s, 2H), 4.21 4.24 (2s, 2H), 4.31 4.35 (2s, 2H), 4.44 (s, 2H), 6.98 (s, 1H), 7.07-7.15 (m, 2H), 7.32-7.35 (m, 2H), 8.34 (t, J=5.8, 1H), 8.80 (brs, 2H).

Example 222N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-(6-methyl-1-oxo-2,3-dihydro-1H-inden-5-yl)-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (261 mg, 0.941 mmol) of Reference Example 125, the compound (193 mg, 1.01 mmol) of Reference Example 19 and the compound (195 mg, 1.10 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 1, step C, the title compound (98 mg, yield 19%) was obtained as a brown solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=7.1, 3H), 2.28 (s, 3H), 2.49-2.54 (m, 2H), 2.88-2.96 (m, 6H), 2.91 (s, 3H), 3.37-3.41 (m, 2H), 3.99 (s, 2H), 4.13-4.31 (m, 4H), 4.42 (s, 2H), 6.97 (s, 1H), 7.06-7.11 (m, 1H), 7.16 (dd, J=9.0, 2.0, 1H), 7.30-7.33 (m, 1H), 7.34 (s, 1H), 8.35 (t, J=5.7, 1H), 8.83 (brs, 2H).

Example 223N²-(5-cyano-4-fluoro-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-(5-cyano-4-fluoro-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (399 mg, 1.50 mmol) of Reference Example 128, the compound (280 mg, 1.52 mmol) of Reference Example 17 and the compound (311 mg, 1.65 mmol) of Reference Example 2, and according to the method of Example 204, step A, the title compound (769 mg, yield 90%) was obtained as a bistered oil.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 0.95 (brs, 3H), 1.35 (s, 9H), 2.35 (s, 3H), 2.87 (s, 3H), 3.04-3.16 (m, 6H), 3.77 (s, 2H), 4.11 4.14 (2s, 2H), 4.23-4.26 (m, 4H), 7.23-7.32 (m, 5H), 7.59 (d, J=6.2, 1H), 8.01 (brs, 1H).

Step BN²-(5-cyano-4-fluoro-2-methylphenyl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (256 mg, 0.452 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (219 mg, yield 90%) was obtained as a colorless amorphous solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.19 (t, J=7.1, 1H), 2.36 (s, 3H), 2.87 (s, 3H), 2.87-2.91 (m, 4H), 3.35-3.37 (m, 2H), 3.85 (s, 2H), 4.12 4.14 (2s, 2H), 4.23-4.26 (m, 4H), 7.24-7.33 (m, 5H), 7.60 (d, J=6.2, 1H), 8.26 (t, J=5.6, 1H), 8.76 (brs, 2H).

Example 224N²-(5-cyano-4-fluoro-2-methylphenyl)-N²-{2-[(4-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-(5-cyano-4-fluoro-2-methylphenyl)-N²-{2-[(4-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (399 mg, 1.50 mmol) of Reference Example 128, the compound (307 mg, 1.52 mmol) of Reference Example 18 and the compound (311 mg, 1.65 mmol) of Reference Example 2, and according to the method of Example 204, step A, the title compound (760 mg, yield 87%) was obtained as a bistered oil.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 0.95 (brs, 3H), 1.35 (s, 9H), 2.35 (s, 3H), 2.88 (s, 3H), 3.04-3.17 (m, 6H), 3.76 (s, 2H), 4.17-4.30 (m, 6H), 7.07-7.14 (m, 2H), 7.29-7.34 (m, 2H), 7.60 (d, J=6.2, 1H), 8.00 (brs, 1H).

Step BN²-(5-cyano-4-fluoro-2-methylphenyl)-N²-{2-[(4-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (253 mg, 0.433 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (209 mg, yield 84%) was obtained as a colorless amorphous solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=7.1, 3H), 2.37 (s, 3H), 2.88 (brs, 7H), 3.34-3.39 (m, 2H), 3.84 (s, 2H), 4.18-4.32 (m, 6H), 7.07-7.14 (m, 2H), 7.30-7.35 (m, 2H), 7.61 (d, J=6.2, 1H), 8.26 (t, J=5.7, 1H), 8.82 (brs, 2H).

Example 225N²-(5-cyano-4-fluoro-2-methylphenyl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-(5-cyano-4-fluoro-2-methylphenyl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (399 mg, 1.50 mmol) of Reference Example 128, the compound (307 mg, 1.52 mmol) of Reference Example 19 and the compound (311 mg, 1.65 mmol) of Reference Example 2, and according to the method of Example 204, step A, the title compound (784 mg, yield 89%) was obtained as a bistered oil.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 0.95 (brs, 3H), 1.35 (s, 9H), 2.35 (s, 3H), 2.86 (s, 3H), 3.04-3.17 (m, 6H), 3.77 (s, 2H), 4.09-4.26 (m, 6H), 7.05-7.10 (m, 2H), 7.14 (dd, J=8.9, 1.8, 2H), 7.28-7.32 (m, 2H), 7.58 (d, J=6.2, 1H), 8.01 (brs, 1H).

Step BN²-(5-cyano-4-fluoro-2-methylphenyl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (261 mg, 0.447 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (222 mg, yield 89%) was obtained as a colorless amorphous solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=7.2, 3H), 2.36 (s, 3H), 2.87 (s, 3H), 2.87-2.91 (m, 4H), 3.34-3.39 (m, 2H), 3.84 (s, 2H), 4.09-4.25 (m, 6H), 7.05-7.11 (m, 2H), 7.15 (dd, J=8.8, 2.0, 1H), 7.29-7.33 (m, 2H), 7.60 (d, J=6.1, 1H), 8.27 (t, J=5.8, 1H), 8.84 (brs, 2H).

Example 226N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[4-fluoro-2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[4-fluoro-2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (513 mg, 0.905 mmol) of Example 223, step A and according to the method of Reference Example 62, step A, the title compound (513 mg, yield 91%) was obtained as a yellow oil.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 0.92 (brs, 3H), 1.34 (s, 9H), 2.34 (s, 3H), 2.66 (s, 3H), 2.86 (s, 3H), 3.03-3.17 (m, 6H), 3.80 (s, 2H), 4.10 4.12 (2s, 2H), 4.23-4.27 (m, 4H), 7.19-7.28 (m, 5H), 7.81 (d, J=6.8, 1H), 8.07 (brs, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[4-fluoro-2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (513 mg, 0.822 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (458 mg, yield 93%) was obtained as a colorless amorphous solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.2, 3H), 2.36 (s, 3H), 2.67 (s, 3H), 2.87 (s, 3H), 2.87-2.91 (m, 4H), 3.34-3.39 (m, 2H), 3.88 (s, 2H), 4.10 4.13 (2s, 2H), 4.23 4.26 (2s, 2H), 4.30 (s, 2H), 7.20-7.28 (m, 5H), 7.81 (d, J=6.8, 1H), 8.32 (t, J=5.8, 1H), 8.79 (brs, 2H).

Example 227N²-{2-[(4-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[4-fluoro-2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[(4-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[4-fluoro-2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (507 mg, 0.867 mmol) of Example 224, step A and according to the method of Reference Example 62, step A, the title compound (487 mg, yield 88%) was obtained as a yellow oil.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 0.92 (brs, 3H), 1.34 (s, 9H), 2.34 (s, 3H), 2.66 (s, 3H), 2.87 (s, 3H), 3.03-3.17 (m, 6H), 3.79 (s, 2H), 4.16-4.34 (m, 6H), 7.07-7.14 (m, 2H), 7.19-7.22 (m, 1H), 7.29-7.34 (m, 1H), 7.81 (d, J=6.7, 1H), 8.06 (brs, 1H).

Step BN²-{2-[(4-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[4-fluoro-2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (487 mg, 0.759 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (397 mg, yield 85%) was obtained as a colorless amorphous solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.1, 3H), 2.36 (s, 3H), 2.67 (s, 3H), 2.87 (s, 3H), 2.87-2.91 (m, 4H), 3.35-3.39 (m, 2H), 3.87 (s, 2H), 4.16-4.38 (m, 6H), 7.07-7.14 (m, 2H), 7.20-7.23 (m, 1H), 7.30-7.35 (m, 1H), 7.81 (d, J=6.8, 1H), 8.32 (t, J=5.8, 1H), 8.83 (brs, 2H).

Example 228N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[4-fluoro-2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[4-fluoro-2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (523 mg, 0.894 mmol) of Example 225, step A and according to the method of Reference Example 62, step A, the title compound (552 mg, yield 96%) was obtained as a yellow oil.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 0.92 (brs, 3H), 1.34 (s, 9H), 2.34 (s, 3H), 2.66 (s, 3H), 2.86 (s, 3H), 3.03-3.17 (m, 6H), 3.80 (s, 2H), 4.10-4.26 (m, 6H), 7.05-7.10 (m, 1H), 7.13-7.15 (m, 1H), 7.19-7.22 (m, 1H), 7.27-7.31 (m, 1H), 7.80 (d, J=6.8, 1H), 8.05 (brs, 1H).

Step BN²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[4-fluoro-2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-W-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (552 mg, 0.860 mmol) obtained in step A and according to the method of Example 1, step C, the title compound (452 mg, yield 85%) was obtained as a colorless amorphous solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.2, 3H), 2.35 (s, 3H), 2.67 (s, 3H), 2.86 (s, 3H), 2.86-2.91 (m, 4H), 3.34-3.39 (m, 2H), 3.88 (s, 2H), 4.07-4.29 (m, 6H), 7.06-7.11 (m, 1H), 7.15 (dd, J=8.8, 1.9, 1H), 7.20-7.23 (m, 1H), 7.28-7.31 (m, 1H), 7.81 (d, J=6.9, 1H), 8.31 (t, J=5.7, 1H), 8.78 (brs, 2H).

Example 229N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(3-methyl-1,2,4-oxadiazol-5-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (305 mg, 1.00 mmol) of Reference Example 129, the compound (187 mg, 1.01 mmol) of Reference Example 17 and the compound (207 mg, 2.02 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 1, step C, the title compound (479 mg, yield 83%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=7.1, 3H), 2.34 (s, 3H), 2.37 (s, 3H), 2.89-2.90 (m, 4H), 2.92 (s, 3H), 3.37-3.42 (m, 2H), 4.00 (s, 2H), 4.17 4.20 (2s, 2H), 4.28 4.31 (2s, 2H), 4.45 (s, 2H), 7.03 (d, J=8.6, 1H), 7.24-7.30 (m, 4H), 7.75 (dd, J=8.5, 1.9, 1H), 7.79 (d, J=1.8, 1H), 8.38 (t, J=5.7, 1H), 8.89 (brs, 2H).

Example 230N²-{2-[(4-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(3-methyl-1,2,4-oxadiazol-5-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (401 mg, 1.31 mmol) of Reference Example 129, the compound (271 mg, 1.34 mmol) of Reference Example 18 and the compound (271 mg, 1.44 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 1, step C, the title compound (491 mg, yield 63%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.2, 3H), 2.34 (s, 3H), 2.37 (s, 3H), 2.8-3.0 (m, 4H), 2.93 (s, 3H), 3.35-3.41 (m, 2H), 3.99 (s, 2H), 4.22-4.35 (m, 4H), 4.44 (s, 2H), 7.05 (d, J=8.5, 1H), 7.07-7.16 (m, 2H), 7.29-7.36 (m, 1H), 7.76 (dd, J=2.1, 8.5, 1H), 7.79 (d, J=2.1, 1H), 8.33 (t, J=5.9, 1H), 8.67 (brs, 2H).

Example 231N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(3-methyl-1,2,4-oxadiazol-5-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (305 mg, 1.00 mmol) of Reference Example 129, the compound (205 mg, 1.01 mmol) of Reference Example 19 and the compound (207 mg, 1.01 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 1, step C, the title compound (498 mg, yield 84%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=7.2, 1H), 2.33 (s, 3H), 2.37 (s, 3H), 2.87-2.91 (m, 4H), 2.91 (s, 3H), 3.37-3.42 (m, 2H), 3.99 (s, 2H), 4.14-4.31 (m, 4H), 4.44 (s, 2H), 7.02-7.11 (m, 2H), 7.16 (dd, J=8.9, 1.9, 1H), 7.30-7.33 (m, 1H), 7.75 (dd, J=8.5, 2.1, 1H), 7.79 (d, J=1.7, 1H), 8.38 (t, J=5.7, 1H), 8.90 (brs, 2H).

Example 232N²-{2-[2,3-dihydro-1H-inden-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(3-methyl-1,2,4-oxadiazol-5-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (438 mg, 1.43 mmol) of Reference Example 129, the compound (269 mg, 1.46 mmol) of Reference Example 23 and the compound (307 mg, 1.63 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 1, step C, the title compound (635 mg, yield 82%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.17 (t, J=7.2, 3H), 2.35 (s, 3H), 2.37 (s, 3H), 2.71 2.79 (2s, 3H), 2.8-3.2 (m, 8H), 3.37-3.42 (m, 2H), 3.97 3.98 (2s, 2H), 4.22 4.40 (2s, 2H), 4.79-4.88 (m, 0.4H), 5.30-5.38 (m, 0.6H), 7.04-7.10 (m, 1H), 7.14-7.17 (m, 2H), 7.21-7.23 (m, 2H), 7.77 (d, J=8.6, 1H), 7.81 (s, 1H), 8.45 (t, J=5.3, 1H), 8.86 (brs, 2H).

Example 233N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3-methyl-8-oxo-5,6,7,8-tetrahydronaphthalen-2-yl)-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (340 mg, 1.17 mmol) of Reference Example 127, the compound (222 mg, 1.20 mmol) of Reference Example 17 and the compound (246 mg, 1.31 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 1, step C, the title compound (477 mg, yield 72%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.2, 3H), 1.90-2.05 (m, 2H), 2.31 (s, 3H), 2.45-2.55 (m, 2H), 2.81 (t, J=5.8, 2H), 2.85-2.95 (m, 4H), 2.87 (s, 3H), 3.33-3.40 (m, 2H), 3.84 (s, 2H), 4.10 (d, J=11.5, 2H), 4.25 (d, J=11.5, 2H), 4.28 (s, 2H), 7.10 (s, 1H), 7.22-7.30 (m, 4H), 7.63 (s, 1H), 8.33 (t, J=5.8, 1H), 8.68 (brs, 2H).

Example 234N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-(3-methyl-8-oxo-5,6,7,8-tetrahydronaphthalen-2-yl)-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (310 mg, 1.06 mmol) of Reference Example 127, the compound (221 mg, 1.09 mmol) of Reference Example 19 and the compound (216 mg, 1.15 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 1, step C, the title compound (522 mg, yield 85%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.2, 3H), 1.90-2.05 (m, 2H), 2.30 (s, 3H), 2.45-2.55 (m, 2H), 2.81 (t, J=5.8, 2H), 2.80-2.95 (m, 4H), 2.86 (s, 3H), 3.33-3.40 (m, 2H), 3.84 (s, 2H), 4.00-4.25 (m, 4H), 4.27 (s, 2H), 7.05-7.11 (m, 1H), 7.11 (s, 1H), 7.13-7.17 (m, 1H), 7.28-7.32 (m, 1H), 7.62 (s, 1H), 8.33 (t, J=5.8, 1H), 8.70 (brs, 2H).

Example 235N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(4-methyl-1,3-thiazol-2-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (386 mg, 1.20 mmol) of Reference Example 130, the compound (226 mg, 1.22 mmol) of Reference Example 17 and the compound (262 mg, 1.39 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 57, step B, the title compound (466 mg, yield 70%) was obtained as a yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.14 (t, J=7.2, 3H), 2.32 (s, 3H), 2.39 (d, J=0.9, 3H), 2.8-3.0 (m, 4H), 2.91 (s, 3H), 3.34-3.40 (m, 2H), 3.93 (s, 2H), 4.14 (d, J=11.4, 2H), 4.28 (d, J=11.4, 2H), 4.35 (s, 2H), 7.07 (d, J=8.4, 1H), 7.21 (d, J=0.9, 1H), 7.23-7.30 (m, 4H), 7.59 (dd, J=2.1, 8.4, 1H), 7.65 (d, J=2.1, 1H), 8.31 (t, J=5.8, 1H), 8.57 (brs, 2H).

Example 236N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(5-methyl-1,3-thiazol-2-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (290 mg, 0.905 mmol) of Reference Example 131, the compound (168 mg, 0.910 mmol) of Reference Example 17 and the compound (186 mg, 0.988 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 57, step B, the title compound (326 mg, yield 65%) was obtained as a yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.14 (t, J=7.2, 3H), 2.31 (s, 3H), 2.46 (d, J=1.1, 3H), 2.8-3.0 (m, 4H), 2.90 (s, 3H), 3.34-3.40 (m, 2H), 3.93 (s, 2H), 4.14 (d, J=11.4, 2H), 4.27 (d, J=11.4, 2H), 4.35 (s, 2H), 7.07 (d, J=8.4, 1H), 7.23-7.30 (m, 4H), 7.51 (d, J=1.1, 1H), 7.55 (dd, J=2.1, 8.4, 1H), 7.60 (d, J=2.1, 1H), 8.31 (broad t, 1H), 8.67 (brs, 2H).

Example 237N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(5-methyl-1,3-thiazol-2-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (293 mg, 0.915 mmol) of Reference Example 131, the compound (186 mg, 0.920 mmol) of Reference Example 19 and the compound (192 mg, 1.02 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 57, step B, the title compound (420 mg, yield 80%) was obtained as a yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.14 (t, J=7.2, 3H), 2.31 (s, 3H), 2.46 (d, J=1.1, 3H), 2.8-3.0 (m, 4H), 2.90 (s, 3H), 3.3-3.4 (m, 2H), 3.92 (s, 2H), 4.09-4.30 (m, 4H), 4.34 (s, 2H), 7.07 (d, J=8.4, 1H), 7.08-7.12 (m, 1H), 7.13-7.17 (m, 1H), 7.28-7.33 (m, 1H), 7.51 (d, J=1.1, 1H), 7.55 (dd, J=2.1, 8.4, 1H), 7.60 (d, J=2.1, 1H), 8.31 (t, J=5.8, 1H), 8.66 (brs, 2H).

Example 238N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(5-methyl-1,3,4-thiadiazol-2-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (368 mg, 1.15 mmol) of Reference Example 132, the compound (221 mg, 1.16 mmol) of Reference Example 17 and the compound (252 mg, 1.34 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 1, step C, the title compound (359 mg, yield 52%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.14 (t, J=7.2, 3H), 2.33 (s, 3H), 2.74 (s, 3H), 2.8-3.0 (m, 4H), 2.91 (s, 3H), 3.33-3.40 (m, 2H), 3.95 (s, 2H), 4.15 (d, J=11.5, 2H), 4.28 (d, J=11.5, 2H), 4.37 (s, 2H), 7.08 (d, J=8.4, 1H), 7.24-7.30 (m, 4H), 7.61 (dd, J=2.1, 8.4, 1H), 7.66 (d, J=2.1, 1H), 8.30 (t, J=5.6, 1H), 8.55 (brs, 2H).

Example 239N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(5-methyl-1,3,4-thiadiazol-2-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (371 mg, 1.15 mmol) of Reference Example 132, the compound (242 mg, 1.20 mmol) of Reference Example 19 and the compound (252 mg, 1.34 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 1, step C, the title compound (389 mg, yield 55%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.14 (t, J=7.2, 3H), 2.32 (s, 3H), 2.74 (s, 3H), 2.8-3.0 (m, 4H), 2.91 (s, 3H), 3.33-3.40 (m, 2H), 3.95 (s, 2H), 4.11-4.31 (m, 4H), 4.36 (s, 2H), 7.06-7.12 (m, 1H), 7.07 (d, J=8.4, 1H), 7.15 (d, J=8.8, 1H), 7.29-7.33 (m, 1H), 7.61 (dd, J=2.1, 8.4, 1H), 7.66 (d, J=2.1, 1H), 8.29 (t, J=5.8, 1H), 8.48 (brs, 2H).

The compounds of Examples 217-239 are shown below.

TABLE 16StructuralLC-MSExampleFormulaTMW(found)217 [Image Omitted]

513.07477 218 [Image Omitted]

564.55492 219 [Image Omitted]

582.54510 220 [Image Omitted]

550.52478 221 [Image Omitted]

568.51496 222 [Image Omitted]

568.51496 223 [Image Omitted]

539.47467 224 [Image Omitted]

557.46485 225 [Image Omitted]

557.46485 226 [Image Omitted]

596.52524 227 [Image Omitted]

614.51542 228 [Image Omitted]

614.51542 229 [Image Omitted]

578.53506 230 [Image Omitted]

596.52524 231 [Image Omitted]

596.52524 232 [Image Omitted]

541.08505 233 [Image Omitted]

564.55492 234 [Image Omitted]

582.54510 235 [Image Omitted]

557.15521 236 [Image Omitted]

557.15521 237 [Image Omitted]

575.14539 238 [Image Omitted]

594.60522 239 [Image Omitted]

612.59540

Example 241N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(1,6-dimethyl-1H-indazol-5-yl)-N¹-[2-(ethylamino)ethyl]glycinamide hydrochlorideStep AN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-[6-methyl-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-5-yl]glycine

To N,N-dimethylformamide (80 ml) were added the compound (6.33 g, 18.2 mmol) of Reference Example 133 and WSC₃(3.70 g, 19.3 mmol), and the mixture was stirred at room temperature for 1 hr. The reaction mixture was ice-cooled, the compound (3.44 g, 18.6 mmol) of Reference Example 17 and N,N-diisopropylethylamine (5.0 ml, 29.4 mmol) were added, and the mixture was stirred at the same temperature for 1 hr. To the reaction mixture was added diluted hydrochloric acid, and the precipitated solid was filtered, washed with water, and dried under reduced pressure to give the title compound (7.44 g, yield 86%) as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.5-1.6 (m, 2H), 1.65-1.80 (m, 1H), 1.85-2.10 (m, 2H), 2.3-2.5 (m, 1H), 2.40 (s, 3H), 2.86 (s, 3H), 3.68-3.80 (m, 1H), 3.84-3.89 (m, 1H), 3.98 (s, 2H), 4.03-4.25 (m, 4H), 4.27 (s, 2H), 5.73 (dd, J=2.4, 9.7, 1H), 7.22-7.27 (m, 4H), 7.46 (s, 1H), 7.54 (s, 1H), 7.92 (s, 1H), 12.47 (brs, 1H).

Step BN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-(6-methyl-1H-indazol-5-yl)glycine ethyl ester

The compound (2.23 g, 4.67 mmol) of step A was dissolved in ethanol (60 ml), concentrated sulfuric acid (0.5 ml) was added at root temperature, and the mixture was heated under reflux for 80 min. The reaction mixture was concentrated under reduced pressure, and the residue was diluted with ethyl acetate. The organic layer was washed with aqueous sodium bicarbonate and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (1.64 g, yield 83%) as a colorless amorphous solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.12 (t, J=7.1, 3H), 2.39 (s, 3H), 2.84 (s, 3H), 3.99 (q, J=7.1, 2H), 4.03-4.21 (m, 4H), 4.22 (d, J=11.8, 2H), 4.25 (s, 2H), 7.25 (brs, 4H), 7.27 (s, 1H), 7.55 (s, 1H), 7.88 (s, 1H), 12.71 (brs, 1H).

Step CN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-(1,6-dimethyl-1H-indazol-5-yl)glycine ethyl ester

The compound (871 mg, 2.07 mmol) of step B was dissolved in N,N-dimethylformamide (19 ml), 60% sodium hydride (109 mg, 2.73 mmol) was added under ice-cooling with stirring, and the mixture was stirred at the same temperature for 1 hr. Then, methyl iodide (0.44 ml) was added, and the mixture was stirred under ice-cooling for 90 min. The reaction mixture was diluted with 10% citric acid, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium hydrogen carbonate and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexaneâ†’ethyl acetate-methanol) to give the title compound (653 mg, yield 73%) as a colorless amorphous solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.19 (t, J=7.1, 3H), 2.52 (s, 3H), 2.92 (s, 3H), 3.99 (s, 3H), 4.05-4.25 (m, 6H), 4.38 (s, 2H), 7.17 (s, 1H), 7.18-7.25 (m, 4H), 7.68 (s, 1H), 7.82 (s, 1H).

In addition, N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-(2,6-dimethyl-2H-indazol-5-yl)glycine ethyl ester (171 mg, yield 19%) was obtained as a colorless solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.18 (t, J=7.2, 3H), 2.45 (s, 3H), 2.91 (s, 3H), 4.08 (d, J=14, 2H), 4.09 (q, J=7.2, 2H), 4.16 (d, J=14, 2H), 4.21 (s, 2H), 4.37 (s, 2H), 7.17-7.30 (m, 4H), 7.45 (s, 1H), 7.51 (s, 1H), 7.70 (s, 1H).

Step DN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-(1,6-dimethyl-1H-indazol-5-yl)glycine

The compound (631 mg, 1.45 mmol) of step C was dissolved in a methanol (5 ml)-tetrahydrofuran (2 ml) mixed solvent, 1N sodium hydroxide (5 ml) was added at room temperature, and the mixture was stirred at room temperature for 70 min. To the reaction mixture was added 1N hydrochloric acid (5 ml), and the solution was concentrated under reduced pressure. The precipitated solid was filtered, washed with water, and dried under reduced pressure to give the title compound (517 mg, yield 88%) as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.41 (s, 3H), 2.86 (s, 3H), 3.95 (s, 3H), 3.97 (s, 2H), 4.07 (d, J=12, 2H), 4.23 (d, J=12, 2H), 4.27 (s, 2H), 7.21-7.28 (m, 4H), 7.37 (s, 1H), 7.53 (s, 1H), 7.85 (s, 1H), 12.49 (brs, 1H).

Step EN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(1,6-dimethyl-1H-indazol-5-yl)-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (262 mg, 0.643 mmol) of step D and the compound (183 mg, 0.972 mmol) of Reference Example 2, and according to the methods of Example 1, step B, and Example 57, step B, the title compound (273 mg, yield 83%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.13 (t, J=7.2, 3H), 2.43 (s, 3H), 2.8-3.0 (m, 4H), 2.87 (s, 3H), 3.30-3.45 (m, 2H), 3.83 (s, 2H), 3.96 (s, 3H), 4.04 (d, J=12, 2H), 4.22 (d, J=12, 2H), 4.25 (s, 2H), 7.25 (brs, 4H), 7.40 (s, 1H), 7.58 (s, 1H), 7.86 (s, 1H), 8.42 (t, J=5.7, 1H), 8.63 (brs, 2H).

Example 242N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(1,6-dimethyl-1H-indazol-5-yl)-N¹-[2-(isopropylamino)ethyl]glycinamide hydrochloride

Using the compound (248 mg, 0.609 mmol) of Example 241, step D, and the compound (182 mg, 0.900 mmol) of Reference Example 3, and according to the methods of Example 1, step B, and Example 57, step B, the title compound (197 mg, yield 61%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.17 (d, J=6.6, 6H), 2.44 (s, 3H), 2.8-3.0 (m, 2H), 2.87 (s, 3H), 3.1-3.3 (m, 1H), 3.34-3.39 (m, 2H), 3.84 (s, 2H), 3.96 (s, 3H), 4.05 (d, J=12, 2H), 4.22 (d, J=12, 2H), 4.27 (s, 2H); 7.25 (brs, 4H), 7.40 (s, 1H), 7.58 (s, 1H), 7.86 (s, 1H), 8.43 (t, J=5.7, 1H), 8.66 (brs, 2H).

Example 243N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2,6-dimethyl-2H-indazol-5-yl)-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-(2,6-dimethyl-2H-indazol-5-yl)glycine ethyl ester (165 mg, 0.379 mmol) obtained in Example 241, step C, and according to the methods of Example 241, steps D and E, the title compound (147 mg, yield 75%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.13 (t, J=7.2, 3H), 2.36 (s, 3H), 2.8-3.0 (m, 4H), 2.87 (s, 3H), 3.30-3.45 (m, 2H), 3.82 (s, 2H), 4.05 (d, J=12, 2H), 4.08 (s, 3H), 4.22 (d, J=12, 2H), 4.24 (s, 2H), 7.25 (brs, 4H), 7.35 (s, 1H), 7.44 (s, 1H), 8.12 (s, 1H), 8.39 (t, J=5.7, 1H), 8.63 (brs, 2H).

Example 244N²-(1,6-dimethyl-1H-indazol-5-yl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochlorideStep AN-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N-[6-methyl-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-5-yl]glycine

Using the compound (601 mg, 1.73 mmol) of Reference Example 133 and the compound (360 mg, 1.78 mmol) of Reference Example 19, and according to the method of Example 241, step A, the title compound (835 mg, yield 97%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.50-1.64 (m, 2H), 1.65-1.81 (m, 1H), 1.86-1.96 (m, 1H), 1.97-2.08 (m, 1H), 2.30-2.43 (m, 1H), 2.40 (s, 3H), 2.85 (s, 3H), 3.65-3.76 (m, 1H), 3.81-3.92 (m, 1H), 3.93-4.30 (m, 4H), 3.98 (s, 2H), 4.26 (s, 2H), 5.73 (dd, J=2.3, 9.7, 1H), 7.04-7.14 (m, 2H), 7.25-7.30 (m, 1H), 7.46 (s, 1H), 7.53 (s, 1H), 7.93 (s, 1H), 12.45 (brs, 1H).

Step BN-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N-(6-methyl-1H-indazol-5-yl)glycine ethyl ester

Using the compound (825 mg, 1.66 mg) of step A, and according to the method of Example 241, step B, the title compound (643 mg, yield 88%) was obtained as a colorless amorphous solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.19 (t, J=7.1, 3H), 2.50 (s, 3H), 2.92 (s, 3H), 4.03-4.20 (m, 4H), 4.10 (q, J=7.1, 2H), 4.17 (s, 2H), 4.38 (s, 2H), 6.86-6.98 (m, 2H), 7.06-7.18 (m, 1H), 7.27 (s, 1H), 7.71 (s, 1H), 7.92 (s, 1H), 9.88 (brs, 1H).

Step CN-(1,6-dimethyl-1H-indazol-5-yl)-N-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}glycine ethyl ester

Using the compound (640 mg, 1.46 mmol) of step B, and according to the method of Example 241, step C, the title compound (456 mg, yield 69%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.19 (t, J=7.1, 3H), 2.52 (s, 3H), 2.91 (s, 3H), 3.99 (s, 3H), 4.03-4.23 (m, 6H), 4.16 (s, 2H), 4.37 (s, 2H), 6.87-6.98 (m, 2H), 7.10-7.16 (m, 1H), 7.18 (s, 1H), 7.67 (s, 1H), 7.82 (s, 1H).

Step DN²-(1,6-dimethyl-1H-indazol-5-yl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (456 mg, 1.01 mmol) of step C, and according to the methods of Example 241, steps D and E, the title compound (410 mg, yield 76%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.13 (t, J=7.2, 3H), 2.43 (s, 3H), 2.8-3.0 (m, 4H), 2.86 (s, 3H), 3.30-3.43 (m, 2H), 3.83 (s, 2H), 3.96 (s, 3H), 3.97-4.22 (m, 4H), 4.24 (s, 2H), 7.04-7.14 (m, 2H), 7.25-7.31 (m, 1H), 7.39 (s, 1H), 7.57 (s, 1H), 7.86 (s, 1H), 8.41 (t, J=5.7, 1H), 8.70 (brs, 2H).

Example 245N²-(2,6-dimethyl-2H-indazol-5-yl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochlorideStep AN-(2,6-dimethyl-2H-indazol-5-yl)-N-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}glycine ethyl ester

As a byproduct of Example 244, step C, the title compound (147 mg, yield 22%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.19 (t, J=7.1, 3H), 2.45 (s, 3H), 2.91 (s, 3H), 3.98-4.17 (m, 6H), 4.14 (s, 3H), 4.20 (s, 2H), 4.36 (s, 2H), 6.87-6.98 (m, 2H), 7.10-7.16 (m, 1H), 7.45 (s, 1H), 7.51 (s, 1H), 7.70 (s, 1H).

Step BN²-(2,6-dimethyl-2H-indazol-5-yl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloric acid

Using the compound (147 mg, 0.324 mmol) of step A, and according to the methods of Example 241, steps D and E, the title compound (101 mg, yield 59%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.13 (t, J=7.2, 3H), 2.36 (s, 3H), 2.8-3.0 (m, 4H), 2.87 (s, 3H), 3.31-3.41 (m, 2H), 3.82 (s, 2H), 3.99-4.21 (m, 4H), 4.08 (s, 3H), 4.23 (s, 2H), 7.03-7.14 (m, 2H), 7.25-7.31 (m, 1H), 7.35 (s, 1H), 7.44 (s, 1H), 8.12 (s, 1H), 8.37 (t, J=5.7, 1H), 8.60 (brs, 2H).

Example 246N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(1-ethyl-6-methyl-1H-indazol-5-yl)-N¹-[2-(ethylamino)ethyl]glycinamide hydrochlorideStep AN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-(1-ethyl-6-methyl-1H-indazol-5-yl)glycine ethyl ester

Using the compound (746 mg, 1.77 mmol) of Example 241, step B and ethyl iodide (0.26 ml, 3.23 mmol), and according to the method of Example 241, step C, the title compound (549 mg, yield 69%) was obtained as a colorless amorphous solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.19 (t, J=7.1, 3H), 1.48 (t, J=7.2, 3H), 2.52 (s, 3H), 2.92 (s, 3H), 4.06-4.15 (m, 4H), 4.16 (s, 2H), 4.20 (d, J=11, 2H), 4.35 (q, J=7.2, 2H), 4.38 (s, 2H), 7.16-7.27 (m, 5H), 7.72 (s, 1H), 7.82 (s, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(1-ethyl-6-methyl-1H-indazol-5-yl)-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (547 mg, 1.09 mmol) obtained in step A and according to the methods of Example 241, steps D and E, the title compound (536 mg, yield 93%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.14 (t, J=7.1, 3H), 1.35 (t, J=7.2, 3H), 2.43 (s, 3H), 2.8-3.0 (m, 4H), 2.87 (s, 3H), 3.33-3.41 (m, 2H), 3.83 (s, 2H), 4.05 (d, J=12, 2H), 4.22 (d, J=12, 2H), 4.25 (s, 2H), 4.35 (q, J=7.2, 2H), 7.25 (brs, 4H), 7.43 (s, 1H), 7.58 (s, 1H), 7.87 (s, 1H), 8.44 (t, J=5.8, 1H), 8.75 (brs, 2H).

Example 247N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2-ethyl-6-methyl-2H-indazol-5-yl)-N¹-[2-(ethylamino)ethyl]glycinamide hydrochlorideStep AN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-(2-ethyl-6-methyl-2H-indazol-5-yl)glycine ethyl ester

As a byproduct of Example 246, step A, the title compound (199 mg, yield 25%) was obtained as a colorless amorphous solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.19 (t, J=7.1, 3H), 1.58 (t, J=7.4, 3H), 2.46 (s, 3H), 2.91 (s, 3H), 4.05-4.15 (m, 4H), 4.19 (d, J=12, 2H), 4.21 (s, 2H), 4.37 (s, 2H), 4.40 (q, J=7.4, 2H), 7.16-7.28 (m, 4H), 7.47 (s, 1H), 7.53 (s, 1H), 7.74 (s, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2-ethyl-6-methyl-2H-indazol-5-yl)-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (198 mg, 0.440 mmol) obtained in step A and according to the methods of Example 241, steps D and E, the title compound (101 mg, yield 43%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); 1.12 (t, J=7.1, 3H), 1.45 (t, J=7.3, 3H), 2.37 (s, 3H), 2.8-3.0 (m, 4H), 2.88 (s, 3H), 3.3-3.4 (m, 2H), 3.82 (s, 2H), 4.05 (d, J=11, 2H), 4.23 (d, J=11, 2H), 4.24 (s, 2H), 4.37 (q, J=7.3, 2H), 7.25 (brs, 4H), 7.36 (s, 1H), 7.44 (s, 1H), 8.17 (s, 1H), 8.39 (broad t, 1H), 8.52 (brs, 2H).

Example 248N²-(1-ethyl-6-methyl-1H-indazol-5-yl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochlorideStep AN-(1-ethyl-6-methyl-1H-indazol-5-yl)-N-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}glycine ethyl ester

Using the compound (1.68 g, 3.82 mmol) of Example 244, step B and ethyl iodide (0.50 ml, 6.25 mmol), and according to the method of Example 241, step C, the title compound (1.22 g, yield 68%) was obtained as a colorless amorphous solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.19 (t, J=7.1, 3H), 1.47 (t, J=7.2, 3H), 2.52 (s, 3H), 2.91 (s, 3H), 4.0-4.2 (m, 6H), 4.16 (s, 2H), 4.35 (q, J=7.2, 2H), 4.37 (s, 2H), 6.87-6.97 (m, 2H), 7.10-7.15 (m, 1H), 7.19 (s, 1H), 7.67 (s, 1H), 7.82 (s, 1H).

Step BN²-(1-ethyl-6-methyl-1H-indazol-5-yl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (1.19 g, 2.55 mmol) of step A, and according to the methods of Example 241, steps D and E, the title compound (634 mg, yield 46%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.13 (t, J=7.2, 3H)), 1.35 (t, J=7.2, 3H), 2.44 (s, 3H), 2.8-3.0 (m, 4H), 2.86 (s, 3H), 3.34-3.40 (m, 2H), 3.85 (s, 2H), 4.00-4.24 (m, 4H), 4.28 (s, 2H), 4.35 (q, J=7.2, 2H), 7.04-7.15 (m, 2H), 7.26-7.30 (m, 1H), 7.44 (s, 1H), 7.61 (s, 1H), 7.88 (s, 1H), 8.44 (broad t, 1H), 8.72 (brs, 2H).

Example 249N²-(2-ethyl-6-methyl-2H-indazol-5-yl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochlorideStep AN-(2-ethyl-6-methyl-2H-indazol-5-yl)-N-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}glycine ethyl ester

As a byproduct of Example 248, step A, the title compound (435 mg, yield 24%) was obtained as a colorless amorphous solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.19 (t, J=7.1, 3H), 1.58 (t, J=7.3, 3H), 2.45 (s, 3H), 2.91 (s, 3H), 4.0-4.2 (m, 6H), 4.20 (s, 2H), 4.36 (s, 2H), 4.40 (q, J=7.3, 2H), 6.87-6.97 (m, 2H), 7.10-7.15 (m, 1H), 7.47 (s, 1H), 7.53 (s, 1H), 7.74 (s, 1H).

Step BN²-(2-ethyl-6-methyl-2H-indazol-5-yl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (434 mg, 0.928 mmol) of step A, and according to the methods of Example 241, steps D and E, the title compound (245 mg, yield 48%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.13 (t, J=7.2, 3H), 1.46 (t, J=7.2, 3H), 2.36 (s, 3H), 2.8-3.0 (m, 4H), 2.87 (s, 3H), 3.34-3.42 (m, 2H), 3.82 (s, 2H), 4.01-4.21 (m, 4H), 4.23 (s, 2H), 4.37 (q, J=7.2, 2H), 7.04-7.14 (m, 2H), 7.26-7.30 (m, 1H), 7.36 (s, 1H), 7.44 (s, 1H), 8.17 (s, 1H), 8.38 (t, J=5.8, 1H), 8.70 (brs, 2H).

Example 250N²-[1-(2,2-difluoroethyl)-6-methyl-1H-indazol-5-yl]-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochlorideStep AN-[1-(2,2-difluoroethyl)-6-methyl-1H-indazol-5-yl]-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine ethyl ester

Using the compound (767 mg, 1.82 mmol) of Example 241, step B and 2,2-difluoroethyl trifluoromethanesulfonate (534 mg, 2.49 mmol), and according to the method of Example 241, step C, the title compound (621 mg, yield 70%) was obtained as a colorless amorphous solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.19 (t, J=7.1, 3H), 2.52 (s, 3H), 2.92 (s, 3H), 4.06-4.22 (m, 8H), 4.38 (s, 2H), 4.63 (dt, J=4.3, 14, 2H), 6.12 (tt, J=4.3, 56, 1H), 7.18-7.26 (m, 5H), 7.70 (s, 1H), 7.89 (s, 1H).

Step BN-[1-(2,2-difluoroethyl)-6-methyl-1H-indazol-5-yl]-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound (621 mg, 1.28 mmol) of step A, and according to the method of Example 241, step D, the title compound (557 mg, yield 95%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 2.40 (s, 3H), 2.86 (s, 3H), 3.98 (s, 2H), 4.07 (d, J=11.5, 2H), 4.22 (d, J=11.5, 2H), 4.27 (s, 2H), 4.82 (dt, J=3.6, 15, 2H), 6.38 (tt, J=3.6, 55, 1H), 7.25 (brs, 4H), 7.48 (s, 1H), 7.56 (s, 1H), 7.98 (s, 1H), 12.47 (brs, 1H).

Step CN²-[1-(2,2-difluoroethyl)-6-methyl-1H-indazol-5-yl]-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (552 mg, 1.21 mmol) of step B and the compound (255 mg, 1.35 mmol) of Reference Example 2, and according to the methods of Example 1, step B, and Example 57, step B, the title compound (482 mg, yield 71%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.13 (t, J=7.2, 3H), 2.43 (s, 3H), 2.8-3.0 (m, 4H), 2.86 (s, 3H), 3.34-3.41 (m, 2H), 3.84 (s, 2H), 4.05 (d, J=11.4, 2H), 4.21 (d, J=11.4, 2H), 4.26 (s, 2H), 4.83 (dt, J=3.5, 15, 2H), 6.39 (tt, J=3.5, 55, 1H), 7.25 (brs, 4H), 7.50 (s, 1H), 7.60 (s, 1H), 7.98 (s, 1H), 8.39 (t, J=5.8, 1H), 8.60 (brs, 2H).

Example 251N²-[1-(2,2-difluoroethyl)-6-methyl-1H-indazol-5-yl]-N²-{2-[(4-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochlorideStep AN-{2-[(4-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N-(6-methyl-1H-indazol-5-yl)glycine ethyl ester

Using the compound (875 mg, 2.52 mmol) of Reference Example 133 and the compound (519 mg, 2.56 mmol) of Reference Example 18, and according to the methods of Example 241, steps m A and B, the title compound (919 mg, yield 83%) was obtained as a pale-yellow amorphous solid

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.20 (t, J=7.1, 3H), 2.50 (s, 3H), 2.93 (s, 3H), 4.10 (q, J=7.1, 2H), 4.13-4.23 (m, 6H), 4.39 (s, 2H), 6.91-6.99 (m, 2H), 7.20-7.26 (m, 1H), 7.28 (s, 1H), 7.71 (s, 1H), 7.93 (s, 1H), 9.85 (brs, 1H).

Step BN-[1-(2,2-difluoroethyl)-6-methyl-1H-indazol-5-yl]-N-{2-[(4-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}glycine ethyl ester

Using the compound (909 mg, 2.07 mmol) of step A and 2,2-difluoroethyl trifluoromethanesulfonate (612 mg, 2.86 mmol), and according to the method of Example 241, step C, the title compound (732 mg, yield 70%) was obtained as a colorless amorphous solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.20 (t, J=7.1, 3H), 2.53 (s, 3H), 2.92 (s, 3H), 4.07-4.23 (m, 8H), 4.38 (s, 2H), 4.63 (dt, J=4.4, 13.6, 2H), 6.12 (tt, J=4.4, 56, 1H), 6.91-6.99 (m, 2H), 7.20-7.25 (m, 2H), 7.69 (s, 1H), 7.90 (s, 1H).

Step CN-[1-(2,2-difluoroethyl)-6-methyl-1H-indazol-5-yl]-N-{2-[(4-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}glycine

Using the compound (732 mg, 1.45 mmol) of step B, and according to the method of Example 241, step D, the title compound (660 mg, yield 96%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 2.41 (s, 3H), 2.87 (s, 3H), 3.97 (s, 2H), 4.12-4.25 (m, 4H), 4.28 (s, 2H), 4.82 (dt, J=3.6, 15, 2H), 6.38 (tt, J=3.6, 55, 1H), 7.05-7.13 (m, 2H), 7.28-7.34 (m, 1H), 7.48 (s, 1H), 7.57 (s, 1H), 7.98 (s, 1H), 12.45 (brs, 1H).

Step DN²-[1-(2,2-difluoroethyl)-6-methyl-1H-indazol-5-yl]-N²-{2-[(4-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (654 mg, 1.38 mmol) of step C and the compound (285 mg, 1.51 mmol) of Reference Example 2, and according to the methods of Example 1, step B, and Example 57, step B, the title compound (599 mg, yield 75%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.12 (t, J=7.2, 3H), 2.43 (s, 3H), 2.8-3.0 (m, 4H), 2.88 (s, 3H), 3.35-3.40 (m, 2H), 3.83 (s, 2H), 4.09-4.24 (m, 4H), 4.27 (s, 2H), 4.83 (dt, J=3.5, 15, 2H), 6.38 (tt, J=3.5, 55, 1H), 7.06-7.12 (m, 2H), 7.28-7.34 (m, 1H), 7.50 (s, 1H), 7.61 (s, 1H), 7.98 (s, 1H), 8.38 (t, J=5.7, 1H), 8.56 (brs, 2H).

Example 252N²-[1-(2,2-difluoroethyl)-6-methyl-1H-indazol-5-yl]-N²-{2-[2,3-dihydro-1H-inden-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochlorideStep AN-{2-[2,3-dihydro-1H-inden-2-yl(methyl)amino]-2-oxoethyl}-N-(6-methyl-1H-indazol-5-yl)glycine ethyl ester

Using the compound (908 mg, 2.61 mmol) of Reference Example 133 and the compound (485 mg, 2.64 mmol) of Reference Example 23, and according to the methods of Example 241, steps A and B, the title compound (971 mg, yield 88%) was obtained as a colorless amorphous solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.19-1.24 (m, 3H), 2.50 (s, 3H), 2.73 2.78 (2s, 3H), 2.80-3.01 (m, 2H), 3.08-3.18 (m, 2H), 4.01 4.05 (2s, 2H), 4.08-4.16 (m, 2H), 4.13 4.25 (2s, 2H), 4.94-5.03 5.50-5.59 (m, 1H), 7.1-7.2 (m, 4H), 7.29 (s, 1H), 7.73 (s, 1H), 7.96 (s, 1H), 9.96 (brs, 1H).

Step BN-[1-(2,2-difluoroethyl)-6-methyl-1H-indazol-5-yl]-N-{2-[2,3-dihydro-1H-inden-2-yl(methyl)amino]-2-oxoethyl}glycine ethyl ester

Using the compound (954 mg, 2.27 mmol) of step A and 2,2-difluoroethyl trifluoromethanesulfonate (607 mg, 3.12 mmol), and according to the method of Example 241, step C, the title compound (747 mg, yield 68%) was obtained as a colorless oil.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.19-1.30 (m, 3H), 2.52 (s, 3H), 2.73 2.78 (2s, 3H), 2.79-3.01 (m, 2H), 3.08-3.18 (m, 2H), 4.01 4.05 (2s, 2H), 4.08-4.16 (m, 2H), 4.12 4.24 (2s, 2H), 4.64 (dt, J=4.3, 13.5, 2H), 4.9-5.0 5.4-5.6 (m, 1H), 6.12 (tt, J=4.3, 56, 1H), 7.1-7.2 (m, 4H), 7.25 (s, 1H), 7.72 (s, 1H), 7.93 (s, 1H).

Step CN-[1-(2,2-difluoroethyl)-6-methyl-1H-indazol-5-yl]-N-{2-[2,3-dihydro-1H-inden-2-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound (747 mg, 1.54 mmol) of step B, and according to the method of Example 241, step D, the title compound (651 mg, yield 93%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 2.42 (s, 3H), 2.64 2.76 (2s, 3H), 2.82-3.10 (m, 4H), 3.87 3.91 (2s, 2H), 4.06 4.19 (2s, 2H), 4.83 (dt, J=3.7, 14, 2H), 4.95-5.05 5.20-5.35 (m, 1H), 6.39 (tt, J=3.7, 55, 1H), 7.13-7.21 (m, 4H), 7.51 (s, 1H), 7.61 (s, 1H), 8.00 8.01 (2s, 1H). 12.67 (brs, 1H).

Step DN²-[1-(2,2-difluoroethyl)-6-methyl-1H-indazol-5-yl]-N²-{2-[2,3-dihydro-1H-inden-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (646 mg, 1.42 mmol) of step C and the compound (303 mg, 1.61 mmol) of Reference Example 2, and according to the methods of Example 1, step B, and Example 57, step B, the title compound (636 mg, yield 80%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.10-1.16 (m, 3H), 2.45 (s, 3H), 2.65 2.74 (2s, 3H), 2.82-3.07 (m, 8H), 3.35-3.42 (m, 2H), 3.76% 3.80 (2s, 2H), 4.03 4.18 (2s, 2H), 4.84 (dt, J=3.6, 15, 2H), 4.85-4.95 5.20-5.35 (m, 1H), 7.12-7.20 (m, 4H), 7.52 (s, 1H), 7.64 (s, 1H), 8.00 8.01 (2s, 1H), 8.51 (t, J=5.8, 1H), 8.54 (brs, 2H).

Example 253N²-[1-(2,2-difluoroethyl)-6-methyl-1H-indazol-5-yl]-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochlorideStep AN-[1-(2,2-difluoroethyl)-6-methyl-1H-indazol-5-yl]-N-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}glycine ethyl ester

Using the compound (1.92 g, 4.37 mmol) of Example 244, step B and 2,2-difluoroethyl trifluoromethanesulfonate (1.49 g, 6.96 mmol), and according to the method of Example 241, step C, the title compound (1.56 g, yield 71%) was obtained as a colorless amorphous solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.19 (t, J=7.1, 3H), 2.52 (s, 3H), 2.91 (s, 3H), 4.0-4.2 (m, 6H), 4.17 (s, 2H), 4.37 (s, 2H), 4.63 (dt, J=4.3, 14, 2H), 6.12 (tt, J=4.3, 56, 1H), 6.87-6.97 (m, 2H), 7.11-7.15 (m, 1H), 7.23 (s, 1H), 7.69 (s, 1H), 7.89 (s, 1H).

Step BN²-[1-(2,2-difluoroethyl)-6-methyl-1H-indazol-5-yl]-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (1.53 g, 3.04 mmol) of step A, and according to the methods of Example 241, steps D and E, the title compound (1.11 g, yield 63%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.13 (t, J=7.2, 3H), 2.43 (s, 3H), 2.8-3.0 (m, 4H), 2.86 (s, 3H), 3.34-3.41 (m, 2H), 3.85 (s, 2H), 4.01-4.24 (m, 4H), 4.26 (s, 2H), 4.83 (dt, J=3.5, 15, 2H), 6.39 (tt, J=3.5, 55, 1H), 7.04-7.14 (m, 2H), 7.26-7.30 (m, 1H), 7.50 (s, 1H), 7.60 (s, 1H), 7.98 (s, 1H), 8.39 (t, J=5.8, 1H), 8.70 (brs, 2H).

Example 254N²-[2-(2,2-difluoroethyl)-6-methyl-2H-indazol-5-yl]-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochlorideStep AN-[2-(2,2-difluoroethyl)-6-methyl-2H-indazol-5-yl]-N-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}glycine ethyl ester

As a byproduct of Example 253, step A, the title compound (280 mg, yield 13%) was obtained as a colorless solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.19 (t, J=7.1, 3H), 2.46 (s, 3H), 2.92 (s, 3H), 4.0-4.2 (m, 6H), 4.19 (s, 2H), 4.36 (s, 2H), 4.67 (dt, J=4.3, 13, 2H), 6.18 (tt, J=4.3, 56, 1H), 6.88-7.00 (m, 2H), 7.11-7.15 (m, 1H), 7.46 (s, 1H), 7.52 (s, 1H), 7.81 (s, 1H).

Step BN-[2-(2,2-difluoroethyl)-6-methyl-2H-indazol-5-yl]-N-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}glycine

Using the compound (274 mg, 0.544 mmol) of step A, and according to the method of Example 241, step D, the title compound (238 mg, yield 92%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 2.34 (s, 3H), 2.86 (s, ³H), 3.97 (s, 2H), 4.03-4.23 (m, 4H), 4.25 (s, 2H), 4.87 (dt, J=3.8, 15, 2H), 6.46 (tt, J=3.8, 55, 1H), 7.04-7.14 (m, 2H), 7.26-7.30 (m, 1H), 7.36 (s, 1H), 7.41 (s, 1H), 8.22 (s, 1H).

Step CN²-[2-(2,2-difluoroethyl)-6-methyl-2H-indazol-5-yl]-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (235 mg, 0.494 mmol) of step B, the compound (111 mg, 0.590 mmol) of Reference Example 2, and according to the methods of Example 1, step B, and Example 57, step B, the title compound (237 mg, yield 82%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.12 (t, J=7.2, 3H), 2.37 (s, 3H), 2.8-3.0 (m, 4H), 2.87 (s, 3H), 3.32-3.40 (m, 2H), 3.82 (s, 2H), 4.00-4.22 (m, 4H), 4.23 (s, 2H), 4.88 (dt, J=3.8, 11, 2H), 6.47 (tt, J=3.8, 55, 1H), 7.04-7.14Â°(m, 2H), 7.26-7.30 (m, 1H), 7.39 (s, 1H), 7.46 (s, 1H), 8.23 (s, 1H), 8.34 (t, J=5.8, 1H), 8.56 (brs, 2H).

Example 255N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(1,3,6-trimethyl-1H-indazol-5-yl)-N¹-[2-(ethylamino)ethyl]glycinamide hydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3-iodo-1,6-dimethyl-1H-indazol-5-yl)-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (484 mg, 1.20 mmol) of Reference Example 136, the compound (223 mg, 1.21 mmol) of Reference Example 17 and the compound (255 mg, 1.35 mmol) of Reference Example 2, and according to the method of Example 204, step A, the title compound (743 mg, yield 88%) was obtained as a colorless amorphous solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.06 (t, J=7.0, 3H), 1.45 (s, 9H), 2.51 (s, 3H), 2.94 (s, 3H), 3.15-3.25 (m, 2H), 3.28-3.35 (m, 2H), 3.40-3.49 (m, 2H), 3.75 (s, 2H), 4.03 (s, 3H), 4.15 (d, J=11.7, 2H), 4.23 (d, J=11.7, 2H), 4.27 (s, 2H), 7.18-7.34 (m, 5H), 7.34 (s, 1H), 8.46 8.75 (2brs, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(1,3,6-trimethyl-1H-indazol-5-yl)-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

The compound (734 mg, 1.04 mmol) of step A, trimethylboroxin (0.19 ml, 1.36 mmol), bis(tricyclohexylphosphine)palladium(II) dichloride (139 mg, 0.188 mmol), and 1.27 mol/l aqueous potassium phosphate solution (2.50 ml, 3.18 mmol) were added to 1,4-dioxane (8 ml), and the mixture was heated under reflux for 10 hr. After cooling to room temperature, the reaction mixture was diluted with ethyl acetate, washed with saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-methanol) to give the title compound (505 mg, yield 82%) as a colorless amorphous solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.03 (t, J=7.0, 3H), 1.45 (s, 9H), 2.48 (s, 3H), 2.49 (s, 3H), 2.94 (s, 3H), 3.10-3.20 (m, 2H), 3.25-3.35 (m, 2H), 3.40-3.46 (m, 2H), 3.80 (s, 2H), 3.93 (s, 3H), 4.04 (d, J=11.4, 2H), 4.20 (d, J=11.4, 2H), 4.21 (s, 2H), 7.13 (s, 1H), 7.16-7.25 (m, 4H), 7.57 (s, 1H), 8.44 8.72 (2brs, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(1,3,6-trimethyl-1H-indazol-5-yl)-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (496 mg, 0.838 mmol) of step B, and according to the method of Example 57, step B, the title compound (363 mg, yield 82%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.14 (t, J=7.2, 3H), 2.38 (s, 3H), 2.42 (s, 3H), 2.8-3.0 (m, 4H), 2.87 (s, 3H), 3.35-3.41 (m, 2H), 3.81 (s, 2H), 3.87 (s, 3H), 4.03 (d, J=11.4, 2H), 4.22 (d, J=11.4, 2H), 4.25 (s, 2H), 7.24 (brs, 4H), 7.32 (s, 1H), 7.54 (s, 1H), 8.51 (t, J=5.9, 1H), 8.64 (brs, 2H).

Example 256N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-(1,3,6-trimethyl-1H-indazol-5-yl)-N¹-[2-(ethylamino)ethyl]glycinamide hydrochlorideStep AN²-(3-iodo-1,6-dimethyl-1H-indazol-5-yl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (484 mg, 1.20 mmol) of Reference Example 136, the compound (243 mg, 1.20 mmol) of Reference Example 19 and the compound (253 mg, 1.34 mmol) of Reference Example 2, and according to the method of Example 204, step A, the title compound (798 mg, yield 92%) was obtained as a colorless amorphous solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.06 (t, J=7.0, 3H), 1.45 (s, 9H), 2.51 (s, 3H), 2.93 (s, 3H), 3.15-3.25 (m, 2H), 3.28-3.35 (m, 2H), 3.41-3.49 (m, 2H), 3.75 (s, 2H), 4.03 (s, 3H), 4.08-4.23 (m, 4H), 4.26 (s, 2H), 6.90-6.99 (m, 2H), 7.13-7.18 (m, 1H), 7.19 (s, 1H), 7.33 (s, 1H), 8.42 8.72 (2brs, 1H).

Step BN²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-(1,3,6-trimethyl-1H-indazol-5-yl)-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (791 mg, 1.10 mmol) of step A, and according to the method of Example 255, step B, the title compound (495 mg, yield 74%) was obtained as a colorless amorphous solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.03 (t, J=7.0, 3H), 1.44 (s, 9H), 2.48 (s, 6H), 2.93 (s, 3H), 3.10-3.20 (m, 2H), 3.25-3.35 (m, 2H), 3.40-3.46 (m, 2H), 3.80 (s, 2H), 3.93 (s, 3H), 3.97-4.15 (m, 4H), 4.17 (s, 2H), 6.87-6.98 (m, 2H), 7.10-7.12 (m, 1H), 7.13 (s, 1H), 7.56 (s, 1H), 8.40 8.68 (2brs, 1H).

Step CN²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-(1,3,6-trimethyl-1H-indazol-5-yl)-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (486 mg, 0.797 mmol) of step B, and according to the method of Example 57, step B, the title compound (361 mg, yield 83%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.13 (t, J=7.2, 3H), 2.38 (s, 3H), 2.42 (s, 3H), 2.8-3.0 (m, 4H), 2.87 (s, 3H), 3.35-3.41 (m, 2H), 3.81 (s, 2H), 3.87 (s, 3H), 3.98-4.20 (m, 4H), 4.23 (s, 2H), 7.04-7.13 (m, 2H), 7.25-7.29 (m, 1H), 7.32 (s, 1H), 7.53 (s, 1H), 8.49 (t, J=5.9, 1H), 8.56 (brs, 2H).

Example 257N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(1,5-dimethyl-1H-indazol-6-yl)-N¹-[2-(ethylamino)ethyl]glycinamide hydrochlorideStep AN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-[5-methyl-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-6-yl]glycine

Using the compound (903 mg, 2.60 mmol) of Reference Example 134 and the compound (595 mg, 3.22 mmol) of Reference Example 17, and according to the method of Example 241, step A, the title compound (1.07 g, yield 86%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.5-1.6 (m, 2H), 1.65-1.80 (m, 1H), 1.85-2.10 (m, 2H), 2.3-2.4 (m, 1H), 2.32 (s, 3H), 2.89 (s, 3H), 3.65-3.75 (m, 1H), 3.80-3.95 (m, 1H), 4.06 (s, 2H), 4.12 (d, J=12, 2H), 4.26 (d, J=12, 2H), 4.32 (s, 2H), 5.65-5.70 (m, 1H), 7.25 (brs, 4H), 7.32 (s, 1H), 7.46 (s, 1H), 7.87 (s, 1H), 12.52 (brs, 1H).

Step BN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-(5-methyl-1H-indazol-6-yl)glycine ethyl ester

Using the compound (1.07 g, 2.39 mmol) of step A, and according to the method of Example 241, step B, the title compound (821 mg, yield 82%) was obtained as a colorless amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 1.21 (t, J=7.2, 3H), 2.43 (s, 3H), 2.94 (s, 3H), 4.07-4.16 (m, 4H), 4.22 (d, J=11.4, 2H), 4.24 (s, 2H), 4.44 (s, 2H), 7.13-7.27 (m, 4H), 7.38 (s, 1H), 7.50 (s, 1H), 7.89 (s, 1H), 9.87 (brs, 1H).

Step CN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-(1,5-dimethyl-1H-indazol-6-yl)glycine ethyl ester

Using the compound (815 mg, 1.93 mmol) of step B, and according to the method of Example 241, step C, the title compound (530 mg, yield 63%) was obtained as a pale-yellow amorphous solid

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.23 (t, J=7.2, 3H), 2.43 (s, 3H), 2.93 (s, 3H), 3.99 (s, 3H), 4.04-4.15 (m, 4H), 4.22 (d, J=11.3, 2H), 4.26 (s, 2H), 4.44 (s, 2H), 7.17-7.27 (m, 5H), 7.46 (s, 1H), 7.79 (s, 1H).

Step DN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(1,5-dimethyl-1H-indazol-6-yl)-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (513 mg, 1.18 mmol) of step C, the compound (319 mg, 1.69 mmol) of Reference Example 2, and according to the methods of Example 241, steps D and E, the title compound (450 mg, yield 74%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.13 (t, J=7.2, 3H), 2.35 (s, 3H), 2.8-3.0 (m, 4H), 2.89 (s, 3H), 3.32-3.42 (m, 2H), 3.92 (s, 5H), 4.09 (d, J=11.6, 2H), 4.25 (d, J=11.6, 2H), 4.32 (s, 2H), 7.25 (brs, 4H), 7.30 (s, 1H), 7.47 (s, 1H), 7.82 (s, 1H), 8.36 (t, J=5.7, 1H), 8.59 (brs, 2H).

Example 258N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2,5-dimethyl-2H-indazol-6-yl)-N¹-[2-(ethylamino)ethyl]glycinamide hydrochlorideStep AN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-(2,5-dimethyl-2H-indazol-6-yl)glycine ethyl ester

As a byproduct of Example 257, step C, the title compound (191 mg, yield 23%) was obtained as a yellow-bistered amorphous solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.22 (t, J=7.2, 3H), 2.40 (s, 3H), 2.93 (s, 3H), 4.08-4.23 (m, 8H), 4.13 (s, 3H), 4.45 (s, 2H), 7.17-7.27 (m, 5H), 7.37 (s, 1H), 7.67 (s, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2,5-dimethyl-2H-indazol-6-yl)-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (181 mg, 0.416 mmol) of step A and the compound (135 mg, 0.717 mmol) of Reference Example 2, and according to the methods of Example 241, steps D and E, the title compound (151 mg, yield 71%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.12 (t, J=7.2, 3H), 2.31 (s, 3H), 2.8-3.0 (m, 4H), 2.89 (s, 3H), 3.86 (s, 2H), 4.07 (s, 3H), 4.09 (d, J=12, 2H), 4.26 (d, J=12, 2H), 4.28 (s, 2H), 7.22 (s, 1H), 7.25 (brs, 4H), 7.40 (s, 1H), 8.09 (s, 1H), 8.32 (t, J=5.8, 1H), 8.55 (brs, 2H).

Example 259N²-(1,5-dimethyl-1H-indazol-6-yl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochlorideStep AN-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N-[5-methyl-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-6-yl]glycine

Using, the compound (749 mg, 2.16 mmol) of Reference Example 134 and the compound (439 mg, 2.17 mmol) of Reference Example 19, and according to the method of Example 241, step A, the title compound (965 mg, yield 90%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.5-1.6 (m, 2H), 1.6-1.8 (m, 1H), 1.8-2.1 (m, 2H), 2.3-2.4 (m, 1H), 2.32 (s, 3H), 2.88 (s, 3H), 3.6-3.8 (m, 1H), 3.8-3.9 (m, 1H), 4.06 (s, 2H), 4.06-4.25 (m, 4H), 4.31 (s, 2H), 5.68 (dd, J=2.4, 9.6, 1H), 7.0-7.2 (m, 4H), 7.23-7.30 (m, 1H), 7.32 (s, 1H), 7.46 (s, 1H), 7.87 (s, 1H), 12.51 (brs, 1H).

Step BN-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N-(5-methyl-1H-indazol-6-yl)glycine ethyl ester

Using the compound (961 mg, 1.94 mmol) of step A, and according to the method of Example 241, step B, the title compound (770 mg, yield 90%) was obtained as a colorless amorphous solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.21 (t, J=7.1, 3H), 2.43 (s, 3H), 2.93 (s, 3H), 4.05-4.22 (m, 6H), 4.23 (s, 2H), 4.43 (s, 2H), 6.88-6.98 (m, 2H), 7.11-7.16 (m, 1H), 7.38 (s, 1H), 7.50 (s, 1H), 7.89 (s, 1H), 9.93 (brs, 1H).

Step CN-(1,5-dimethyl-1H-indazol-6-yl)-N-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}glycine ethyl ester

Using the compound (750 mg, 1.71 mmol) of step B, and according to the method of Example 241, step C, the title compound (546 mg, yield 63%) was obtained as a colorless amorphous solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.21 (t, J=7.1, 3H), 2.43 (s, 3H), 2.92 (s, 3H), 3.99 (s, 3H), 4.04-4.21 (m, 6H), 4.25 (s, 2H), 4.42 (s, 2H), 6.86-6.98 (m, 2H), 7.10-7.18 (m, 1H), 7.25 (s, 1H), 7.46 (s, 1H), 7.79 (s, 1H).

Step DN²-(1,5-dimethyl-1H-indazol-6-yl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (536 mg, 1.18 mmol) of step C and the compound (327 mg, 1.74 mmol) of Reference Example 2, and according to the methods of Example 241, steps D and E, the title compound (557 mg, yield 89%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.12 (t, J=7.2, 3H), 2.35 (s, 3H), 2.8-3.0 (m, 4H), 2.88 (s, 3H), 3.3-3.5 (m, 2H), 3.92 (s, 5H), 4.04-4.28 (m, 4H), 4.31 (s, 2H), 7.04-7.15 (m, 2H), 7.27-7.30 (m, 1H), 7.30 (s, 1H), 7.47 (s, 1H), 7.82 (s, 1H), 8.34 (t, J=5.8, 1H), 8.55 (brs, 2H).

Example 260N²-(2,5-dimethyl-2H-indazol-6-yl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochlorideStep AN-(2,5-dimethyl-2H-indazol-6-yl)-N-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}glycine ethyl ester

As a byproduct of Example 259, step C, the title compound (180 mg, yield 23%) was obtained as a pale-yellow amorphous solid

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.22 (t, J=7.1, 3H), 2.40 (s, 3H), 2.93 (s, 3H), 4.05-4.20 (m, 6H), 4.13 (s, 3H), 4.18 (s, 2H), 4.44 (s, 2H), 6.86-6.96 (m, 2H), 7.09-7.14 (m, 1H), 7.37 (s, 2H), 7.67 (s, 1H).

Step BN²-(2,5-dimethyl-2H-indazol-6-yl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (175 mg, 0.386 mmol) of step A and the compound of Reference Example 2 (122 mg, 0.648 mmol), and according to the methods of Example 241, steps D and E, the title compound (134 mg, yield 65%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.12 (t, J=7.2, 3H), 2.31 (s, 3H), 2.8-3.0 (m, 4H), 2.88 (s, 3H), 3.34-3.42 (m, 2H), 3.86 (s, 2H), 4.03-4.32 (m, 4H), 4.07 (s, 3H), 4.27 (s, 2H), 7.04-7.15 (m, 2H), 7.21 (s, 1H), 7.27-7.31 (m, 1H), 7.40 (s, 1H), 8.09 (s, 1H), 8.31 (t, J=5.9, 1H), 8.55 (brs, 2H).

Example 261N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(1,3,5-trimethyl-1H-indazol-6-yl)-N¹-[2-(ethylamino)ethyl]glycinamide hydrochlorideStep AN-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N-(3-iodo-1,5-dimethyl-1H-indazol-6-yl)glycine

Using the compound (2.55 g, 6.32 mmol) of Reference Example 135 and the compound (1.37 g, 7.42 mmol) of Reference Example 17, and according to the method of Example 241, step A, the title compound (3.32 g, yield 98%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 2.35 (s, 3H), 2.89 (s, 3H), 3.94 (s, 3H), 4.07 (s, 2H), 4.10 (d, J=11.7, 2H), 4.25 (d, J=11.7, 2H), 4.33 (s, 2H), 7.11 (s, 1H), 7.24 (s, 1H), 7.25 (brs, 4H), 12.4 (brs, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3-iodo-1,5-dimethyl-1H-indazol-6-yl)-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (861 mg, 1.61 mmol) of step A, and according to the method of Example 1, step B, the title compound (859 mg, yield 76%) was obtained as a colorless amorphous solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 0.97 (t, J=7.0, 3H), 1.41 (brs, 9H), 2.43 (s, 3H), 2.96 (s, 3H), 3.00-3.22 (m, 2H), 3.22-3.30 (m, 2H), 3.33-3.39 (m, 2H), 3.93 (s, 2H), 4.00 (s, 3H), 4.09 (d, J=11.4, 2H), 4.22 (s, 2H), 4.23 (d, J=11.4, 2H), 7.18-7.27 (m, 6H), 7.98 8.15 (2brs, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(1,3,5-trimethyl-1H-indazol-6-yl)-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (406 mg, 0.577 mmol) of step B, and according to the method of Example 255, step B, the title compound (315 mg, yield 93%) was obtained as a colorless amorphous solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 0.97 (t, J=7.1, 3H), 1.42 (brs, 9H), 2.41 (s, 3H), 2.49 (s, 3H), 2.96 (s, 3H), 3.0-3.1 (m, 2H), 3.1-3.3 (m, 2H), 3.34-3.41 (m, 2H), 3.90 (s, 5H), 4.08 (d, J=12, 2H), 4.21 (s, 2H), 4.22 (d, J=12, 2H), 7.17-7.26 (m, 5H), 7.41 (s, 1H), 8.09 8.28 (2brs, 1H).

Step DN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(1,3,5-trimethyl-1H-indazol-6-yl)-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (313 mg, 0.838 mmol) of step C, and according to the method of Example 57, step B, the title compound (156 mg, yield 56%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.14 (t, J=7.2, 3H), 2.35 (s, 3H), 2.38 (s, 3H), 2.8-3.0 (m, 4H), 2.88 (s, 3H), 3.35-3.41 (m, 2H), 3.83 (s, 3H), 3.92 (s, 2H), 4.09 (d, J=11.4, 2H), 4.25 (d, J=11.4, 2H), 4.32 (s, 2H), 7.22 (s, 1H), 7.25 (brs, 4H), 7.40 (s, 1H), 8.38 (t, J=5.8, 1H), 8.77 (brs, 2H).

Example 262N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-(1,3,5-trimethyl-1H-indazol-6-yl)-N¹-[2-(ethylamino)ethyl]glycinamide hydrochlorideStep AN²-(3-iodo-1,5-dimethyl-1H-indazol-6-yl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (799 mg, 1.98 mmol) of Reference Example 135, the compound (418 mg, 2.06 mmol) of Reference Example 19 and the compound (433 mg, 2.30 mmol) of Reference Example 2, and according to the methods of Example 241, step A, and Example 1, step B, the title compound (1.38 g, yield 97%) was obtained as a colorless amorphous solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 0.97 (t, J=7.0, 3H), 1.41 (brs, 9H), 2.43 (s, 3H), 2.95 (s, 3H), 3.0-3.1 (m, 2H), 3.1-3.3 (m, 2H), 3.34-3.39 (m, 2H), 3.94 (s, 2H), 4.00 (s, 3H), 4.02-4.22 (m, 4H), 4.20 (s, 2H), 6.89-6.98 (m, 2H), 7.12-7.16 (m, 1H), 7.23 (s, 2H), 7.93 8.10 (2brs, 1H).

Step BN²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-(1,3,5-trimethyl-1H-indazol-6-yl)-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (508 mg, 0.704 mmol) of step A, and according to the method of Example 255, step B, the title compound (399 mg, yield 93%) was obtained as a colorless amorphous solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 0.96 (t, J=7.1, 3H), 1.42 (brs, 9H), 2.41 (s, 3H), 2.49 (s, 3H), 2.95 (s, 3H), 3.0-3.1 (m, 2H), 3.1-3.3 (m, 2H), 3.34-3.41 (m, 2H), 3.90 (s, 5H), 3.98-4.22 (m, 4H), 4.15 (s, 2H), 6.88-6.98 (m, 2H), 7.11-7.15 (m, 1H), 7.19 (s, 1H), 7.41 (s, 1H), 8.03 8.24 (2brs, 1H).

Step CN²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-(1,3,5-trimethyl-1H-indazol-6-yl)-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (397 mg, 0.651 mmol) of step B, and according to the method of Example 57, step B, the title compound (153 mg, yield 43%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.14 (t, J=7.2, 3H), 2.35 (s, 3H), 2.38 (s, 3H), 2.8-3.0 (m, 4H), 2.88 (s, 3H), 3.35-3.41 (m, 2H), 3.84 (s, 3H), 3.92 (s, 2H), 4.04-4.27 (m, 4H), 4.32 (s, 2H), 7.05-7.16 (m, 2H), 7.23 (s, 1H), 7.27-7.31 (m, 1H), 7.41 (s, 1H), 8.38 (t, J=5.8, 1H), 8.78 (brs, 2H).

Example 263N²-{2-[2,3-dihydro-1H-inden-2-yl(methyl)amino]-2-oxoethyl}-N²-(1,3,5-trimethyl-1H-indazol-6-yl)-N¹-[2-(ethylamino)ethyl]glycinamide hydrochlorideStep AN²-{2-[2,3-dihydro-1H-inden-2-yl(methyl)amino]-2-oxoethyl}-N²-(3-iodo-1,5-dimethyl-1H-indazol-6-yl)-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (587 mg, 1.46 mmol) of Reference Example 135, the compound (272 mg, 1.48 mmol) of Reference Example 23 and the compound (358 mg, 1.90 mmol) of Reference Example 2, and according to the methods of Example 241, step A, and Example 1, step B, the title compound (874 mg, yield 88%) was obtained as a colorless solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 0.97 (t, J=7.0, 3H), 1.42 (brs, 9H), 2.44 (s, 3H), 2.72 2.80 (2s, 3H), 2.82-2.90 (m, 1H), 3.0-3.3 (m, 7H), 3.3-3.4 (m, 2H), 3.92 3.96 4.07 (3brs, 4H), 4.03 4.04 (2s, 3H), 4.61 5.58 (2brs, 1H), 7.1-7.3 (m, 6H), 7.99 8.19 (2brs, 1H).

Step BN²-{2-[2,3-dihydro-1H-inden-2-yl(methyl)amino]-2-oxoethyl}-N²-(1,3,5-trimethyl-1H-indazol-6-yl)-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (863 mg, 1.23 mmol) of step A, and according to the method of Example 255, step B, the title compound (664 mg, yield 91%) was obtained as a colorless amorphous solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 0.97 (t, J=6.9, 3H), 1.42 (brs, 9H), 2.42 (s, 3H), 2.50 (s, 3H), 2.70 2.80 (2s, 3H), 2.82-2.90 (m, 1H), 2.98-3.45 (m, 9H), 3.80-4.06 (m, 4H), 3.93 3.94 (2s, 3H), 4.61 5.59 (2brs, 1H), 7.1-7.3 (m, 5H), 7.43 (s, 1H), 8.11 8.32 (2brs, 1H).

Step CN²-{2-[2,3-dihydro-1H-inden-2-yl(methyl)amino]-2-oxoethyl}-N²-(1,3,5-trimethyl-1H-indazol-6-yl)-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (660 mg, 1.12 mmol) of step B, and according to the method of Example 57, step B, the title compound (425 mg, yield 72%) was obtained as a colorless solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.13-1.17 (m, 3H), 2.37 (s, 3H), 2.39 (s, 3H), 2.66 2.77 (2s, 3H), 2.85-3.10 (m, 8H), 3.3-3.4 (m, 2H), 3.82 3.87 (2s, 2H), 3.84 3.86 (2s, 3H), 4.09 4.25 (2s, 2H), 4.93-5.05 5.25-5.38 (2m, 1H), 7.13-7.22 (m, 4H), 7.24 7.28 (2s, 1H), 7.42 (s, 1H), 8.44-8.52 (m, 1H), 8.73 (brs, 2H).

Example 264N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3-ethyl-1,5-dimethyl-1H-indazol-6-yl)-N¹-[2-(ethylamino)ethyl]glycinamide hydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(1,5-dimethyl-3-vinyl-1H-indazol-6-yl)-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

To toluene (8 ml) were added the compound (583 mg, 0.829 mmol) of Example 261, step B, tri-n-butylvinyltin (415 mg, 1.31 mmol), bis(triphenylphosphine)palladium(II)dichloride (74 mg, 0.105 mmol) and lithium chloride (94 mg, 2.22 mmol), and the mixture was heated under reflux for 100 min. The reaction mixture was cooled, diluted with ethyl acetate, washed with saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-methanol) to give the title compound (446 mg, yield 89%) as a yellow amorphous solid.

¹H-NMR (300 MHz, CDCl₃); Î´(ppm) 0.96 (t, J=6.9, 3H), 1.41 (brs, 9H), 2.43 (s, 3H), 2.96 (s, 3H), 3.0-3.1 (m, 2H), 3.1-3.3 (m, 2H), 3.3-3.4 (m, 2H), 3.93 (s, 2H), 3.95 (s, 3H), 4.08 (d, J=11, 2H), 4.22 (s, 2H), 4.23 (d, J=11, 2H), 5.44 (dd, J=1.2, 12, 1H), 6.00 (dd, J=1.2, 18, 1H), 6.95 (dd, J=12, 18, 1H), 7.15-7.28 (m, 5H), 7.69 (s, 1H), 8.0 8.1 (2brs, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3-ethyl-1,5-dimethyl-1H-indazol-6-yl)-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

The compound (439 mg, 0.727 mmol) of step A was dissolved in an ethanol (15 ml)-tetrahydrofuran (1 ml) mixed solvent, 10% palladium carbon (containing water) (0.40 g) was added, and the mixture was stirred under a hydrogen atmosphere at room temperature for 5 hr. The reaction mixture was filtered through celite, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-methanol) to give the title compound (392 mg, yield 89%) as a colorless amorphous solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 0.96 (t, J=7.1, 3H), 1.36 (t, J=7.5, 3H), 1.42 (brs, 9H), 2.41 (s, 3H), 2.91 (q, J=7.5, 2H), 2.96 (s, 3H), 3.0-3.1 (m, 2H), 3.1-3.3 (m, 2H), 3.35-3.41 (m, 2H), 3.91 (s, 5H), 4.08 (d, J=11.3, 2H), 4.21 (s, 2H), 4.23 (d, J=11.3, 2H), 7.17-7.26 (m, 5H), 7.45 (s, 1H), 8.08 8.28 (2brs, 1H).

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3-ethyl-1,5-dimethyl-1H-indazol-6-yl)-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (382 mg, 0.631 mmol) of step B, and according to the method of Example 57, step B, the title compound (265 mg, yield 77%) was obtained as a pale-yellow solid.

¹H-NMR (300 MHz, DMSO-d₆); Î´(ppm) 1.13 (t, J=7.1, 3H), 1.26 (t, J=7.5, 3H), 2.35 (s, 3H), 2.8-3.0 (m, 4H), 2.82 (q, J=7.5, 2H), 2.88 (s, 3H), 3.33-3.40 (m, 2H), 3.84 (s, 3H), 3.91 (s, 2H), 4.08 (d, J=11.5, 2H), 4.25 (d, J=11.5, 2H), 4.31 (s, 2H), 7.22 (s, 1H), 7.25 (brs, 4H), 7.44 (s, 1H), 8.37 (t, J=5.9, 1H), 8.70 (brs, 2H).

The compounds of Examples 241-264 are shown below.

TABLE 17StructuralLC-MSExampleFormulaTMW(found)241 [Image Omitted]

514.06478 242 [Image Omitted]

528.09492 243 [Image Omitted]

514.06478 244 [Image Omitted]

532.05496 245 [Image Omitted]

532.05496 246 [Image Omitted]

528.09492 247 [Image Omitted]

528.09492 248 [Image Omitted]

546.08510 249 [Image Omitted]

546.08510 250 [Image Omitted]

564.07528 251 [Image Omitted]

582.06546 252 [Image Omitted]

563.08527 253 [Image Omitted]

582.06546 254 [Image Omitted]

582.06546 255 [Image Omitted]

528.09492 256 [Image Omitted]

546.08510 257 [Image Omitted]

514.06478 258 [Image Omitted]

514.06478 259 [Image Omitted]

532.05496 260 [Image Omitted]

532.05496 261 [Image Omitted]

528.09492 262 [Image Omitted]

546.08510 263 [Image Omitted]

527.10491 264 [Image Omitted]

542.12506

Example 265N²-[1-(2,2-difluoroethyl)-5-methyl-1H-indazol-6-yl]-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochlorideStep AN-[1-(2,2-difluoroethyl)-5-methyl-1H-indazol-6-yl]-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine ethyl ester

Using the compound (1.25 g, 2.97 mmol) of Example 257, step B and 2,2-difluoroethyl trifluoromethanesulfonate (859 mg, 4.01 mmol), and according to the method of Example 241, step C, the title compound (982 mg, yield 68%) was obtained as a colorless amorphous solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.21 (t, J=7.1, 3H), 2.43 (s, 3H), 2.93 (s, 3H), 4.10 (d, J=11.4, 2H), 4.12 (q, J=7.1, 2H), 4.22 (d, J=11.4, 2H), 4.24 (s, 2H), 4.44 (s, 2H), 4.63 (dt, J=4.3, 14, 2H), 6.10 (tt, J=4.3, 56, 1H), 7.18-7.26 (m, 5H), 7.47 (s, 1H), 7.86 (s, 1H).

Step BN-[1-(2,2-difluoroethyl)-5-methyl-1H-indazol-6-yl]-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound (975 mg, 2.01 mmol) of step A, and according to the method of Example 241, step D, the title compound (843 mg, yield 92%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 2.33 (s, 3H), 2.87 (s, 3H), 4.05 (s, 2H), 4.06 (d, J=11.5, 2H), 4.24 (d, J=11.5, 2H), 4.32 (s, 2H), 4.78 (dt, J=3.6, 15, 2H), 6.35 (tt, J=3.6, 55, 1H), 7.2-7.3 (m, 4H), 7.36 (s, 1H), 7.47 (s, 1H), 7.92 (s, 1H), 12.48 (brs, 1H).

Step CN²-[1-(2,2-difluoroethyl)-5-methyl-1H-indazol-6-yl]-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (325 mg, 0.710 mmol) of step B and the compound (177 mg, 0.940 mmol) of Reference Example 2, and according to the methods of Example 1, step B, and Example 57, step B, the title compound (272 mg, yield 68%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.13 (t, J=7.2, 3H), 2.36 (s, 3H), 2.8-3.0 (m, 4H), 2.88 (s, 3H), 3.35-3.39 (m, 2H), 3.92 (s, 2H), 4.09 (d, J=11.4, 2H), 4.24 (d, J=11.4, 2H), 4.33 (s, 2H), 4.80 (dt, J=3.6, 15, 2H), 6.37 (tt, J=3.6, 55, 1H), 7.25 (brs, 4H), 7.41 (s, 1H), 7.49 (s, 1H), 7.94 (s, 1H), 8.35 (t, J=5.8, 1H), 8.61 (brs, 2H).

Example 266N²-[2-(2,2-difluoroethyl)-5-methyl-2H-indazol-6-yl]-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochlorideStep AN-[2-(2,2-difluoroethyl)-5-methyl-2H-indazol-6-yl]-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine ethyl ester

As a byproduct of Example 265, step A, the title compound (346 mg, yield 24%) was obtained as a colorless amorphous solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.22 (t, J=7.1, 3H), 2.40 (s, 3H), 2.94 (s, 3H), 4.10-4.26 (m, 8H), 4.46 (s, 2H), 4.65 (dt, J=4.4, 13, 2H), 6.19 (tt, J=4.4, 56, 1H), 7.18-7.26 (m, 4H), 7.37 (s, 1H), 7.40 (s, 1H), 7.78 (s, 1H).

Step BN-[2-(2,2-difluoroethyl)-5-methyl-2H-indazol-6-yl]-N-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}glycine

Using the compound (340 mg, 0.700 mmol) of step A, and according to the method of Example 241, step D, the title compound (267 mg, yield 83%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 2.29 (s, 3H), 2.88 (s, 3H), 4.01 (s, 2H), 4.11 (d, J=11.5, 2H), 4.26 (d, J=11.5, 2H), 4.31 (s, 2H), 4.85 (dt, J=3.9, 15, 2H), 6.46 (tt, J=3.9, 55, 1H), 7.18 (s, 1H), 7.22-7.28 (m, 4H), 7.43 (s, 1H), 8.18 (s, 1H), 12.48 (brs, 1H).

Step CN²-[1-(2,2-difluoroethyl)-5-methyl-2H-indazol-6-yl]-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (264 mg, 0.577 mmol) of step B and the compound (152 mg, 0.807 mmol) of Reference Example 2, and according to the methods of Example 1, step B, and Example 57, step B, the title compound (220 mg, yield 68%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.11 (t, J=7.3, 3H), 2.32 (s, 3H), 2.8-3.0 (m, 4H), 2.90 (s, 3H), 3.34-3.40 (m, 2H), 3.88 (s, 2H), 4.10 (d, J=11.4, 2H), 4.26 (d, J=11.4, 2H), 4.29 (s, 2H), 4.86 (dt, J=3.8, 15, 2H), 6.47 (tt, J=3.8, 55, 1H), 7.22 (s, 1H), 7.23-7.29 (m, 4H), 7.45 (s, 1H), 8.19 (s, 1H), 8.29 (t, J=5.8, 1H), 8.39 (brs, 2H).

Example 267N²-[1-(2,2-difluoroethyl)-5-methyl-1H-indazol-6-yl]-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochlorideStep AN-[1-(2,2-difluoroethyl)-5-methyl-1H-indazol-6-yl]-N-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}glycine ethyl ester

Using the compound (1.46 g, 3.32 mmol) of Example 259, step B, and 2,2-difluoroethyl trifluoromethanesulfonate (957 mg, 4.47 mmol), and according to the method of Example 241, step C, the title compound (1.09 g, yield 65%) was obtained as a colorless amorphous solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.21 (t, J=7.1, 3H), 2.43 (s, 3H), 2.93 (s, 3H), 4.04-4.21 (m, 6H), 4.23 (s, 2H), 4.43 (s, 2H), 4.64 (dt, J=4.3, 14, 2H), 6.10 (tt, J=4.3, 55, 1H), 6.88-6.98 (m, 2H), 7.11-7.16 (m, 1H), 7.26 (s, 1H), 7.48 (s, 1H), 7.86 (s, 1H).

Step BN-[1-(2,2-difluoroethyl)-5-methyl-1H-indazol-6-yl]-N-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}glycine

Using the compound (1.08 mg, 2.14 mmol) of step A, and according to the method of Example 241, step D, the title compound (925 mg, yield 91%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 2.32 (s, 3H), 2.86 (s, 3H), 4.04-4.26 (m, 4H), 4.05 (s, 2H), 4.31 (s, 2H), 4.79 (dt, J=3.6, 15, 2H), 6.35 (tt, J=3.6, 55, 1H), 7.04-7.15 (m, 2H), 7.26-7.31 (m, 1H), 7.36 (s, 1H), 7.47 (s, 1H), 7.92 (s, 1H), 12.48 (brs, 1H).

Step CN²-[1-(2,2-difluoroethyl)-5-methyl-1H-indazol-6-yl]-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (322 mg, 0.677 mmol) of step B, and according to the methods of Example 1, step B, and Example 57, step B, the title compound (268 mg, yield 68%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.12 (t, J=7.2, 3H), 2.36 (s, 3H), 2.8-3.0 (m, 4H), 2.88 (s, 3H), 3.3-3.4 (m, 2H), 3.91 (s, 2H), 4.05-4.26 (m, 4H), 4.31 (s, 2H), 4.80 (dt, J=3.7, 15, 2H), 6.37 (tt, J=3.7, 55, 1H), 7.05-7.15 (m, 2H), 7.26-7.31 (m, 1H), 7.41 (s, 1H), 7.49 (s, 1H), 7.94 (s, 1H), 8.34 (broad t, 1H), 8.60 (brs, 2H).

Example 268N²-[2-(2,2-difluoroethyl)-5-methyl-2H-indazol-6-yl]-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochlorideStep AN-[2-(2,2-difluoroethyl)-5-methyl-2H-indazol-6-yl]-N-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}glycine ethyl ester

As a byproduct of Example 267, step A, the title compound (313 mg, yield 19%) was obtained as a colorless amorphous solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.23 (t, J=7.2, 3H), 2.40 (s, 3H), 2.94 (s, 3H), 4.08-4.22 (m, 8H), 4.45 (s, 2H), 4.65 (dt, J=4.4, 13, 2H), 6.19 (tt, J=4.4, 56, 1H), 6.87-6.97 (m, 2H), 7.11-7.15 (m, 1H), 7.36 (s, 1H), 7.40 (s, 1H), 7.78 (s, 1H).

Step BN-[2-(2,2-difluoroethyl)-5-methyl-2H-indazol-6-yl]-N-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}glycine

Using the compound (308 mg, 0.612 mmol) of step A, and according to the method of Example 241, step D, the title compound (202 mg, yield 69%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 2.29 (s, 3H), 2.87 (s, 3H), 4.00 (s, 2H), 4.07-4.27 (m, 4H), 4.30 (s, 2H), 4.85 (dt, J=3.9, 15, 2H), 6.46 (tt, J=3.9, 55, 1H), 7.04-7.16 (m, 2H), 7.17 (s, 1H), 7.27-7.31 (m, 1H), 7.43 (s, 1H), 8.18 (s, 1H), 12.45 (brs, 1H).

Step CN²-[2-(2,2-difluoroethyl)-5-methyl-2H-indazol-6-yl]-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (201 mg, 0.423 mmol) of step B and the compound (103 mg, 0.547 mmol) of Reference Example 2, and according to the methods of Example 1, step B, and Example 57, step B, the title compound (172 mg, yield 70%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.12 (t, J=7.2, 3H), 2.32 (s, 3H), 2.8-3.0 (m, 4H), 2.89 (s, 3H), 3.30-3.42 (m, 2H), 3.88 (s, 2H), 4.06-4.25 (m, 4H), 4.28 (s, 2H), 4.86 (dt, J=3.8, 15, 2H), 6.47 (tt, J=3.8, 55, 1H), 7.05-7.16 (m, 2H), 7.22 (s, 1H), 7.27-7.32 (m, 1H), 7.45 (s, 1H), 8.19 (s, 1H), 8.29 (t, J=5.8, 1H), 8.55 (brs, 2H).

Example 269N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-(2,3,5-trimethyl-2H-indazol-6-yl)-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (146 mg, 0.501 mmol) of Reference Example 137, the compound (102 mg, 0.503 mmol) of Reference Example 19 and the compound (106 mg, 0.563 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 57, step B, the title compound (191 mg, yield 70%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.13 (t, J=7.2, 3H), 2.31 (s, 3H), 2.52 (s, 3H), 2.8-3.0 (m, 4H), 2.88 (s, 3H), 3.31-3.43 (m, 2H), 3.87 (s, 2H), 3.97 (s, 3H), 4.01-4.24 (m, 4H), 4.27 (s, 2H), 7.05-7.15 (m, 2H), 7.10 (s, 1H), 7.27-7.31 (m, 1H), 7.38 (s, 1H), 8.32 (t, J=5.9, 1H), 8.56 (brs, 2H).

Example 270N²-(2-ethyl-3,5-dimethyl-2H-indazol-6-yl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (182 mg, 0.596 mmol) of Reference Example 138, the compound (124 mg, 0.612 mmol) of Reference Example 19 and the compound (132 mg, 0.701 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 57, step B, the title compound (236 mg, yield 71%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.13 (t J=7.1, 3H), 1.37 (t, J=7.2, 3H), 2.31 (s, 3H), 2.52 (s, 3H), 2.8-3.0 (m, 4H), 2.88 (s, 3H), 3.85 (s, 2H), 4.03-4.11 (m, 2H), 4.17-4.32 (m, 4H), 4.26 (s, 2H), 7.05-7.15 (m, 2H), 7.13 (s, 1H), 7.27-7.31 (m, 1H), 7.36 (s, 1H), 8.32 (t, J=5.8, 1H), 8.62 (brs, 2H).

Example 271N²-(1-ethyl-3,5-dimethyl-1H-indazol-6-yl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (82 mg, 0.269 mmol) of Reference Example 139, the compound (55 mg, 0.271 mmol) of Reference Example 19 and the compound (70 mg, 0.372 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 57, step B, the title compound (85 mg, yield 56%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.13 (t, J=7.3, 3H), 1.30 (t, J=7.2, 3H), 2.34 (s, 3H), 2.39 (s, 3H), 2.8-3.0 (m, 4H), 2.88 (s, 3H), 3.33-3.38 (m, 2H), 3.91 (s, 2H), 4.02-4.11 (m, 2H), 4.16-4.28 (m, 2H), 4.22 (q, J=7.2, 2H), 4.30 (s, 2H), 7.04-7.15 (m, 2H), 7.23 (s, 1H), 7.25-7.31 (m, 1H), 7.40 (s, 1H), 8.35 (t, J=5.8, 1H), 8.70 (brs, 2H).

Example 272N²-[2-(2,2-difluoroethyl)-3,5-dimethyl-2H-indazol-6-yl]-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (185 mg, 0.542 mmol) of Reference Example 140, the compound (106 mg, 0.574 mmol) of Reference Example 17 and the compound (131 mg, 0.696 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 57, step B, the title compound (271 mg, yield 86%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.13 (t, J=7.2, 3H), 2.32 (s, 3H), 2.55 (s, 3H), 2.8-3.0 (m, 4H), 2.89 (s, 3H), 3.32-3.45 (m, 2H), 3.87 (s, 2H), 4.10 (d, J=11.4, 2H), 4.26 (d, J=11.4, 2H), 4.29 (s, 2H), 4.80 (dt, J=3.8, 15, 2H), 6.45 (dt, J=3.8, 55, 1H), 7.12 (s, 1H), 7.23-7.29 (m, 4H), 7.39 (s, H), 8.31 (t, J=5.9, 1H), 8.64 (brs, 2H).

Example 273N²-[2-(2,2-difluoroethyl)-3,5-dimethyl-2H-indazol-6-yl]-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (192 mg, 0.563 mmol) of Reference Example 140, the compound (118 mg, 0.582 mmol) of Reference Example 19 and the compound (147 mg, 0.563 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 57, step B, the title compound (264 mg, yield 79%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.13 (t, J=7.2, 3H), 2.31 (s, 3H), 2.55 (s, 3H), 2.8-3.0 (m, 4H), 2.89 (s, 3H), 3.30-3.45 (m, 2H), 3.87 (s, 2H), 4.04-4.25 (m, 4H), 4.27 (s, 2H), 4.79 (dt, J=3.7, 15, 2H), 6.44 (dt, J=3.7, 55, 1H), 7.05-7.16 (m, 2H), 7.12 (s, 1H), 7.26-7.32 (m, 1H), 7.39 (s, H), 8.29 (t, J=6.0, 1H), 8.56 (brs, 2H).

Example 274N²-(3-ethyl-2,5-dimethyl-2H-indazol-6-yl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (123 mg, 0.403 mmol) of Reference Example 141, the compound (82 mg, 0.405 mmol) of Reference Example 19 and the compound (94 mg, 0.499 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 57, step B, the title compound (150 mg, yield 66%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.12 (t, J=7.2, 3H), 1.22 (t, J=7.6, 3H), 2.31 (s, 3H), 2.8-3.0 (m, 4H), 2.88 (s, 3H), 2.98 (q, J=7.6, 2H), 3.34-3.42 (m, 2H), 3.86 (s, 2H), 3.99 (s, 3H), 4.02-4.11 (m, 2H), 4.17-4.25 (m, 2H), 4.26 (s, 2H), 7.05-7.15 (m, 2H), 7.12 (s, 1H), 7.27-7.31 (m, 1H), 7.41 (s, 1H), 8.32 (t, J=5.8, 1H), 8.54 (brs, 2H).

Example 275N²-(2,3-diethyl-5-methyl-2H-indazol-6-yl)-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (129 mg, 0.404 mmol) of Reference Example 142, the compound (76 mg, 0.412 mmol) of Reference Example 17 and the compound (104 mg, 0.552 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 57, step B, the title compound (170 mg, yield 76%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.13 (t, J=7.2, 3H), 1.23 (t, J=7.5, 3H), 1.41 (t, J=7.2, 3H), 2.32 (s, 3H), 2.8-3.0 (m, 4H), 2.89 (s, 3H), 2.99 (q, J=7.5, 2H), 3.34-3.40 (m, 2H), 3.86 (s, 2H), 4.10 (d, J=11.6, 2H), 4.26 (d, J=11.6, 2H), 4.29 (s, 2H), 4.30 (q, J=7.2, 2H), 7.15 (s, 1H), 7.2-7.3 (m, 4H), 7.42 (s, 1H), 8.35 (t, J=5.8, 1H), 8.78 (brs, 2H).

Example 276N²-(2,3-diethyl-5-methyl-2H-indazol-6-yl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (131 mg, 0.410 mmol) of Reference Example 142, the compound (86 mg, 0.424 mmol) of Reference Example 19 and the compound (104 mg, 0.552 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 57, step B, the title compound (160 mg, yield 68%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.13 (t, J=7.2, 3H), 1.23 (t, J=7.5, 3H), 1.40 (t, J=7.2, 3H), 2.32 (s, 3H), 2.8-3.0 (m, 4H), 2.88 (s, 3H), 2.99 (q, J=7.5, 2H), 3.34-3.41 (m, 2H), 3.86 (s, 2H), 4.05-4.24 (m, 4H), 4.27 (s, 2H), 4.30 (q, J=7.2, 2H), 7.05-7.13 (m, 2H), 7.15 (s, 1H), 7.27-7.31 (m, 1H), 7.40 (s, 1H), 8.34 (t, J=5.8, 1H), 8.76 (brs, 2H).

Example 277N²-[2-(2,2-difluoroethyl)-3-ethyl-5-methyl-2H-indazol-6-yl]-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (206 mg, 0.580 mmol) of Reference Example 143, the compound (110 mg, 0.596 mmol) of Reference Example 17 and the compound (138 mg, 0.733 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 57, step B, the title compound (286 mg, yield 83%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.12 (t, J=7.2, 3H), 1.23 (t, J=7.5, 3H), 2.32 (s, 3H), 2.8-3.0 (m, 4H), 2.89 (s, 3H), 3.02 (q, J=7.5, 2H), 3.34-3.40 (m, 2H), 3.87 (s, 2H), 4.10 (d, J=11.4, 2H), 4.26 (d, J=11.4, 2H), 4.29 (s, 2H), 4.80 (dt, J=3.9, 15, 2H), 6.48 (tt, J=3.9, 55, 1H), 7.14 (s, 1H), 7.24-7.27 (m, 4H), 7.44 (s, 1H), 8.31 (t, J=5.8, 1H), 8.69 (brs, 2H).

Example 278N²-[2-(2,2-difluoroethyl)-3-ethyl-5-methyl-2H-indazol-6-yl]-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxo-ethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (196 mg, 0.552 mmol) of Reference Example 143, the compound (113 mg, 0.558 mmol) of Reference Example 19 and the compound (130 mg, 0.563 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 57, step B, the title compound (259 mg, yield 77%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.12 (t, J=7.2, 3H), 1.23 (t, J=7.5, 3H), 2.32 (s, 3H), 2.8-3.0 (m, 4H), 2.89 (s, 3H), 3.02 (q, J=7.5, 2H), 3.3-3.5 (m, 2H), 3.87 (s, 2H), 4.06-4.24 (m, 4H), 4.28 (s, 2H), 4.80 (dt, J=3.9, 15, 2H), 6.47 (tt, J=3.9, 55, 1H), 7.05-7.16 (m, 2H), 7.13 (s, 1H), 7.27-7.31 (m, 1H), 7.43 (s, 1H), 8.30 (t, J=5.6, 1H), 8.64 (brs, 2H).

Example 279N²-[1-(2,2-difluoroethyl)-3-ethyl-5-methyl-1H-indazol-6-yl]-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (178 mg, 0.501 mmol) of Reference Example 144, the compound (106 mg, 0.523 mmol) of Reference Example 19 and the compound (114 mg, 0.606 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 57, step B, the title compound (124 mg, yield 41%) was obtained as a yellow-bistered solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.13 (t, J=7.2, 3H), 1.27 (t, J=7.6, 3H), 2.36 (s, 3H), 2.8-3.0 (m, 4H), 2.84 (q, J=7.6, 2H), 2.87 (s, 3H), 3.34-3.41 (m, 2H), 3.90 (s, 2H), 4.04-4.26 (m, 4H), 4.31 (s, 2H), 4.70 (dt, J=3.6, 15, 2H), 6.33 (tt, J=3.6, 55, 1H), 7.04-7.14 (m, 2H), 7.24-7.30 (m, 1H), 7.33 (s, 1H), 7.47 (s, 1H), 8.35 (t, J=5.6, 1H), 8.67 (brs, 2H).

Example 280N²-[1-(2,2-difluoroethyl)-7-methyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-yl]-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (391 mg, 1.10 mmol) of Reference Example 145, the compound (207 mg, 1.12 mmol) of Reference Example 17 and the compound (227 mg, 1.21 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 205, step B, the title compound (536 mg, yield 77%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=7.2, 3H), 2.27 (s, 3H), 2.50-2.56 (m, 2H), 2.74-2.79 (m, 2H), 2.8-3.0 (m, 4H), 2.88 (s, 3H), 3.34-3.42 (m, 2H), 3.81 (s, 2H), 4.08 (d, J=11.4, 2H), 4.23 (s, 2H), 4.24â€³(d, J=11.4, 2H), 4.31 (dt, J=4.1, 15, 2H), 6.20 (tt, J=4.1, 56, 1H), 7.02 (s, 1H), 7.08 (s, 1H), 7.23-7.29 (m, 4H), 8.40 (t, J=5.7, 1H), 8.82 (brs, 2H).

Example 281N²-[1-(2,2-difluoroethyl)-7-methyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-yl]-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (395 mg, 1.11 mmol) of Reference Example 145, the compound (228 mg, 1.13 mmol) of Reference Example 19 and the compound (229 mg, 1.22 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 205, step B, the title compound (549 mg, yield 76%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=7.2, 3H), 2.27 (s, 3H), 2.50-2.57 (m, 2H), 2.74-2.79 (m, 2H), 2.8-3.0 (m, 4H), 2.87 (s, 3H), 3.34-3.42 (m, 2H), 3.81 (s, 2H), 4.03-4.28 (m, 4H), 4.21 (s, 2H), 4.31 (dt, J=4.1, 14, 2H), 6.20 (tt, J=4.1, 56, 1H), 7.02 (s, 1H), 7.05-7.16 (m, 2H), 7.07 (s, 1H), 7.27-7.32 (m, 1H), 8.38 (t, J=5.8, 1H), 8.75 (brs, 2H).

Example 282N²-[2-(2,2-difluoroethyl)-6-methyl-3-oxo-2,3-dihydro-1H-isoindol-5-yl]-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (297 mg, 0.868 mmol) of Reference Example 146, the compound (163 mg, 0.883 mmol) of Reference Example 17 and the compound (180 mg, 0.956 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 205, step B, the title compound (453 mg, yield 85%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.14 (t, J=7.2, 3H), 2.37 (s, 3H), 2.8-3.0 (m, 4H), 2.87 (s, 3H), 3.32-3.40 (m, 2H), 3.90 (s, 2H), 3.93 (dt, J=3.5, 16, 2H), 4.10 (d, J=11.4, 2H), 4.25 (d, J=11.4, 2H), 4.31 (s, 2H), 4.46 (s, 2H), 6.27 (tt, J=3.5, 15, 1H), 7.24-7.28 (m, 4H), 7.36 (s, 1H), 7.47 (s, 1H), 8.28 (t, J=5.8, 1H), 8.64 (brs, 2H).

Example 283N²-[2-(2,2-difluoroethyl)-6-methyl-3-oxo-2,3-dihydro-1H-isoindol-5-yl]-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (306 mg, 0.894 mmol) of Reference Example 146, the compound (190 mg, 0.938 mmol) of Reference Example 19 and the compound (213 mg, 1.13 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 205, step B, the title compound (426 mg, yield 75%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.14 (t, J=7.2, 3H), 2.37 (s, 3H), 2.8-3.0 (m, 4H), 2.86 (s, 3H), 3.90 (s, 2H), 3.93 (dt, J=3.6, 16, 2H), 4.04-4.27 (m, 4H), 4.30 (s, 2H), 4.46 (s, 2H), 6.27 (tt, J=3.6, 55, 1H), 7.05-7.16 (m, 2H), 7.27-7.32 (m, 1H), 7.36 (s, 1H), 7.47 (s, 1H), 8.27 (t, J=5.7, 1H), 8.57 (brs, 2H).

Example 284N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2-ethyl-6-methyl-3-oxo-2,3-dihydro-1H-isoindol-5-yl)-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (237 mg, 0.774 mmol) of Reference Example 147, the compound (145 mg, 0.785 mmol) of Reference Example 17 and the compound (161 mg, 0.855 mmol) of Reference Example 2, and according to the methods of Example 204, step A, to and Example 205, step B, the title compound (366 mg, yield 82%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.12-1.17 (m, 6H), 2.36 (s, 3H), 2.8-3.0 (m, 4H), 2.87 (s, 3H), 3.32-3.39 (m, 2H), 3.50 (q, J=7.2, 2H), 3.89 (s, 2H), 4.10 (d, J=11.4, 2H), 4.25 (d, J=11.4, 2H), 4.30 (s, 2H), 4.34 (s, 2H), 7.23-7.29 (m, 4H), 7.32 (s, 1H), 7.43 (s, 1H), 8.29 (t, J=5.7, 1H), 8.65 (brs, 2H).

Example 285N²-(2-ethyl-6-methyl-3-oxo-2,3-dihydro-1H-isoindol-5-yl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (251 mg, 0.819 mmol) of Reference Example 147, the compound (171 mg, 0.844 mmol) of Reference Example 19 and the compound (201 mg, 1.07 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 205, step B, the title compound (350 mg, yield 72%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.11-1.17 (m, 6H), 2.36 (s, 3H), 2.8-3.0 (m, 4H), 2.86 (s, 3H), 3.32-3.40 (m, 2H), 3.50 (q, J=7.2, 2H), 3.89 (s, 2H), 4.04-4.26 (m, 4H), 4.29 (s, 2H), 4.34 (s, 2H), 7.05-7.16 (m, 2H), 7.27-7.33 (m, 1H), 7.32 (s, 1H), 7.43 (s, 1H), 8.28 (t, J=5.7, 1H), 8.63 (brs, 2H).

Example 286N²-{5-[5-(difluoromethyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl}-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-{5-[amino(hydroxyimino)methyl]-2-methylphenyl}-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

To ethanol (20 ml) were added the compound (1.10 g, 2.00% mmol) of Example 2, step A, sodium acetate (347 mg, 4.23 mmol) and hydroxylammonium chloride (292 mg, 4.20 mmol) and the mixture was heated under reflux for 210 min. The reaction mixture was cooled, diluted with an ethyl acetate-hexane=1:1 mixed solvent, washed with saturated aqueous sodium hydrogen carbonate and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure to give a colorless amorphous solid (1.19 g).

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.03 (t, J=7.1, 3H), 1.40 (brs, 9H), 1.80 (brs, 1H), 2.33 (s, 3H), 2.94 (s, 3H), 3.05-3.20 (m, 2H), 3.20-3.35 (m, 2H), 3.37-3.43 (m, 2H), 3.81 (s, 2H), 4.12 (d, J=11.4, 2H), 4.20 (s, 2H), 4.22 (d, J=11.4, 2H), 4.95 (brs, 2H), 7.16-7.28 (m, 6H), 7.56 (brs, 1H), 8.36 8.59 (2brs, 1H).

Step BN²-{5-[5-(difluoromethyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl}-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

The compound (406 mg, 0.698 mmol) of step A, difluoroacetic acid (0.12 ml, 1.90 mmol) and WSC (530 mg, 2.76 mmol) were dissolved in 1,4-dioxane (5 ml) and the mixture was heated under reflux for 5 hr. The reaction mixture was diluted with an ethyl acetate-hexane=1:1 mixed solvent, and the organic layer was washed with water, 10% aqueous citric acid solution, diluted aqueous sodium hydroxide solution and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the residue was purified by silica gel column chromatography (ethyl acetate-hexaneâ†’ethyl acetate-methanol) to give the title compound (97 mg, yield 22%) as a pale-yellow amorphous solid

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.05 (t, J=7.0, 3H), 1.43 (brs, 9H), 2.41 (s, 3H), 2.95 (s, 3H), 3.10-3.25 (m, 2H), 3.25-3.40 (m, 2H), 3.41-3.47 (m, 2H), 3.83 (s, 2H), 4.18 (d, J=11.4, 2H), 4.25 (d, J=11.4, 2H), 4.30 (s, 2H), 6.84 (t, J=52, 1H), 7.19-7.32 (m, 5H), 7.72 (d, J=7.5, 1H), 7.96 (d, J=1.5, 1H), 8.33 8.60 (2brs, 1H).

Step CN²-{5-[5-(difluoromethyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl}-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (96 mg, 0.150 mmol) of step B, and according to the method of Example 1, step C, the title compound (86 mg, yield 93%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.14 (t, J=7.2, 3H), 2.35 (s, 3H), 2.8-3.0 (m, 4H), 2.88 (s, 3H), 3.35-3.40 (m, 2H), 3.95 (s, 2H), 4.14 (d, J=11.5, 2H), 4.27 (d, J=11.5, 2H), 4.37 (s, 2H), 7.26 (brs, 4H), 7.33 (d, J=7.9, 1H), 7.55 (t, J=52, 1H), 7.57 (dd, J=1.4, 7.9, 1H), 7.78 (d, J=1.4, 1H), 8.33 (broad t, 1H), 8.68 (brs, 2H).

Example 287N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-{2-methyl-5-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-{2-methyl-5-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl}-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

To N,N-dimethylformamide (5 ml) were added the compound (350 mg, 0.602 mmol) of Example 286, step A, triethylamine (0.12 ml, 0.86 mmol) and trifluoroacetic acid anhydride (0.090 ml, 0.64 mmol), and the mixture was stirred with heating at 100Â° C. for 90 min. The reaction mixture was cooled, and diluted with an ethyl acetate-hexane=1:1 mixed solvent. The organic layer was washed with water, 10% aqueous citric acid solution, saturated aqueous sodium hydrogen carbonate and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the residue was purified by silica gel column chromatography (ethyl acetate-hexaneâ†’ethyl acetate-methanol) to give the title compound (235 mg, yield 59%) as a pale-yellow amorphous solid

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.05 (t, J=7.0, 3H), 1.43 (brs, 9H), 2.42 (s, 3H), 2.96 (s, 3H), 3.10-3.25 (m, 2H), 3.25-3.35 (m, 2H), 3.41-3.47 (m, 2H), 3.83 (s, 2H), 4.19 (d, J=11.7, 2H), 4.26 (d, J=11.7, 2H), 4.32 (s, 2H), 7.19-7.28 (m, 4H), 7.31 (d, J=7.8, 1H), 7.72 (d, J=7.8, 1H), 7.94 (d, J=1.6, 1H), 8.30 8.60 (2brs, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-{2-methyl-5-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (233 mg, 0.353 mmol) of step B, and according to the method of Example 1, step C, the title compound (197 mg, yield 88%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.2, 3H), 2.36 (s, 3H), 2.8-3.0 (m, 4H), 2.88 (s, 3H), 3.35-3.40 (m, 2H), 3.96 (s, 2H), 4.14 (d, J=11.4, 2H), 4.27 (d, J=11.4, 2H), 4.37 (s, 2H), 7.26 (brs, 4H), 7.35 (d, J=7.8, 1H), 7.58 (dd, J=1.4, 7.8, 1H), 7.77 (d, J=1.4, 1H), 8.34 (t, J=6.0, 1H), 8.66 (brs, 2H).

Example 288N²-{4-[5-(difluoromethyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl}-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-{4-[amino(hydroxyimino)methyl]-2-methylphenyl}-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (1.18 g, 2.15 mmol) of Example 62, step A, and according to the method of Example 286, step A, the title compound (1.30 g) was obtained as a colorless amorphous solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.01 (t, J=7.1, 3H), 1.42 (brs, 9H), 1.72 (brs, 1H), 2.33 (s, 3H), 2.95 (s, 3H), 3.09-3.13 (m, 2H), 3.15-3.30 (m, 2H), 3.35-3.41 (m, 2H), 3.86 (s, 2H), 4.15 (d, J=11.4, 2H), 4.21 (s, 2H), 4.25 (d, J=11.4, 2H), 4.82 (brs, 2H), 7.20-7.28 (m, 6H), 7.43 (s, 1H), 8.09 8.30 (2brs, 1H).

Step BN²-{4-[5-(difluoromethyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl}-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (406 mg, 0.698 mmol) of step A, and according to the methods of Example 286, step B, and Example 1, step C, the title compound (78 mg, yield 18%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.2, 3H), 2.34 (s, 3H), 2.8-3.0 (m, 4H), 2.92 (s, 3H), 3.36-3.41 (m, 2H), 3.98 (s, 2H), 4.16 (d, J=11.5, 2H), 4.29 (d, J=11.5, 2H), 4.41 (s, 2H), 7.10 (d, J=8.4, 1H), 7.24-7.30 (m, 4H), 7.52 (t, J=52, 1H), 7.73 (dd, J=2.0, 8.4, 1H), 7.77 (d, J=2.0, 1H), 8.33 (broad t, 1H), 8.68 (brs, 2H).

The compounds of Examples 265-288 are shown below.

TABLE 18StructuralLC-MSExampleFormulaTMW(found)265 [Image Omitted]

564.07528 266 [Image Omitted]

564.07528 267 [Image Omitted]

582.06546 268 [Image Omitted]

582.06546 269 [Image Omitted]

546.08510 270 [Image Omitted]

560.11524 271 [Image Omitted]

560.11524 272 [Image Omitted]

578.10542 273 [Image Omitted]

596.09560 274 [Image Omitted]

560.11524 275 [Image Omitted]

556.14520 276 [Image Omitted]

574.13538 277 [Image Omitted]

592.12556 278 [Image Omitted]

610.11574 279 [Image Omitted]

610.11574 280 [Image Omitted]

629.57557 281 [Image Omitted]

647.56575 282 [Image Omitted]

615.54543 283 [Image Omitted]

633.53561 284 [Image Omitted]

579.56507 285 [Image Omitted]

597.55525 286 [Image Omitted]

614.51542 287 [Image Omitted]

632.51560 288 [Image Omitted]

614.51542

Example 289N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-{2-methyl-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (355 mg, 0.610 mmol) of Example 288, step A, and according to the methods of Example 287, step A, and Example 1, step C, the title compound (83 mg, yield 22%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.2, 3H), 2.34 (s, 3H), 2.8-3.0 (m, 4H), 2.92 (s, 3H), 3.3-3.4 (m, 2H), 3.99 (s, 2H), 4.17 (d, J=11.6, 2H), 4.29 (d, J=11.6, 2H), 4.42 (s, 2H), 7.09 (d, J=8.4, 1H), 7.2-7.3 (m, 4H), 7.75 (d, J=8.4, 1H), 7.77 (s, 1H), 8.34 (t, J=5.7, 1H), 8.65 (brs, 2H).

Example 290N²-{5-[5-(difluoromethyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl}-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-(5-cyano-2-methylphenyl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (534 mg, 2.15 mmol) of Reference Example 61, the compound (442 mg, 2.18 mmol) of Reference Example 19 and the compound (452 mg, 2.40 mmol) of Reference Example 2, and according to the method of Example 204, step A, the title compound (1.07 g, yield 88%) was obtained as a pale-yellow amorphous solid

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.05 (t, J=7.1, 3H), 1.41 (brs, 9H), 2.39 (s, 3H), 2.96 (s, 3H), 3.13-3.19 (m, 2H), 3.20-3.35 (m, 2H), 3.38-3.44 (m, 2H), 3.82 (s, 2H), 4.14-4.28 (m, 4H), 4.24 (s, 2H), 6.92-7.00 (m, 2H), 7.16-7.20 (m, 1H), 7.22-7.25 (m, 2H), 7.48 (s, 1H), 8.02 8.36 (2brs, 1H).

Step BN²-{5-[amino(hydroxyimino)methyl]-2-methylphenyl}-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (1.04 g, 1.84 mmol) of step A, and according to the method of Example 286, step A, the title compound (1.08 g, yield 98%) was obtained as a colorless amorphous solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.04 (t, J=7.1, 3H), 1.40 (brs, 9H), 1.75 (brs, 1H), 2.33 (s, 3H), 2.94 (s, 3H), 3.1-3.2 (m, 2H), 3.2-3.3 (m, 2H), 3.38-3.43 (m, 2H), 3.80 (s, 2H), 4.06-4.23 (m, 4H), 4.19 (s, 2H), 4.95 (brs, 2H), 6.90-6.98 (m, 2H), 7.13-7.19 (m, 2H), 7.24-7.26 (m, 1H), 7.56 (brs, 1H), 8.34 8.57 (2brs, 1H).

Step CN²-{5-[5-(difluoromethyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl}-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl) (ethyl)amino]ethyl}glycinamide

Using the compound (1.06 g, 1.77 mmol) of step B, difluoroacetic anhydride (463 mg, 2.66 mmol), and according to the method of Example 287, step A, the title compound (838 mg, yield 72%) was obtained as a colorless amorphous solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.05 (t, J=7.1, 3H), 1.43 (brs, 9H), 2.41 (s, 3H), 2.95 (s, 3H), 3.10-3.25 (m, 2H), 3.25-3.35 (m, 2H), 3.41-3.47 (m, 2H), 3.82 (s, 2H), 4.12-4.26 (m, 4H), 4.30 (s, 2H), 6.85 (t, J=52, 1H), 6.90-6.98 (m, 2H), 7.13-7.18 (m, 1H), 7.30 (d, J=7.9, 1H), 7.72 (d, J=7.5, 1H), 7.95 (d, J=1.4, 1H), 8.30 8.58 (2brs, 1H).

Step DN²-{5-[5-(difluoromethyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl}-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl) (methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (821 mg, 1.24 mmol) of step C, and according to the method of Example 205, step B, the title compound (670 mg, yield 85%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.2, 3H), 2.35 (s, 3H), 2.8-3.0 (m, 4H), 2.88 (s, 3H), 3.35-3.40 (m, 2H), 3.95 (s, 2H), 4.08-4.29 (m, 4H), 4.36 (s, 2H), 7.05-7.16 (m, 2H), 7.28-7.32 (m, 1H), 7.33 (d, J=8.0, 1H), 7.55 (t, J=52, 1H), 7.57 (dd, J=1.6, 8.0, 1H), 7.78 (d, J=1.6, 1H), 8.34 (t, J=5.8, 1H), 8.75 (brs, 2H).

Example 291N²-{4-[5-(difluoromethyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl}-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-(4-cyano-2-methylphenyl)-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (524 mg, 2.11 mmol) of Reference Example 68, the compound (434 mg, 2.14 mmol) of Reference Example 19 and the compound (445 mg, 2.36 mmol) of Reference Example 2, and according to the method of Example 204, step A, the title compound (1.04 g, yield 87%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.01 (t, J=7.1, 3H), 1.39 (brs, 9H), 2.33 (s, 3H), 2.98 (s, 3H), 3.06-3.12 (m, 2H), 3.15-3.30 (m, 2H), 3.34-3.40 (m, 2H), 3.92 (s, 2H), 4.09-4.26 (m, 4H), 4.29 (s, 2H), 6.92-7.00 (m, 2H), 7.14-7.20 (m, 2H), 7.39 (d, J=1.8, 1H), 7.41 (s, 1H), 7.87 8.08 (2brs, 1H).

Step BN²-{4-[5-(difluoromethyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl}-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (982 mg, 1.73 mmol) of step A, and according to the methods of Example 286, step A, Example 290, step C, and Example 205, step B, the title compound (451 mg, yield 41%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.2, 3H), 2.34 (s, 3H), 2.8-3.0 (m, 4H), 2.91 (s, 3H), 3.35-3.41 (m, 2H), 3.97 (s, 2H), 4.12-4.31 (m, 4H), 4.40 (s, 2H), 7.05-7.11 (m, 1H), 7.10 (d, J=8.6, 1H), 7.14-7.18 (m, 1H), 7.29-7.33 (m, 1H), 7.52 (t, J=52, 1H), 7.73 (dd, J=1.8, 8.6, 1H), 7.76 (d, J=1.8, 1H), 8.33 (t, J=5.8, 1H), 8.72 (brs, 2H).

Example 292N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-{5-[5-(hydroxymethyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochlorideStep AN²-{5-[5-(chloromethyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl}-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

The compound (4.82 g, 8.04 mmol) of Example 290, step B was dissolved in 1,4-dioxane (70 ml), magnesium oxide (355 mg, 8.81 mmol) and chloroacetyl chloride (0.67 ml, 8.42 mmol) were added at room temperature, and the mixture was stirred at 100Â° C. for 1 hr. After cooling to room temperature, the reaction mixture was diluted with ethyl acetate, and the organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (3.40 g, yield 64%) as a pale-yellow amorphous solid

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.05 (t, J=7.2, 3H), 1.43 (brs, 9H), 2.40 (s, 3H), 2.95 (s, 3H), 3.10-3.24 (m, 2H), 3.24-3.36 (m, 2H), 3.41-3.47 (m, 2H), 3.81 (s, 2H), 4.09-4.25 (m, 4H), 4.28 (s, 2H), 4.72 (s, 2H), 6.90-7.01 (m, 2H), 7.13-7.18 (m, 1H), 7.29 (d, J=7.7, 1H), 7.70 (d, J=8.2, 1H), 7.93 (s, 1H), 8.32 8.60 (2brs, 1H).

Step BN²-[5-{5-[(acetoxy)methyl]-1,2,4-oxadiazol-3-yl}-2-methylphenyl]-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

To N,N-dimethylformamide (40 ml) were added the compound (3.39 g, 5.15 mmol) of step A and sodium acetate (1.37 g, 16.7 mmol), and the mixture was stirred at 60Â° C. for 5 hr. After cooling to room temperature, ethyl acetate-hexane=1:1 mixed solvent and water were added to the reaction mixture, and the organic layer was extracted. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (3.15 g, yield 90%) as a pale-yellow amorphous solid

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.05 (t, J=7.2, 3H), 1.43 (brs, 9H), 2.22 (s, 3H), 2.40 (s, 3H), 2.94 (s, 3H), 3.10-3.24 (m, 2H), 3.24-3.35 (m, 2H), 3.41-3.47 (m, 2H), 3.81 (s, 2H), 4.09-4.32 (m, 4H), 4.28 (s, 2H), 5.33 (s, 2H), 6.89-6.99 (m, 2H), 7.13-7.18 (m, 1H), 7.28 (d, J=8.2, 1H), 7.70 (d, J=7.7, 1H), 7.94 (s, 1H), 8.32 8.61 (2brs, 1H).

Step CN²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-{5-[5-(hydroxymethyl)-1,2,4-oxadiazol-3-yl]-2-methylphenyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

The compound (535 mg, 0.785 mmol) of step B was dissolved in a 2N hydrochloric acid-ethanol solution (8 ml) at room temperature, and the mixture was stirred at the same temperature for 24 hr. To the reaction mixture was added diluted aqueous ammonia to alkalify the solution, and the organic layer was extracted with dichloromethane, and dried over sodium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (NH silica gel use, ethyl acetate-methanol) to give a colorless amorphous solid (363 mg). This was dissolved in ethanol (1 ml), and 2N hydrochloric acid-ethanol (0.34 ml) was added. To the solution was added diethyl ether, and the precipitated solid was filtered, washed with diethyl ether, and dried under reduced pressure to give the title compound (357 mg, yield 79%) as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.14 (t, J=7.2, 3H), 2.34 (s, 3H), 2.8-3.0 (m, 4H), 2.88 (s, 3H), 3.30-3.41 (m, 2H), 3.93 (s, 2H), 4.09-4.29 (m, 4H), 4.34 (s, 2H), 4.79 (s, 2H), 6.09 (brs, 1H), 7.05-7.18 (m, 2H), 7.28-7.33 (m, 2H), 7.54 (d, J=9.2, 1H), 7.77 (s, 1H), 8.32 (t, J=5.7, 1H), 8.65 (brs, 2H).

Example 293N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2-methyl-4-pyrimidin-5-ylphenyl)-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(4-iodo-2-methylphenyl)-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (6.33 g, 18.1 mmol) of Reference Example 121, the compound (3.51 g, 19.0 mmol) of Reference Example 17 and the compound (3.47 g, 19.0 mmol) of Reference Example 2, and according to the method of Example 204, step A, the title compound (11.24 g, yield 96%) was obtained as a brown oil.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 0.94 (brs, 3H), 1.36 1.39 (2s, 11H), 2.20 (s, 3H), 2.87 (s, 3H), 3.02-3.15 (m, 4H), 3.76 (s, 2H), 4.08-4.26 (m, 6H), 6.87 (d, J=8.4, 1H), 7.23-7.28 (m, 4H), 7.35-7.38 (m, 1H), 7.43 (s, 1H).

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2-methyl-4-pyrimidin-5-ylphenyl)-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (325 mg, 0.500 mmol) of step A and pyrimidine-5-boronic acid (74 mg, 0.600 mmol), and according to the methods of Example 255, step B, and Example 1, step C, the title compound (167 mg, yield 58%) was obtained as a yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=7.3, 3H), 2.35 (s, 3H), 2.87-2.90 (m, 2H), 3.36-3.41 (m, 3H), 3.84 (brs, 4H), 3.94 (s, 2H), 4.13-4.16 (m, 2H), 4.26-4.29 (m, 2H), 4.36 (s, 2H), 7.17 (d, J=8.4, 1H), 7.24-7.30 (m, 4H), 7.52-7.54 (m, 1H), 7.58 (s, 1H), 8.33-8.37 (m, 1H), 8.82 (brs, 2H), 9.09 (s, 2H), 9.12 (s, 1H).

Example 294N²-[4-(6-aminopyridin-3-yl)-2-methylphenyl]-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide trihydrochloride

Using the compound (325 mg, 0.500 mmol) of Example 293, step A and 2-amino-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine (132 mg, 0.600 mmol), and according to the methods of Example 255, step B, and Example 1, step C, the title compound (197 mg, yield 63%) was obtained as a brown solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=7.2, 3H), 2.32 (s, 3H), 2.89 (brs, 3H), 3.90 (s, 2H), 4.11-4.14 (m, 2H), 4.26-4.32 (m, 4H), 7.07 (d, J=9.2, 1H), 7.14 (d, J=8.4, 1H), 7.24-7.29 (m, 4H), 7.35-7.38 (m, 1H), 7.42 (s, 1H), 8.07 (brs, 1H), 8.20-8.26 (m, 2H), 8.33-8.35 (m, 1H), 8.79 (brs, 2H).

Example 295N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-{4-[5-(methyloxycarbonyl)pyridin-2-yl]-2-methylphenyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[4-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-2-methylphenyl]-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

The compound (2.16 g, 3.33 mmol) of Example 293, step A, bis(neopentylglycolate)diboron (827 mg, 3.66 mmol), bis(tricyclohexylphosphine)palladium(II)dichloride (123 mg, 0.167 mmol) and potassium acetate (490 mg, 5.00 mmol) were dissolved in 1,4-dioxane (7 ml), and the mixture was heated under reflux for 5 hr. The reaction mixture was diluted with ethyl acetate, and the organic layer was washed with water and saturated brine, and dried over sodium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (2.04 g, yield 97%) as a crude brown oil.

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-{4-[5-(methoxycarbonyl)pyridin-2-yl]-2-methylphenyl}-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

The compound (510 mg, 0.802 mmol) obtained in step A, 6-bromonicotinic acid methyl ester (208 mg, 0.962 mmol), bis(tricyclohexylphosphine)palladium(II)dichloride (59 mg, 0.080 mmol) and 1.27 mol/l aqueous potassium phosphate solution (0.95 ml) were dissolved in 1,4-dioxane (4 ml), and the mixture was heated under reflux for 8 hr. The reaction mixture was diluted with ethyl acetate, and the organic layer was washed with water and saturated brine, and dried over sodium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-methanol) to give the title compound (37.5 mg, yield 71%) as a brown oil.

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-{4-[5-(methyloxycarbonyl)pyridin-2-yl]-2-methylphenyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (78 mg, 0.118 mmol) of step B, and according to the method of Example 1, step C, the title compound (25 mg, yield 33%) was obtained as a yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=7.3, 3H), 2.36 (s, 3H), 2.86-2.91 (m, 7H), 3.37-3.42 (m, 2H), 3.90 (s, 3H), 3.98-4.23 (m, 4H), 4.27-4.42 (m, 4H), 7.09 (d, J=8.6, 1H), 7.24-7.30 (m, 4H), 7.89-7.91 (m, 1H), 7.97 (s, 1H), 8.08 (d, J=8.4, 1H), 8.33-8.41 (m, 2H), 8.89 (brs, 2H), 9.08 (s, 1H).

Example 296N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-{4-[4-(ethoxycarbonyl)-1,3-thiazol-2-yl]-2-methylphenyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-{4-[4-(ethoxycarbonyl)-1,3-thiazol-2-yl]-2-methylphenyl}-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (510 mg, 0.802 mmol) of Example 295, step A and ethyl 2-bromothiazole-4-carboxylate (227 mg, 0.962 mmol), and according to the method of Example 295, step B, the title compound (282 mg, yield 52%) was obtained as a brown oil.

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-{4-[4-(ethoxycarbonyl)-1,3-thiazol-2-yl]-2-methylphenyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (36 mg, 0.053 mmol) of step A, and according to the method of Example 1, step C, the title compound (14 mg, yield 40%) was obtained as a yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=7.2, 3H), 1.33 (t, J=7.4, 3H), 2.34 (s, 3H), 2.87-2.91 (m, 7H), 3.37-3.41 (m, 2H), 3.91-3.96 (m, 2H), 4.14-4.17 (m, 2H), 4.27-4.39 (m, 6H), 7.07 (d, J=8.4, 1H), 7.24-7.30 (m, 4H), 7.64-7.71 (m, 2H), 8.36 (t, J=5.7, 1H), 8.47 (s, 1H), 8.81 (brs, 2H).

Example 297N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(6-oxo-1,6-dihydropyridazin-3-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide

Using the compound (510 mg, 0.802 mmol) of Example 295, step A and 3-chloro-6-methoxypyridazine (139 mg, 0.962 mmol), and according to the method of Example 295, step B, N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[4-(6-methoxypyridazin-3-yl)-2-methylphenyl]-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide (250 mg) was obtained as a brown oil. Using this oil (210 mg, 0.332 mmol), and according to the method of Example 46, step B, the title compound (92 mg, yield 53%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 0.91 (t, J=7.1, 3H), 2.31 (s, 3H), 2.40-2.48 (m, 4H), 2.89 (s, 3H), 3.10-3.15 (m, 2H), 3.84 (s, 2H), 4.11-4.14 (m, 2H), 4.25-4.30 (m, 4H), 6.95 (d, J=9.7, 1H), 7.11 (d, J=8.5, 1H), 7.23-7.29 (m, 4H), 7.54-7.57 (m, 1H), 7.62 (s, 1H), 7.96-8.02 (m, 2H).

Example 298N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(2-oxopyrrolidin-1-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(2-oxopyrrolidin-1-yl)phenyl]-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

The compound (650 mg, 1.00 mmol) of Example 293, step A, 2-pyrrolidone (128 mg, 1.50 mmol), copper iodide(I) (19 mg, 0.10 mmol), N,Nâ€²-dimethylethylenediamine (0.022 ml, 0.20 mmol) and potassium phosphate (425 mg, 2.00 mmol) were dissolved in toluene (4.0 ml), and the mixture was heated under reflux for 7 hr. The reaction mixture was diluted with ethyl acetate and water, and the organic layer was extracted. The organic layer was washed with saturated brine and dried over sodium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (542 mg, yield 89%) as a brown oil.

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(2-oxopyrrolidin-1-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (542 mg, 0.893 mmol) of step A, and according to the method of Example 1, step C, the title compound (391 mg, yield 40%) was obtained as a brown solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.16-1.19 (m, 3H), 2.01-2.07 (m, 2H), 2.29 (s, 3H), 2.45 (t, J=8.0, 2H), 2.87-2.92 (m, 9H), 3.32-3.41 (m, 2H), 3.86 (brs, 2H), 4.07-4.10 (m, 2H), 4.23-4.29 (m, 4H), 7.17 (d, J=8.7, 1H), 7.23-7.28 (m, 4H), 7.31-7.33 (m, 1H), 7.39 (s, 1H), 8.40 (t, J=5.7, 1H), 8.82 (brs, 3H).

Example 299N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-(2-oxoimidazolidin-1-yl)phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (650 mg, 1.00 mmol) of Example 293, step A and ethyleneurea (129 mg, 1.50 mmol), and according to the methods of Example 298, step A, and Example 1, step C, the title compound (150 mg, yield 26%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=7.1, 3H), 2.30 (s, 3H), 2.88-2.91 (m, 7H), 3.35-3.39 (m, 4H), 3.57 (s, 2H), 3.88 (s, 2H), 4.07-4.10 (m, 2H), 4.22-4.33 (m, 4H), 7.21-7.40 (m, 7H), 8.44-8.51 (m, 1H), 8.82 (brs, 2H).

Example 300N²-{4-[4-(aminocarbonyl)-2-oxopyrrolidin-1-yl]-2-methylphenyl}-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycine amide 2 hydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-{4-[4-(methoxycarbonyl)-2-oxopyrrolidin-1-yl]-2-methylphenyl}-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (650 mg, 1.00 mmol) of Example 293, step A and methyl 5-oxopyrrolidine-3-carboxylate (215 mg, 1.50 mmol), and according to the method of Example 298, step A, the title compound (480 mg, yield 72%) was obtained as a brown oil (480 mg).

Step BN²-{4-[4-(aminocarbonyl)-2-oxopyrrolidin-1-yl]-2-methylphenyl}-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

The compound (480 mg, 0.722 mmol) of step A was dissolved in a methanol (1.5 ml)-tetrahydrofuran (1.5 ml) mixed solvent. Then, 1N aqueous sodium hydroxide solution (3.0 ml) was added, and the mixture was stirred at room temperature for 1 hr. To the reaction mixture was added 10% aqueous citric acid solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over sodium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure to give a crude pale-yellow oil (497 mg). This oil was dissolved in N,N-dimethylformamide (7 ml), 3H-[1,2,3]triazolo[4,5-b]pyridin-3-ol (147 mg, 1.08 mmol) and WSC (208 mg, 1.08 mmol) were added at room temperature, and the mixture was stirred at the same temperature for 30 min. Then, to the reaction mixture was added 28% aqueous ammonia (0.72 ml), and the mixture was successively stirred at room temperature for 3 hr. The reaction mixture was diluted with ethyl acetate and water, and the organic layer was extracted. The organic layer was washed with saturated brine and dried over sodium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane-*ethyl acetate-methanol) to give the title compound (312 mg, yield 67%) as a colorless amorphous solid.

Step CN²-{4-[4-(aminocarbonyl)-2-oxopyrrolidin-1-yl]-2-methylphenyl}-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (312 mg, 0.480 mmol) of step B, and according to the method of Example 1, step C, the title compound (274 mg, yield 92%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.0, 3H), 2.28 (s, 3H), 2.56-2.70 (m, 2H), 2.87 (brs, 7H), 3.17-3.18 (m, 1H), 3.36-3.40 (m, 2H), 3.55-3.57 (m, 2H), 3.79-3.85 (m, 2H), 4.06-4.09 (m, 2H), 4.22-4.26 (m, 4H), 7.11-7.16 (m, 2H), 7.25-7.32 (m, 5H), 7.38 (s, 1H), 7.61 (s, 1H), 8.36 (brs, 1H), 8.72 (brs, 2H).

Example 301N²-{4-[5-(aminocarbonyl)pyridin-2-yl]-2-methylphenyl}-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (238 mg, 0.361 mmol) of Example 295, step B, and according to the methods of Example 300, step B, and Example 1, step C, the title compound (138 mg, yield 62%) was obtained as a yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.17 (t, J=6.4, 3H), 2.36 (s, 3H), 2.87-2.93 (m, 7H), 3.36-3.42 (m, 2H), 3.98 (s, 2H), 4.15-4.18 (m, 2H), 4.28-4.31 (m, 2H), 4.41 (m, 2H), 7.09 (d, J=8.6, 1H), 7.24-7.30 (m, 4H), 7.69 (s, 1H), 7.87-7.90 (m, 1H), 7.95 (s, 1H), 8.10 (d, J=8.5, 1H), 8.29 (s, 1H), 8.37-8.41 (m, 2H), 8.81 (brs, 2H), 9.05 (s, 1H).

Example 302N²-{4-[4-(aminocarbonyl)-1,3-thiazol-2-yl]-2-methylphenyl}-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (181 mg, 0.267 mmol) of Example 296, step A, and according to the methods of Example 300, step B, and Example 1, step C, the title compound (65 mg, yield 39%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.1, 3H), 2.34 (s, 3H), 2.87-2.91 (m, 7H), 3.36-3.41 (m, 2H), 3.96 (s, 2H), 4.14-4.17 (m, 2H), 4.27-4.30 (m, 2H), 4.38 (s, 2H), 7.06 (d, J=8.5, 1H), 7.24-7.30 (m, 4H), 7.65 (s, 2H), 7.69-7.72 (m, 2H), 7.78-7.84 (m, 2H), 8.17 (s, 1H), 8.35 (t, J=5.8, 1H), 8.75 (brs, 2H).

Example 303N²-{4-[4-(aminocarbonyl)-1H-pyrazol-1-yl]-2-methylphenyl}-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (650 mg, 1.00 mmol) of Example 293, step A and ethyl 4-pyrazolecarboxylate (210 mg, 1.50 mmol), and according to the methods of Example 298, step A, Example 300, step B, and Example 1, step C, the title compound (79 mg, yield 13%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.1, 3H), 2.34 (s, 3H), 2.87-2.89 (m, 7H), 3.34-3.41 (m, 2H), 3.90 (s, 2H), 4.11-4.14 (m, 2H), 4.25-4.31 (m, 4H), 7.17-7.29 (m, 6H), 7.49-7.52 (m, 1H), 7.59 (s, 1H), 7.70 (brs, 1H), 8.07 (s, 1H), 8.33 (t, J=5.8, 1H), 8.76-8.79 (m, 3H).

Example 304N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[4-{4-[(dimethylamino)carbonyl]-1,3-thiazol-2-yl}-2-methylphenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (247 mg, 0.364 mmol) of Example 296, step A and 50% aqueous dimethylamine solution (0.36 ml), and according to the methods of Example 300, step B, and Example 1, step C, the title compound (111 mg, yield 47%) was obtained as a yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.3, 3H), 2.33 (s, 3H), 2.88-2.91 (m, 7H), 3.01 (s, 3H), 3.16 (s, 3H), 3.36-3.40 (m, 2H), 3.95 (s, 2H), 4.13-4.16 (m, 2H), 4.27-4.29 (m, 2H), 4.38 (s, 2H), 7.08 (d, J=8.5, 1H), 7.24-7.29 (m, 4H), 7.63-7.69 (m, 2H), 7.99 (s, 1H), 8.33 (t, J=5.8, 1H), 8.76 (brs, 2H).

Example 305N²-{4-[5-(aminocarbonyl)-1,3-thiazol-2-yl]-2-methylphenyl}-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-{4-[5-(ethoxycarbonyl)-1,3-thiazol-2-yl]-2-methylphenyl}-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (1.69 g, 2.66 mmol) of Example 295, step A and ethyl 2-bromothiazole-5-carboxylate (754 mg, 3.19 mmol), and according to the method of Example 295, step B, the title compound (246 mg, yield 14%) was obtained.

Step BN²-{4-[5-(aminocarbonyl)-1,3-thiazol-2-yl]-2-methylphenyl}-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (246 mg, 0.362 mmol) of step A, and according to the methods of Example 300, step B, and Example 1, step C, the title compound (202 mg, yield 90%) was obtained as a yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=7.2, 3H), 2.33 (s, 3H), 2.86-2.91 (m, 5H), 3.37-3.41 (m, 2H), 3.96 (s, 2H), 4.15-4.18 (m, 2H), 4.27-4.30 (m, 2H), 4.40 (s, 2H), 7.05 (d, J=8.5, 1H), 7.24-7.30 (m, 4H), 7.59-7.70 (m, 3H), 8.16 (brs, 1H), 8.34-8.38 (m, 2H), 8.87 (brs, 2H).

Example 306N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-4-{5-[(methylamino)carbonyl]-1,3-thiazol-2-yl]phenyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (120 mg, 0.177 mmol) of Example 305, step A, and 50% aqueous methylamine solution (0.195 ml), and according to the methods of Example 300, step B, and Example 1, step C, the title compound (105 mg, yield 93%) was obtained as a yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=7.1, 3H), 2.32 (s, 3H), 2.78 (s, 3H), 2.88-2.91 (m, 7H), 3.37-3.41 (m, 2H), 3.96 (s, 2H), 4.15-4.17 (m, 2H), 4.27-4.30 (m, 2H), 4.39 (s, 2H), 7.04 (d, J=8.5, 1H), 7.24-7.30 (m, 4H), 7.64-7.67 (m, 1H), 7.70 (s, 1H), 8.35-8.37 (m, 2H), 8.70-8.73 (m, 1H), 8.88 (brs, 2H).

Example 307N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[4-{5-[(dimethylamino)carbonyl]-1,3-thiazol-2-yl}-2-methylphenyl]-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (120 mg, 0.177 mmol) of Example 305, step A and 50% aqueous dimethylamine solution (0.195 ml), and according to the methods of Example 300, step B, and Example 1, step C, the title compound (106 mg, yield 92%) was obtained as a yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=7.3, 3H), 2.33 (s, 3H), 2.88-2.91 (m, 7H), 3.38-3.41 (m, 2H), 3.96 (s, 2H), 4.15-4.18 (m, 2H), 4.27-4.30 (m, 2H), 4.40 (s, 2H), 7.05 (d, J=8.5, 1H), 7.24-7.30 (m, 4H), 7.66-7.71 (m, 2H), 8.17 (s, 1H), 8.36 (t, J=5.8, 1H), 8.90 (brs, 2H).

Example 308N²-{4-[4-(aminocarbonyl)-1,3-thiazol-2-yl]-2-methylphenyl}-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochlorideStep AN²-[4-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-2-methylphenyl]-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-{2-[(tert-butoxycarbonyl)(ethyl)amino]ethyl}glycinamide

Using the compound (887 mg, 2.54 mmol) of Reference Example 121, the compound (520 mg, 2.57 mmol) of Reference Example 19 and the compound (526 mg, 2.79 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 295, step A, the title compound (1.24 g, yield 75%) was obtained as a brown oil.

Step BN²-{4-[4-(aminocarbonyl)-1,3-thiazol-2-yl]-2-methylphenyl}-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (611 mg, 0.935 mmol) of step A and ethyl 2-bromothiazole-4-carboxylate (265 mg, 1.12 mmol), and according to the methods of Example 295, step B, Example 300, step B, and Example 1, step C, the title compound (85 mg, yield 14%) was obtained as a yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=7.3, 3H), 2.34 (s, 3H), 2.89-2.90 (m, 7H), 3.37-3.41 (m, 2H), 3.96 (s, 2H), 4.12-4.30 (m, 4H), 4.38 (s, 2H), 7.05-7.11 (m, 2H), 7.15-7.17 (m, 1H), 7.29-7.33 (m, 1H), 7.65 (s, 1H), 7.69-7.72 (m, 1H), 7.78 (s, 1H), 7.83 (s, 1H), 8.18 (s, 1H), 8.35 (t, J=5.8, 1H), 8.85 (brs, 2H).

Example 309N²-{4-[4-(aminocarbonyl)-1,3-oxazol-2-yl]-2-methylphenyl}-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (547 mg, 0.836 mmol) of Example 295, step A, and methyl 2-chlorooxazole-4-carboxylate (176 mg, 1.00 mmol), and according to the methods of Example 295, step B, Example 300, step B, and Example 1, step C, the title compound (208 mg, yield 41%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=7.2, 3H), 2.33 (s, 3H), 2.88-2.91 (m, 7H), 3.37-3.41 (m, 2H), 3.96 (s, 2H), 4.15-4.17 (m, 2H), 4.27-4.30 (m, 2H), 4.40 (s, 2H), 7.09 (d, J=8.6, 1H), 7.24-7.30 (m, 4H), 7.54 (s, 1H), 7.64-7.70 (m, 2H), 7.75 (s, 1H), 8.36 (t, J=5.8, 1H), 8.59 (s, 1H), 8.87 (brs, 2H).

Example 310N²-{4-[4-(aminocarbonyl)-1,3-oxazol-2-yl]-2-methylphenyl}-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide dihydrochloride

Using the compound (559 mg, 0.855 mmol) of Example 308, step A and methyl-2-chlorooxazole-4-carboxylate (180 mg, 1.03 mmol), and according to the methods of Example 295, step B, Example 300, step B, and Example 1, step C, the title compound (223 mg, yield 42%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.16 (t, J=7.3, 3H), 2.33 (s, 3H), 2.89-2.91 (m, 7H), 3.36-3.41 (m, 2H), 3.96 (s, 2H), 4.12-4.30 (m, 6H), 7.06-7.11 (m, 2H), 7.15-7.17 (m, 1H), 7.29-7.33 (m, 1H), 7.54 (s, 1H), 7.64-7.74 (m, 2H), 7.75 (s, 1H), 8.34 (t, J=5.5, 1H), 8.59 (s, 1H), 8.83 (brs, 2H).

Example 311N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3,5-dimethyl-1,2-benzisoxazol-6-yl)-N¹-{2-[(2-fluoroethyl)amino]ethyl}glycinamide hydrochlorideStep AN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3,5-dimethyl-1,2-benzisoxazol-6-yl)-N¹-[2-{[(2-nitrophenyl)sulfonyl]amino}ethyl]glycinamide

Using the compound (278 mg, 1.00 mmol) of Reference Example 117, the compound (186 mg, 1.01 mmol) of Reference Example 17 and N-(2-aminoethyl)-2-nitrobenzenesulfonamide (270 mg, 1.10 mmol), and according to the method of Example 204, step A, a yellow solid (557 mg, yield 88%) was obtained.

Step BN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3,5-dimethyl-1,2-benzisoxazol-6-yl)-N¹-[2-{(2-fluoroethyl)[(2-nitrophenyl)sulfonyl]amino}ethyl]glycinamide

The compound (557 mg, 0.876 mmol) of step A, 2-fluoroethanol (84 mg, 1.31 mmol) and triphenylphosphine (345 mg, 1.31 mmol) were dissolved in tetrahydrofuran (4.4 ml), and the mixture was stirred at room temperature. Thereto was slowly added a 40% diisopropyl azodicarboxylate-toluene solution (0.70 ml), and the mixture was stirred at the same temperature for 12 hr. The reaction mixture was diluted with ethyl acetate, and the organic layer was washed with water and saturated brine, and dried over sodium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane) to give the title compound (561 mg, yield 94%) as a yellow solid.

Step CN²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3,5-dimethyl-1,2-benzisoxazol-6-yl)-N¹-{2-[(2-fluoroethyl)amino]ethyl}glycinamide hydrochloride

Using the compound (561 mg, 0.823 mmol) of step B, and according to the methods of Example 40, step E, and Example 57, step B, the title compound (304 mg, yield 69%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 2.35 (s, 3H), 2.45 (s, 3H), 2.90 (s, 3H), 3.24-3.39 (m, 2H), 3.40-3.42 (m, 2H), 3.96 (s, 4H), 4.12-4.15 (m, 2H), 4.26-4.29 (m, 2H), 4.38 (s, 2H), 4.64-4.78 (m, 2H), 7.22-7.28 (m, 5H), 7.52 (s, 1H), 8.30 (t, J=5.8, 1H), 9.08 (brs, 2H).

Example 312N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3,5-dimethyl-1,2-benzisoxazol-6-yl)-N¹-{2-[(2,2-difluoroethyl)amino]ethyl}glycinamide hydrochloride

Using the compound (533 mg, 0.838 mmol) of Example 311, step A and 2,2-difluoroethanol (103 mg, 1.26 mmol), and according to the methods of Example 311, step B, Example 40, step E, and Example 57, step B, the title compound (53 mg, yield 11%) was obtained as a pale-yellow solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 2.35 (s, 3H), 2.45 (s, 3H), 2.90 (s, 3H), 3.04 (brs, 2H), 3.96 (s, 2H), 4.12-4.15 (m, 2H), 4.26-4.29 (m, 2H), 4.38 (s, 2H), 6.28-6.57 (m, 1H), 7.21-7.29 (m, 5H), 7.52 (s, 1H), 8.32 (t, J=5.8, 1H), 9.46 (brs, 2H).

The compounds of Examples 289-312 are shown below.

TABLE 19StructuralLC-MSExampleFormulaTMW(found)289 [Image Omitted]

632.51560 290 [Image Omitted]

632.51560 291 [Image Omitted]

632.51560 292 [Image Omitted]

576.06540 293 [Image Omitted]

574.55502 294 [Image Omitted]

625.03516 295 [Image Omitted]

631.59559 296 [Image Omitted]

651.65579 297 [Image Omitted]

517.62518 298 [Image Omitted]

579.56507 299 [Image Omitted]

580.55508 300 [Image Omitted]

622.59550 301 [Image Omitted]

616.58544 302 [Image Omitted]

622.61550 303 [Image Omitted]

605.56533 304 [Image Omitted]

650.66578 305 [Image Omitted]

622.61550 306 [Image Omitted]

636.64564 307 [Image Omitted]

650.66578 308 [Image Omitted]

640.60568 309 [Image Omitted]

606.54534 310 [Image Omitted]

624.53552 311 [Image Omitted]

533.04497 312 [Image Omitted]

551.03515

Example 313N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]-N¹-(2-aminoethyl)glycinamide hydrochloride

Using the compound (963 mg, 3.15 mmol) of Reference Example 62, the compound (653 mg, 3.22 mmol) of Reference Example 19 and tert-butyl (2-aminoethyl)carbamate (635 mg, 3.96 mmol), and according to the methods of Example 204, step A, and Example 57, step B, the title compound (1.28 g, yield 76%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 2.33 (s, 3H), 2.65 (s, 3H), 2.78-2.83 (m, 2H), 2.88 (s, 3H), 3.29-3.37 (m, 2H), 3.91 (s, 2H), 4.07-4.28 (m, 4H), 4.33 (s, 2H), 7.05-7.17 (m, 2H), 7.26-7.32 (m, 2H), 7.51 (dd, J=1.4, 7.8, 1H), 7.75 (d, J=1.4, 1H), 7.89 (brs, 3H), 8.28 (t, J=5.8, 1H).

Example 314N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2-methyl-8,9,10,11-tetrahydro-7H-azepino[1,2-b]indazol-3-yl)-N¹-[2-(ethylamino)ethyl]glycinamide

Using the compound (277 mg, 0.836 mmol) of Reference Example 148, the compound (156 mg, 0.845 mmol) of Reference Example 17 and the compound (175 mg, 0.930 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 46, step B, the title compound (287 mg, yield 65%) was obtained as a colorless solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 0.99 (t, J=7.2, 3H), 1.50 (brs, 1H), 1.68-1.78 (m, 2H), 1.80-1.89 (m, 2H), 1.89-2.00 (m, 2H), 2.42 (s, 3H), 2.56 (q, J=7.2, 2H), 2.72 (t, J=5.9, 2H), 2.94 (s, 3H), 3.01-3.05 (m, 2H), 3.38-3.44 (m, 2H), 3.78 (s, 2H), 4.16 (d, J=11.3, 2H), 4.23 (d, J=11.3, 2H), 4.24 (s, 2H), 4.47-4.51 (m, 2H), 7.19-7.28 (m, 4H), 7.32 (s, 1H), 7.42 (s, 1H), 8.43 (t, J=5.6, 1H).

Example 315N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-(2-methyl-8,9,10,11-tetrahydro-7H-azepino[1,2-b]indazol-3-yl)-N¹-[2-(ethylamino)ethyl]glycinamide

Using the compound (256 mg, 0.773 mmol) of Reference Example 148, the compound (166 mg, 0.819 mmol) of Reference Example 19 and the compound (169 mg, 0.898 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 46, step B, the title compound (299 mg, yield 70%) was obtained as a colorless solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 0.99 (t, J=7.2, 3H), 1.39 (brs, 1H), 1.69-1.78 (m, 2H), 1.80-1.89 (m, 2H), 1.89-1.99 (m, 2H), 2.42 (s, 3H), 2.56 (q, J=7.2, 2H), 2.72 (t, J=5.9, 2H), 2.93 (s, 3H), 3.01-3.05 (m, 2H), 3.38-3.43 (m, 2H), 3.78 (s, 2H), 4.09-4.21 (m, 4H), 4.23 (s, 2H), 4.47-4.51 (m, 2H), 6.88-6.99 (m, 2H), 7.13-7.17 (m, 1H), 7.33 (s, 1H), 7.41 (s, 1H), 8.40 (t, J=5.7, 1H).

Example 316N²-{2-[2,3-dihydro-1H-inden-2-yl(methyl)amino]-2-oxoethyl}-N²-(2-methyl-8,9,10,11-tetrahydro-7H-azepino[1,2-b]indazol-3-yl)-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (298 mg, 0.899 mmol) of Reference Example 148, the compound (167 mg, 0.909 mmol) of Reference Example 23 and the compound (188 mg, 0.999 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 57, step B, the title compound (294 mg, yield 58%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.09-1.19 (m, 3H), 1.57-1.67 (m, 2H), 1.67-1.78 (m, 2H), 1.82-1.93 (m, 2H), 2.34 (s, 3H), 2.65 2.77 (2s, 3H), 2.6-3.2 (m, 10H), 3.34-3.42 (m, 2H), 3.76 3.81 (2s, 2H), 4.06 4.21 (2s, 2H), 4.41-4.50 (m, 2H), 4.96-5.06 5.26-5.36 (2m, 1H), 7.11-7.23 (m, 5H), 7.41 (s, 1H), 8.46 (t, J=5.6, 1H), 8.76 (brs, 2H).

Example 317N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(2-methyl-7,8,9,10-tetrahydropyrido[1,2-b]indazol-3-yl)-N¹-[2-(ethylamino)ethyl]glycinamide

Using the compound (300 mg, 0.945 mmol) of Reference Example 149, the compound (183 mg, 0.991 mmol) of Reference Example 17 and the compound (200 mg, 1.06 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 46, step B, the title compound (335 mg, yield 68%) was obtained as a colorless solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.00 (t, J=7.2, 3H), 1.2-1.7 (broad, 1H), 1.94-2.03 (m, 2H), 2.09-2.18 (m, 2H), 2.42 (s, 3H), 2.56 (q, J=7.2, 2H), 2.72 (t, J=5.9, 2H), 2.94 (s, 3H), 3.04 (t, J=6.2, 2H), 3.38-3.43 (m, 2H), 3.78 (s, 2H), 4.16 (d, J=11.3, 2H), 4.24 (d, J=11.3, 2H), 4.25 (s, 2H), 4.39 (t, J=5.9, 2H), 7.19-7.27 (m, 4H), 7.35 (s, 1H), 7.42 (s, 1H), 8.44 (t, J=5.6, 1H).

Example 318N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-(2-methyl-7,8,9,10-tetrahydropyrido[1,2-b]indazol-3-yl)-N¹-[2-(ethylamino)ethyl]glycinamide

Using the compound (285 mg, 0.898 mmol) of Reference Example 149, the compound (190 mg, 0.938 mmol) of Reference Example 19 and the compound (190 mg, 1.01 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 46, step B, the title compound (352 mg, yield 73%) was obtained as a colorless solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.00 (t, J=7.2, 3H), 1.2-1.7 (broad, 1H), 1.95-2.03 (m, 2H), 2.10-2.18 (m, 2H), 2.42 (s, 3H), 2.57 (q, J=7.2, 2H), 2.72 (t, J=6.1, 2H), 2.93 (s, 3H), 3.04 (t, J=6.4, 2H), 3.38-3.44 (m, 2H), 3.78 (s, 2H), 4.10-4.23 (m, 4H), 4.24 (s, 2H), 4.39 (t, J=6.2, 2H), 6.88-6.98 (m, 2H), 7.13-7.17 (m, 1H), 7.35 (s, 1H), 7.42 (s, 1H), 8.41 (t, J=5.7, 1H).

Example 319N²-{2-[2,3-dihydro-1H-inden-2-yl(methyl)amino]-2-oxoethyl}-N²-(2-methyl-7,8,9,10-tetrahydropyrido[1,2-b]indazol-3-yl)-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (324 mg, 1.02 mmol) of Reference Example 149, the compound (190 mg, 1.03 mmol) of Reference Example 23 and the compound (214 mg, 1.14 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 57, step B, the title compound (390 mg, yield 69%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.11-1.17 (m, 3H), 1.86-1.95 (m, 2H), 2.01-2.10 (m, 2H), 2.34 (s, 3H), 2.65 2.77 (2s, 3H), 2.84-3.11 (m, 10H), 3.34-3.42 (m, 2H), 3.79 3.83 (2s, 2H), 4.08 4.23 (2s, 2H), 4.30 (t, J=5.7, 2H), 4.97-5.07 5.26-5.36 (2m, 1H), 7.11-7.23 (m, 5H), 7.41 (s, 1H), 8.44 (t, J=5.4, 1H), 8.74 (brs, 2H).

Example 320N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(8-methyl-2,3-dihydro-1H-pyrrolo[1,2-b]indazol-7-yl)-N¹-[2-(ethylamino)ethyl]glycinamide

Using the compound (120 mg, 0.396 mmol) of Reference Example 150, the compound (76 mg, 0.412 mmol) of Reference Example 17 and the compound (87 mg, 0.462 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 46, step B, the title compound (132 mg, yield 66%) was obtained as a colorless solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.01 (t, J=7.2, 3H), 1.69 (brs, 1H), 2.42 (s, 3H), 2.57 (q, J=7.2, 2H), 2.68-2.78 (m, 4H), 2.94 (s, 3H), 3.13 (t, J=7.2, 2H), 3.38-3.44 (m, 2H), 3.79 (s, 2H), 4.17 (d, J=11.8, 2H), 4.24 (d, J=11.8, 2H), 4.26 (s, 2H), 4.39 (t, J=7.2, 2H), 7.18-7.27 (m, 4H), 7.37 (s, 1H), 7.46 (s, 1H), 8.46 (t, J=5.9, 1H).

Example 321N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-(8-methyl-2,3-dihydro-1H-pyrrolo[1,2-b]indazol-7-yl)-N¹-[2-(ethylamino)ethyl]glycinamide

Using the compound (113 mg, 0.373 mmol) of Reference Example 150, the compound (79 mg, 0.390 mmol) of Reference Example 19 and the compound (85 mg, 0.451 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 46, step B, the title compound (112 mg, yield 58%) was obtained as a colorless solid.

¹H-NMR (400 MHz, CDCl₃); Î´(ppm) 1.01 (t, J=7.2, 3H), 1.64 (brs, 1H), 2.42 (s, 3H), 2.57 (q, J=7.2, 2H), 2.67-2.78 (m, 4H), 2.94 (s, 3H), 3.13 (t, J=7.4, 2H), 3.38-3.44 (m, 2H), 3.78 (s, 2H), 4.10-4.24 (m, 4H), 4.25 (s, 2H), 4.39 (t, J=7.4, 2H), 6.88-6.99 (m, 2H), 7.13-7.17 (m, 1H), 7.37 (s, 1H), 7.45 (s, 1H), 8.44 (t, J=5.6, 1H).

Example 322N²-{5-[4-(aminocarbonyl)-1,3-thiazol-2-yl]-2-methylphenyl}-N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (309 mg, 0.884 mmol) of Reference Example 151, the compound (171 mg, 0.926 mmol) of Reference Example 17 and the compound (190 mg, 1.01 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 57, step B, the title compound (323 mg, yield 62%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.13 (t, J=7.2, 3H), 2.33 (s, 3H), 2.8-3.0 (m, 4H), 2.89 (s, 3H), 3.96 (s, 2H), 4.14 (d, J=11.6, 2H), 4.27 (d, J=11.6, 2H), 4.35 (s, 2H), 7.23-7.29 (m, 5H), 7.56 (d, J=7.7, 1H), 7.70 (brs, 1H), 7.71 (s, 1H), 7.84 (brs, 1H), 8.24 (s, 1H), 8.36 (t, J=5.6, 1H), 8.52 (brs, 2H).

Example 323N²-{5-[4-(aminocarbonyl)-1,3-thiazol-2-yl]-2-methylphenyl}-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (323 mg, 0.925 mmol) of Reference Example 151, the compound (193 mg, 0.952 mmol) of Reference Example 19 and the compound (195 mg, 1.04 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 57, step B, the title compound (377 mg, yield 67%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.14 (t, J=7.2, 3H), 2.32 (s, 3H), 2.8-3.0 (m, 4H), 2.89 (s, 3H), 3.35-3.42 (m, 2H), 3.95 (s, 2H), 4.09-4.30 (m, 4H), 4.34 (s, 2H), 7.04-7.17 (m, 2H), 7.26 (d, J=8.2, 1H), 7.28-7.32 (m, 1H), 7.55 (d, J=8.2, 1H), 7.70 (brs, 2H), 7.84 (brs, 1H), 8.24 (s, 1H), 8.37 (t, J=5.7, 1H), 8.65 (brs, 2H).

Example 324N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-{4-[(methylamino)carbonyl]-1,3-thiazol-2-yl}phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (364 mg, 1.00 mmol) of Reference Example 152, the compound (193 mg, 1.01 mmol) of Reference Example 17 and the compound (210 mg, 1.12 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 57, step B, the title compound (508 mg, yield 85%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.15 (t, J=7.2, 3H), 2.33 (s, 3H), 2.83 (d, J=4.6, 3H), 2.84-2.97 (m, 4H), 2.89 (s, 3H), 3.35-3.42 (m, 2H), 3.97 (s, 2H), 4.14 (d, J=11.3, 2H), 4.27 (d, J=11.3, 2H), 4.36 (s, 2H), 7.22-7.29 (m, 5H), 7.58 (d, J=7.7, 1H), 7.70 (s, 1H), 8.22 (s, 1H), 8.38-8.48 (m, 2H), 8.81 (brs, 2H).

Example 325N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N²-[2-methyl-5-{4-[(methylamino)carbonyl]-1,3-thiazol-2-yl}phenyl]-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (363 mg, 0.999 mmol) of Reference Example 152, the compound (209 mg, 1.03 mmol) of Reference Example 19 and the compound (211 mg, 1.12 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 57, step B, the title compound (480 mg, yield 78%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.14 (t, J=7.2, 3H), 2.33 (s, 3H), 2.83 (d, J=4.6, 3H), 2.84-2.98 (m, 4H), 2.89 (s, 3H), 3.35-3.42 (m, 2H), 3.96 (s, 2H), 4.08-4.30 (m, 4H), 4.34 (s, 2H), 7.05-7.18 (m, 2H), 7.27 (d, J=7.7, 1H), 7.28-7.31 (m, 1H), 7.58 (d, J=7.7, 1H), 7.70 (s, 1H), 8.22 (s, 1H), 8.38 (t, J=5.4, 1H), 8.43 (q, J=4.6, 1H), 8.64 (brs, 2H).

Example 326N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-[5-{4-[(dimethylamino)carbonyl]-1,3-thiazol-2-yl}-2-methylphenyl]-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (378 mg, 1.00 mmol) of Reference Example 153, the compound (194 mg, 1.01 mmol) of Reference Example 17 and the compound (214 mg, 1.14 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 57, step B, the title compound (447 mg, yield 73%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.14 (t, J=7.2, 3H), 2.32 (s, 3H), 2.8-3.0 (m, 4H), 2.90 (s, 3H), 3.02 (s, 3H), 3.15 (s, 3H), 3.35-3.41 (m, 2H), 3.94 (s, 2H), 4.14 (d, J=11.3, 2H), 4.27 (d, J=11.3, 2H), 4.37 (s, 2H), 7.22-7.29 (m, 5H), 7.46 (d, J=7.7, 1H), 7.66 (s, 1H), 8.05 (s, 1H), 8.37 (t, J=5.7, 1H), 8.66 (brs, 2H).

Example 327N²-[5-{4-[(dimethylamino)carbonyl]-1,3-thiazol-2-yl}-2-methylphenyl]-N²-{2-[(5-fluoro-1,3-dihydro-2H-isoindol-2-yl)(methyl)amino]-2-oxoethyl}-N¹-[2-(ethylamino)ethyl]glycinamide hydrochloride

Using the compound (378 mg, 1.00 mmol) of Reference Example 153, the compound (207 mg, 1.02 mmol) of Reference Example 19 and the compound (216 mg, 1.15 mmol) of Reference Example 2, and according to the methods of Example 204, step A, and Example 57, step B, the title compound (409 mg, yield 65%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.14 (t, J=7.2, 3H), 2.31 (s, 3H), 2.8-3.0 (m, 4H), 2.89 (s, 3H), 3.02 (s, 3H), 3.15 (s, 3H), 3.34-3.42 (m, 2H), 3.94 (s, 2H), 4.08-4.30 (m, 4H), 4.36 (s, 2H), 7.05-7.17 (m, 2H), 7.25 (d, J=7.7, 1H), 7.27-7.32 (m, 1H), 7.46 (d, J=7.7, 1H), 7.66 (s, 1H), 8.05 (s, 1H), 8.36 (t, J=5.6, 1H), 8.66 (brs, 2H).

Example 328N²-{2-[1,3-dihydro-2H-isoindol-2-yl(methyl)amino]-2-oxoethyl}-N²-(3,6-dimethyl-1,2-benzisoxazol-5-yl)-N¹-[(2S)-pyrrolidin-2-ylmethyl]glycinamide dihydrochloride

Using the compound (357 mg, 0.874 mmol) of Example 180, step A, and the compound (304 mg, 1.28 mmol) of Reference Example 12, and according to the methods of Example 1, steps B and C, the title compound (389 mg, yield 79%) was obtained as a colorless solid.

¹H-NMR (400 MHz, DMSO-d₆); Î´(ppm) 1.4-1.5 (m, 1H), 1.70-1.85 (m, 3H), 2.46 (s, 3H), 2.47 (s, 3H), 2.87 (s, 3H), 3.01-3.08 (m, 2H), 3.30-3.55 (m, 3H), 3.88 (s, 2H), 4.08 (d, J=11.4, 2H), 4.23 (d, J=11.4, 2H), 4.27 (s, 2H), 7.25 (brs, 4H), 7.49 (s, 1H), 7.66 (s, 1H), 8.46 (t, J=6.1, 1H), 8.56 (brs, 1H), 9.14 (brs, 1H).

The compounds of Examples 313-328 are shown below.

TABLE 20StructuralLC-MSExampleFormulaTMW(found)313 [Image Omitted]

532.01496 314 [Image Omitted]

531.69532 315 [Image Omitted]

549.68550 316 [Image Omitted]

567.17531 317 [Image Omitted]

517.67518 318 [Image Omitted]

535.66536 319 [Image Omitted]

553.14517 320 [Image Omitted]

503.64504 321 [Image Omitted]

521.63522 322 [Image Omitted]

586.15550 323 [Image Omitted]

604.14568 324 [Image Omitted]

600.18564 325 [Image Omitted]

618.17582 326 [Image Omitted]

614.20578 327 [Image Omitted]

632.19596 328 [Image Omitted]

563.52491

The pharmacological test results of the compounds of the Examples are shown below.

Experimental Example 1Measurement of Enzyme Inhibitory Activity

The enzyme inhibitory activity of the compounds of the Examples was measured using the hydrolysis activity of S-Adenosyl-L-Homocysteine as an index. The measurement method was modification of the method of Henry H. Richards et al. (J. Biol. Chem. 253, 4476-4480, 1978). That is, S-Adenosyl-L-Homocysteine (10 Î¼M) and Adenosine Deaminase (Roche) (4 units) were added to 50 mM phosphate buffer (pH 7.2, containing 1 mM EDTA) with the total amount being 200 Î¼l, and to the solution were added a test substance and then Human-recombinant-S-Adenosyl-L-Homocysteine Hydrolase (50 ng, Diazyme Laboratories) to start the reaction, and the mixture was incubated at 37Â° C. for 15 min. The reaction was quenched by the addition of 1N aqueous perchloric solution (20 Î¼l), and the mixture was centrifuged under the conditions of 10000 rpm, 5 min, 4Â° C. The supernatant was collected, and the amount of S-Adenosyl-L-Homocysteine after the reaction was quantified by HPLC. The column used was a reversed-phase column. The detailed conditions of HPLC were as follows.

column used: Wakopak^RHandyODS 150*4.6 mm (Wako Pure Chemical Industries, Ltd.)
elution condition: 1.0 ml/min
elution solvent: 0.1M acetate buffer (pH 4.0) containing 10 mM 1-heptanesulfonic acid containing 4% acetonitrile wavelength: 258 nm (UV)
The inhibitory rate was determined with the amount of decrease in S-Adenosyl-L-Homocysteine before and after the reaction without using the test substance as 100%.

Inhibitory rate (%)={(amount of decrease of S-Adenosyl-L-Homocysteine in the presence of test substance)/(amount of decrease of S-Adenosyl-L-Homocysteine in the absence of test substance)}Ã—100

The results are shown in the following Table.

TABLE 21ExampleIC50 (nM)16829215171619193320392189244626565652574264103654784348517871888438953924812910176631774618015181161843718581908819151192461932920465205482103421151214232154721633229352314624192426243724715253202564725930279662843328758289762985030137303413082630923328150

Experimental Example 2Measurement of Homocysteine Synthesis Inhibitory Activity In Vivo

A sample was orally administered to BALB/c mouse and, 1 hr later, methionine water (50 g/L) was orally administered at a proportion of 10 ml/kg. 30 min later, blood samples were collected with heparin from the abdominal vein and plasma was obtained. The plasma homocysteine concentration was measured by treating the plasma with tributylphosphine, removing protein with 10% trichloroacetic acid (TCA), fluorescent labeling the supernatant with 4-fluoro-7-sulfobenzofurazan ammonium salt (SBD-F) under alkali conditions, and quantifying by HPLC. The homocysteine synthesis inhibitory rate of the sample was determined with the difference in the homocysteine value between methionine water-loaded animal and methionine water-unloaded animal as 100%. The detailed conditions of HPLC were as follows.

column used: Wakopak^RHandyODS 150*4.6 mm (Wako Pure Chemical Industries, Ltd.)
elution condition: 1.0 ml/min
elution solvent: 0.1M phosphate buffer (pH 6.0) 2% methanol
wavelength: ex 385 nm em 515 nm

The results at a dose of 10 mg/kg are shown in the following Table.

TABLE 22Exampleactivity1A2A20A21A24B57A(2HCl salt)64A65A88B89B92A105B136A176A184A185A215A229A241A244A245B253A254B268C292B304AActivity:A: homocysteine synthesis inhibitory rate â‰§ 40%B: 40% > homocysteine synthesis inhibitory rate â‰§ 20%C: 20% > homocysteine synthesis inhibitory rate

Experimental Example 3Infarct Volume Suppressive and Motor Function Improving Effects in Mouse Ischemic Stroke Model

Mouse was fixed under isoflurane anesthesia and the scalp was incised. Rose Bengal (7.5 mg/kg) was administered i.v., and green light (550 nm, Hamamatsu Photonics, K.K.) was immediately irradiated at 2 mm side and 1 mm above the bregma for 5 min. Thereafter, the scalp was bonded with an instant glue. To the test drug and control groups was given the first administration after the mice awoke, and they were subjected to the administration again the next day. Two days later, motor function was evaluated by Rota-rod (up to 60 sec, walking time on Rota-Rod was measured). Then the brain was removed, sliced in 1 mm, the site of infaction was decided by 1% TTC staining and the volume was measured by image analysis. The infarct volume suppression rate (%) and walking time (%) on Rota-Rod with Vehicle 100% at the dose of 10 mg/kg are shown in the following Table. In addition, walking time (sec) on Rota-Rod and infarct volume suppression rate (mm³) when 3-deazaadenosine was used as a test drug are shown in FIG. 1 and FIG. 2.

TABLE 23infarct volumewalking timesuppression rate (%)(%)Example 2026240Example 6530250Example 18322240Example 21519340Example 24426330Example 253162303-deazaadenosine14170

INDUSTRIAL APPLICABILITY

The compound of the present invention and a compound having an S-adenosyl-L-homocysteine hydrolase inhibitory action can be medicaments effective for the treatment of ischemic stroke.

This application is based on Japanese patent application No. 2009-235752 filed in Japan, the contents of which are incorporated in full herein.