This invention relates to a new process to prepare optically active substituted alpha-amino-indan derivatives useful as synthetic intermediates for the preparation of active pharmaceuticals.

According to the prior art document WO98/27055, optically active substituted alpha-amino-indan derivatives are prepared from an optically active non-substituted alpha-amino-indane with a four steps process in order to obtain optically active alpha-amino-indan substituted compounds. This process involves a Friedel & Craft reaction and a Bayer-Villiger reaction. However, these two reactions show some limitations such as low yields and safety issues.

According to this document optically active substituted alpha-amino-indan derivatives are also prepared from a racemic substituted alpha-amino-indan compounds with an optical resolution process. The limitations of this process are the low yields.

This invention describes a new process for yielding to optically active substituted alpha-amino-indane compounds of general formula (I) hereunder: [Image Omitted]

wherein:

m is an integer equal to 0, 1, 2 or 3, preferably m is 0,

R₁is a hydrogen atom, an alkyl group having from 1 to 20 carbon atoms, an aryl group having from 6 to 20 carbon atoms, an alkylaryl group having from 6 to 20 carbon atoms, an alkaloyl group, an aryloyl group, preferably R1 is an alkyl group having from 1 to 20 carbon atoms, and more preferably R1 is an alkyl group having from 1 to 4 carbon atoms, especially a methyl group,

which comprise

- an asymmetric hydrogenation reaction of an en-amide derivative of formula (III)

wherein m and R1 are as defined above,

R2 is a hydrogen atom, an alkyl group having from 1 to 20 carbon atoms, an aryl group having from 6 to 20 carbon atoms, an alkylaryl group having from 6 to 20 carbon atoms, preferably R2 is an alkyl group having from 1 to 20 carbon atoms, and more preferably an alkyl group having from 1 to 4 carbon atoms, especially a methyl in presence of hydrogen and an optically active catalyst, preferably an optically active asymmetric hydrogenation catalyst,

in order to obtain an amide derivative of formula (II) [Image Omitted]

- a hydrolysis reaction of the amide derivative of formula (II) obtained in the previous step,

in order to obtain optically active substituted alpha-indanyl amide derivatives of formula (I).

The derivatives of formula (I) can be in a (R) configuration or in a (S) configuration. In the same way, the derivatives of formula (II) can be in a (R) configuration or in a (S) configuration.

In the present application the term alkyl means a straight or branched alkyl group having from 1 to 20 carbon atoms (such as but not limited to methyl, ethyl, n-propyl, isopropyl, n-butyl, iso-butyl, sec-butyl, tert-butyl), optionally substituted with a lower alkyl group or a functional group.

The term aryl means an aryl group having from 6 to 20 carbon atoms (such as but not limited to phenyl, tolyl, xylyl, cumenyl, naphthyl), optionally substituted with a lower alkyl group or a functional group, or a fused aryl or a heteroaryl group having from 6 to 20 carbon atoms (such as but not limited to furyl, thienyl, pyrrolyl, imidazolyl, pyridyl, pyrazyl, pyrimidinyl, indolyl, carbazolyl, isoxazolyl, isothiazolyl).

The term alkylaryl means an alkylaryl group having from 6 to 20 carbon atoms (such as but not limited to benzyl, phenethyl, naphthylmethyl) optionally substituted with a lower alkyl group or a functional group.

The term alkaloyl means preferably â€”COR1 wherein R1 is an alkyl group as defined above (such as but not limited to acetyl, propionyl or pivaloyl).

The term aryloyl means preferably â€”COR1 wherein R1 is an aryl group as defined above (such as but not limited to benzoyl or phenylacetyl).

The term lower alkyl means a straight or branched alkyl group having from 1 to 8 carbons atoms (such as but not limited to methyl, ethyl, n-propyl, isopropyl, n-butyl, iso-butyl, sec-butyl or tert-butyl).

The term functional group means an halogen, â€”OH, â€”OR3, â€”CN, â€”COOR3, â€”COR3, â€”CONR3R4, â€”OCOR3, â€”NH2, â€”NHR3, â€”NR3R4, â€”NHCOR3 and â€”N(COR3)2, â€”NO2, â€”SH, â€”SR3, wherein R3 and R4 are independently a lower alkyl, an alkylaryl or an aryl group as defined previously. The term halogen means an atom like chlore, brome, fluor or iode.

The optically active catalyst used in the asymmetric hydrogenation of the en-amide derivative of formula (III) is represented by a chiral phosphine transition metal complexe of formula (VIIA) or formula (VIIB):
M(X)_j(Z)_i(L*)(Y)_nâ€ƒâ€ƒ(VIIA)
or
[M(X)(L*)]₂(X)₃Sâ€ƒâ€ƒ(VIIB)

wherein

M is a transition metal selected in the group comprising ruthenium (Ru), rhodium (Rh) and iridium (Ir) preferably M is ruthenium or rhodium.

X is a halogen atom selected in the group comprising chlorine (Cl), bromine (Br), fluorine (F) and iodine (I), preferably X is chlorine or bromine.

Z is an aryl group having from 6 to 20 carbon atoms or an unsaturated organic group, cyclic or not, selected in the group comprising olefine, diene and cyano, preferably diene and most preferably cyclooctadiene (COD).

L* is a chiral ligand selected in the group comprising the chiral diphosphine derivatives, the chiral atropoisomeric diphosphine derivatives, the chiral monodentate phosphoramidine derivatives, the chiral biphospholane derivatives, the chiral ferrotane derivatives and the chiral ferrocenyl phosphine derivatives,

Y is an anion such as ClO₄^âˆ’, BF₄^âˆ’, PF₆^âˆ’, SbF₆^âˆ’, preferably BF4^âˆ’.

S is a dialkyl ammnonium, preferably a dimethy ammonium.

j is an integer equal to 0 or 1.

i is an integer equal to 0, 1, 2 or 4.

n is an integer equal to 1 or 2.

The transition metal preferably means ruthenium or rhodium.

The aryl group is a benzene optionally substituted with an alkyl.

The olefin is selected in the group comprising pi-allyl and 1,3,5,7-cyclooctatetraene and the diene is selected in the group comprising 1,3-butadiene, 2,5-norbornadiene, 1,5-cyclooctadiene (COD) and cyclopentadiene.

The chiral diphosphine is selected in the group comprising BICP, DuPHOS, MiniPHOS, BDPMI, TangPHOS, P-PHOS, Tol-P-PHOS, Xyl-P-PHOS and BPE.

The chiral atropoisomeric diphosphine is selected in the group comprising BINAP, TolBINAP, MeOBIPHEP, BINAPO, SYNPHOS and BINAPO optionally ortho-substituted with an alkyl or an aryl.

The chiral monodentate phosphoramidine is selected in the group comprising Monophos and Ethylmonophos.

The chiral bisphospholane is selected in the group comprising Tangphos, Duphos, Me-Duphos, Me-BPE, Et-BPE, Binaphane and Malphos.

The chiral ferrocenyl phosphine is JOSIPHOS.

The chiral ligand is preferably a chiral atropoisomeric diphosphine or a chiral bisphospholane, most preferably BINAP, MeOBIPHEP, Tangphos, Me-BPE, Et-BPE or Binaphane.

The wellknown abbreviations listed above have the following meaning:

Concerning the chiral diphosphine derivatives:

BICP: (R,R)-2,2â€²1-bis-diphenylphosphanyl-bicyclopentyl and other isomers.
MiniPHOS: 1,3-diphenyl-[1,3]diphospholane and other isomers.
BDPMI: 2-Imidazolidinone, 4,5-bis[(diphenylphosphino)methyl]-1,3-dimethyl-, (4S,5S)â€” and other isomers.
TangPHOS: 2,2â€²-Biphospholane, 1,1â€²-bis(1,1-dimethylethyl)-, (1S,1â€²S,2R,2â€²R) and other isomers.
P-PHOS: 3,3â€²-Bipyridine, 4,4â€²-bis(diphenylphosphino)-2,2â€², 6,6â€²-tetramethoxy-, (3S); or 3,3â€²-Bipyridine, 4,4â€²-bis(diphenylphosphino)-2,2â€²,6,6â€²-tetramethoxy-, (3R);
Tol-P-PHOS: 3,3â€²-Bipyridine, 4,4â€²-bis(di-(4-methylphenyl)-phosphino)-2,2â€²,6,6â€²-tetramethoxy-, (3S); or 3,3â€²-Bipyridine, 4,4â€²-bis(di-(4-methylphenyl)-phosphino)-2,2â€²,6,6â€²-tetramethoxy-, (3R);
Xyl-P-Phos: 3,3â€²-Bipyridine, 4,4â€²-bis(di-(3,5-dimethylphenyl)-phosphino)-2,2â€²,6,6â€²-tetramethoxy-, (3S); or 3,3â€²-Bipyridine, 4,4â€²-bis(di-(3,5-dimethylphenyl)-phosphino)-2,2â€²,6,6â€²-tetramethoxy-, (3R).
BPE: 1,2-bis(substituted-phospholano)ethane and other isomers.
Me-BPE 1,2-(2,5-dimethylphospholano)ethane and other isomers

Concerning the atropoisomeric chiral diphosphines derivative:

BINAP: (R)-2,2â€²-Bis(diphenylphosphino)-1,1â€²-binaphthyl or (S)-2,2â€²-Bis(diphenylphosphino)-1,1â€²-binaphthyl
TolBINAP: (R)-2,2â€²-Bis(di-p-tolylphosphino)-1,1â€²-binaphthyl or (S)-2,2â€²-Bis(di-p-tolylphosphino)-1,1â€²-binaphthyl;
MeOBIPHEP: (R)-2,2â€²-bis-diphenylphosphanyl-6,6â€²-dimethoxy-biphenyl or (S)-2,2â€²-bis-diphenylphosphanyl-6,6â€²-dimethoxy-biphenyl;
BINAPO: (R)-[1,1â€²-Binaphthalene]-2,2â€²-diyl bis(diphenylphosphinite) or (S)-[1,1â€²-Binaphthalene]-2,2â€²-diyl bis(diphenylphosphinite);
SYNPHOS: â€”(R)-[2,3,2â€²,3â€²-tetrahydro-5,5â€²-bi(1,4-benzodioxin)-6,6â€²-diyl]bis(diphenylphosphane) or â€”(S)-[2,3,2â€²,3â€²-tetrahydro-5,5â€²-bi(1,4-benzodioxin)-6,6â€²-diyl]bis(diphenylphosphane)

Concerning the chiral monodentate phosphoramidine derivative:

Monophos: Dinaphtho [2,1-d:1â€²,2â€²-f] [1,3,2]dioxaphosphepin-4-amine, N,N-dimethyl-, (2aR);or Dinaphtho [2,1-d:1â€²,2â€²-f] [1,3,2]dioxaphosphepin-4-amine, N,N-dimethyl-,(11bS);

Concerning the chiral bisphospholane derivative:

Me-Duphos: 1,2-bis-((2R,5R)-2,5-dimethylphospholano)benzene or 1,2-bis-((2S,5S)-2,5-dimethylphospholano)benzene;
DupHOS: bis(substituted-phospholano)benzene;

Concerning the chiral ferrocenyl phosphine derivative:

JOSIPHOS: (R)-1-[(S)-2-diphenylphosphino)-ferrocenyl]ethyldicyclohexylphosphine or (S)-1-[(R)-2-diphenylphosphino)-ferrocenyl]ethyldicyclohexylphosphine.

According to a preferred embodiment of the invention, the optically active catalyst of formula (VII) is Ru(COD) (MeOBIPHEP)BF₄^âˆ’, Ru(COD) (BINAP)BF₄^âˆ’ or Rh(COD) (Me-BPE)BF4^âˆ’. The catalyst can be in situ prepared or can a preformed complex.

The solvant used during the assymetric hydrogenation is selected in the group comprising ether such as tetrahydrofuran (THF), tetrahydropyran and diethyl ether, aromatic hydrocarbon such as benzene and toluene, halogenated hydrocarbon such as dichloromethane, alcohol such as-methanol, ethanol or isopropanol. According to a preferred embodiment of the invention the solvant used is an alcohol, more preferably methanol.

The molar ratio of the en-amide derivative of formula (III) to the optically active catalyst (VII) used during the asymmetric hydrogenation is from 100/1 to 10000/1, preferably from 100/1 to 1000/1, more preferably from 200/1 to 1000/1, especially from 500/1 to 1000/1.

The hydrogen pressure used during the asymmetric hydrogenation is from 0,5 to 20 bar, preferably from 0,5 to 10 bar, more preferably 1 to 8 bar, especially from 4 to 8 bar.

The temperature range used during the asymmetric hydrogenation is from âˆ’20 to 100Â° C., preferably from 20 to 100Â° C., more preferably from 20Â° C. to 60Â° C. and especially from 40Â° C. to 60Â° C., for a period of time in the range of 10 min to three days, preferably of one hour to three days, more preferably 1 hours to 1 day and especially 4 hours to 1 day.

The step of the hydrolysis reaction of the amide derivative of formula (II) obtained at the end of the assymetric hydrogenation is performed in presence of an organic acid or a mineral acid such as hydrochloric acid, sulfuric acid or hydrobromic acid, preferably sulfuric acid, according to methods described in the literature to obtain alpha-aminoindan derivatives of formula (I) in an appropriate solvent, preferably an alcohol and more preferably methanol.

According to a preferred embodiment of the invention, the en-amide derivative of formula (III) is prepared by the two following step:

- an acylation reaction of an alpha-hydroxyimino-indane derivative of formula (V):

wherein R₁and m are as defined above

in presence of an organic anhydride of formula (VI):
R₂OCâ€”Oâ€”CORâ€²₂â€ƒâ€ƒ(VI)

wherein R₂and Râ€²₂identical or different are a hydrogen atom, an alkyl group having from 1 to 20 carbon atoms, an aryl group having from 6 to 20 carbon atoms, an alkylaryl group having from 6 to 20 carbon atoms, preferably R2 and Râ€²2 are an alkyl group having from 1 to 20 carbon atoms, and more preferably a methyl. in order to obtain an Nâ€”(O-acylimino)-indane derivative of formula (IV): [Image Omitted]

wherein R₁, m and R₂are as defined above,

- a hydrogenolyse-acylation reaction of the Nâ€”(O-acylimino)-indane derivative of formula (IV) obtained in the previous step,

in presence of an organic anhydride of formula (VI) as defined above and of an heterogeneous catalyst based on a metal transition selected in the group comprising Pt, Pd, Ir, Rh and Ni,

in order to obtain an en-amide derivative of formula (III).

The molar ratio of the organic anhydride of formula (VI) to the alpha-hydroxyimino-indane derivative of formula (V) used during the acylation reaction is from 1:1 to 5:1, and is more preferably 1.5:1 to 2:1.

The acylation reaction is performed under a temperature range from 0 to 80Â° C., preferably 20Â° C. to 40Â° C., for a period of time in the range of 1 to 8 hours, preferably 2 to 4 hours.

The heterogeneous catalyst used during the hydrogenolyse-acylation reaction of the derivative of formula (IV) is selected in the group comprising PtO₂, Pt/C, Pd/C, Pd(OH)₂/C, Ir/C, Rh/C and Raney Ni.

Preferably the heterogeneous catalyst is Ir/C.

The effective amount of the heterogeneous catalyst used during the hydrogenolyse-acylation is in an amount from 0.1% to 30% for 1 mole of the Nâ€”(O-acylimino)-indane derivative of formula (IV).

The reaction of hydrogenolyse-acylation is performed with a hydrogen pressure range from 0.5 to 20 bars under a temperature range from âˆ’20 to 150Â° C., preferably 20 to 120Â° C., for a period of time in the range from 10 min to three days, preferably from 1 to 24 hours.

The molar ratio of the organic anhydride of formula (VI) to the Nâ€”(O-acylimino)-indane derivative of formula (IV) used during the hydrogenolyse-acylation reaction is from 1:1 to 5:1 and preferably 1.5:1 to 2:1.

The acylation reaction of the derivative of formula (V) and the hydrogenolyse-acylation reaction of the derivative of formula (IV) are respectively performed in an aprotic non-basic solvent selected in the group comprising ether like tetrahydrofuran (THF) and diethyl ether, organic acid alkyl ester like ethyl acetate, aromatic hydrocarbon like toluene, and halogenated hydrocarbon like methylene chloride. Preferably the aprotic non-basic solvent is an ether, more preferably THF.

The organic anhydride of formula (VI) used during the acylation reaction and the hydrogenolyse-acylation reaction is selected in the group comprising dialkyl anhydride, diaryl anhydride and alkylarylanhydride, and is preferably an acetic anhydride. The preferred organic anhydride is acetic anhydride.

The derivatives of formula (V) (alpha-hydroxyimino-indane) or (IV) (Nâ€”(O-acylimino)-indane)) may be used as a syn-form, anti-form or a mixed form of both.

In a preferred embodiment, the two step previously described (the acylation reaction of the derivatives of formula (V) and the hydrogenolyse-acylation reaction of derivatives of formula (IV)) are carried out in one step (also called â€œone potâ€ process).

Thus, the derivative of formula (III) is obtained directly from the derivative of formula (V) without isolating specifically the derivative of formula (IV).

The present invention has also for object the en-amide derivative of formula (III): [Image Omitted]

wherein

m is an integer equal to 0, 1, 2 or 3,

R₁is a hydrogen atom, an alkyl group having from 1 to 20 carbon atoms, an aryl group having from 6 to 20 carbon atoms, an alkylaryl group having from 6 to 20 carbon atoms, an alkaloyl group, an aryloyl group, preferably R1 is an alkyl group having from 1 to 20 carbon atoms, more preferably R1 is an alkyl group having from 1 to 4 carbon atoms,

R₂is an hydrogen, an alkyl group having from 1 to 20 carbon atoms, an aryl group having from 6 to 20 carbon atoms, an alkylaryl group having from 6 to 20 carbon atoms, preferably R₂is an alkyl group having from 1 to 20 carbon atoms.

The present invention has also for object the optically active substituted alpha-indanyl amide derivatives of formula (I): [Image Omitted]

wherein

m is an integer equal to 0, 1, 2 or 3,

m is an integer equal to 0, 1, 2 or 3,

R₁is a hydrogen atom, an alkyl group having from 1 to 20 carbon atoms, an aryl group having from 6 to 20 carbon atoms, an alkylaryl group having from 6 to 20 carbon atoms, an alkaloyl group, an aryloyl group, preferably R1 is an alkyl group having from 1 to 20 carbon atoms, and more preferably R1 is an alkyl group having from 1 to 4 carbon atoms,

as synthetic intermediates for the preparation of active pharmaceuticals.

The FIG. 1 is an illustration of the different steps of the new process of the invention for the synthesis of substituted alpha-aminoindan derivatives. The first step of the process relates to acetylation of the corresponding oxime function of the derivatives of formula (V) in the presence of an organic anhydride of formula (VI) in an appropriate solvent to obtain the derivatives of formula (IV).

The second step of the process relates to a hydrogenolyse-acylation of the intermediates of formula (IV) in presence of a heterogeneous catalyst based on a metal transition and an organic anhydride of formula (VI) in an appropriate solvent to obtain the derivatives of formula (III).

The third step of the process relates to an asymmetric hydrogenation reaction of the derivatives of formula (III) in presence of hydrogen and optically active catalyst of formula (VII) and an appropriate solvent to obtain optically active alpha-indanyl amide derivatives of formula (II).

The fourth step is a hydrolysis reaction of derivatives of formula (II) to obtain alpha-amino-indan derivatives of formula (I).

The invention will be better understood from the experimental details described in the following examples, which will not limit the scope of the invention in any way.

EXAMPLE 1 Acetylation Reaction: Preparation of Indan-1-on-(O-acetyloxime), Methoxy-6 of Formula (IV) (in which R1=R2=CH₃, m=0).

6-methoxy-indan-1-one-oxime of formula (V) (in which R₁=CH₃, m=0) (30 g, 0.169 mol) is partially dissolved in 180 ml of THF at room temperature. To this solution, acetic anhydride of formula (VI) in which R₂=Râ€²₂=CH₃(47.9 ml, 0.508 mol) is added in 15 minutes at 20Â° C. The reaction mixture is stirred between 20-30Â° C. during 2 hours and is then concentrated. A colorless liquid is obtained which can solidify. The residue is dissolved in methylene chloride (60 ml). The organic layer is washed with water (60 ml) twice. The organic layer is respectively separated from the aqueous layer, is dried over MgSO4, is filtered off and is concentrated to obtain 56 g of a white solid product (the indan-1-on-(O-acetyloxime), methoxy-6 of formula (IV)). This product is partially dissolved in MTBE (tert-butyl-methyl ether) (60 ml), is warmed at 55Â° C. MTBE (195 ml) is added again slowly to dissolve completely the product. The solution is warmed at reflux temperature during 5 mn. The solution is cooled at room temperature (20Â° C.) and the solid is filtered off. The solid is dried under vacuum.

28.8 g of white solid (the indan-1-on-(O-acetyloxime), methoxy-6 of formula (IV)) is obtained. The yield is 77%.

EXAMPLE 2 The Preparation of the Acetamide, N-(2,3-dihydro-6-methoxy-1H-inden-1-yl) of Formula (III) in which R1=R2=CH3, m=0.

This example illustrates a â€œone potâ€ process from oxime derivative of formula (V) (in which R₁=CH₃, m=0).

25 g (0.141 mol) of 6-methoxy-indan-1-one-oxime of formula (V) (in which R₁=CH₃, m=0) was dissolved in 190 ml of THF.

The mixture is stirred at room temperature until complete dissolution of the product. Then 40 ml of acetic anhydride of formula (VI) in which R₂=Râ€²₂=CH₃are added drop wise. The reaction mixture is stirred at a temperature between 20-30Â° C. during 2 hours. 2.5 g of the Ir-carbon (5%) catalyst is added to this reaction mixture. The hydrogenation is carried out at a hydrogen pressure of 7.4 bars at 70-80Â° C. during 2 hours 15 minutes. After the catalyst Ir/C is filtered off, the filtrate was concentrated to dryness under reduced pressure. The residue is dissolved in 400 ml of toluene and concentrated to dryness under reduced pressure. The residue is dissolved in 75 ml of toluene, the mixture is stirred at a temperature 20Â° C. during 15 mn. The mixture is filtered. The solid is dried under reduced pressure at a temperature of 40-45Â° C.

The compound Acetamide, N-(2,3-dihydro-6-methoxy-1H-inden-1-yl)- is obtained with 84% yield. The chemical purity is 98.4%.

EXAMPLE 3 Preparation of N-(6-methoxy-indan-1-yl)-acetamide (R) of Formula (II) (in which R₁=R2=CH₃and m=0.)

The molar ratio of the en-amide derivative of formula (III) to the catalyst (VII) during the asymmetric hydrogenation is 500/1.

3 g (0.0148 mol) of N-(6-methoxy-3H-inden-1-yl)-acetamide of formula (III) (in which R₁=CH₃and m=0) was dissolved in 30 ml of methanol and 24 mg (2.95 10^âˆ’5mol) of (R)â€”Ru(OAc)₂(MeOBIPHEP) of formule (VII) are added. The reaction mixture is flushed with nitrogen (5 times) and is warmed to 40Â° C. The hydrogenation is carried out with a hydrogen pressure of 8 bars at a temperature of 40Â° C. during 27 hours. The reaction mixture is concentrated until complete removal of the methanol.

50 ml of toluene are added to the residue and concentrated to dryness. The operation is repeated with 10 ml and 5 ml of toluene. The solid is dried under vacuum.

The yield is 89% and the enantiomeric excess (e.e.) is 84.5%. Then the product is recrystallized in 15 ml of toluene. The yield is 80% and the enantiomeric excess (e.e.) is >98%.

EXAMPLE 4 Preparation of N-(6-methoxy-indan-1-yl)-acetamide (R) of Formula (II) (in which R₁=CH₃and m=0.)

The reaction is carried out in the same manner as in example 3, except that the molar ratio of the en-amide derivative of formula (III) to the catalyst (VII) during the asymmetric hydrogenation is 100/1 and the hydrogenation is carried out at 30Â° C. The yield is 95% and the enantiomeric excess (e.e.) is 86.6%. Then the product is recrystallized in toluene. The yield is 77% and the enantiomeric excess is 98, 2%.

EXAMPLE 5 Preparation of 6-methoxy-indan-1-ylamine (R) of Formula (I) (in which R₁=CH₃and m=0.)

1.5 g of N-(6-methoxy-indan-1-yl)-acetamide (R) of formula (II) (in which R₁=CH₃and m=0) is dissolved in methanol (13 ml). To this methanolic solution of the product a solution of hydrochloric acid 36% is added (2.2 ml). The mixture is warmed at 90Â° C. during 8 hours.

After the mixture is cooled down to 25Â° C., a solution of hydrochloric acid (1.1 ml) is added again and the mixture is warmed at 90Â° C. during 7 hours. After the mixture is cooled down to 25Â° C., the same operation is repeated with the solution of hydrochloric acid (0.5 ml) and the mixture is warmed at 90Â° C. during 6 hours. The mixture is concentrated to remove the methanol. Water is added (6.5 ml) to the residue and the mixture is concentrated until the complete removal of methanol. The mixture is warmed at 60Â° C. and water (7 ml) is added to complete dissolution of the product. Toluene (8 ml) is added to the solution. After removal of the organic layers, the aqueous layer is basified with soda 30% until a pH range 12 to 13 in presence of xylenes (5 ml) at a temperature 22Â° C. The aqueous layer is separated and re-extracted with xylenes (8 ml) 3 times. All organic layers are mixed and concentrated to dryness. The product is obtained with 65% yield.

Asymmetric hydrogenation reactions were performed using different ligand and conditions according to the protocol of Example 3. The results are summarized in the following table for each example.

chiralPressureTemp.Ex.ligandS/CH₂barÂ° C.Time% e.e.6(1S, 1Sâ€²,11062545mn93.8% (R)2R,Râ€²) Tangphos [Image Omitted]

7(1S, 1Sâ€²,1000122518h89.8% (R)2R,Râ€²) Tangphos [Image Omitted]

8(S) Binaphane11062545mn95.8% (R) [Image Omitted]

9(R,R)11062510-12h72.3% (R) [Image Omitted]

10(S,S)1106251-1 h 3084.2% (S) preformed catalyst [Image Omitted]

11(R, R) MeBPE11062515mn97.9% (R) preformed catalyst [Image Omitted]

12(R, R) MeBPE11062530mn98.2% (R) [Image Omitted]

13(R, R) MeBPE1000065024h95.2% (R) preformed catalyt [Image Omitted]

14(R, R) EtBPE11062545mn97% (R) [Image Omitted]