Resolution process for (R)-(-)-2-hydroxy-2-(2-chlorophenyl) acetic acid
AssigneeSanofi-Aventis
InventorsJózsef Bálint, Marianna Csatáriné Nagy, Zsolt Dombrády, Elemér Fogassy, Antal Gajáry, Charles Suba
Life of this patent
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Abstract
The subject of the present invention is the preparation of the (R)-(−)-2-hydroxy-2-(2-chlorophenyl)acetic acid of the formula (I) by the resolution of the corresponding racemic compound by using the compounds of the general formula (II).
Claims15
Process for the preparation of (R)-(−)-2-hydroxy-2-(2-chlorophenyl)acetic acid of formula I:
- wherein racemic 2-hydroxy-2-(2-chlorophenyl)acetic acid is resolved with a substituted amine of formula (II):
- where R1 means hydroxy-methyl group or carboxyl group, R2 means phenyl group, nitro-phenyl group or a C1-C4 alkyl group substituted with an amino group, R3 means hydroxyl group or hydrogen atom.
(1S, 2S)-(+)-1-phenyl-2-amino-1,3-propanediol(S)-(+)-2-hydroxy-2-(2-chlorophenyl)acetic acid salt.
(1R, 2R)-(−)-threo-1-(4-nitrophenyl)-2-amino-1,3-propanediol (R)-(−)-2-hydroxy-2-(2-chlorophenyl)acetic acid salt.
Process for the preparation of (R)-(−)-2-hydroxy-2-(2-chlorophenyl)acetic acid of formula I:
- wherein racemic 2-hydroxy-2-(2-chlorophenyl)acetic acid is resolved with a substituted amine of formula (II):
- where R1 means hydroxy-methyl group or carboxyl group, R2 means phenyl group, nitro-phenyl group or a C1-C4 alkyl group substituted with an amino group, and R3 means hydroxyl group or hydrogen atom;
- and wherein a pair of diastereomeric salts of the racemic 2-hydroxy-2-(2-chlorophenyl)acetic acid and the compound of formula (II) is formed in an organic solvent or in a mixture of water and one or more organic solvents, and one of the salts of the pair of diastereomeric salts which is separated due to its different solubility from the pair of diastereomeric salts is obtained from the reaction mixture, and the compound of the formula (I) is obtained from the salt or from the mother liquor.
Process for the preparation of (R)-(−)-2-hydroxy-2-(2-chlorophenyl)acetic acid of formula I:
- wherein racemic 2-hydroxy-2-(2-chlorophenyl)acetic acid is resolved with a substituted amine of formula (II):
- where R1 means hydroxy-methyl group or carboxyl group, R2 means phenyl group, nitro-phenyl group or a C1-C4 alkyl group substituted with an amino group, and R3 means hydroxyl group or hydrogen atom;
- and wherein the optical purity of the crude compound of the formula (I) obtained by resolution is increased by selective crystallization.
Process for the preparation of (R)-(−)-2-hydroxy-2-(2-chlorophenyl)acetic acid of formula I:
- wherein racemic 2-hydroxy-2-(2-chlorophenyl)acetic acid is resolved with a substituted amine of formula (II):
- where R1 means hydroxy-methyl group or carboxyl group, R2 means phenyl group, nitro-phenyl group or a C1-C4 alkyl group substituted with an amino group, and R3 means hydroxyl group or hydrogen atom;
- and wherein the optical purity of the crude compound of the formula (I) obtained by resolution is increased by selective crystallization;
- and wherein the selective crystallization is carried out in toluene or in isopropyl-acetate.
Process for the preparation of (R)-(−)-2-hydroxy-2-(2-chlorophenyl)acetic acid of formula I:
- wherein racemic 2-hydroxy-2-(2-chlorophenyl)acetic acid is resolved with a substituted amine of formula (II):
- where R1 means hydroxy-methyl group or carboxyl group, R2 means phenyl group, nitro-phenyl group or a C1-C4 alkyl group substituted with an amino group, and R3 means hydroxyl group or hydrogen atom;
- and wherein the optical purity of the crude compound of the formula (I) obtained by resolution is increased by selective crystallization;
- and wherein the compound of increased optical purity of the formula (I) obtained by selective crystallization is separated from the solvent at a temperature between +40° and +100° C.
Process for the preparation of (R)-(−)-2-hydroxy-2-(2-chlorophenyl)acetic acid of formula I:
- wherein racemic 2-hydroxy-2-(2-chlorophenyl)acetic acid is resolved with a substituted amine of formula (II):
- where R1 means hydroxy-methyl group or carboxyl group, R2 means phenyl group, nitro-phenyl group or a C1-C4 alkyl group substituted with an amino group, and R3 means hydroxyl group or hydrogen atom;
- and wherein the (S)-(+)-2-hydroxy-2-(2-chlorophenyl)acetic acid obtained by resolution is subjected to racemisation and then it is returned to the resolution process;
- and wherein the racemisation is carried out with an alkali metal hydroxide.
Process for the preparation of (R)-(−)-2-hydroxy-2-(2-chlorophenyl)acetic acid of formula I:
- wherein racemic 2-hydroxy-2-(2-chlorophenyl)acetic acid is resolved with a substituted amine of formula (II):
- where R1 means hydroxy-methyl group or carboxyl group, R2 means phenyl group, nitro-phenyl group or a C1-C4 alkyl group substituted with an amino group, and R3 means hydroxyl group or hydrogen atom;
- and wherein the (S)-(+)-2-hydroxy-2-(2-chlorophenyl)acetic acid obtained by resolution is subjected to racemisation and then it is returned to the resolution process;
- and wherein the racemisation is carried out in water in the presence of a small quantity of aprotic solvent.
Dependencies are inferred from the claim text.