IP Library Granted Patent US 7,109,356
Granted Patent B2
US 7,109,356 · App. 10/718,925 · Granted Sep 19, 2006

Process for racemization

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Quick Facts
Patent No.
US 7,109,356
App. No.
10/718,925
Granted
Sep 19, 2006
Kind
B2
Abstract

The invention relates to the racemization process of the optically active [2-(2-thienyl)ethylamino](2-halogenophenyl)acetamides of general formula (VII) by using basic compounds. The resulting racemic compounds of general formula (VII) can thus be recycled into synthesis of the therapeutically useful compounds of general formula (VI).

Claims (13)

1. A process for the racemization of the optically active compounds of formula (VII)—wherein X is halogen

which comprises reacting said compound or an acid addition salt thereof with an organic or inorganic base at a temperature between 40° C. and 60° C.

2. A process according to claim 1 wherein the inorganic base is an alkali metal hydroxide.

3. A process according to claim 1 wherein the organic base is an alkali metal alcoholate.

4. A process according to claim 1 wherein the racemisation is performed in an organic solvent.

5. A process according to claim 1 wherein an acid addition salt of a levorotatory compound of formula (VII) is reacted with an organic or inorganic base.

6. A process according to claim 1 , wherein an acid addition salt of a dextrorotatory compound of formula (VII) is reacted with an organic or inorganic base.

7. A process according to claim 4 wherein the organic solvent is an alcohol or aromatic carbohydrate.

8. A process according to claim 1 wherein the organic or inorganic base is used in an amount of 5–500 mol %, based on the levorotatory compound of formula (VII).

9. A process according to claim 1 wherein the organic or inorganic base is used in an amount of 5–500 mol %, based on the dextrorotatory compound of formula (VII).

10. A process according to claim 1 , wherein the compound of formula VII is a mixture of the levorotatory and dextrorotatory compounds.

11. A process according to claim 1 wherein the mole ratio of the base to the compound of formula (VII) is from 1:3.5 to 1:0.2.

12. A process according to claim 11 wherein the reaction is carried out over a period of about 20–30 minutes.

Assignments (3)
CHANGE OF NAME Recorded Jun 20, 2012
From: SANOFI-AVENTIS
To: SANOFI
Reel/Frame 028413/0927 →
CHANGE OF NAME Recorded Jul 22, 2005
From: SANOFI-SYNTHELABO
To: SANOFI-AVENTIS
Reel/Frame 016345/0189 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 23, 2005
From: BAKONYI, MARIA; BAI, TIBORNE; DOMBRADY, ZSOLT; GASPAR, KATALIN; SUPIC, ATTILA
To: SANOFI-SYNTHELABO
Reel/Frame 016051/0108 →