IP Library Granted Patent US 12,077,514
Granted Patent B2
US 12,077,514 · App. 17/414,214 · Granted Sep 3, 2024

Method for racemisation of (5R)-4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4H¬isoxazol-3-yl]-2-methyl-benzoic acid

Inventor: Harald Schmitt (Mainz, DE)
Assignee: Intervet Inc.
C07D261/04C07B55/00
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Quick Facts
Patent No.
US 12,077,514
App. No.
17/414,214
Granted
Sep 3, 2024
Kind
B2
Abstract

The present invention relates to a method for racemizing (5R)-4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4H-isoxazol-3-yl]-2-methyl-benzoic acid.

Claims (22)

1. A Method for racemizing a mixture containing (5R)-4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4H-isoxazol-3-yl]-2-methyl-benzoic acid according to Formula (1a) and (5S)-4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4H-isoxazol-3-yl]-2-methyl-benzoic acid according to Formula (1b)

wherein the mixture has an enantiomeric excess of the compound according to Formula (1a) comprising the step of:

(i) reacting the mixture with an alkaline compound in an organic solvent obtaining a reacted mixture

wherein step (i) is carried out in the absence of phase transfer catalysts and wherein the organic solvent is 2 propanol and wherein the alkaline compound is potassium hydroxide, cesium hydroxide or potassium tert-butanolate.

2. The Method according to claim 1 , further comprising the steps of:

(ii) acidifying the reacted mixture from step (i), to form a result mixture and

(iii) separating the result mixture from step (ii) into a compound mixture and supernatant.

3. The Method according to claim 1 , further comprising the preceding steps of (a) reacting (5RS)-4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4H-isoxazol-3-yl]-2-methyl-benzoic acid with a compound of Formula (2A), (2B) or (2C)

wherein R is an alkyl with 1 or 2 carbon atoms,

wherein X is Cl or Br;

in an organic solvent is 2-propanol to form a precipitate and a supernatant solution, and

(b) separating the supernatant solution containing the mixture containing (5R)-4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4H-isoxazol-3-yl]-2-methyl-benzoic acid according to Formula (1a) and (5S)-4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4H-isoxazol-3-yl]-2-methyl-benzoic acid according to Formula (1b) from the precipitate.

4. The Method according to claim 3 , wherein in step (a) R of Formula (2A) is methyl or R of Formula (2A) is ethyl.

5. The Method according to claim 3 , wherein step (a) comprises heating (5RS)-4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4H-isoxazol-3-yl]2-methyl-benzoic acid with the compound of Formula (2A), (2b) or (2C) in the solvent to an elevated temperature.

6. The Method according to claim 3 , wherein in step (b) the separation of the supernatant solution from step (a) from the precipitate is carried out via filtration.

7. The method according to claim 2 , further comprising the preceding steps of

(a) reacting (5RS)-4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4H-isoxazol-3-yl]-2-methyl-benzoic acid with a compound of Formula (2A), (2B) or (2C)

wherein R is an alkyl with 1 or 2 carbon atoms,

wherein X is Cl or Br;

in an organic solvent is 2-propanol to form a precipitate and a supernatant solution, and

(b) separating the supernatant solution containing the mixture containing (5R)-4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4H-isoxazol-3-yl]-2-methyl-benzoic acid according to Formula (1a) and (5S)-4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4H-isoxazol-3-yl]-2-methyl-benzoic acid according to Formula (1b) from the precipitate.

8. The method according to claim 7 , wherein in step (a) R of Formula (2A) is methyl or R of Formula (2A) is ethyl.

Assignments (2)
CHANGE OF ADDRESS Recorded Sep 26, 2023
From: INTERVET INC.
To: INTERVET INC.
Reel/Frame 065028/0818 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 15, 2021
From: SCHMITT, HARALD
To: INTERVET INC.
Reel/Frame 056551/0704 →
Priority Claims (1)
EP 18215357 · Dec 21, 2018 · regional
Continuity (1)
Related Publication 20220041564A1 · Feb 10, 2022