IP Library Granted Patent US 8,981,110
Granted Patent B2
US 8,981,110 · App. 14/237,213 · Granted Mar 17, 2015

Process for the preparation of olmesartan medoxomil

Inventors: Rajendra Vishwanath Firke (Maharashtra, IN); Ujjwal Komalsing Sisodiya (Maharashtra, IN); Chandrakant Shriram Bhangale (Maharashtra, IN); Radhakrishna Bhikaji Shivdavkar (Maharashtra, IN); Himanshu Madhav Godbole (Maharashtra, IN); Girij Pal Singh (Maharashtra, IN)
Assignee: Lupin Limited
C07D405/14
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Quick Facts
Patent No.
US 8,981,110
App. No.
14/237,213
Granted
Mar 17, 2015
Kind
B2
Abstract

The present invention provides novel process for preparation of olmesartan medoxomil (I) substantially free of olmesartan acid impurity (II) comprising, reacting trityl olmesartan medoxomil (III) with acid, filtering the precipitate of trityl alcohol, subjecting the filtrate to agitated thin film drying and recovering olmesartan medoxomil (I).

Claims (24)

1. A process for preparation of olmesartan medoxomil (I) comprising:

a) reacting trityl olmesartan medoxomil (III) with an acid,

b) filtering the precipitate of trityl alcohol,

c) subjecting the filtrate to agitated thin film drying, and

d) recovering olmesartan medoxomil (I).

2. A process for preparation of olmesartan medoxomil (I) substantially free of olmesartan acid impurity (II) comprising:

a) reacting trityl olmesartan medoxomil (III) with an acid,

b) filtering the precipitate of trityl alcohol,

c) subjecting the filtrate to agitated thin film drying,

d) recovering olmesartan medoxomil (I), and

e) optionally crystallizing olmesartan medoxomil (I) from an organic solvent.

3. A process according to claim 1 wherein, acid is selected from acetic acid, propionic acid, trifluoroacetic acid and hydrochloric acid.

4. A process according to claim 3 wherein, acid is acetic acid.

5. A process according to claim 1 wherein, step (a) is carried out in solvent selected from methanol, ethanol, acetone, ethyl acetate, tetrahydrofuran, 1,4-dioxane, water and mixtures thereof.

6. A process according to claim 5 , wherein solvent is water.

7. A process according to claim 1 wherein, step (a) is carried out at a temperature of 0-100° C.

8. A process according to claim 7 wherein, temperature is 20-60° C.

9. A process according to claim 7 wherein, temperature is 40-45° C.

10. A process according to claim 1 wherein, the feed rate of subjecting the filtrate to agitated thin film dryer is at 4 to 10 ml per minute.

11. A process according to claim 1 wherein, heating medium for agitated thin film dryer is jacketed hot water of temperature of 40-90° C.

12. A process according to claim 11 wherein, temperature is 45-50° C.

13. A process according to claim 1 wherein, the agitated thin film drying is carried out at a vacuum of 20-100 mm/Hg.

14. A process according to claim 13 wherein, vacuum is 70-75 mm/Hg.

15. A process according to claim 2 wherein olmesartan medoxomil (I) is crystallized from an organic solvent selected from acetone, acetonitrile, ethyl acetate or mixtures thereof.

Assignments (2)
CHANGE OF ADDRESS Recorded Jan 27, 2017
From: LUPIN LIMITED
To: LUPIN LIMITED
Reel/Frame 041936/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 5, 2014
From: FIRKE, RAJENDRA VISHWANATH; SISODIA, UJJWAL KOMALSING; BHANGALE, CHANDRAKANT SHRIRAM; SHIVDAVKAR, RADHAKRISHNA BHIKAJI; GODBOLE, HIMANSHU MADHAV; SINGH, GIRIJ PAL
To: LUPIN LIMITED
Reel/Frame 032147/0854 →
Priority Claims (1)
IN 1041/KOL/2011 · Aug 5, 2011 · national
Continuity (1)
Related Publication 20140179930A1 · Jun 26, 2014