WO2009084028A3 - Improved process for manufacturing anhydrous (e)-3-[2-butyl-1- {(4-carboxyphenyl) methyl}-1h-imidazole-5-yl]-(thiophen-2- ylmethyl)prop-2-enoic acid methane sulfonate - Google Patents
Improved process for manufacturing anhydrous (e)-3-[2-butyl-1- {(4-carboxyphenyl) methyl}-1h-imidazole-5-yl]-(thiophen-2- ylmethyl)prop-2-enoic acid methane sulfonate Download PDFInfo
- Publication number
- WO2009084028A3 WO2009084028A3 PCT/IN2008/000803 IN2008000803W WO2009084028A3 WO 2009084028 A3 WO2009084028 A3 WO 2009084028A3 IN 2008000803 W IN2008000803 W IN 2008000803W WO 2009084028 A3 WO2009084028 A3 WO 2009084028A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- carboxyphenyl
- thiophen
- ylmethyl
- prop
- imidazole
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
The present invention relates to a simple efficient and cost effective process for commercial manufacture of (E)-3-[2-Butyl-1-{(4-carboxyphenyl) methyl}-1H-imidazole-5-yl]- 2-(thiophen-2-ylmethyl)prop-2-enoic acid and its conversion to substantially pure anhydrous mesylate salt as shown in Formula (I), with a purity level of 99.85% and single individual impurity of less than 0.10 %.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IN2861CH2007 | 2007-12-03 | ||
| IN2861/CHE/2007 | 2007-12-03 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2009084028A2 WO2009084028A2 (en) | 2009-07-09 |
| WO2009084028A3 true WO2009084028A3 (en) | 2010-12-02 |
Family
ID=40824843
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/IN2008/000803 Ceased WO2009084028A2 (en) | 2007-12-03 | 2008-12-02 | Improved process for manufacturing anhydrous (e)-3-[2-butyl-1- {(4-carboxyphenyl) methyl}-1h-imidazole-5-yl]-(thiophen-2- ylmethyl)prop-2-enoic acid methane sulfonate |
Country Status (1)
| Country | Link |
|---|---|
| WO (1) | WO2009084028A2 (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101333216A (en) * | 2008-08-03 | 2008-12-31 | 浙江华海药业股份有限公司 | Novel saltforming process of eprosartan mesylate |
| WO2011051975A1 (en) | 2009-10-30 | 2011-05-05 | Matrix Laboratories Ltd | An improved process for the preparation of pure eprosartanand its pharmaceutical acceptable salts |
| CN102584709B (en) * | 2011-12-19 | 2016-08-17 | 浙江华海药业股份有限公司 | A kind of preparation technology of the Eprosartan intermediate aryl imidazole aldehyde of improvement |
| CN104788382A (en) * | 2015-04-21 | 2015-07-22 | 浙江华海药业股份有限公司 | Method for preparing eprosartan midbody impurity EP2A |
| CN106916139A (en) * | 2017-05-09 | 2017-07-04 | 浙江华海致诚药业有限公司 | A kind of preparation method of improved Eprosartan intermediate |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5185351A (en) * | 1989-06-14 | 1993-02-09 | Smithkline Beecham Corporation | Imidazolyl-alkenoic acids useful as angiotensin II receptor antagonists |
| WO1997036874A1 (en) * | 1996-03-29 | 1997-10-09 | Smithkline Beecham Corporation | Eprosartan dihydrate and a process for its production and formulation |
| WO1998035963A1 (en) * | 1997-02-14 | 1998-08-20 | Smithkline Beecham Corporation | Process for preparing eprosartan |
| WO2008078330A1 (en) * | 2006-12-27 | 2008-07-03 | Hetero Drugs Limited | Improved process for eprosartan |
-
2008
- 2008-12-02 WO PCT/IN2008/000803 patent/WO2009084028A2/en not_active Ceased
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5185351A (en) * | 1989-06-14 | 1993-02-09 | Smithkline Beecham Corporation | Imidazolyl-alkenoic acids useful as angiotensin II receptor antagonists |
| WO1997036874A1 (en) * | 1996-03-29 | 1997-10-09 | Smithkline Beecham Corporation | Eprosartan dihydrate and a process for its production and formulation |
| WO1998035963A1 (en) * | 1997-02-14 | 1998-08-20 | Smithkline Beecham Corporation | Process for preparing eprosartan |
| WO2008078330A1 (en) * | 2006-12-27 | 2008-07-03 | Hetero Drugs Limited | Improved process for eprosartan |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2009084028A2 (en) | 2009-07-09 |
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