WO2008001392A3 - An improved process for the preparation of pantoprazole and its pharmaceutically acceptable salts - Google Patents
An improved process for the preparation of pantoprazole and its pharmaceutically acceptable salts Download PDFInfo
- Publication number
- WO2008001392A3 WO2008001392A3 PCT/IN2007/000265 IN2007000265W WO2008001392A3 WO 2008001392 A3 WO2008001392 A3 WO 2008001392A3 IN 2007000265 W IN2007000265 W IN 2007000265W WO 2008001392 A3 WO2008001392 A3 WO 2008001392A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- preparation
- pantoprazole
- improved process
- pharmaceutically acceptable
- acceptable salts
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
The present invention related to an improved process for the preparation of Pantoprazole sodium sesquihydrate comprising the reaction of 5-difluoromethoxy-2-mercapto benzimidazole with 2-chloromethyl-3,4-dimethoxy pyridine hydrochloride in an aqueous alkali, which upon oxidation with sodium hypochlorite having pH of about 8.5-9.0 and assay of about 3.0-3.5 in chloro solvent followed by reaction with sodium hydroxide in acetone. The invention also relates to the process for the preparation of pantoprazole sodium sesquihydrate form-I.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IN1121/CHE/2006 | 2006-06-30 | ||
IN1121CH2006 | 2006-06-30 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2008001392A2 WO2008001392A2 (en) | 2008-01-03 |
WO2008001392A3 true WO2008001392A3 (en) | 2009-09-24 |
Family
ID=38846112
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/IN2007/000265 WO2008001392A2 (en) | 2006-06-30 | 2007-06-29 | An improved process for the preparation of pantoprazole and its pharmaceutically acceptable salts |
Country Status (1)
Country | Link |
---|---|
WO (1) | WO2008001392A2 (en) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
MXPA05013316A (en) | 2003-06-10 | 2006-03-17 | Teva Pharma | Process for preparing 2-[(pyridinyl)methyl]sulfinyl-substituted benzimidazoles and novel chlorinated derivatives of pantoprazole. |
US7682828B2 (en) | 2003-11-26 | 2010-03-23 | Whitehead Institute For Biomedical Research | Methods for reprogramming somatic cells |
US20100210847A1 (en) * | 2007-07-17 | 2010-08-19 | Ranbaxy Laboratories Limited | Process for the preparation of pantoprazole sodium and pantoprazole sodium sesquihydrate |
WO2010012063A1 (en) | 2008-07-31 | 2010-02-04 | Labbell Inc. | Method of detecting bioactive molecules in a fluid sample |
CN102584790B (en) * | 2011-12-31 | 2014-04-02 | 江苏奥赛康药业股份有限公司 | S-pantoprazole sodium trihydrate, and preparation method and application thereof |
CN103214459B (en) * | 2013-03-22 | 2014-11-12 | 海南中化联合制药工业股份有限公司 | Pantoprazole sodium crystalline compound, pharmaceutical composition and preparation method thereof |
CN114853678A (en) * | 2022-03-31 | 2022-08-05 | 山东科源制药股份有限公司 | Synthesis method of lansoprazole bulk drug intermediate H-benzimidazole |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1411053A1 (en) * | 2000-04-14 | 2004-04-21 | Esteve Quimica, S.A. | Method for obtaining derivatives of (pyridil substituted)methyl]thio]benzimidazol |
WO2004063188A1 (en) * | 2003-01-15 | 2004-07-29 | Cipla Limited | Paharmaceutical process and compounds prepared thereby |
US20040186139A1 (en) * | 2002-09-02 | 2004-09-23 | Dr. Reddy's Laboratories Limited | Process for preparation of crystalline form-1 of pantoprazole sodium sesquihydrate |
WO2004111029A2 (en) * | 2003-06-10 | 2004-12-23 | Teva Pharmaceutical Industries Ltd. | Process for preparing 2-[(pyridinyl)methyl]sulfinyl-substituted benzimidazoles and novel chlorinated derivatives of pantoprazole |
WO2006040778A1 (en) * | 2004-10-15 | 2006-04-20 | Matrix Laboratories Ltd | Process for preparations and purification of pantoprazole sesquihydrate |
-
2007
- 2007-06-29 WO PCT/IN2007/000265 patent/WO2008001392A2/en active Search and Examination
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1411053A1 (en) * | 2000-04-14 | 2004-04-21 | Esteve Quimica, S.A. | Method for obtaining derivatives of (pyridil substituted)methyl]thio]benzimidazol |
US20040186139A1 (en) * | 2002-09-02 | 2004-09-23 | Dr. Reddy's Laboratories Limited | Process for preparation of crystalline form-1 of pantoprazole sodium sesquihydrate |
WO2004063188A1 (en) * | 2003-01-15 | 2004-07-29 | Cipla Limited | Paharmaceutical process and compounds prepared thereby |
WO2004111029A2 (en) * | 2003-06-10 | 2004-12-23 | Teva Pharmaceutical Industries Ltd. | Process for preparing 2-[(pyridinyl)methyl]sulfinyl-substituted benzimidazoles and novel chlorinated derivatives of pantoprazole |
WO2006040778A1 (en) * | 2004-10-15 | 2006-04-20 | Matrix Laboratories Ltd | Process for preparations and purification of pantoprazole sesquihydrate |
Also Published As
Publication number | Publication date |
---|---|
WO2008001392A2 (en) | 2008-01-03 |
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