TNSN96148A1 - Methode pour la synthese d'un benzimidazole. - Google Patents
Methode pour la synthese d'un benzimidazole.Info
- Publication number
- TNSN96148A1 TNSN96148A1 TNTNSN96148A TNSN96148A TNSN96148A1 TN SN96148 A1 TNSN96148 A1 TN SN96148A1 TN TNSN96148 A TNTNSN96148 A TN TNSN96148A TN SN96148 A TNSN96148 A TN SN96148A TN SN96148 A1 TNSN96148 A1 TN SN96148A1
- Authority
- TN
- Tunisia
- Prior art keywords
- fact
- reaction sequence
- benzimidazole
- synthesis
- pyrmethyl
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 5
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 title 1
- 230000015572 biosynthetic process Effects 0.000 title 1
- 238000003786 synthesis reaction Methods 0.000 title 1
- 238000006243 chemical reaction Methods 0.000 abstract 3
- 239000002904 solvent Substances 0.000 abstract 2
- PSEPRWKZZJWRCB-UHFFFAOYSA-N (4-methoxy-3,5-dimethylpyridin-2-yl)methanol Chemical compound COC1=C(C)C=NC(CO)=C1C PSEPRWKZZJWRCB-UHFFFAOYSA-N 0.000 abstract 1
- SUBDBMMJDZJVOS-UHFFFAOYSA-N 5-methoxy-2-{[(4-methoxy-3,5-dimethylpyridin-2-yl)methyl]sulfinyl}-1H-benzimidazole Chemical compound N=1C2=CC(OC)=CC=C2NC=1S(=O)CC1=NC=C(C)C(OC)=C1C SUBDBMMJDZJVOS-UHFFFAOYSA-N 0.000 abstract 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 abstract 1
- XURCIPRUUASYLR-UHFFFAOYSA-N Omeprazole sulfide Chemical compound N=1C2=CC(OC)=CC=C2NC=1SCC1=NC=C(C)C(OC)=C1C XURCIPRUUASYLR-UHFFFAOYSA-N 0.000 abstract 1
- 230000003993 interaction Effects 0.000 abstract 1
- 238000002955 isolation Methods 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 229960000381 omeprazole Drugs 0.000 abstract 1
- 238000000746 purification Methods 0.000 abstract 1
- 239000000376 reactant Substances 0.000 abstract 1
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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
UN PROCEDE POUR LA FABRICATION D'OMEPRAZOLE A PARTIR D'ALCOOL DE PYRMETHYLE EN PASSANT PAR LE CHLORURE DE PYRMETHYLE ET LE PYRMETAZOLE CARACTERISE PAR LE FAIT QUE LA SEQUENCE ENTIERE DE REACTION EST EFFECTUEE SANS AUCUNE ISOLATION OU PURIFICATION DES INTERMEDIAIRES. CE PROCEDE EST EGALEMENT CARACTERISE PAR LE FAIT QUE LES REACTIONS SE FONT DANS UN SEUL SYSTEME A SOLVANT, COMMUN A L'ENSEMBLE DE LA SEQUENCE DE REACTION, CE SOLVANT ETANT INERTE FACE AUX REACTANTS FORMES AU COURS DU PROCEDE ET UTILISES DANS CELUI-CI. LE PROCEDE DE LA PRESENTE INVENTION PEUT EGALEMENT COMPRENDRE UNE ETAPE DE PURIFICATION SUPPLEMENTAIRE.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE9504503A SE521100C2 (sv) | 1995-12-15 | 1995-12-15 | Förfarande för framställning av en bensimidazolförening |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TNSN96148A1 true TNSN96148A1 (fr) | 2005-03-15 |
Family
ID=20400614
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TNTNSN96148A TNSN96148A1 (fr) | 1995-12-15 | 1996-12-02 | Methode pour la synthese d'un benzimidazole. |
Country Status (39)
| Country | Link |
|---|---|
| US (1) | US5958955A (fr) |
| EP (1) | EP0868423B1 (fr) |
| JP (1) | JP3523267B2 (fr) |
| KR (1) | KR100433436B1 (fr) |
| CN (1) | CN1113879C (fr) |
| AR (1) | AR004834A1 (fr) |
| AT (1) | ATE205201T1 (fr) |
| AU (1) | AU704422B2 (fr) |
| CA (1) | CA2238864C (fr) |
| CO (1) | CO4750654A1 (fr) |
| CZ (1) | CZ288661B6 (fr) |
| DE (2) | DE868423T1 (fr) |
| DK (1) | DK0868423T3 (fr) |
| DZ (1) | DZ2137A1 (fr) |
| EE (1) | EE03768B1 (fr) |
| EG (1) | EG23859A (fr) |
| ES (1) | ES2125210T3 (fr) |
| HR (1) | HRP960581B1 (fr) |
| HU (1) | HUP9900110A3 (fr) |
| IL (1) | IL124856A (fr) |
| IS (1) | IS1891B (fr) |
| MA (1) | MA24026A1 (fr) |
| MX (1) | MX9804603A (fr) |
| MY (1) | MY115661A (fr) |
| NO (1) | NO314306B1 (fr) |
| NZ (1) | NZ324482A (fr) |
| PL (1) | PL186132B1 (fr) |
| PT (1) | PT868423E (fr) |
| RU (1) | RU2166502C2 (fr) |
| SE (1) | SE521100C2 (fr) |
| SI (1) | SI0868423T1 (fr) |
| SK (1) | SK282347B6 (fr) |
| TN (1) | TNSN96148A1 (fr) |
| TR (1) | TR199801070T2 (fr) |
| TW (1) | TW460474B (fr) |
| UA (1) | UA62921C2 (fr) |
| WO (1) | WO1997022603A1 (fr) |
| YU (1) | YU49420B (fr) |
| ZA (1) | ZA9610067B (fr) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE521100C2 (sv) * | 1995-12-15 | 2003-09-30 | Astra Ab | Förfarande för framställning av en bensimidazolförening |
| US6699885B2 (en) * | 1996-01-04 | 2004-03-02 | The Curators Of The University Of Missouri | Substituted benzimidazole dosage forms and methods of using same |
| US6489346B1 (en) | 1996-01-04 | 2002-12-03 | The Curators Of The University Of Missouri | Substituted benzimidazole dosage forms and method of using same |
| US5840737A (en) | 1996-01-04 | 1998-11-24 | The Curators Of The University Of Missouri | Omeprazole solution and method for using same |
| US6645988B2 (en) | 1996-01-04 | 2003-11-11 | Curators Of The University Of Missouri | Substituted benzimidazole dosage forms and method of using same |
| SK283805B6 (sk) | 1996-09-09 | 2004-02-03 | Slovakofarma, A. S. | Spôsob prípravy omeprazolu |
| US6303787B1 (en) * | 1998-05-27 | 2001-10-16 | Natco Pharma Limited | Intermediates and an improved process for the preparation of Omeprazole employing the said intermediates |
| SI20019A (sl) * | 1998-07-13 | 2000-02-29 | LEK, tovarna farmacevtskih in kemi�nih izdelkov, d.d. | Izboljšan postopek sinteze 5-metoksi -2-/(4-metoksi-3,5-dimetil-2-piridil)metil/ sulfinil-1H-benzimidazola |
| US6166213A (en) * | 1998-08-11 | 2000-12-26 | Merck & Co., Inc. | Omeprazole process and compositions thereof |
| UA72748C2 (en) * | 1998-11-10 | 2005-04-15 | Astrazeneca Ab | A novel crystalline form of omeprazole |
| IL142703A (en) | 1998-11-10 | 2006-04-10 | Astrazeneca Ab | Crystalline form of omeprazole |
| DE19951960C2 (de) * | 1999-10-28 | 2002-06-27 | Gruenenthal Gmbh | Verfahren zur Herstellung als Ulkustherapeutika geeigneter Benzimidazol-Derivate |
| RU2247120C2 (ru) * | 1999-10-28 | 2005-02-27 | Грюненталь Гмбх | Способ получения противоязвенных терапевтических средств |
| US20040006111A1 (en) * | 2002-01-25 | 2004-01-08 | Kenneth Widder | Transmucosal delivery of proton pump inhibitors |
| SE0203092D0 (en) * | 2002-10-18 | 2002-10-18 | Astrazeneca Ab | Method for the synthesis of a benzimidazole compound |
| US8993599B2 (en) | 2003-07-18 | 2015-03-31 | Santarus, Inc. | Pharmaceutical formulations useful for inhibiting acid secretion and methods for making and using them |
| US8906940B2 (en) | 2004-05-25 | 2014-12-09 | Santarus, Inc. | Pharmaceutical formulations useful for inhibiting acid secretion and methods for making and using them |
| US8815916B2 (en) | 2004-05-25 | 2014-08-26 | Santarus, Inc. | Pharmaceutical formulations useful for inhibiting acid secretion and methods for making and using them |
| US8691995B2 (en) | 2004-12-16 | 2014-04-08 | Cipla Limited | Process |
| CN100393712C (zh) * | 2006-01-23 | 2008-06-11 | 中国科学院成都有机化学有限公司 | 苯并咪唑型质子泵抑止剂及其前体的改进制备和分离纯化方法 |
| WO2007122686A1 (fr) * | 2006-04-14 | 2007-11-01 | Eisai R & D Management Co., Ltd. | Composes benzimidazole |
| CA2889878A1 (fr) * | 2007-02-21 | 2008-08-28 | Cipla Limited | Procede pour la preparation de esomeprazole magnesium dihydrate |
| CN101492459B (zh) * | 2008-01-25 | 2011-04-27 | 山东轩竹医药科技有限公司 | 含烷氧乙酰基二氢异噁唑并吡啶化合物 |
| CN101497603B (zh) * | 2008-01-30 | 2012-11-07 | 山东轩竹医药科技有限公司 | 含有被烷氧烷胺氧基取代的吡啶的苯并咪唑衍生物 |
| CN103664885A (zh) * | 2013-12-12 | 2014-03-26 | 武汉工程大学 | 苯并咪唑型质子泵抑制剂中间体的制备方法 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US461997A (en) * | 1891-10-27 | Sand-pump or other pipes | ||
| SE7804231L (sv) * | 1978-04-14 | 1979-10-15 | Haessle Ab | Magsyrasekretionsmedel |
| JPS6150978A (ja) * | 1984-08-16 | 1986-03-13 | Takeda Chem Ind Ltd | ピリジン誘導体およびその製造法 |
| US4619997A (en) * | 1984-09-06 | 1986-10-28 | The Upjohn Company | Substituted 2-pyridylmethylthio and sulfinyl-benzimidazoles as gastric antisecretory agents |
| IL76839A (en) * | 1984-10-31 | 1988-08-31 | Byk Gulden Lomberg Chem Fab | Picoline derivatives,processes for the preparation thereof and pharmaceutical compositions containing the same |
| SE9002043D0 (sv) * | 1990-06-07 | 1990-06-07 | Astra Ab | Improved method for synthesis |
| NZ244301A (en) * | 1991-09-20 | 1994-08-26 | Merck & Co Inc | Preparation of 2-pyridylmethylsulphinylbenzimidazole and pyridoimidazole derivatives from the corresponding sulphenyl compounds |
| SE521100C2 (sv) * | 1995-12-15 | 2003-09-30 | Astra Ab | Förfarande för framställning av en bensimidazolförening |
-
1995
- 1995-12-15 SE SE9504503A patent/SE521100C2/sv not_active IP Right Cessation
-
1996
- 1996-05-12 UA UA98052782A patent/UA62921C2/uk unknown
- 1996-11-29 ZA ZA9610067A patent/ZA9610067B/xx unknown
- 1996-12-02 AR ARP960105459A patent/AR004834A1/es active IP Right Grant
- 1996-12-02 TN TNTNSN96148A patent/TNSN96148A1/fr unknown
- 1996-12-03 TW TW085114881A patent/TW460474B/zh not_active IP Right Cessation
- 1996-12-04 YU YU64296A patent/YU49420B/sh unknown
- 1996-12-04 DZ DZ960182A patent/DZ2137A1/fr active
- 1996-12-04 MA MA24415A patent/MA24026A1/fr unknown
- 1996-12-05 RU RU98110659/04A patent/RU2166502C2/ru not_active IP Right Cessation
- 1996-12-05 EP EP96942702A patent/EP0868423B1/fr not_active Expired - Lifetime
- 1996-12-05 CN CN96199057A patent/CN1113879C/zh not_active Expired - Fee Related
- 1996-12-05 AU AU11550/97A patent/AU704422B2/en not_active Ceased
- 1996-12-05 SI SI9630367T patent/SI0868423T1/xx unknown
- 1996-12-05 TR TR1998/01070T patent/TR199801070T2/xx unknown
- 1996-12-05 NZ NZ324482A patent/NZ324482A/xx unknown
- 1996-12-05 HU HU9900110A patent/HUP9900110A3/hu unknown
- 1996-12-05 CA CA002238864A patent/CA2238864C/fr not_active Expired - Fee Related
- 1996-12-05 WO PCT/SE1996/001603 patent/WO1997022603A1/fr not_active Ceased
- 1996-12-05 US US08/776,222 patent/US5958955A/en not_active Expired - Lifetime
- 1996-12-05 PL PL96327334A patent/PL186132B1/pl not_active IP Right Cessation
- 1996-12-05 ES ES96942702T patent/ES2125210T3/es not_active Expired - Lifetime
- 1996-12-05 DE DE0868423T patent/DE868423T1/de active Pending
- 1996-12-05 CZ CZ19981685A patent/CZ288661B6/cs not_active IP Right Cessation
- 1996-12-05 JP JP52269797A patent/JP3523267B2/ja not_active Expired - Fee Related
- 1996-12-05 IL IL12485696A patent/IL124856A/en not_active IP Right Cessation
- 1996-12-05 EE EE9800183A patent/EE03768B1/xx not_active IP Right Cessation
- 1996-12-05 SK SK768-98A patent/SK282347B6/sk not_active IP Right Cessation
- 1996-12-05 PT PT96942702T patent/PT868423E/pt unknown
- 1996-12-05 DK DK96942702T patent/DK0868423T3/da active
- 1996-12-05 KR KR10-1998-0704454A patent/KR100433436B1/ko not_active Expired - Fee Related
- 1996-12-05 AT AT96942702T patent/ATE205201T1/de not_active IP Right Cessation
- 1996-12-05 DE DE69615052T patent/DE69615052T2/de not_active Expired - Fee Related
- 1996-12-09 HR HR960581A patent/HRP960581B1/xx not_active IP Right Cessation
- 1996-12-11 CO CO96065025A patent/CO4750654A1/es unknown
- 1996-12-13 MY MYPI96005252A patent/MY115661A/en unknown
- 1996-12-14 EG EG112296A patent/EG23859A/xx active
-
1998
- 1998-05-22 IS IS4750A patent/IS1891B/is unknown
- 1998-06-08 NO NO19982624A patent/NO314306B1/no not_active IP Right Cessation
- 1998-06-09 MX MX9804603A patent/MX9804603A/es not_active IP Right Cessation
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