SV2002000126A - NEW PROCEDURE FOR OBTAINING DERIVATIVES OF 2- (2-PIRIDINILMETILSULFINIL) -1H-BENZIMIDAZOL REF. A-149206 - Google Patents
NEW PROCEDURE FOR OBTAINING DERIVATIVES OF 2- (2-PIRIDINILMETILSULFINIL) -1H-BENZIMIDAZOL REF. A-149206Info
- Publication number
- SV2002000126A SV2002000126A SV2000000126A SV2000000126A SV2002000126A SV 2002000126 A SV2002000126 A SV 2002000126A SV 2000000126 A SV2000000126 A SV 2000000126A SV 2000000126 A SV2000000126 A SV 2000000126A SV 2002000126 A SV2002000126 A SV 2002000126A
- Authority
- SV
- El Salvador
- Prior art keywords
- piridinilmetilsulfinil
- benzimidazol
- ref
- obtaining derivatives
- new procedure
- Prior art date
Links
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 3
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 abstract 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
- 210000000481 breast Anatomy 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical group 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 230000001175 peptic effect Effects 0.000 abstract 1
- 239000002798 polar solvent Substances 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- 239000001294 propane Substances 0.000 abstract 1
- 239000002904 solvent 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
- 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)
Abstract
PROCEDIMIENTO DE OBTENCION DE DERIVADOS DE 2-(2- PIRIDINILMETILSULFINIL)-1H-BENZIMIDAZOL DE FORMULA GENERAL (I), DONDE R= H O ALQUILO; R'= CADENA ALQUILICA INTERRUMPIDA O NO POR 0, R''=ALQUILO O ALCOXI; R'''=H O ALCOXI SUBSTITUIDO O NO, CARACTERIZADO PORQUE SE LLEVA A CABO MEDIANTE LA SUBSTITUCION DE UN HALOGENO EN LA POSICION 4 DEL ANILLO DE PIRIDINA DE LOS COMPUESTOS DE FORMULA GENERAL(VIII) POR 3-METOXI PROPANO O METANOL EN PRESENCIA DE UNA BASE Y EN EL SENO DE UNA MEZCLA DE DISOLVENTES CONSTITUIDA POR EL CORRESPONDIENTE ALCOHOL R'OH Y OTRO DISOLVENTE POLAR APROTICO. ES UTIL EN EL TRATAMIENTO O PREVENCION DE LAS ULCERAS PEPTICAS.PROCEDURE FOR OBTAINING DERIVATIVES OF 2- (2- PIRIDINILMETILSULFINIL) -1H-BENZIMIDAZOL OF GENERAL FORMULA (I), WHERE R = H OR RENT; R '= ALKYL CHAIN INTERRUPTED OR NOT BY 0, R' '= RENT OR ALCOXI; R '' '= HO ALCOXI SUBSTITUTED OR NOT, CHARACTERIZED BECAUSE IT IS CARRIED OUT BY REPLACING A HALOGEN IN POSITION 4 OF THE PIRIDINE RING OF THE GENERAL FORMULA COMPOUNDS (VIII) BY 3-METOXI PROPANE OR METHANOL IN THE PRESENCE OF A BASE AND IN THE BREAST OF A MIXTURE OF SOLVENTS CONSTITUTED BY THE CORRESPONDING ALCOHOL R'OH AND ANOTHER APROTIC POLAR SOLVENT. IT IS USEFUL IN THE TREATMENT OR PREVENTION OF PEPTIC ULCERAS.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ES009901579A ES2166269B1 (en) | 1999-07-14 | 1999-07-14 | NEW PROCEDURE FOR OBTAINING DERIVATIVES OF 2- (2-PIRIDINILMETILSULFINIL) -1H-BENZIMIDAZOL. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SV2002000126A true SV2002000126A (en) | 2002-02-05 |
Family
ID=8309223
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SV2000000126A SV2002000126A (en) | 1999-07-14 | 2000-07-13 | NEW PROCEDURE FOR OBTAINING DERIVATIVES OF 2- (2-PIRIDINILMETILSULFINIL) -1H-BENZIMIDAZOL REF. A-149206 |
Country Status (6)
| Country | Link |
|---|---|
| AU (1) | AU5558800A (en) |
| EG (1) | EG23175A (en) |
| ES (1) | ES2166269B1 (en) |
| SV (1) | SV2002000126A (en) |
| TN (1) | TNSN00153A1 (en) |
| WO (1) | WO2001004109A1 (en) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2187248B1 (en) * | 2000-08-25 | 2004-01-16 | Sint Quimica Sa | NEW PROCEDURE FOR OBTAINING DERIVATIVES OF 2- (2-PIRIDINILMETILSULFINIL) -1H-BENZIMIDAZOL. |
| ES2185459B1 (en) * | 2000-10-02 | 2003-12-16 | Dinamite Dipharma Spa | PROCEDURE FOR OBTAINING PANTOPRAZOL AND INTERMEDIATE COMPOUNDS FOR THE SAME. |
| WO2003101452A1 (en) * | 2002-06-03 | 2003-12-11 | Aurobindo Pharma Ltd. | Process for the preparation of highly pure rabeprazole sodium salt |
| EP1572680A2 (en) | 2002-12-19 | 2005-09-14 | Eva Pharmaceutical Industries Ltd. | Solid states of pantoprazole sodium, known pantoprazole sodium hydrates, processes for their preparation. |
| US7683177B2 (en) | 2003-06-10 | 2010-03-23 | Teva Pharmaceutical Industries Ltd | Process for preparing 2-[(pyridinyl)methyl]sulfinyl-substituted benzimidazoles and novel chlorinated derivatives of pantoprazole |
| AU2003288703A1 (en) * | 2003-12-05 | 2005-06-24 | Hetero Drugs Limited | A process for the preparation of substitited pyridinylmethylsulfinyl- benzimidazole enantiomers |
| SE0400410D0 (en) | 2004-02-20 | 2004-02-20 | Astrazeneca Ab | New compounds |
| US7557217B2 (en) | 2004-06-30 | 2009-07-07 | Eisai R&D Management Co., Ltd. | Process for production of benzimidazole derivative salt precipitate |
| AU2005315390B2 (en) * | 2004-12-16 | 2011-10-27 | Cipla Limited | Process for the preparation of pantoprazole sodium |
| ES2264362B1 (en) * | 2004-12-22 | 2007-11-01 | Laboratorios Viñas S.A. | "PROCEDURE FOR OBTAINING DERIVATIVES OF 2- (2-PIRIDINILMETILSUFINIL-1H-BENZIMIDAZOLES"). |
| ATE473222T1 (en) * | 2005-02-21 | 2010-07-15 | Ltd Cipla | NEW METHOD FOR SYNTHESIS OF PROTON PUMP INHIBITORS |
| ES2273564B1 (en) * | 2005-03-22 | 2008-04-01 | Quimica Sintetica, S.A. | PROCEDURE FOR THE PREPARATION OF PANTOPRAZOLE. |
| JP2008534578A (en) * | 2005-03-30 | 2008-08-28 | ルピン・リミテッド | Improved preparation of rabeprazole sodium |
| MX2010010049A (en) * | 2008-03-18 | 2010-10-04 | Reddys Lab Ltd Dr | Dexlansoprazole process and polymorphs. |
| KR20130087509A (en) | 2010-06-24 | 2013-08-06 | 씨아이피엘에이 엘티디. | Salt and polymorphs of dexrabeprazole |
| CN102993181B (en) * | 2012-12-26 | 2014-07-23 | 山东大学 | Preparation method of esomeprazole and preparation method of esomeprazole salt |
| CN104098516B (en) * | 2013-04-15 | 2016-12-28 | 北大方正集团有限公司 | A kind of intermediate for preparing esomeprazole or its sodium salt and preparation method thereof |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2023609A6 (en) * | 1990-11-29 | 1992-01-16 | Inke Sa | Process for obtaining 2-[[[3-methyl-4-(2,2,2- trifluoroethoxy)-2-pyridinyl]methyl]sulphinyl]-1H- benzimidazole |
| ES2036948B1 (en) * | 1991-11-21 | 1994-09-01 | Genesis Para La Investigacion | PROCEDURE FOR OBTAINING COMPOUNDS DERIVED FROM PIRIDINE. |
| ES2037608B1 (en) * | 1991-12-02 | 1994-04-01 | Techquin Etablissment | PROCEDURE FOR OBTAINING 2 (((3-METHYL-4- (2,2,2, -TRIFLUOROETOXI) -2-PIRIDINIL) -METIL) SULFINIL) -1H-BENZIMIDAZOLE ". |
| ES2037609B1 (en) * | 1991-12-02 | 1994-04-01 | Techquin Etablissment | PROCEDURE FOR OBTAINING 2 - ((((3-METHYL-4- (2,2,2-TRIFLUROETOXI) -2-PIRIDINIL) -METIL) SULFINIL) -1H-BENZIMIDAZOLE. |
| ES2060541B1 (en) * | 1993-02-26 | 1995-11-16 | Vinas Lab | NEW PROCEDURE FOR THE SYNTHESIS OF A DERIVATIVE OF 2- (2-PIRIDILMETILSUFINIL) BENCIMIDAZOLE, AND NEW INTERMEDIATE PRODUCTS OBTAINED WITH THE SAME. |
-
1999
- 1999-07-14 ES ES009901579A patent/ES2166269B1/en not_active Expired - Fee Related
-
2000
- 2000-07-10 AU AU55588/00A patent/AU5558800A/en not_active Abandoned
- 2000-07-10 WO PCT/IB2000/000927 patent/WO2001004109A1/en not_active Ceased
- 2000-07-12 EG EG20000903A patent/EG23175A/en active
- 2000-07-13 SV SV2000000126A patent/SV2002000126A/en not_active Application Discontinuation
- 2000-07-31 TN TNTNSN00153A patent/TNSN00153A1/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ES2166269A1 (en) | 2002-04-01 |
| WO2001004109A1 (en) | 2001-01-18 |
| TNSN00153A1 (en) | 2002-05-30 |
| ES2166269B1 (en) | 2003-04-01 |
| AU5558800A (en) | 2001-01-30 |
| EG23175A (en) | 2004-06-30 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| SV2002000126A (en) | NEW PROCEDURE FOR OBTAINING DERIVATIVES OF 2- (2-PIRIDINILMETILSULFINIL) -1H-BENZIMIDAZOL REF. A-149206 | |
| MXPA06001273A (en) | Novel compounds. | |
| DE60318030D1 (en) | PIPERAZINE SUBSTITUTED ARYL BENZODIAZEPINES AND THEIR USE AS DOPAMINE RECEPTOR ANTAGONISTS FOR THE TREATMENT OF PSYCHOSIS | |
| CY1113054T1 (en) | DIAMIN PRODUCERS | |
| TW200510441A (en) | Novel compounds | |
| NO20041504L (en) | Lactam derivatives as antagonists of human 11CBY receptors. | |
| ATE416157T1 (en) | INHIBITORS OF INTEGRIN ALPHA-V-BETA-6 | |
| ATE300543T1 (en) | CONDENSED PYRAZINEDIONE DERIVATIVES AS PDE5 INHIBITERS | |
| GB9923077D0 (en) | Sapogenin derivatives and their use | |
| ES2166046T3 (en) | DERIVATIVES OF ARILACRILAMIDE AS AGONISTS OR ANTAGONISTS OF 5HT1. | |
| DK380279A (en) | PROCEDURE FOR PREPARING BENZIMIDAZOLE CARBAMATES | |
| DK1222159T3 (en) | Intermediates for the preparation of a benzofuran or benzothiophene derivative nitrated at position 5 and use thereof | |
| ES2172029T3 (en) | 3-AMINO-1-CIANOFENIL-URACILOS. | |
| ES2091899T3 (en) | PROCEDURE FOR OBTAINING NITROGUANIDINE DERIVATIVES. | |
| BR0209901A (en) | Processes for the synthesis of 2,3-dihydro-1,4-dioxino- [2,3-f] quinoline derivatives | |
| DE60002583D1 (en) | BENZOFURYL PIPERAZINE AS SEROTONIN AGONISTS | |
| AR041481A1 (en) | ARILPROPIONIC-OXAZOL ACID DERIVATIVES AND ITS USE AS PPAR AGONISTS | |
| ES2071479T3 (en) | DERIVATIVES OF INDANO. | |
| DE60131001D1 (en) | OXAZOLYLARYLPROPIONIC ACID DERIVATIVES AND THEIR USE AS PPAR AGONISTS | |
| DE69819742D1 (en) | INDOLDER DERIVATIVES AS 5-HT1B AND 5-HT1D AGONISTS | |
| DE69819266D1 (en) | Piperidine and piperazine derivatives as 5-HT1 receptor agonists | |
| KR940019705A (en) | 2- [4- (4-Azolylbutyl) -1-piperazinyl] -5-hydroxy-pyramidine derivatives, their preparation and their use as medicinal products | |
| ES2074966B1 (en) | PROCEDURE FOR OBTAINING 3- (2- (4- (6-FLUORO-BENZO (D) ISOXAZOL-3-IL) PIPERIDIN-1-IL) -ETIL) -2-METHYL-6,7,8,9- TETRAHIDRO-4H-PIRIDO- (1,2-A) PIRIMIDIN-4-ONA. | |
| ES2104509B1 (en) | NEW COMPOUNDS DERIVED FROM 2- (3,4-DISSTITUTED-1-PIPERAZINYL) -5-FLUOROPYRIMIDINE. | |
| DE69906243D1 (en) | 2-indanemethanol derivatives and their use as fragrances |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG | Grant | ||
| FD | Lapse |