ES8404993A1 - Procedimiento para preparar derivados de piridina - Google Patents
Procedimiento para preparar derivados de piridinaInfo
- Publication number
- ES8404993A1 ES8404993A1 ES525122A ES525122A ES8404993A1 ES 8404993 A1 ES8404993 A1 ES 8404993A1 ES 525122 A ES525122 A ES 525122A ES 525122 A ES525122 A ES 525122A ES 8404993 A1 ES8404993 A1 ES 8404993A1
- Authority
- ES
- Spain
- Prior art keywords
- preparation
- omeprazole
- intermediates
- formula
- image
- 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.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/89—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members with hetero atoms directly attached to the ring nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/62—Oxygen or sulfur atoms
- C07D213/63—One oxygen atom
- C07D213/68—One oxygen atom attached in position 4
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Compounds Of Unknown Constitution (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
PROCEDIMIENTO PARA LA OBTENCION DE DERIVADOS DE PIRIDINA, DE FORMULA (I), EN LA QUE R ES HIDROGENO O METILO.CONSISTE EN LA REACCION DE UN COMPUESTO DE FORMULA (II), EN LA QUE R ES EL MISMO QUE EN LA FORMULA (I), CON UN AGENTE DE NITRACION, TAL COMO ACIDO NITRICO EN ACIDO SULFURICO; SEGUIDA DEL TRATAMIENTO DEL COMPUESTO FORMADO CON UNA DISOLUCION DE ANION METOXIDO EN METANOL, PREPARADA A PARTIR DE METANOL E HIDROXIDO SODICO.ESTOS COMPUESTOS TIENEN APLICACION COMO INTERMEDIOS EN LA PREPARACION DE MEDICAMENTOS QUE TIENEN EFECTOS CITROPROTECTORES GASTROINTESTINALES, E INHIBIDORES DELA SECRECION DEL ACIDO GASTRICO.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SE8204879A SE8204879D0 (sv) | 1982-08-26 | 1982-08-26 | Novel chemical intermediates |
Publications (2)
Publication Number | Publication Date |
---|---|
ES525122A0 ES525122A0 (es) | 1984-05-16 |
ES8404993A1 true ES8404993A1 (es) | 1984-05-16 |
Family
ID=20347627
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES525122A Expired ES8404993A1 (es) | 1982-08-26 | 1983-08-24 | Procedimiento para preparar derivados de piridina |
Country Status (28)
Country | Link |
---|---|
US (2) | US4544750A (es) |
EP (1) | EP0103553B1 (es) |
JP (1) | JPS5959662A (es) |
KR (1) | KR880000091B1 (es) |
AT (1) | ATE40884T1 (es) |
AU (1) | AU560028B2 (es) |
CA (1) | CA1234118A (es) |
CY (1) | CY1328A (es) |
DD (1) | DD233126A5 (es) |
DE (2) | DE3379222D1 (es) |
DK (1) | DK381583A (es) |
ES (1) | ES8404993A1 (es) |
FI (1) | FI79701C (es) |
GB (1) | GB2126226B (es) |
GR (1) | GR79374B (es) |
HK (1) | HK19486A (es) |
HU (1) | HU189738B (es) |
IE (1) | IE55865B1 (es) |
IL (1) | IL69175A (es) |
IS (1) | IS1438B6 (es) |
MY (1) | MY8600503A (es) |
NO (1) | NO164093C (es) |
NZ (1) | NZ204959A (es) |
OA (1) | OA07498A (es) |
PH (1) | PH17786A (es) |
PT (1) | PT77249B (es) |
SE (1) | SE8204879D0 (es) |
ZA (1) | ZA835143B (es) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2060541A1 (es) * | 1993-02-26 | 1994-11-16 | Vinas Lab | Nuevo procedimiento para la sintesis de un derivado de 2-(2-piridilmetilsufinil) bencimidazol, y nuevos productos intermedios obtenidos con el mismo. |
ES2067407A1 (es) * | 1991-11-21 | 1995-03-16 | Genesis Para La Investigacion | Perfeccionamientos en el objeto de la patente 9102594 por procedimiento de obtencion de derivados de piridina. |
Families Citing this family (56)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SE8404065D0 (sv) * | 1984-08-10 | 1984-08-10 | Haessle Ab | Novel biologically active compounds |
SE8504409D0 (sv) * | 1985-09-24 | 1985-09-24 | Haessle Ab | Novel chemical intermediates |
ES2053533T3 (es) * | 1986-04-17 | 1994-08-01 | Ici Plc | Derivados de esteres de acido piridil-acrilico, un proceso para su preparacion y su uso como fungicidas. |
US5221316A (en) * | 1986-04-17 | 1993-06-22 | Imperial Chemical Industries Plc | Fungicides |
US4920230A (en) * | 1987-06-29 | 1990-04-24 | Takeda Chemical Industries, Ltd. | Method of producing nitrogen-containing heteroaromatic compounds having an alkoxy group |
AT391693B (de) * | 1988-11-15 | 1990-11-12 | Cl Pharma | Verfahren zur herstellung von 3-5-dimethyl-4methoxypyridinderivaten sowie neues zwischenprodukt hierfuer |
US4965269A (en) * | 1989-12-20 | 1990-10-23 | Ab Hassle | Therapeutically active chloro substituted benzimidazoles |
ES2026761A6 (es) * | 1990-10-31 | 1992-05-01 | Genesis Para La Investigacion | Procedimiento de obtencion del omeprazol. |
SE9301830D0 (sv) * | 1993-05-28 | 1993-05-28 | Ab Astra | New compounds |
ES2097089B1 (es) * | 1995-02-01 | 1997-12-16 | Esteve Quimica Sa | Procedimiento para la preparacion de 2-hidroximetil-3,5-dimetil-4-metoxipiridina. |
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 |
US6437139B1 (en) | 1997-05-06 | 2002-08-20 | Pdi-Research Laboratories, Inc. | Synthesis of pharmaceutically useful pyridine derivatives |
CA2204580A1 (en) * | 1997-05-06 | 1998-11-06 | Michel Zoghbi | Synthesis of pharmaceutically useful pyridine derivatives |
WO1999033807A2 (en) * | 1997-12-24 | 1999-07-08 | Pdi-Research Laboratories, Inc. | Synthesis of pharmaceutically useful pyridine derivatives (intermediates) employing free radical substitution reactions to functionalize the 2-position of the pyridine |
GB9717849D0 (en) * | 1997-08-23 | 1997-10-29 | Seal Sands Chemicals Limited | Preparation of pyridene derivatives |
US6174548B1 (en) | 1998-08-28 | 2001-01-16 | Andrx Pharmaceuticals, Inc. | Omeprazole formulation |
US6096340A (en) * | 1997-11-14 | 2000-08-01 | Andrx Pharmaceuticals, Inc. | Omeprazole formulation |
US6350876B2 (en) | 1998-01-26 | 2002-02-26 | Kuraray Co., Ltd. | 4-chloro-3,5-dimethyl-2-sulfonyl pyridines |
KR100396431B1 (ko) * | 1998-01-26 | 2003-09-02 | 가부시키가이샤 구라레 | 2-술포닐피리딘 유도체 및 2-[((2-피리딜)메틸)티오]-1h-벤즈이 |
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 |
WO2000000474A1 (en) * | 1998-06-26 | 2000-01-06 | Russinsky Limited | Pyridine building blocks as intermediates in the synthesis of pharmaceutically active compounds |
US6733778B1 (en) | 1999-08-27 | 2004-05-11 | Andrx Pharmaceuticals, Inc. | Omeprazole formulation |
US6362202B1 (en) | 1999-03-02 | 2002-03-26 | Sepracor Inc. | Methods and compositions using (−) norcisapride in combination with proton pump inhibitors or H2 receptor antagonists |
US6353005B1 (en) | 1999-03-02 | 2002-03-05 | Sepracor, Inc. | Method and compositions using (+) norcisapride in combination with proton pump inhibitors or H2 receptor antagonist |
US6555139B2 (en) | 1999-06-28 | 2003-04-29 | Wockhardt Europe Limited | Preparation of micron-size pharmaceutical particles by microfluidization |
US6245913B1 (en) | 1999-06-30 | 2001-06-12 | Wockhardt Europe Limited | Synthetic procedure for 5-methoxy-2-[(4-methoxy-3,5-dimethyl-2-pyridinyl)-methylthio]-IH-benzimidazole hydrochloride and its conversion to omeprazole |
US6262085B1 (en) | 1999-08-26 | 2001-07-17 | Robert R. Whittle | Alkoxy substituted Benzimidazole compounds, pharmaceutical preparations containing the same, and methods of using the same |
US6312712B1 (en) | 1999-08-26 | 2001-11-06 | Robert R. Whittle | Method of improving bioavailability |
US6369087B1 (en) | 1999-08-26 | 2002-04-09 | Robert R. Whittle | Alkoxy substituted benzimidazole compounds, pharmaceutical preparations containing the same, and methods of using the same |
US6780880B1 (en) | 1999-08-26 | 2004-08-24 | Robert R. Whittle | FT-Raman spectroscopic measurement |
US6326384B1 (en) | 1999-08-26 | 2001-12-04 | Robert R. Whittle | Dry blend pharmaceutical unit dosage form |
US6268385B1 (en) | 1999-08-26 | 2001-07-31 | Robert R. Whittle | Dry blend pharmaceutical formulations |
US6262086B1 (en) | 1999-08-26 | 2001-07-17 | Robert R. Whittle | Pharmaceutical unit dosage form |
US6316020B1 (en) | 1999-08-26 | 2001-11-13 | Robert R. Whittle | Pharmaceutical formulations |
US6312723B1 (en) | 1999-08-26 | 2001-11-06 | Robert R. Whittle | Pharmaceutical unit dosage form |
GB9921578D0 (en) * | 1999-09-13 | 1999-11-17 | Cipla Limited | Omeprazole synthesis |
ES2171116B1 (es) | 2000-04-14 | 2003-08-01 | Esteve Quimica Sa | Procedimiento para la obtencion de derivados de (((piridil sustituido)metil)tio)bencimidazol. |
AU2000258410A1 (en) * | 2000-07-28 | 2003-12-02 | Herbex, Produtos Quimicos, Sa | New method for the preparation of the anti-ulcer compounds omeprazole, lansoprazole and pantoprazole |
ATE429431T1 (de) | 2001-05-11 | 2009-05-15 | Tibotec Pharm Ltd | 2-amino-benzoxazol-suphonamide als breitspektrum- hiv-protease-inhibitoren |
WO2003063840A2 (en) * | 2002-01-25 | 2003-08-07 | Santarus, Inc. | Transmucosal delivery of proton pump inhibitors |
FR2848555B1 (fr) | 2002-12-16 | 2006-07-28 | Negma Gild | Enantiomere(-)du tenatoprazole et son application en therapeutique |
US8993599B2 (en) | 2003-07-18 | 2015-03-31 | 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 |
US8906940B2 (en) | 2004-05-25 | 2014-12-09 | Santarus, Inc. | Pharmaceutical formulations useful for inhibiting acid secretion and methods for making and using them |
CN100376574C (zh) * | 2006-06-14 | 2008-03-26 | 浙江大学 | 泰妥拉唑的制备方法 |
EA200900985A1 (ru) | 2007-01-31 | 2009-12-30 | Крка, Товарна Здравил, Д. Д., Ново Место | Способ получения оптически чистого омепразола |
CN101648912B (zh) * | 2009-09-14 | 2012-07-04 | 南京第一农药集团有限公司 | 一种4-硝基-3,5-二甲基吡啶-n-氧化物的连续化制备方法 |
CN101648907B (zh) * | 2009-09-14 | 2011-08-03 | 南京第一农药集团有限公司 | 2-氯甲基-4-甲氧基-3,5-二甲基吡啶盐酸盐的纯化方法 |
CN102603620B (zh) * | 2012-01-13 | 2014-10-29 | 江苏中邦制药有限公司 | 一种氯甲基吡啶或其吡啶衍生物盐酸盐的合成方法 |
WO2021061991A1 (en) | 2019-09-24 | 2021-04-01 | Prolacta Bioscience, Inc. | Compositions and methods for treatment of inflammatory and immune diseases |
CN112142653B (zh) * | 2020-10-22 | 2022-02-11 | 成都百泉生物医药科技有限公司 | 奥美拉唑中间体的制备方法 |
CN113307773A (zh) * | 2021-06-17 | 2021-08-27 | 上海毕得医药科技股份有限公司 | 6-溴-3-甲氧基-1-苯基-1h-吲唑及其合成方法和应用 |
CN114805193B (zh) * | 2022-04-19 | 2023-06-20 | 南京红太阳医药研究院有限公司 | 一种奥美拉唑中间体的制备方法 |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2735851A (en) * | 1956-02-21 | Alkanolpykroine-n-oxides | ||
US2663711A (en) * | 1951-12-08 | 1953-12-22 | Du Pont | Process for the preparation of pyridine alcohols from pyridine n-oxides |
GB1564502A (en) * | 1975-07-31 | 1980-04-10 | Smith Kline French Lab | Guanidines thioureas and 1,1-diamino-2-nitroethylene derivatives |
SE7804231L (sv) * | 1978-04-14 | 1979-10-15 | Haessle Ab | Magsyrasekretionsmedel |
US4472409A (en) * | 1981-11-05 | 1984-09-18 | Byk Gulden Lomberg Chemische Fabrik Gesellschaft Mit Beschrankter Haftung | 2-Pyridylmethyl thio(sulfinyl)benzimidazoles with gastric acid secretion inhibiting effects |
KR840002371A (ko) * | 1981-11-05 | 1984-06-25 | 귄터 미카엘, 헤르페르트 수키 | 치환된 벤즈 이미다졸의 제조방법 |
-
1982
- 1982-08-26 SE SE8204879A patent/SE8204879D0/xx unknown
-
1983
- 1983-06-30 DE DE8383850185T patent/DE3379222D1/de not_active Expired
- 1983-06-30 AT AT83850185T patent/ATE40884T1/de not_active IP Right Cessation
- 1983-06-30 DE DE198383850185T patent/DE103553T1/de active Pending
- 1983-06-30 EP EP83850185A patent/EP0103553B1/en not_active Expired
- 1983-07-06 IL IL69175A patent/IL69175A/xx not_active IP Right Cessation
- 1983-07-06 CA CA000431863A patent/CA1234118A/en not_active Expired
- 1983-07-14 ZA ZA835143A patent/ZA835143B/xx unknown
- 1983-07-20 AU AU17101/83A patent/AU560028B2/en not_active Expired
- 1983-07-20 NZ NZ204959A patent/NZ204959A/en unknown
- 1983-07-20 OA OA58065A patent/OA07498A/xx unknown
- 1983-07-28 IE IE1787/83A patent/IE55865B1/en not_active IP Right Cessation
- 1983-08-02 NO NO832794A patent/NO164093C/no not_active IP Right Cessation
- 1983-08-08 PH PH29368A patent/PH17786A/en unknown
- 1983-08-18 DD DD83254056A patent/DD233126A5/de unknown
- 1983-08-19 DK DK381583A patent/DK381583A/da not_active Application Discontinuation
- 1983-08-24 ES ES525122A patent/ES8404993A1/es not_active Expired
- 1983-08-25 JP JP58154250A patent/JPS5959662A/ja active Granted
- 1983-08-25 GB GB08322866A patent/GB2126226B/en not_active Expired
- 1983-08-25 CY CY1328A patent/CY1328A/xx unknown
- 1983-08-25 HU HU832987A patent/HU189738B/hu unknown
- 1983-08-25 FI FI833047A patent/FI79701C/fi not_active IP Right Cessation
- 1983-08-25 PT PT77249A patent/PT77249B/pt unknown
- 1983-08-26 KR KR1019830004003A patent/KR880000091B1/ko not_active IP Right Cessation
- 1983-08-26 US US06/526,900 patent/US4544750A/en not_active Expired - Lifetime
- 1983-08-26 IS IS2845A patent/IS1438B6/is unknown
- 1983-08-26 GR GR72304A patent/GR79374B/el unknown
-
1985
- 1985-02-01 US US06/697,396 patent/US4620008A/en not_active Expired - Lifetime
-
1986
- 1986-03-20 HK HK194/86A patent/HK19486A/xx not_active IP Right Cessation
- 1986-12-30 MY MY503/86A patent/MY8600503A/xx unknown
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2067407A1 (es) * | 1991-11-21 | 1995-03-16 | Genesis Para La Investigacion | Perfeccionamientos en el objeto de la patente 9102594 por procedimiento de obtencion de derivados de piridina. |
ES2105953A1 (es) * | 1991-11-21 | 1997-10-16 | Genesis Para La Investigacion | Perfeccionamientos en el objeto de la patente de invencion 9102594 por procedimiento de obtencion de compuestos derivados de piridina. |
ES2060541A1 (es) * | 1993-02-26 | 1994-11-16 | Vinas Lab | Nuevo procedimiento para la sintesis de un derivado de 2-(2-piridilmetilsufinil) bencimidazol, y nuevos productos intermedios obtenidos con el mismo. |
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