ES2175167T3 - Procedimiento para la preparacion de cefdinir. - Google Patents
Procedimiento para la preparacion de cefdinir.Info
- Publication number
- ES2175167T3 ES2175167T3 ES96943357T ES96943357T ES2175167T3 ES 2175167 T3 ES2175167 T3 ES 2175167T3 ES 96943357 T ES96943357 T ES 96943357T ES 96943357 T ES96943357 T ES 96943357T ES 2175167 T3 ES2175167 T3 ES 2175167T3
- Authority
- ES
- Spain
- Prior art keywords
- cefdinir
- pct
- date
- preparation
- sec
- 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 - Lifetime
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D501/00—Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
Abstract
LA PRESENTE INVENCION TRATA DE UN NUEVO COMPUESTO INTERMEDIO CRISTALINO DE CEFDINIR CON FORMULA (II) QUE SE PUEDE UTILIZAR MUY BIEN PARA PREPARAR UN ANTIBIOTICO DE CEFALOSPORINA, CEFDINIR, EN LA CUAL PH SIGNIFICA FENILO, P - TSOH REPRESENTA ACIDO P TOLUENSULFONICO Y DMAC REPRESENTA N,N - DIMETILACETAMIDA, TAMBIEN TRATA DE UN PROCEDIMIENTO PARA SU PREPARACION Y DE UN PROCEDIMIENTO PARA PREPARAR CEFDINIR UTILIZANDO EL COMPUESTO DE FORMULA (II). SEGUN LA PRESENTE INVENCION, CEFDINIR SE PUEDE PREPARAR CON UN BUEN RENDIMIENTO Y CON EXCELENTE COLOR Y PUREZA.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1019950058694A KR0174432B1 (ko) | 1995-12-27 | 1995-12-27 | 신규한 결정성 세프디니르 중간체 및 그의 제조방법 |
KR1019950058695A KR0174431B1 (ko) | 1995-12-27 | 1995-12-27 | 세프디니르의 제조방법 |
Publications (1)
Publication Number | Publication Date |
---|---|
ES2175167T3 true ES2175167T3 (es) | 2002-11-16 |
Family
ID=26631527
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES96943357T Expired - Lifetime ES2175167T3 (es) | 1995-12-27 | 1996-12-26 | Procedimiento para la preparacion de cefdinir. |
Country Status (9)
Country | Link |
---|---|
US (1) | US6093814A (es) |
EP (1) | EP0874853B1 (es) |
JP (1) | JP3948628B2 (es) |
AT (1) | ATE218572T1 (es) |
DE (1) | DE69621649T2 (es) |
DK (1) | DK0874853T3 (es) |
ES (1) | ES2175167T3 (es) |
PT (1) | PT874853E (es) |
WO (1) | WO1997024358A1 (es) |
Families Citing this family (35)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5883247A (en) * | 1996-06-10 | 1999-03-16 | Hoffmann-La Roche Inc. | Preparation of cephem and isooxacephem derivatives |
AT405283B (de) | 1997-04-04 | 1999-06-25 | Biochemie Gmbh | Neues kristallines 7-(z)-(2-(2-aminothiazol-4-yl) -2-hydroxyiminoacetamido)-3-vinyl-3-cephem-4- carbonsäure dicyclohexylammoniumsalz und verfahren zu dessen herstellung |
US20080113025A1 (en) * | 1998-11-02 | 2008-05-15 | Elan Pharma International Limited | Compositions comprising nanoparticulate naproxen and controlled release hydrocodone |
JP4544692B2 (ja) * | 2000-04-13 | 2010-09-15 | 大塚化学株式会社 | 3−ビニル−セフェム化合物の製造方法 |
KR100451672B1 (ko) * | 2001-06-05 | 2004-10-08 | 한미약품 주식회사 | 결정성 세프디니르 산부가염, 이의 제조방법 및 이를이용한 세프디니르의 제조방법 |
ITMI20012364A1 (it) * | 2001-11-09 | 2003-05-09 | Antibioticos Spa | Processo di sintesi della cefixima via alchil-o arilsolfonati |
JP2005516011A (ja) * | 2001-12-13 | 2005-06-02 | ランバクシー ラボラトリーズ リミテッド | 結晶二水化セフニディールカリウム |
EA200401428A1 (ru) * | 2002-04-26 | 2006-04-28 | Рэнбакси Лабораториз Лимитед | Способ получения цефдинира |
ITMI20020913A0 (it) * | 2002-04-29 | 2002-04-29 | Acs Dobfar Spa | Nuova forma cristallina del cefdinir |
KR20050087776A (ko) * | 2002-08-13 | 2005-08-31 | 산도즈 아게 | 세프디니르 중간체 |
ITMI20022076A1 (it) * | 2002-10-01 | 2004-04-02 | Antibioticos Spa | Sali di intermedi del cefdinir. |
EP1609793A4 (en) * | 2003-03-24 | 2008-06-25 | Sandoz Ag | NOVEL 7- 2- (2-AMINOTHIAZOLE-4-YL) -2-HYDROXYIMIN OACETAMIDO-3-VINYL-3-CEPHEM-4-CARBOXYLIC ACID CRYSTAL (SYNTHETIC ISOMER) AND PROCESS FOR PREPARING THE SAME |
WO2004104010A1 (en) * | 2003-05-20 | 2004-12-02 | Ranbaxy Laboratories Limited | Crystalline form of cefdinir |
US20050137182A1 (en) * | 2003-06-02 | 2005-06-23 | Ramesh Dandala | Novel crystalline form of cefdinir |
US20040242556A1 (en) * | 2003-06-02 | 2004-12-02 | Ramesh Dandala | Novel crystalline form of cefdinir |
US20050113355A1 (en) * | 2003-09-12 | 2005-05-26 | Duerst Richard W. | Cefdinir pyridine salt |
US20050059818A1 (en) * | 2003-09-12 | 2005-03-17 | Duerst Richard W. | Polymorph of a pharmaceutical |
US20050059819A1 (en) * | 2003-09-12 | 2005-03-17 | Duerst Richard W. | Cefdinir pyridine salt |
US20060211676A1 (en) * | 2004-03-16 | 2006-09-21 | Devalina Law | Crystalline anhydrous cefdinir and crystalline cefdinir hydrates |
US20060142563A1 (en) * | 2004-03-16 | 2006-06-29 | Devalina Law | Crystalline anhydrous cefdinir and crystalline cefdinir hydrates |
US20060142261A1 (en) * | 2004-03-16 | 2006-06-29 | Devalina Law | Crystalline anhydrous cefdinir and crystalline cefdinir hydrates |
US20050209211A1 (en) * | 2004-03-16 | 2005-09-22 | Devalina Law | Trihemihydrate, anhydrate and novel hydrate forms of Cefdinir |
US20060069079A1 (en) * | 2004-09-27 | 2006-03-30 | Sever Nancy E | Stable amorphous cefdinir |
US20050245738A1 (en) * | 2004-05-03 | 2005-11-03 | Lupin Ltd | Stable bioavailable crystalline form or cefdinir and a process for the preparation thereof |
WO2006010978A1 (en) * | 2004-06-30 | 2006-02-02 | Wockhardt Limited | Cefdinir polymorphic forms, and imidazole salt |
WO2006018807A1 (en) * | 2004-08-16 | 2006-02-23 | Ranbaxy Laboratories Limited | Crystalline forms of cefdinir |
MX2007006018A (es) * | 2004-11-30 | 2007-06-07 | Astellas Pharma Inc | Suspension farmaceutica oral novedosa de cristal de cefdinir. |
KR20080064990A (ko) * | 2005-10-31 | 2008-07-10 | 테바 파마슈티컬 인더스트리즈 리미티드 | 세프디니르의 제조방법 |
US20070128268A1 (en) * | 2005-12-07 | 2007-06-07 | Herwig Jennewein | Pharmaceutical compositions comprising an antibiotic |
US8466096B2 (en) * | 2007-04-26 | 2013-06-18 | Afton Chemical Corporation | 1,3,2-dioxaphosphorinane, 2-sulfide derivatives for use as anti-wear additives in lubricant compositions |
ITMI20071628A1 (it) | 2007-08-06 | 2007-11-05 | Acs Dobfar Spa | Sintesi di 3-alchenilcefalosporine e nuovi intermedi utili ad esse correlati |
KR101058135B1 (ko) * | 2008-04-04 | 2011-08-24 | 대웅바이오 주식회사 | 세프디니르 합성에 유용한 중간체 및 이를 이용하여세프디니르를 제조하는 방법 |
CN101481383B (zh) * | 2008-12-31 | 2012-01-11 | 杭州奥默医药技术有限公司 | 头孢地尼酸式复盐化合物及制备方法 |
CN102020664B (zh) * | 2010-11-30 | 2012-12-12 | 浙江工业大学 | 一种头孢地尼的合成方法 |
CN103319503A (zh) * | 2013-06-09 | 2013-09-25 | 四川方向药业有限责任公司 | 一种头孢地尼的制备方法 |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DK162718C (da) * | 1982-09-30 | 1992-05-11 | Fujisawa Pharmaceutical Co | Analogifremgangsmaade til fremstilling af 7-substitueret-3-vinyl-3-cephemforbindelser |
IL99898A (en) * | 1990-11-09 | 1996-10-31 | Eisai Co Ltd | 7-Noble-3- Compounds Transformed Carbamoylloxy |
TW212181B (es) * | 1992-02-14 | 1993-09-01 | Hoechst Ag | |
EP0720611A1 (en) * | 1994-07-22 | 1996-07-10 | Antibioticos S.P.A. | Glutaryl 7-aca derivatives and processes for obtaining them |
-
1996
- 1996-12-26 ES ES96943357T patent/ES2175167T3/es not_active Expired - Lifetime
- 1996-12-26 WO PCT/KR1996/000250 patent/WO1997024358A1/en active IP Right Grant
- 1996-12-26 DE DE69621649T patent/DE69621649T2/de not_active Expired - Lifetime
- 1996-12-26 EP EP96943357A patent/EP0874853B1/en not_active Expired - Lifetime
- 1996-12-26 US US09/068,719 patent/US6093814A/en not_active Expired - Lifetime
- 1996-12-26 PT PT96943357T patent/PT874853E/pt unknown
- 1996-12-26 JP JP52423097A patent/JP3948628B2/ja not_active Expired - Lifetime
- 1996-12-26 DK DK96943357T patent/DK0874853T3/da active
- 1996-12-26 AT AT96943357T patent/ATE218572T1/de not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
JP2000502700A (ja) | 2000-03-07 |
US6093814A (en) | 2000-07-25 |
EP0874853A1 (en) | 1998-11-04 |
DE69621649T2 (de) | 2002-09-19 |
WO1997024358A1 (en) | 1997-07-10 |
DK0874853T3 (da) | 2002-09-23 |
EP0874853B1 (en) | 2002-06-05 |
JP3948628B2 (ja) | 2007-07-25 |
PT874853E (pt) | 2002-09-30 |
DE69621649D1 (de) | 2002-07-11 |
ATE218572T1 (de) | 2002-06-15 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FG2A | Definitive protection |
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