JPH0143757B2 - - Google Patents

Info

Publication number
JPH0143757B2
JPH0143757B2 JP56021600A JP2160081A JPH0143757B2 JP H0143757 B2 JPH0143757 B2 JP H0143757B2 JP 56021600 A JP56021600 A JP 56021600A JP 2160081 A JP2160081 A JP 2160081A JP H0143757 B2 JPH0143757 B2 JP H0143757B2
Authority
JP
Japan
Prior art keywords
formula
group
amino
compound
cef
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
Application number
JP56021600A
Other languages
English (en)
Japanese (ja)
Other versions
JPS56128786A (en
Inventor
Rene Heymes
Didier Pronine
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sanofi Aventis France
Original Assignee
Roussel Uclaf SA
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Roussel Uclaf SA filed Critical Roussel Uclaf SA
Publication of JPS56128786A publication Critical patent/JPS56128786A/ja
Publication of JPH0143757B2 publication Critical patent/JPH0143757B2/ja
Granted legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D277/587—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with aliphatic hydrocarbon radicals substituted by 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, said aliphatic radicals being substituted in the alpha-position to the ring by a hetero atom, e.g. with m >= 0, Z being a singly or a doubly bound hetero atom
    • 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
    • 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
    • C07D501/14—Compounds having a nitrogen atom directly attached in position 7
    • C07D501/16—Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
    • C07D501/20—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids
    • C07D501/24—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids with hydrocarbon radicals, substituted by hetero atoms or hetero rings, attached in position 3
    • C07D501/26—Methylene radicals, substituted by oxygen atoms; Lactones thereof with the 2-carboxyl group
    • C07D501/34—Methylene radicals, substituted by oxygen atoms; Lactones thereof with the 2-carboxyl group with the 7-amino radical acylated by carboxylic acids containing hetero rings
    • 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
    • C07D501/14—Compounds having a nitrogen atom directly attached in position 7
    • C07D501/16—Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
    • C07D501/20—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids
    • C07D501/24—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids with hydrocarbon radicals, substituted by hetero atoms or hetero rings, attached in position 3
    • C07D501/36—Methylene radicals, substituted by sulfur atoms
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/50—Improvements relating to the production of bulk chemicals
    • Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Communicable Diseases (AREA)
  • Animal Behavior & Ethology (AREA)
  • Oncology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Cephalosporin Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
JP2160081A 1980-02-18 1981-02-18 Novel oxime derivatives of 3-alkyloxy or 3-alkylthiomethyl-7-aminothiazolylacetamidocephalosporanic acid, their manufacture, their use as drug, drug containing them and novel intermediate Granted JPS56128786A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR8003479A FR2476087A1 (fr) 1980-02-18 1980-02-18 Nouvelles oximes derivees de l'acide 3-alkyloxy ou 3-alkyl-thiomethyl 7-amino thiazolyl acetamido cephalosporanique, leur procede de preparation et leur application comme medicaments
FR8214575A FR2532313A2 (fr) 1980-02-18 1982-08-25 Nouvelles oximes derivees de l'acide 3-alkyloxy ou 3-alkylthio-methyl 7-aminothiazolyl acetamido cephalosporanique, leur procede de preparation et leur application comme medicaments

Publications (2)

Publication Number Publication Date
JPS56128786A JPS56128786A (en) 1981-10-08
JPH0143757B2 true JPH0143757B2 (en, 2012) 1989-09-22

Family

ID=26221608

Family Applications (3)

Application Number Title Priority Date Filing Date
JP2160081A Granted JPS56128786A (en) 1980-02-18 1981-02-18 Novel oxime derivatives of 3-alkyloxy or 3-alkylthiomethyl-7-aminothiazolylacetamidocephalosporanic acid, their manufacture, their use as drug, drug containing them and novel intermediate
JP58019848A Expired - Lifetime JPH0794462B2 (ja) 1980-02-18 1983-02-10 ３−アルキルオキシ又は３−アルキルチオメチル−７−アミノチアゾリルアセトアミドセファロスポラン酸の新規なオキシム誘導体、それらの製造法及びそれらを含む薬剤
JP63051810A Expired - Lifetime JPH0639476B2 (ja) 1980-02-18 1988-03-07 ３‐アルキルオキシ又は３‐アルキルチオメチル‐７‐アミノチアゾリルアセトアミドセフアロスポラン酸の新規なオキシム誘導体

Family Applications After (2)

Application Number Title Priority Date Filing Date
JP58019848A Expired - Lifetime JPH0794462B2 (ja) 1980-02-18 1983-02-10 ３−アルキルオキシ又は３−アルキルチオメチル−７−アミノチアゾリルアセトアミドセファロスポラン酸の新規なオキシム誘導体、それらの製造法及びそれらを含む薬剤
JP63051810A Expired - Lifetime JPH0639476B2 (ja) 1980-02-18 1988-03-07 ３‐アルキルオキシ又は３‐アルキルチオメチル‐７‐アミノチアゾリルアセトアミドセフアロスポラン酸の新規なオキシム誘導体

Country Status (14)

Country Link
US (1) US4992431A (en, 2012)
EP (1) EP0034536B1 (en, 2012)
JP (3) JPS56128786A (en, 2012)
AT (1) ATE10941T1 (en, 2012)
AU (1) AU542325B2 (en, 2012)
CA (1) CA1181740A (en, 2012)
DE (3) DE3167891D1 (en, 2012)
ES (2) ES8206520A1 (en, 2012)
FR (2) FR2476087A1 (en, 2012)
GR (1) GR73815B (en, 2012)
HU (1) HU185628B (en, 2012)
PT (1) PT72512B (en, 2012)
SU (1) SU1194279A3 (en, 2012)
ZA (1) ZA81800B (en, 2012)

Families Citing this family (45)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4409215A (en) * 1979-11-19 1983-10-11 Fujisawa Pharmaceutical Co., Ltd. 7-Acylamino-3-substituted cephalosporanic acid derivatives and processes for the preparation thereof
US5243043A (en) * 1980-02-18 1993-09-07 Roussel Uclaf Cephalosporins
FR2482587A1 (fr) * 1980-05-14 1981-11-20 Poudres & Explosifs Ste Nale Procede de synthese de chloroformiates a-chlores et nouveaux chloroformiates a-chlores
JPS5759894A (en) * 1980-09-30 1982-04-10 Sankyo Co Ltd Cephalosporin for oral administration
US4486425A (en) * 1980-09-30 1984-12-04 Sankyo Company Limited 7-[2-(2-Aminothiazol-4-yl)-2-(syn)-methoxyiminoacetamido]-3-methoxymethyl-3-cephem-4-carboxylates
FR2499995A1 (fr) * 1981-02-13 1982-08-20 Roussel Uclaf Nouvelles oximes derivees de l'acide 3-alkyloxy ou 3-alkylthiomethyl 7-amino thiazolylacetamido cephalosporanique, leur preparation, leur application comme medicaments, les compositions les renfermant et les nouveaux intermediaires obtenus.
JPS5896091A (ja) * 1981-12-01 1983-06-07 Sankyo Co Ltd ３−アルコキシメチルセフアロスポリン類の製造法
JPS5965094A (ja) * 1982-10-06 1984-04-13 Sumitomo Chem Co Ltd セフアロスポリン化合物の製造法
JPS5984889A (ja) * 1982-11-05 1984-05-16 Sumitomo Chem Co Ltd セフアロスポリン誘導体およびその製造方法
US4499088A (en) * 1983-01-04 1985-02-12 Fujisawa Pharmaceutical Co., Ltd. Cephem compounds
JPS58159496A (ja) * 1983-03-02 1983-09-21 Kyoto Yakuhin Kogyo Kk セフエム系化合物
FR2551058B1 (fr) * 1983-08-26 1986-09-26 Poudres & Explosifs Ste Nale Procede de preparation de chloroformiates a-chlores
GB8329030D0 (en) * 1983-10-31 1983-11-30 Fujisawa Pharmaceutical Co Cephem compounds
GB8400024D0 (en) * 1984-01-03 1984-02-08 Glaxo Group Ltd Cephalosporin antibiotics
JPH0631259B2 (ja) * 1984-02-17 1994-04-27 三共株式会社 経口用セフアロスポリン化合物
JPH0613530B2 (ja) * 1984-06-08 1994-02-23 武田薬品工業株式会社 セフエム化合物
JPS6140291A (ja) * 1984-07-31 1986-02-26 Shionogi & Co Ltd ヒドロキシアルキルチオセフアロスポリン
JPS63269027A (ja) * 1987-04-25 1988-11-07 Sukegawa Denki Kogyo Kk シース型測温ケーブルの接続端子
DK637888A (da) * 1987-11-24 1989-05-25 Hoffmann La Roche Carboxylsyreestere
DE3804841A1 (de) * 1988-02-17 1989-08-31 Hoechst Ag Cephalosporinderivate und verfahren zu ihrer herstellung
IT1224252B (it) * 1988-04-08 1990-09-26 Sclavo Spa Metodo di protezione del gruppo carbossilico nella chimica dei composti beta lattamici
DK492289A (da) * 1988-10-07 1990-04-08 Sankyo Co 3-aryloxymethyl-cephalosporinderivater og fremgangsmaade til fremstilling deraf samt farmaceutisk middel indeholdende derivaterne
DE3901405A1 (de) * 1989-01-19 1990-07-26 Hoechst Ag Cephalosporinderivate und verfahren zu ihrer herstellung
DE3910093A1 (de) * 1989-03-29 1990-10-04 Hoechst Ag Cephalosporinderivate und verfahren zu ihrer herstellung
DE3919259A1 (de) * 1989-06-13 1990-12-20 Hoechst Ag Kristalline cephem-saeureadditionssalze und verfahren zu ihrer herstellung
YU48484B (sh) * 1991-05-24 1998-09-18 Hoechst Aktiengesellschaft Kristalne kiselinske adicione soli diastereomerno čistih 1-(2,2-dimetilpropioniloksi)-etilestara 3-cefem-4-karbonske kiseline
ES2215161T3 (es) * 1991-09-07 2004-10-01 Aventis Pharma Deutschland Gmbh Diastereoisomero del ester 1-(isopropoxicarboniloxi)-etilico del acido 3-cefem-4-carboxilico y procedimiento para su preparacion.
TW212181B (en, 2012) * 1992-02-14 1993-09-01 Hoechst Ag
DE59308295D1 (de) * 1992-05-21 1998-04-30 Hoechst Ag Verfahren zur Spaltung von Cephalosporin Prodrugestern zu 7-Amino-3-methoxymethylceph-3-em-4-carbonsäure
FR2716110B1 (fr) 1994-02-16 1996-04-05 Roussel Uclaf Compositions cosmétiques ou pharmaceutiques comprenant des liposomes.
WO2000068234A2 (en) * 1999-05-07 2000-11-16 Ranbaxy Laboratories Limited Process for the preparation of cefpodoxime acid
ES2260031T3 (es) * 1999-08-06 2006-11-01 Janssen Pharmaceutica N.V. Derivados de 6-azauracilo que inhiben la interleucina-5.
IL159300A0 (en) * 2001-06-11 2004-06-01 Xenoport Inc Prodrugs of gaba analogs, compositions and uses thereof
US7186855B2 (en) 2001-06-11 2007-03-06 Xenoport, Inc. Prodrugs of GABA analogs, compositions and uses thereof
US7232924B2 (en) 2001-06-11 2007-06-19 Xenoport, Inc. Methods for synthesis of acyloxyalkyl derivatives of GABA analogs
US8048917B2 (en) 2005-04-06 2011-11-01 Xenoport, Inc. Prodrugs of GABA analogs, compositions and uses thereof
US6818787B2 (en) 2001-06-11 2004-11-16 Xenoport, Inc. Prodrugs of GABA analogs, compositions and uses thereof
KR20070026295A (ko) * 2003-08-25 2007-03-08 레박스 파마슈티칼즈, 엘엘씨 경구 신경치료 세파졸린 조성물
EP1621536A1 (en) 2004-07-27 2006-02-01 Aventis Pharma S.A. Amino cyclic urea derivatives, preparation thereof and pharmaceutical use thereof as kinase inhibitors
FR2896504B1 (fr) 2006-01-23 2012-07-13 Aventis Pharma Sa Nouveaux derives d'uree cyclique, leur preparation et leur utilisation pharmaceutique comme inhibiteurs de kinases
JP5013795B2 (ja) * 2006-09-25 2012-08-29 Ｍｅｉｊｉ Ｓｅｉｋａファルマ株式会社 経口投与用カルバペネム
FR2907453B1 (fr) 2006-10-24 2008-12-26 Sanofi Aventis Sa Nouveaux derives du fluorene,compositions les contenant et utilisation
AR077405A1 (es) 2009-07-10 2011-08-24 Sanofi Aventis Derivados del indol inhibidores de hsp90, composiciones que los contienen y utilizacion de los mismos para el tratamiento del cancer
FR2949467B1 (fr) 2009-09-03 2011-11-25 Sanofi Aventis Nouveaux derives de 5,6,7,8-tetrahydroindolizine inhibiteurs d'hsp90, compositions les contenant et utilisation
CN102417451B (zh) * 2011-12-20 2013-12-04 浙江国邦药业有限公司 一种合成（r，s）1-溴代乙基乙酸酯的制备方法

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS502518B1 (en, 2012) * 1970-12-24 1975-01-27
GB1399086A (en) * 1971-05-14 1975-06-25 Glaxo Lab Ltd Cephalosporin compounds
DE2760484C2 (en, 2012) * 1976-04-14 1992-12-03 Takeda Chemical Industries, Ltd., Osaka, Jp
JPS6011713B2 (ja) * 1976-09-08 1985-03-27 武田薬品工業株式会社 セフアロスポリン誘導体およびその製造法
GB1565941A (en) * 1977-02-08 1980-04-23 Toyama Chemical Co Ltd Process for producing 7-(substituted)amino-3-substituted thiomethyl cephem carboxylic acids
JPS53103493A (en) * 1977-02-18 1978-09-08 Takeda Chem Ind Ltd Cephalosporin derivatives and process for their preparation
PH17188A (en) * 1977-03-14 1984-06-14 Fujisawa Pharmaceutical Co New cephem and cepham compounds and their pharmaceutical compositions and method of use
DE2714880A1 (de) * 1977-04-02 1978-10-26 Hoechst Ag Cephemderivate und verfahren zu ihrer herstellung
DE2716677C2 (de) * 1977-04-15 1985-10-10 Hoechst Ag, 6230 Frankfurt Cephemderivate und Verfahren zu ihrer Herstellung
FR2410655A1 (fr) * 1977-12-05 1979-06-29 Roussel Uclaf Nouvelles oximes derivees de l'acide 3-substitue 7-amino thiazolyl acetamido cephalosporanique, leur procede de preparation et leur application comme medicaments
US4409215A (en) * 1979-11-19 1983-10-11 Fujisawa Pharmaceutical Co., Ltd. 7-Acylamino-3-substituted cephalosporanic acid derivatives and processes for the preparation thereof
ZA806977B (en) * 1979-11-19 1981-10-28 Fujisawa Pharmaceutical Co 7-acylamino-3-vinylcephalosporanic acid derivatives and processes for the preparation thereof
JPS5759894A (en) * 1980-09-30 1982-04-10 Sankyo Co Ltd Cephalosporin for oral administration

Also Published As

Publication number Publication date
ZA81800B (en) 1982-02-24
PT72512B (fr) 1982-10-21
US4992431A (en) 1991-02-12
EP0034536A3 (en) 1981-11-04
FR2532313A2 (fr) 1984-03-02
ES509128A0 (es) 1983-01-01
EP0034536A2 (fr) 1981-08-26
GR73815B (en, 2012) 1984-04-18
FR2476087A1 (fr) 1981-08-21
ES499487A0 (es) 1982-08-16
CA1181740A (fr) 1985-01-29
AU6738181A (en) 1981-08-27
JPS58170789A (ja) 1983-10-07
JPH0639476B2 (ja) 1994-05-25
JPS6452784A (en) 1989-02-28
JPS56128786A (en) 1981-10-08
DE3177186D1 (de) 1990-06-28
DE3167891D1 (en) 1985-02-07
ES8206520A1 (es) 1982-08-16
PT72512A (fr) 1981-03-01
ES8302003A1 (es) 1983-01-01
JPH0794462B2 (ja) 1995-10-11
FR2476087B1 (en, 2012) 1983-07-18
HU185628B (en) 1985-03-28
SU1194279A3 (ru) 1985-11-23
AU542325B2 (en) 1985-02-21
FR2532313B2 (en, 2012) 1985-03-22
EP0034536B1 (fr) 1984-12-27
ATE10941T1 (de) 1985-01-15
DE3177185D1 (de) 1990-06-28

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