FI109027B - Menetelmä kefeemi-esilääke-esterien valmistamiseksi, menetelmässä käyttökelpoisia yhdisteitä, menetelmä näiden yhdisteiden valmistamiseksi ja niiden käyttö - Google Patents

Menetelmä kefeemi-esilääke-esterien valmistamiseksi, menetelmässä käyttökelpoisia yhdisteitä, menetelmä näiden yhdisteiden valmistamiseksi ja niiden käyttö Download PDF

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Publication number
FI109027B
FI109027B FI930604A FI930604A FI109027B FI 109027 B FI109027 B FI 109027B FI 930604 A FI930604 A FI 930604A FI 930604 A FI930604 A FI 930604A FI 109027 B FI109027 B FI 109027B
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FI
Finland
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formula
compound
acid
ethyl
preparation
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FI930604A
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English (en)
Finnish (fi)
Swedish (sv)
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FI930604A (fi
FI930604A0 (fi
Inventor
Rudolf Lattrell
Rolf Hoerlein
Theodor Wollmann
Gerd Fischer
Ulrich Stache
Elisabeth Defossa
Uwe Gerlach
Norbert Krass
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Hoechst Ag
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Publication of FI930604A publication Critical patent/FI930604A/fi
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D501/00Heterocyclic 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
    • C07D501/14Compounds having a nitrogen atom directly attached in position 7
    • C07D501/16Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
    • C07D501/207-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids
    • C07D501/247-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
    • C07D501/26Methylene radicals, substituted by oxygen atoms; Lactones thereof with the 2-carboxyl group
    • C07D501/34Methylene radicals, substituted by oxygen atoms; Lactones thereof with the 2-carboxyl group with the 7-amino radical acylated by carboxylic acids containing hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D277/00Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/20Heterocyclic 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
    • C07D277/587Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D501/00Heterocyclic 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
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/55Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

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  • 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)
  • Plural Heterocyclic Compounds (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Diaphragms For Electromechanical Transducers (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
FI930604A 1992-02-14 1993-02-11 Menetelmä kefeemi-esilääke-esterien valmistamiseksi, menetelmässä käyttökelpoisia yhdisteitä, menetelmä näiden yhdisteiden valmistamiseksi ja niiden käyttö FI109027B (fi)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE4204349 1992-02-14
DE4204349 1992-02-14

Publications (3)

Publication Number Publication Date
FI930604A0 FI930604A0 (fi) 1993-02-11
FI930604A FI930604A (fi) 1993-08-15
FI109027B true FI109027B (fi) 2002-05-15

Family

ID=6451660

Family Applications (1)

Application Number Title Priority Date Filing Date
FI930604A FI109027B (fi) 1992-02-14 1993-02-11 Menetelmä kefeemi-esilääke-esterien valmistamiseksi, menetelmässä käyttökelpoisia yhdisteitä, menetelmä näiden yhdisteiden valmistamiseksi ja niiden käyttö

Country Status (13)

Country Link
US (2) US5589594A (ja)
EP (1) EP0555769B1 (ja)
JP (1) JP3426629B2 (ja)
KR (1) KR100265191B1 (ja)
AT (1) ATE184609T1 (ja)
CA (1) CA2089441C (ja)
DE (1) DE59309776D1 (ja)
DK (1) DK0555769T3 (ja)
ES (1) ES2137201T3 (ja)
FI (1) FI109027B (ja)
GR (1) GR3032076T3 (ja)
HU (1) HU219587B (ja)
TW (1) TW212181B (ja)

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ATE218572T1 (de) * 1995-12-27 2002-06-15 Hanmi Pharmaceutical Co Ltd Verfahren zur herstellung von cefdinir
US5883247A (en) * 1996-06-10 1999-03-16 Hoffmann-La Roche Inc. Preparation of cephem and isooxacephem derivatives
ITMI20012363A1 (it) * 2001-11-09 2003-05-09 Antibioticos Spa Metodo per la sintesi di catene laterali di cefalosporine
GB0416380D0 (en) * 2004-07-22 2004-08-25 Sandoz Ag Organic compounds
CN100448856C (zh) * 2006-06-26 2009-01-07 山东金城医药化工股份有限公司 一种催化合成ae-活性酯的工艺
ITMI20071628A1 (it) 2007-08-06 2007-11-05 Acs Dobfar Spa Sintesi di 3-alchenilcefalosporine e nuovi intermedi utili ad esse correlati
WO2011029596A1 (en) 2009-09-11 2011-03-17 Lonza Ltd Process for preparing 2-aminothiazol-4-yl-acetic acid derivates
US9409904B2 (en) 2011-08-01 2016-08-09 Yissum Research Development Company Of The Hebrew University Of Jerusalem Ltd Compounds and compositions for use in augmentation of glucose
CN102659713B (zh) * 2012-05-07 2014-03-05 山东金城柯瑞化学有限公司 头孢地尼侧链酸活性酯的制备方法

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DK154939C (da) * 1974-12-19 1989-06-12 Takeda Chemical Industries Ltd Analogifremgangsmaade til fremstilling af thiazolylacetamido-cephemforbindelser eller farmaceutisk acceptable salte eller estere deraf
JPS5760345B2 (ja) * 1974-12-19 1982-12-18 Takeda Chemical Industries Ltd
US4203899A (en) * 1974-12-19 1980-05-20 Takeda Chemical Industries, Ltd. Thiazolylacetamido compounds
US4668783A (en) * 1974-12-19 1987-05-26 Takeda Chemical Industries, Ltd. Thiazolylacetamido cephalosporin compounds
US4298606A (en) * 1974-12-19 1981-11-03 Takeda Chemical Industries, Ltd. Thiazolylacetamido compounds
DE2760123C2 (de) * 1976-01-23 1986-04-30 Roussel-Uclaf, Paris 7-Aminothiazolyl-syn-oxyiminoacetamidocephalosporansäuren, ihre Herstellung und sie enthaltende pharmazeutische Zusammensetzungen
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
US4120690A (en) * 1976-11-22 1978-10-17 Gulf Oil Corporation 2-Acylaminothiazol-4-ylacetamides as post-emergent selective herbicides
DE2714880A1 (de) * 1977-04-02 1978-10-26 Hoechst Ag Cephemderivate und verfahren zu ihrer herstellung
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
FR2476087A1 (fr) * 1980-02-18 1981-08-21 Roussel Uclaf 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
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
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
US4948898A (en) * 1982-06-03 1990-08-14 Hoffmann-La Roche Inc. Process for the manufacture of 1-sulpho-2-oxoazetidine derivatives
JPS604189A (ja) * 1983-06-20 1985-01-10 Sankyo Co Ltd β−ラクタム系化合物の製造法
JPS604190A (ja) * 1983-06-21 1985-01-10 Sankyo Co Ltd セフアロスポリン誘導体の製法
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DE3804841A1 (de) * 1988-02-17 1989-08-31 Hoechst Ag Cephalosporinderivate und verfahren zu ihrer herstellung
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DE3905119A1 (de) * 1989-02-20 1990-08-23 Bayer Ag Substituierte acrylsaeureester
DE3919259A1 (de) * 1989-06-13 1990-12-20 Hoechst Ag Kristalline cephem-saeureadditionssalze und verfahren zu ihrer herstellung
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WO1992007840A1 (en) * 1990-11-02 1992-05-14 Taisho Pharmaceutical Co., Ltd. Thiazole thioester derivative
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
EP0531875B1 (de) * 1991-09-07 2004-03-24 Aventis Pharma Deutschland GmbH Diastereomer des 3-Cephem-4-carbonsäure-1-(-isopropoxycarbonyloxy)ethylesters und Verfahren zu dessen Herstellung

Also Published As

Publication number Publication date
DK0555769T3 (da) 2000-03-20
ATE184609T1 (de) 1999-10-15
FI930604A (fi) 1993-08-15
JPH069650A (ja) 1994-01-18
CA2089441C (en) 2004-01-20
KR930017908A (ko) 1993-09-20
EP0555769B1 (de) 1999-09-15
JP3426629B2 (ja) 2003-07-14
KR100265191B1 (ko) 2000-09-15
DE59309776D1 (de) 1999-10-21
EP0555769A2 (de) 1993-08-18
US5589594A (en) 1996-12-31
CA2089441A1 (en) 1993-08-15
US5637721A (en) 1997-06-10
ES2137201T3 (es) 1999-12-16
HUT64350A (en) 1993-12-28
HU219587B (hu) 2001-05-28
FI930604A0 (fi) 1993-02-11
GR3032076T3 (en) 2000-03-31
TW212181B (ja) 1993-09-01
HU9300374D0 (en) 1993-04-28
EP0555769A3 (en) 1993-11-24

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