ES8107231A1 - Procedimiento para la preparacion de compuestos de cefem y cefam - Google Patents

Procedimiento para la preparacion de compuestos de cefem y cefam

Info

Publication number
ES8107231A1
ES8107231A1 ES494634A ES494634A ES8107231A1 ES 8107231 A1 ES8107231 A1 ES 8107231A1 ES 494634 A ES494634 A ES 494634A ES 494634 A ES494634 A ES 494634A ES 8107231 A1 ES8107231 A1 ES 8107231A1
Authority
ES
Spain
Prior art keywords
preparation
cephem
processes
chem
hydrogen
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
ES494634A
Other languages
English (en)
Other versions
ES494634A0 (es
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.)
Fujisawa Pharmaceutical Co Ltd
Original Assignee
Fujisawa Pharmaceutical Co Ltd
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 Fujisawa Pharmaceutical Co Ltd filed Critical Fujisawa Pharmaceutical Co Ltd
Publication of ES8107231A1 publication Critical patent/ES8107231A1/es
Publication of ES494634A0 publication Critical patent/ES494634A0/es
Granted legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/44—Iso-indoles; Hydrogenated iso-indoles
    • C07D209/48—Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C17/00—Preparation of halogenated hydrocarbons
    • C07C17/26—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton
    • C07C17/263—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by condensation reactions
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles 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
    • C07D249/12—Oxygen or sulfur atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D257/00—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms
    • C07D257/02—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D257/04—Five-membered rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
    • C07D285/01—Five-membered rings
    • C07D285/02—Thiadiazoles; Hydrogenated thiadiazoles
    • C07D285/04—Thiadiazoles; Hydrogenated thiadiazoles not condensed with other rings
    • C07D285/08—1,2,4-Thiadiazoles; Hydrogenated 1,2,4-thiadiazoles
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
    • C07D295/20—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carbonic acid, or sulfur or nitrogen analogues thereof
    • C07D295/21—Radicals derived from sulfur analogues of carbonic acid

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Cephalosporin Compounds (AREA)
  • Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

PROCEDIMIENTO DE OBTENCION DE COMPUESTOS DE CEFEM Y CEFAM. CONSISTE EN HACER REACCIONAR UN COMPUESTO DE FORMULA GENERAL (I) CON UN COMPUESTO DE FORMULA R ELEVADO A 46 (SIENDO R ELEVADO A 6 PIRIDINA). OPCIONALMENTE SE SOMETE AL COMPUESTO RESULTANTE A ELIMINACION DEL GRUPO PROTECTOR DE CARBOXI, O BIEN SE ELIMINA EL GRUPO PROTECTOR DEL AMINO. SE OBTIENE EL COMPUESTO (II). ACCION ANTIMICROBIANA CONTRA UNA AMPLIA VARIEDAD DE MICROORGANISMOS PATOGENOS QUE INCLUYEN BACTERIAS GRAM-NEGATIVAS Y GRAM-POSITIVAS. *FORMULA* B
ES494634A 1978-12-29 1980-08-29 Procedimiento para la preparacion de compuestos de cefem y cefam Granted ES494634A0 (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB7850334 1978-12-29
GB7935538 1979-10-12
AU23283/84A AU2328384A (en) 1978-12-29 1984-01-13 1,2,4-thiadiazole derivatives

Publications (2)

Publication Number Publication Date
ES8107231A1 true ES8107231A1 (es) 1981-08-16
ES494634A0 ES494634A0 (es) 1981-08-16

Family

ID=32965859

Family Applications (3)

Application Number Title Priority Date Filing Date
ES487358A Granted ES487358A0 (es) 1978-12-29 1979-12-28 Un procedimiento para la preparacion de compuestos de cefem y cefam
ES494634A Granted ES494634A0 (es) 1978-12-29 1980-08-29 Procedimiento para la preparacion de compuestos de cefem y cefam
ES494635A Expired ES8107207A1 (es) 1978-12-29 1980-08-29 Procedimiento de preparacion de derivados de tiadiazol

Family Applications Before (1)

Application Number Title Priority Date Filing Date
ES487358A Granted ES487358A0 (es) 1978-12-29 1979-12-28 Un procedimiento para la preparacion de compuestos de cefem y cefam

Family Applications After (1)

Application Number Title Priority Date Filing Date
ES494635A Expired ES8107207A1 (es) 1978-12-29 1980-08-29 Procedimiento de preparacion de derivados de tiadiazol

Country Status (8)

Country Link
US (1) US4331665A (es)
EP (2) EP0064582B1 (es)
JP (1) JPH02223572A (es)
AU (2) AU536842B2 (es)
DE (1) DE2967410D1 (es)
DK (1) DK554279A (es)
ES (3) ES487358A0 (es)
MX (1) MX5973E (es)

Families Citing this family (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1592149A (en) * 1976-10-08 1981-07-01 Fujisawa Pharmaceutical Co 3 7-disubstituted-3-cephem-4-carboxylic acid compounds and processes for preparation thereof
US4390534A (en) * 1978-12-29 1983-06-28 Fujisawa Pharmaceutical Co., Ltd. Cephem and cepham compounds
MA18891A1 (fr) * 1979-07-05 1981-04-01 Ciba Geigy Ag Composes d'amino-thiadiazolyle,procede pour leur preparation
EP0025017A1 (de) * 1979-08-28 1981-03-11 Ciba-Geigy Ag Polyazathiaverbindungen, Verfahren zu ihrer Herstellung, pharmazeutische Präparate enthaltend solche Verbindungen und Verwendung von letzteren
GR75644B (es) * 1980-06-18 1984-08-02 Fujisawa Pharmaceutical Co
GR78245B (es) * 1980-09-12 1984-09-26 Ciba Geigy Ag
US4338452A (en) * 1980-09-17 1982-07-06 Eli Lilly And Company 1-and 2-(1-Alkyl-1H-tetrazol-5-yl-methyl)-1H-tetrazol-5-thiols and 1-cyanomethyl tetrazole-5-thiol
US4431642A (en) * 1980-12-01 1984-02-14 Fujisawa Pharmaceutical Co., Ltd. Cephem compounds
US4521413A (en) * 1981-09-14 1985-06-04 Fujisawa Pharmaceutical Co., Ltd. Cephem compounds
US4563449A (en) * 1982-07-19 1986-01-07 Fujisawa Pharmaceutical Co., Ltd. Cephem compounds
DE3247613A1 (de) * 1982-12-23 1984-07-05 Hoechst Ag, 6230 Frankfurt Cephalosporinderivate und verfahren zu ihrer herstellung
DE3300593A1 (de) * 1983-01-11 1984-07-12 Bayer Ag, 5090 Leverkusen Neue cephalosporine und verfahren zu ihrer herstellung
US4529490A (en) * 1983-05-23 1985-07-16 General Electric Company Photopolymerizable organic compositions and diaryliodonium ketone salts used therein
US4690921A (en) * 1983-10-11 1987-09-01 Yamanouchi Pharmaceutical Co., Ltd. Cephalosporin compounds and salts thereof
EP0150609A3 (en) * 1983-12-30 1986-04-23 Glaxo Group Limited Cephalosporin antibiotics
IE61679B1 (en) * 1987-08-10 1994-11-16 Fujisawa Pharmaceutical Co Water-soluble antibiotic composition and water-soluble salts of new cephem compounds
GB9104238D0 (en) * 1990-03-16 1991-04-17 Ici Pharma 3-tetrazolylthiomethyl cephalosporin antibiotics
JPH11101520A (ja) 1997-09-29 1999-04-13 Sharp Corp エアサイクル式空気調和装置
US7186855B2 (en) 2001-06-11 2007-03-06 Xenoport, Inc. Prodrugs of GABA analogs, compositions and uses thereof
US8048917B2 (en) 2005-04-06 2011-11-01 Xenoport, Inc. Prodrugs of GABA analogs, compositions and uses thereof
CA2932121A1 (en) * 2007-11-30 2009-06-11 Newlink Genetics Corporation Ido inhibitors
MX352760B (es) 2011-09-09 2017-12-07 Merck Sharp & Dohme Corp Star Metodos para tratar infecciones intrapulmonares.
US8809314B1 (en) 2012-09-07 2014-08-19 Cubist Pharmacueticals, Inc. Cephalosporin compound
US8476425B1 (en) 2012-09-27 2013-07-02 Cubist Pharmaceuticals, Inc. Tazobactam arginine compositions
US20140275000A1 (en) 2013-03-15 2014-09-18 Cubist Pharmaceuticals, Inc. Ceftolozane pharmaceutical compositions
MX2020004205A (es) 2013-03-15 2021-11-16 Merck Sharp & Dohme Llc Composiciones antibioticas de ceftolozano.
US9872906B2 (en) 2013-03-15 2018-01-23 Merck Sharp & Dohme Corp. Ceftolozane antibiotic compositions
WO2015035376A2 (en) 2013-09-09 2015-03-12 Calixa Therapeutics, Inc. Treating infections with ceftolozane/tazobactam in subjects having impaired renal function
US20150094293A1 (en) 2013-09-27 2015-04-02 Calixa Therapeutics, Inc. Solid forms of ceftolozane
JP2015174837A (ja) * 2014-03-14 2015-10-05 国立大学法人 千葉大学 ベンゾフラン誘導体の製造方法
JP6243056B2 (ja) * 2014-10-02 2017-12-06 富士フイルム株式会社 ５−アミノ−３置換−１，２，４−チアジアゾールの製造方法
US10059680B2 (en) 2014-12-18 2018-08-28 Merck Sharp & Dohme Corp. Thiadiazolyl-oximinoacetic acid derivative compounds
WO2016109259A2 (en) 2014-12-30 2016-07-07 Merck Sharp & Dohme Corp. Synthesis of cephalosporin compounds

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4093803A (en) * 1971-05-14 1978-06-06 Glaxo Laboratories Limited 7β-[2-Etherified oximino-2-(thienyl-, furyl- or pyridylacetamido)] cephalosporins
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
GB1592149A (en) 1976-10-08 1981-07-01 Fujisawa Pharmaceutical Co 3 7-disubstituted-3-cephem-4-carboxylic acid compounds and processes for preparation thereof
PH17188A (en) * 1977-03-14 1984-06-14 Fujisawa Pharmaceutical Co New cephem and cepham compounds and their pharmaceutical compositions and method of use
FR2387235A1 (fr) * 1978-01-23 1978-11-10 Fujisawa Pharmaceutical Co Procede de preparation de composes d'acide 3,7-disubstitue-3-cephem-4-carboxylique et nouveaux produits ainsi obtenus, ayant une forte activite antibacterienne
US4268509A (en) * 1978-07-10 1981-05-19 Fujisawa Pharmaceutical Co., Ltd. New cephem compounds and processes for preparation thereof

Also Published As

Publication number Publication date
DE2967410D1 (en) 1985-04-18
MX5973E (es) 1984-09-11
EP0013762A3 (en) 1980-10-01
DK554279A (da) 1980-06-30
JPH02223572A (ja) 1990-09-05
ES8102140A1 (es) 1980-12-16
AU5408379A (en) 1980-07-03
ES487358A0 (es) 1980-12-16
EP0013762B1 (en) 1985-03-13
ES494635A0 (es) 1981-08-16
ES494634A0 (es) 1981-08-16
US4331665A (en) 1982-05-25
AU536842B2 (en) 1984-05-24
ES8107207A1 (es) 1981-08-16
EP0064582A1 (en) 1982-11-17
EP0013762A2 (en) 1980-08-06
AU2328384A (en) 1984-05-10
EP0064582B1 (en) 1985-12-11

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