DK594383D0 - CEPHEMERY DERIVATIVES, OR THEIR PHYSIALLY ACCEPTABLE ACID ADDITION SALTS, THEIR PREPARATION AND USE - Google Patents

CEPHEMERY DERIVATIVES, OR THEIR PHYSIALLY ACCEPTABLE ACID ADDITION SALTS, THEIR PREPARATION AND USE

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Publication number
DK594383D0
DK594383D0 DK5943/83A DK594383A DK594383D0 DK 594383 D0 DK594383 D0 DK 594383D0 DK 5943/83 A DK5943/83 A DK 5943/83A DK 594383 A DK594383 A DK 594383A DK 594383 D0 DK594383 D0 DK 594383D0
Authority
DK
Denmark
Prior art keywords
denotes
acid addition
acceptable acid
general formula
group
Prior art date
Application number
DK5943/83A
Other languages
Danish (da)
Other versions
DK594383A (en
Inventor
Rudolf Lattrell
Walter Duerckheimer
Reiner Kirrstetter
Wilfried Schwab
Norbert Klesel
Original Assignee
Hoechst Ag
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 Hoechst Ag filed Critical Hoechst Ag
Publication of DK594383D0 publication Critical patent/DK594383D0/en
Publication of DK594383A publication Critical patent/DK594383A/en

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Classifications

    • 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
    • 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
    • C07D501/38Methylene radicals, substituted by nitrogen atoms; Lactams thereof with the 2-carboxyl group; Methylene radicals substituted by nitrogen-containing hetero rings attached by the ring nitrogen atom; Quaternary compounds thereof
    • C07D501/46Methylene radicals, substituted by nitrogen atoms; Lactams thereof with the 2-carboxyl group; Methylene radicals substituted by nitrogen-containing hetero rings attached by the ring nitrogen atom; Quaternary compounds thereof with the 7-amino radical acylated by carboxylic acids containing hetero rings
    • 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
    • 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
    • C07D501/577-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids with a further substituent in position 7, e.g. cephamycines
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Oncology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Communicable Diseases (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Cephalosporin Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Rigid Pipes And Flexible Pipes (AREA)
  • Bakery Products And Manufacturing Methods Therefor (AREA)
  • Solid-Sorbent Or Filter-Aiding Compositions (AREA)
  • Treatment Of Liquids With Adsorbents In General (AREA)

Abstract

For the Contracting States : BE, CH, DE, FR, GB, IT, LI, LU, NL, SE 1. Cephem derivatives of the general formula see diagramm : EP0111935,P10,F1 and physiologically acceptable acid addition salts thereof in which R**1 denotes hydrogen, R**2 denotes hydrogen, R**3 denotes C1 -C4 -alkyl optionally substituted by fluorine, A denotes a quinolinium or an isoquinolinium radical, each of which can also be substituted once or twice by C1 -C4 -alkyl and in which the R**3O group is in the syn position. For the Contracting State : AT A process for the preparation of cephem derivatives of the general formula I see diagramm : EP0111935,P11,F1 and physiologically acceptable acid addition salts thereof in which R**1 denotes hydrogen, R**2 denotes hydrogen, R**3 denotes C1 -C4 -alkyl optionally substituted by fluorine, A denotes a quinolinium or an isoquinolinium radical, each of which can also be substituted once or twice by C1 -C4 -alkyl and in which the R**3O group is in the syn position, which comprises a) reacting a compound of the general formula II see diagramm : EP0111935,P11,F2 or salts thereof or a reactive derivative of the compound II in which R**1, R**2 and R**3 have the abovementioned meaning and R**8 denotes an amino group or a protected amino group and R**9 denotes a group which can be replaced by quinoline, isoquinoline or substituted quinolines or isoquinolines corresponding to the radicals A of the formula I, with quinoline, isoquinoline or one of their derivatives, and alpha) splitting off a protective group which is present where appropriate and beta) if necessary, converting the resulting product into a physiologically acceptable acid addition salt, or b) reacting a 7-aminocephen compound of the general formula III see diagramm : EP0111935,P12,F3 or acid addition salts thereof in which R**2 and A have the abovementioned meaning, it also being possible for the amino group to be present in the form of a reactive derivative, with a 2-(2-aminothiazol-4-yl)-2-syn-oximinoacetic acid of the general formula IV see diagramm : EP0111935,P12,F4 in which R**1, R**3 and R**8 have the above meaning, or with an activated derivative of this compound, and alpha) splitting off a protective group which is present where appropriate and beta) if necessary, converting the resulting product into a physiologically acceptable acid addition salt
DK594383A 1982-12-23 1983-12-22 CEPHEMERY DERIVATIVES, OR THEIR PHYSIALLY ACCEPTABLE ACID ADDITION SALTS, THEIR PREPARATION AND USE DK594383A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE19823247614 DE3247614A1 (en) 1982-12-23 1982-12-23 CEPHALOSPORINE DERIVATIVES AND METHOD FOR THEIR PRODUCTION

Publications (2)

Publication Number Publication Date
DK594383D0 true DK594383D0 (en) 1983-12-22
DK594383A DK594383A (en) 1984-06-24

Family

ID=6181485

Family Applications (1)

Application Number Title Priority Date Filing Date
DK594383A DK594383A (en) 1982-12-23 1983-12-22 CEPHEMERY DERIVATIVES, OR THEIR PHYSIALLY ACCEPTABLE ACID ADDITION SALTS, THEIR PREPARATION AND USE

Country Status (19)

Country Link
EP (1) EP0111935B1 (en)
JP (1) JPS59130294A (en)
KR (1) KR840007015A (en)
AT (1) ATE37881T1 (en)
AU (1) AU2280983A (en)
CS (1) CS249132B2 (en)
DD (1) DD216026A5 (en)
DE (2) DE3247614A1 (en)
DK (1) DK594383A (en)
ES (1) ES8406494A1 (en)
FI (1) FI834710A (en)
GR (1) GR81360B (en)
HU (1) HU189792B (en)
IL (1) IL70519A0 (en)
NO (1) NO834775L (en)
NZ (1) NZ206659A (en)
PH (1) PH20088A (en)
PT (1) PT77877B (en)
ZA (1) ZA839526B (en)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DK500285A (en) * 1984-11-02 1986-05-03 Glaxo Group Ltd cephalosporin antibiotics
DE3585434D1 (en) * 1984-12-27 1992-04-02 Banyu Pharma Co Ltd CEPHALOSPORINE COMPOUNDS.
NO166283C (en) * 1985-03-01 1991-06-26 Takeda Chemical Industries Ltd METHOD OF ANALOGUE FOR THE PREPARATION OF THERAPEUTIC ACTIVE 7BETA- (2- (5-AMINO-1,2,4-THIADIAZOL-3-YL) -2 (Z) -SUBSTITUTE TOXYIMINOACETAMIDO) -3- (HETEROCYCLYLMETHYL) -CYLMETHYL-Methyl-3 .
GB2183630A (en) * 1985-10-31 1987-06-10 Glaxo Group Ltd Cephalosporin antibiotics
CA1296012C (en) * 1986-03-19 1992-02-18 Susumu Nakagawa 6,7-dihydroxy-isoquinoline derivatives
JPH0645631B2 (en) * 1986-03-19 1994-06-15 萬有製薬株式会社 New cefalosporin derivative
US4814328A (en) * 1986-03-19 1989-03-21 Banyu Pharmaceutical Co., Ltd. Cephalosporin derivatives, and antibacterial agents
AU1228588A (en) * 1987-02-02 1988-08-24 Teijin Limited Cephalosporin compounds or their salts, process for their preparation, and parmaceutical compositions
WO1988005777A1 (en) * 1987-02-03 1988-08-11 Teijin Limited Cephalosporin compounds or their salts, process for their preparation, and pharmaceutical compositions
DE3910421A1 (en) * 1989-03-31 1990-10-04 Hoechst Ag POLAR CEPHALOSPORINE DERIVATIVES AND METHOD FOR THE PRODUCTION THEREOF
TW200305422A (en) 2002-03-18 2003-11-01 Shionogi & Co Broad spectrum cefem compounds

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2760484C2 (en) * 1976-04-14 1992-12-03 Takeda Chemical Industries, Ltd., Osaka, Jp
DE2714880A1 (en) * 1977-04-02 1978-10-26 Hoechst Ag CEPHEMDER DERIVATIVES AND PROCESS FOR THEIR PRODUCTION
US4396619A (en) * 1981-09-08 1983-08-02 Eli Lilly And Company Cephalosporin betaines
US4396620A (en) * 1981-09-08 1983-08-02 Eli Lilly And Company Cephalosporin quinolinium betaines
US4402955A (en) * 1981-10-02 1983-09-06 Eli Lilly And Company Dioximino cephalosporin antibiotics
US4450270A (en) * 1981-10-02 1984-05-22 Eli Lilly And Company Dioximino cephalosporin antibiotics

Also Published As

Publication number Publication date
IL70519A0 (en) 1984-03-30
PT77877A (en) 1984-01-01
NO834775L (en) 1984-06-25
NZ206659A (en) 1986-11-12
CS249132B2 (en) 1987-03-12
ZA839526B (en) 1984-08-29
KR840007015A (en) 1984-12-04
EP0111935A3 (en) 1985-07-03
DE3378212D1 (en) 1988-11-17
ES528247A0 (en) 1984-08-01
AU2280983A (en) 1984-06-28
DD216026A5 (en) 1984-11-28
FI834710A (en) 1984-06-24
FI834710A0 (en) 1983-12-21
HUT34036A (en) 1985-01-28
EP0111935A2 (en) 1984-06-27
ES8406494A1 (en) 1984-08-01
GR81360B (en) 1984-12-11
ATE37881T1 (en) 1988-10-15
HU189792B (en) 1986-07-28
DK594383A (en) 1984-06-24
DE3247614A1 (en) 1984-07-05
PT77877B (en) 1986-04-21
JPS59130294A (en) 1984-07-26
EP0111935B1 (en) 1988-10-12
PH20088A (en) 1986-09-24

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Legal Events

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