ZA894470B - Substituted 3-aminosydnone imines,a process for their preparation and their use - Google Patents

Substituted 3-aminosydnone imines,a process for their preparation and their use

Info

Publication number
ZA894470B
ZA894470B ZA894470A ZA894470A ZA894470B ZA 894470 B ZA894470 B ZA 894470B ZA 894470 A ZA894470 A ZA 894470A ZA 894470 A ZA894470 A ZA 894470A ZA 894470 B ZA894470 B ZA 894470B
Authority
ZA
South Africa
Prior art keywords
substituted
preparation
atoms
formula
image
Prior art date
Application number
ZA894470A
Inventor
Karl Schoenafinger
Schoenafinger Karl
Rudi Beyerle
Beyerle Rudi
Helmut Bohn
Bohn Helmut
Melitta Just
Just Melitta
Original Assignee
Cassella Farbwerke Mainkur 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 Cassella Farbwerke Mainkur Ag filed Critical Cassella Farbwerke Mainkur Ag
Publication of ZA894470B publication Critical patent/ZA894470B/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D271/00Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
    • C07D271/02Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
    • C07D271/041,2,3-Oxadiazoles; Hydrogenated 1,2,3-oxadiazoles
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/04Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Cardiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Engineering & Computer Science (AREA)
  • Animal Behavior & Ethology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Peptides Or Proteins (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyrrole Compounds (AREA)

Abstract

Substituted 3-aminosydnone imines of the formula I <IMAGE> and their pharmacologically acceptable acid addition salts, in which A is, for example, -CH5-, R is hydrogen or the radical -COR<5>, R<2>, R<3> are alkyl with 1 to 4 C atoms, R<5> is, for example, an aliphatic radical with 1 to 4 C atoms, are prepared by cyclisation of a compound of the formula II <IMAGE> and, where appropriate, subsequent acylation and have valuable pharmacological properties.
ZA894470A 1988-06-14 1989-06-13 Substituted 3-aminosydnone imines,a process for their preparation and their use ZA894470B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE3820210A DE3820210A1 (en) 1988-06-14 1988-06-14 SUBSTITUTED 3-AMINO-DYNONOMINES, PROCESS FOR THEIR PREPARATION AND THEIR USE

Publications (1)

Publication Number Publication Date
ZA894470B true ZA894470B (en) 1990-02-28

Family

ID=6356514

Family Applications (1)

Application Number Title Priority Date Filing Date
ZA894470A ZA894470B (en) 1988-06-14 1989-06-13 Substituted 3-aminosydnone imines,a process for their preparation and their use

Country Status (13)

Country Link
EP (1) EP0346694B1 (en)
JP (1) JP2898302B2 (en)
KR (1) KR910000719A (en)
AT (1) ATE85054T1 (en)
CA (1) CA1335989C (en)
DE (2) DE3820210A1 (en)
DK (1) DK247389A (en)
ES (1) ES2053868T3 (en)
GR (1) GR3007514T3 (en)
HU (1) HUT55389A (en)
IE (1) IE891900L (en)
PT (1) PT90840B (en)
ZA (1) ZA894470B (en)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4015236A1 (en) * 1990-05-13 1991-11-14 Cassella Ag SUBSTITUTED 3-AMINO-DYNONOMINES, PROCESS FOR THEIR PREPARATION AND THEIR USE
DE59001784D1 (en) * 1989-11-30 1993-07-22 Cassella Ag SUBSTITUTED 3-AMINOSYDNONIMINE, METHOD FOR THE PRODUCTION AND USE THEREOF.
DE4031373A1 (en) * 1990-10-04 1992-04-09 Cassella Ag 3-PIPERAZINO-SYDNONIMINE, METHOD FOR THE PRODUCTION AND THEIR USE
FR2703047B1 (en) * 1993-03-25 1995-06-09 Hoechst Lab NITERATED DERIVATIVES OF SYDNONIMINE, THEIR PREPARATION PROCESS AND THEIR APPLICATION AS A MEDICAMENT.
DE4337335A1 (en) * 1993-11-02 1995-05-04 Cassella Ag Process for the preparation of Sydnoniminium hydrogen sulfate
JPH08321345A (en) * 1995-05-24 1996-12-03 Yazaki Corp Connector housing
WO1998047896A1 (en) * 1997-04-22 1998-10-29 Chugai Seiyaku Kabushiki Kaisha Sydononimine derivatives

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1695897C3 (en) * 1966-07-04 1979-02-15 Takeda Chemical Industries Ltd N-acyl-sydnonimines, their salts, processes for their preparation and medicaments containing these compounds
JPS5836922B2 (en) * 1976-07-02 1983-08-12 株式会社クボタ reaping harvester
DE2930736A1 (en) * 1979-07-28 1981-02-12 Cassella Ag PHARMACOLOGICALLY ACTIVE, SUBSTITUTED 3-AMINO-SYDNONIMINE, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE
JPS5859977A (en) * 1981-10-06 1983-04-09 Banyu Pharmaceut Co Ltd Novel n-acylsydnoneimine derivative and its preparation
JPS5998076A (en) * 1982-11-26 1984-06-06 Hiroyoshi Hidaka Novel sydnoneimine compound and its preparation
DE3522191A1 (en) * 1985-06-21 1987-01-15 Cassella Ag PHOTOSTABILIZATION OF SYDNONIMINES
DE3526068A1 (en) * 1985-07-20 1987-01-22 Cassella Ag SUBSTITUTED 3-AMINO-SYDNONIMINE, METHOD FOR THE PRODUCTION THEREOF, THEIR USE AND PHARMACEUTICAL PREPARATIONS CONTAINING THE SAME
DE3702083A1 (en) * 1987-01-24 1988-08-04 Cassella Ag ALLYLMERCAPTOACETYL SYDNONIMINE, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE

Also Published As

Publication number Publication date
EP0346694A1 (en) 1989-12-20
IE891900L (en) 1989-12-14
DK247389D0 (en) 1989-05-22
DE3820210A1 (en) 1989-12-21
PT90840B (en) 1994-11-30
GR3007514T3 (en) 1993-08-31
JPH0236180A (en) 1990-02-06
KR910000719A (en) 1991-01-30
JP2898302B2 (en) 1999-05-31
DE58903385D1 (en) 1993-03-11
EP0346694B1 (en) 1993-01-27
CA1335989C (en) 1995-06-20
PT90840A (en) 1989-12-29
ES2053868T3 (en) 1994-08-01
HUT55389A (en) 1991-05-28
DK247389A (en) 1989-12-15
ATE85054T1 (en) 1993-02-15

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