IE873089L - Pyrrolo-benzimidazoles - Google Patents

Pyrrolo-benzimidazoles

Info

Publication number
IE873089L
IE873089L IE873089A IE308987A IE873089L IE 873089 L IE873089 L IE 873089L IE 873089 A IE873089 A IE 873089A IE 308987 A IE308987 A IE 308987A IE 873089 L IE873089 L IE 873089L
Authority
IE
Ireland
Prior art keywords
group
phenyl
atom
substituted
alkoxy
Prior art date
Application number
IE873089A
Original Assignee
S C Johnson Inc
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 S C Johnson Inc filed Critical S C Johnson Inc
Publication of IE873089L publication Critical patent/IE873089L/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/30Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
    • C07D209/32Oxygen atoms
    • C07D209/34Oxygen atoms in position 2
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • 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)
  • Public Health (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Hematology (AREA)
  • Diabetes (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

Pyrrolobenzimidazoles of the formula <IMAGE> in which A and B together with the two intermediate carbon atoms represent an imidazo group of the formula <IMAGE> in which R1 represents a hydrogen atom or an alkyl group which is optionally substituted by a phenyl group and R2 represents a hydrogen atom, an alkyl group which is optionally substituted by a phenyl, pyridyl or thienyl group, a vinylene group which is substituted at the end by a phenyl or pyridyl group, a phenyl group which is optionally substituted by a halogen atom, or a hydroxyl, alkoxy, mercapto, alkylmercapto, alkylsulphinyl, alkylsulphonyl, cyano, amino, alkylamino, dialkylamino, alkanoylamino or nitro group, it being possible for a hydroxyphenyl group to be substituted additionally by one or two alkyl groups or an aminophenyl group to be substituted by one or two halogen atoms, a phenyl group disubstituted by halogen atoms, or hydroxyl, alkoxy, mercapto, alkylmercapto, alkylsulphinyl or alkylsulphonyl groups, it being possible for the substituents of the phenyl ring to be identical or different, a 5- or 6-membered heteroaromatic ring bonded via a carbon atom and which contains an oxygen, sulphur or nitrogen atom, two or three nitrogen atoms or a nitrogen atom and an oxygen or sulphur atom, to which one or two 1,4-butadienyl groups can be additionally bonded via two adjacent carbon atoms, where in this case the bonding can also take place via a fused-on phenyl ring and in the case of the pyridines these can additionally be substituted by an amino, alkylamino, dialkylamino, alkanoylamino or morpholino group or by two halogen atoms or by a halogen atom and an amino or morpholino group and in the case of the quinolines can be additionally mono- or disubstituted by a halogen atom, or an alkoxy or phenyl group, it being possible for the substituents to be identical or different, a 5- to 7-membered saturated imino-, N-alkylimino- or N-alkanoylimino-alkylene ring bonded via a carbon atom, or a 1,2,3,4-tetrahydroquinolyl or 5,6,7,8-tetrahydroquinolyl group, R3 represents an alkyl group which is optionally substituted by a phenyl group, an alkyl group or an alkyl group which is substituted from position 2 by a hydroxyl, alkoxy or pyridinium group, R4 and R5, which can be identical or different, represent hydrogen atoms, alkyl groups or cycloalkyl groups, and their acid addition salts, for pharmaceutical use in particular their physiologically tolerable acid addition salts with inorganic or organic acids, which have useful pharmacological properties, in particular a slight influence on the blood pressure, a positive inotropic effect and an antithrombotic effect. The novel compounds can be prepared by methods known per se. [EP0268178A1]
IE873089A 1986-11-18 1987-11-17 Pyrrolo-benzimidazoles IE873089L (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE19863639466 DE3639466A1 (en) 1986-11-18 1986-11-18 NEW PYRROLO-BENZIMIDAZOLES, MEDICINAL PRODUCTS CONTAINING THESE COMPOUNDS AND METHOD FOR THE PRODUCTION THEREOF

Publications (1)

Publication Number Publication Date
IE873089L true IE873089L (en) 1988-05-18

Family

ID=6314255

Family Applications (1)

Application Number Title Priority Date Filing Date
IE873089A IE873089L (en) 1986-11-18 1987-11-17 Pyrrolo-benzimidazoles

Country Status (14)

Country Link
EP (1) EP0268178A1 (en)
JP (1) JPS63135385A (en)
KR (1) KR890003688A (en)
AU (1) AU8129987A (en)
DD (1) DD272081A5 (en)
DE (1) DE3639466A1 (en)
DK (1) DK602487A (en)
FI (1) FI875076A (en)
HU (1) HUT47277A (en)
IE (1) IE873089L (en)
IL (1) IL84509A0 (en)
NO (1) NO874780L (en)
PT (1) PT86154B (en)
ZA (1) ZA878590B (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3531678A1 (en) * 1985-09-05 1987-03-12 Boehringer Mannheim Gmbh NEW PYRROLO-BENZIMIDAZOLES, METHOD FOR THEIR PRODUCTION AND MEDICINAL PRODUCTS CONTAINING THESE COMPOUNDS
DE3803775A1 (en) * 1988-02-09 1989-08-17 Boehringer Mannheim Gmbh NEW SUBSTITUTED LACTAME, METHOD FOR THE PRODUCTION THEREOF, AND MEDICINAL PRODUCTS CONTAINING THESE COMPOUNDS
DE3932953A1 (en) * 1989-10-03 1991-04-11 Boehringer Mannheim Gmbh NEW 2-BICYCLO-BENZIMIDAZOLES, METHOD FOR THEIR PRODUCTION AND MEDICINAL PRODUCTS CONTAINING THESE COMPOUNDS
DE4027592A1 (en) * 1990-08-31 1992-03-05 Beiersdorf Ag NEW PYRROLOBENZIMIDAZOLE, IMIDAZOBENZOXAZINONE AND IMIDAZOCHINOLONE, PROCESS FOR THEIR PREPARATION AND THEIR USE AND THE COMPOUNDS CONTAINING PREPARATIONS
EP1598353A1 (en) * 2004-05-17 2005-11-23 Boehringer Ingelheim International GmbH Pyrrolobenzimidazolones and their use as antiproliferative agents

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PL144822B1 (en) * 1984-05-12 1988-07-30 Boehringer Mannheim Gmbh Method of obtaining novel pyrolobenzimidazoles
DE3445669A1 (en) * 1984-12-14 1986-06-19 Boehringer Mannheim Gmbh, 6800 Mannheim NEW PYRROLO-BENZIMIDAZOLES, METHOD FOR THEIR PRODUCTION AND MEDICINAL PRODUCTS CONTAINING THESE COMPOUNDS
DE3501497A1 (en) * 1985-01-18 1986-07-24 Boehringer Mannheim Gmbh, 6800 Mannheim NEW PYRROLO-BENZIMIDAZOLES, METHOD FOR THE PRODUCTION THEREOF AND MEDICINAL PRODUCTS CONTAINING THESE COMPOUNDS AND INTERMEDIATE PRODUCTS

Also Published As

Publication number Publication date
IL84509A0 (en) 1988-04-29
AU8129987A (en) 1988-05-19
JPS63135385A (en) 1988-06-07
NO874780L (en) 1988-05-19
FI875076A (en) 1988-05-19
KR890003688A (en) 1989-04-17
DE3639466A1 (en) 1988-05-19
FI875076A0 (en) 1987-11-17
EP0268178A1 (en) 1988-05-25
PT86154A (en) 1987-12-01
ZA878590B (en) 1989-07-26
DD272081A5 (en) 1989-09-27
PT86154B (en) 1990-11-20
DK602487A (en) 1988-05-19
DK602487D0 (en) 1987-11-17
NO874780D0 (en) 1987-11-17
HUT47277A (en) 1989-02-28

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