FI810535L - NYA BENZOXAZOLER OCH BENZTIAZOLER DERAS FRAMSTAELLNING OCH DERAS ANVAENDNING SAOSOM LAEKEMEDEL - Google Patents

NYA BENZOXAZOLER OCH BENZTIAZOLER DERAS FRAMSTAELLNING OCH DERAS ANVAENDNING SAOSOM LAEKEMEDEL

Info

Publication number
FI810535L
FI810535L FI810535A FI810535A FI810535L FI 810535 L FI810535 L FI 810535L FI 810535 A FI810535 A FI 810535A FI 810535 A FI810535 A FI 810535A FI 810535 L FI810535 L FI 810535L
Authority
FI
Finland
Prior art keywords
carbon atoms
substituted
group
general formula
hydrogen atom
Prior art date
Application number
FI810535A
Other languages
Finnish (fi)
Other versions
FI73426C (en
FI73426B (en
Inventor
Norbert Hauel
Joachim Heider
Herbert Stein
Volkhard Austel
Manfred Reiffen
Willi Diederen
Walter Haarmann
Original Assignee
Thomae Gmbh Dr K
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 Thomae Gmbh Dr K filed Critical Thomae Gmbh Dr K
Publication of FI810535L publication Critical patent/FI810535L/en
Application granted granted Critical
Publication of FI73426B publication Critical patent/FI73426B/en
Publication of FI73426C publication Critical patent/FI73426C/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D263/00Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/52Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings condensed with carbocyclic rings or ring systems
    • C07D263/54Benzoxazoles; Hydrogenated benzoxazoles
    • C07D263/58Benzoxazoles; Hydrogenated benzoxazoles 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 in position 2
    • 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
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/04Antihaemorrhagics; Procoagulants; Haemostatic agents; Antifibrinolytic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/04Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/08Vasodilators for multiple indications
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/12Antihypertensives
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C205/00Compounds containing nitro groups bound to a carbon skeleton
    • C07C205/49Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups
    • C07C205/56Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups having nitro groups bound to carbon atoms of six-membered aromatic rings and carboxyl groups bound to acyclic carbon atoms of the carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C59/00Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
    • C07C59/40Unsaturated compounds
    • C07C59/76Unsaturated compounds containing keto groups
    • C07C59/84Unsaturated compounds containing keto groups containing six membered aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D237/00Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
    • C07D237/02Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
    • C07D237/04Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having less than three double bonds between ring members or between ring members and non-ring members

Abstract

1. Claims for the Contracting States : BE, CH, DE, FR, GB, IT, LI, LU, NL Benzoxazoles of general formula see diagramm : EP0034743,P9,F2 in which R1 represents a hydrogen atom ; a straight or branched alkyl group with 1 to 7 carbon atoms which can be substituted by an alkoxy group with 1 to 3 carbon atoms ; a cycloalkyl group with 3 to 7 carbon atoms ; an alkyl group with 1 to 3 carbon atoms substituted by a phenyl group which can be substituted by one or two alkoxy groups with 1 to 3 carbon atoms ; or a phenyl group which can be substituted by an alkyl or alkoxy group each with 1 to 3 carbon atoms, by a trifluormethyl, nitro or cyano group or by a fluorine, chlorine or bromine atom ; and in addition one of the mono-substituted phenyl groups mentioned above can be substituted by one or two alkyl groups with 1 to 3 carbon atoms or by an alkoxy group with 1 to 3 carbon atoms or by a fluorine, chlorine or bromine atom ; and R2 represents a hydrogen atom or an alkyl group with 1 to 3 carbon atoms ; and their optically active antipodes as well as their physiologically compatible acid addition salts with inorganic or organic acids. 1. Claims for the Contracting State : AT Process for producing benzoxazoles of general formula see diagramm : EP0034743,P10,F4 in which R1 represents a hydrogen atom ; a straight or branched alkyl group with 1 to 7 carbon atoms which can be substituted by an alkoxy group with 1 to 3 carbon atoms ; a cycloalkyl group with 3 to 7 carbon atoms ; an alkyl group with 1 to 3 carbon atoms substituted by a phenyl group which can be substituted by one or two alkoxy groups with 1 to 3 carbon atoms ; or a phenyl group which can be substituted by an alkyl or alkoxy group each with 1 to 3 carbon atoms, by a trifluormethyl, nitro or cyano group or by a fluorine, chlorine or bromine atom ; and additionally one of the mono-substituted phenyl groups mentioned above can be substituted by one or two alkyl groups with 1 to 3 carbon atoms or by an alkoxy group with 1 to 3 carbon atoms or by a fluorine, chlorine or bromine atom ; and R2 represents a hydrogen atom or an alkyl group with 1 to 3 carbon atoms ; and their optically active antipodes as well as their physiologically compatible acid addition salts with inorganic or organic acids characterised in that see diagramm : EP0034743,P11,F1 in which R1 and R2 are as defined in the introduction, X represents a mercapto, alkylmercapto, arylmercapto or aralkylmercapto group, and Y represents a hydrogen atom or an acyl radical, is cyclised ; or b) a carboxylic acid of general formula see diagramm : EP0034743,P11,F3 in which R1 and R2 are as defined in the introduction, or its amides, esters, thioester or halides, is reacted with hydrazine ; and if desired a compound of general formula I, in which R1 represents a hydrogen atom, obtained according to processes a) or b) is subsequently converted by means of alkylation into a corresponding compound of general formula I, in which R1 is defined as in the introduction with the exception of the hydrogen atom and the phenyl radicals mentioned in the introduction, and/or a racemate obtained, of general formula I, is separated by means of racemate separation into its optically active antipodes, and/or a compound obtained, of general formula I, is converted into its physiologically compatible acid addition salts with inorganic or organic acids.
FI810535A 1980-02-22 1981-02-20 FARING PROOF FOR PHARMACOLOGICAL PROPERTIES OF BENSOX AZOLER OR BENSTIAZOLER. FI73426C (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE3006671 1980-02-22
DE19803006671 DE3006671A1 (en) 1980-02-22 1980-02-22 NEW BENZOXAZOLES, THEIR PRODUCTION AND THEIR USE AS MEDICINAL PRODUCTS

Publications (3)

Publication Number Publication Date
FI810535L true FI810535L (en) 1981-08-23
FI73426B FI73426B (en) 1987-06-30
FI73426C FI73426C (en) 1987-10-09

Family

ID=6095308

Family Applications (1)

Application Number Title Priority Date Filing Date
FI810535A FI73426C (en) 1980-02-22 1981-02-20 FARING PROOF FOR PHARMACOLOGICAL PROPERTIES OF BENSOX AZOLER OR BENSTIAZOLER.

Country Status (19)

Country Link
EP (1) EP0034743B1 (en)
JP (1) JPS56131581A (en)
AT (1) ATE7696T1 (en)
AU (1) AU543524B2 (en)
CA (1) CA1166252A (en)
DE (2) DE3006671A1 (en)
DK (1) DK151018C (en)
ES (3) ES8206519A1 (en)
FI (1) FI73426C (en)
GR (1) GR74154B (en)
HK (1) HK50785A (en)
IE (1) IE51012B1 (en)
IL (1) IL62181A (en)
NO (1) NO157895C (en)
NZ (1) NZ196313A (en)
PH (1) PH21232A (en)
PT (1) PT72546B (en)
SG (1) SG885G (en)
ZA (1) ZA811130B (en)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA1199027A (en) * 1981-11-12 1986-01-07 Stuart D. Mills Heterocyclic derivatives of pyridazinone, thiadiazinone, oxadiazinone and triazinone
JPH11503110A (en) * 1995-02-17 1999-03-23 スミスクライン・ビーチャム・コーポレイション IL-8 receptor antagonist
US6262113B1 (en) 1996-03-20 2001-07-17 Smithkline Beecham Corporation IL-8 receptor antagonists
US6211373B1 (en) 1996-03-20 2001-04-03 Smithkline Beecham Corporation Phenyl urea antagonists of the IL-8 receptor
BR9709952A (en) * 1996-06-27 1999-08-10 Smithkline Beecham Corp Il-8 receptor antagonists
BR9709938A (en) 1996-06-27 1999-08-10 Smithkline Beecham Corp Il-8 receptor antagonists
UY32138A (en) 2008-09-25 2010-04-30 Boehringer Ingelheim Int SUBSTITUTED AMIDES 2- (2,6-DICLORO-PHENYLAMINE) -6-FLUORO-1-METHYL-1H-BENCIMIDAZOL-5-CARBOXYL AND ITS PHARMACEUTICALLY ACCEPTABLE SALTS
UY32470A (en) 2009-03-05 2010-10-29 Boehringer Ingelheim Int DERIVATIVES OF 2- {2-CHLORINE-5 - [(REPLACED) METHYL] PHENYLAMINE} -1-METHYL] PHENYLAMINE} -1-METHYLBENCIMIDAZOL-5-CARBOXAMIDES-N- (SUBSTITUTED) AND ITS PHYSIOLOGICALLY ACCEPTABLE SALTS, COMPOSITIONS AND APPLIANCE
US8759537B2 (en) 2010-08-20 2014-06-24 Boehringer Ingelheim International Gmbh 3H-imidazo [4, 5-C] pyridine-6-carboxamides as anti-inflammatory agents
US8586604B2 (en) 2010-08-20 2013-11-19 Boehringer Ingelheim International Gmbh Inhibitors of the microsomal prostaglandin E2 synthase-1
US8466186B2 (en) 2010-12-10 2013-06-18 Boehringer Ingelheim International Gmbh Compounds
US8674113B2 (en) 2010-12-10 2014-03-18 Boehringer Ingelheim International Gmbh Compounds
US8486968B2 (en) 2010-12-10 2013-07-16 Boehringer Ingelheim International Gmbh Compounds

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2516040C2 (en) * 1974-06-10 1984-12-20 Dr. Karl Thomae Gmbh, 7950 Biberach Benzimidazoles, processes for their preparation and pharmaceuticals containing them
DE2436279A1 (en) * 1974-07-27 1976-02-12 Henkel & Cie Gmbh Imidazoline and tetrahydropyrimidine derivs - prepd e.g. by reacting 2-cyano-benzoxazoles with alkylene diamines

Also Published As

Publication number Publication date
NZ196313A (en) 1984-07-06
DK73781A (en) 1981-08-23
IE51012B1 (en) 1986-09-03
NO157895C (en) 1988-06-08
DK151018C (en) 1988-06-20
ES8302700A1 (en) 1983-01-16
ZA811130B (en) 1982-10-27
JPS6334154B2 (en) 1988-07-08
AU543524B2 (en) 1985-04-26
PH21232A (en) 1987-08-21
JPS56131581A (en) 1981-10-15
EP0034743A1 (en) 1981-09-02
NO810586L (en) 1981-08-24
CA1166252A (en) 1984-04-24
DK151018B (en) 1987-10-12
IE810343L (en) 1981-08-22
ES499378A0 (en) 1982-08-16
ES509533A0 (en) 1983-01-16
GR74154B (en) 1984-06-06
ES8302699A1 (en) 1983-01-16
AU6751981A (en) 1981-08-27
PT72546A (en) 1981-03-01
NO157895B (en) 1988-02-29
PT72546B (en) 1982-10-21
ATE7696T1 (en) 1984-06-15
ES509532A0 (en) 1983-01-16
EP0034743B1 (en) 1984-05-30
HK50785A (en) 1985-07-12
ES8206519A1 (en) 1982-08-16
FI73426C (en) 1987-10-09
SG885G (en) 1985-11-15
FI73426B (en) 1987-06-30
DE3006671A1 (en) 1981-08-27
IL62181A (en) 1984-10-31
DE3163797D1 (en) 1984-07-05
IL62181A0 (en) 1981-03-31

Similar Documents

Publication Publication Date Title
FI810535L (en) NYA BENZOXAZOLER OCH BENZTIAZOLER DERAS FRAMSTAELLNING OCH DERAS ANVAENDNING SAOSOM LAEKEMEDEL
BR8701368A (en) PROCESS OF PREPARATION OF SOLID POLYMERIC COMPOUNDS, COMPOUNDS SO OBTAINED, AND STABILIZED POLYMERIC COMPOUNDS
DK0485204T3 (en) Process for Preparation of 3-Alkoxymethyl-Cephalosporin Derivatives
HUT34193A (en) Process for the production of substituted 6-aryl-1,2,4-triazolo/4,3-b/-pyridazin-derivatives and of pharmaceutic products containing such compounds
FI822697L (en) OVERFLOWER PROCESSING FOR FRAMSTAZNING AV BENZOTIAZINKARBOXAMIDER
DE3061105D1 (en) Pyrazolin-5-on-yl-methyl-(di)thiophosphoric acid esters, process for their preparation and their use as pesticides

Legal Events

Date Code Title Description
MM Patent lapsed
MM Patent lapsed

Owner name: DR. KARL THOMAE GESELLSCHAFT MIT