YU63089A - Process for preparing new alcanophenones - Google Patents

Process for preparing new alcanophenones

Info

Publication number
YU63089A
YU63089A YU00630/89A YU63089A YU63089A YU 63089 A YU63089 A YU 63089A YU 00630/89 A YU00630/89 A YU 00630/89A YU 63089 A YU63089 A YU 63089A YU 63089 A YU63089 A YU 63089A
Authority
YU
Yugoslavia
Prior art keywords
optionally
lower alkyl
salt
denotes
obtainable according
Prior art date
Application number
YU00630/89A
Original Assignee
Ciba Geigy 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 Ciba Geigy Ag filed Critical Ciba Geigy Ag
Priority to SI8910630A priority Critical patent/SI8910630B/en
Publication of YU63089A publication Critical patent/YU63089A/en
Priority to HR940505A priority patent/HRP940505B1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/04Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom 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
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/08Bronchodilators
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/08Antiallergic agents
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D311/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
    • C07D311/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D311/04Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
    • C07D311/22Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 4
    • C07D311/24Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 4 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pulmonology (AREA)
  • Hematology (AREA)
  • Diabetes (AREA)
  • Pain & Pain Management (AREA)
  • Obesity (AREA)
  • Immunology (AREA)
  • Rheumatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyrane Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)

Abstract

Substituted alkanophenones of the general formula <IMAGE> in which R1 denotes optionally fluorinated lower alkyl, R2 represents hydrogen, optionally fluorinated lower alkyl or lower alkenyl, X denotes lower alkylene, oxy, thio or a direct bond, alk represents lower alkylene, n stands for 1 or 2, R3 denotes phenyl which is unsubstituted or substituted by optionally fluorinated lower alkyl, etherified or esterified hydroxyl, optionally lower alkylated amino and/or optionally esterified or amidated carboxyl or denotes lower alkyl which is optionally fluorinated or substituted by optionally esterified or amidated carboxyl, R4 represents optionally esterified or amidated carboxyl or 5-tetrazolyl and R5 stands for hydrogen or lower alkyl, have leukotriene-antagonist properties and can be used as antiallergic pharmaceutical active compounds. The process for their preparation is characterised in that an epoxide of the formula <IMAGE> in which R1, R2, X, alk, n and R3 have the above meanings, is reacted with a thiol of the formula <IMAGE> in which R4 and R5 have the above meanings, or a salt thereof and, if desired, a compound obtainable according to the process is converted into another compound of the formula I, a stereoisomer mixture obtainable according to the process is resolved into the components and/or a free compound obtainable according to the process is converted into a salt or a salt obtainable according to the process is converted into the free compound or into another salt.
YU00630/89A 1988-03-29 1989-03-27 Process for preparing new alcanophenones YU63089A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
SI8910630A SI8910630B (en) 1988-03-29 1989-03-27 Process for obtaining novel alkanophenones
HR940505A HRP940505B1 (en) 1988-03-29 1994-09-08 Process for the preparation of new alkanophenones

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH118688 1988-03-29
CH385788 1988-10-14

Publications (1)

Publication Number Publication Date
YU63089A true YU63089A (en) 1990-12-31

Family

ID=25686932

Family Applications (1)

Application Number Title Priority Date Filing Date
YU00630/89A YU63089A (en) 1988-03-29 1989-03-27 Process for preparing new alcanophenones

Country Status (19)

Country Link
EP (1) EP0335315B1 (en)
JP (1) JP2777183B2 (en)
KR (1) KR0125933B1 (en)
AT (1) ATE107639T1 (en)
AU (1) AU623383B2 (en)
CA (1) CA1340463C (en)
CY (1) CY1967A (en)
DE (1) DE58907920D1 (en)
DK (1) DK148989A (en)
ES (1) ES2056137T3 (en)
FI (1) FI94342C (en)
HK (1) HK192696A (en)
HU (2) HU202852B (en)
IE (1) IE66248B1 (en)
IL (1) IL89713A0 (en)
NO (1) NO171555C (en)
NZ (1) NZ228477A (en)
PT (1) PT90125B (en)
YU (1) YU63089A (en)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0419411A3 (en) * 1989-09-19 1991-09-04 Ciba-Geigy Ag Additional alkanophenones
EP0419410A3 (en) * 1989-09-19 1991-08-14 Ciba-Geigy Ag Alkanophenones
US6596260B1 (en) * 1993-08-27 2003-07-22 Novartis Corporation Aerosol container and a method for storage and administration of a predetermined amount of a pharmaceutically active aerosol
EE04004B1 (en) 1995-04-14 2003-04-15 Glaxo Wellcome Inc. Fluticasone propionate metered dose inhaler
ATE258813T1 (en) 1995-04-14 2004-02-15 Smithkline Beecham Corp DEVICE FOR THE DOSED INHALATION OF BECLOMETHASONE DIPROPRIONATE
TR199701167T1 (en) 1995-04-14 1998-03-21 Glaxo Wellcome Inc. Metered dose inhaler for albuterol.
EP1366777B1 (en) * 1995-04-14 2005-06-15 SmithKline Beecham Corporation Metered dose inhaler for salmeterol
IT1320162B1 (en) 2000-02-09 2003-11-18 Rotta Research Lab DERIVATIVES OF THYROSIN WITH ANTI LEUKOTRIENIC ACTIVITY, PROCEDURES FOR THEIR PREPARATION AND THEIR PHARMACEUTICAL USE.
ATE358672T1 (en) * 2000-10-23 2007-04-15 Arizona Biomedical Res Commiss ANTITUMOR COMPOUNDS BASED ON REGULATION OF PROTEIN PRENYLATION
JP4691988B2 (en) 2002-10-03 2011-06-01 小野薬品工業株式会社 LPA receptor antagonist
ATE528276T1 (en) * 2003-12-19 2011-10-15 Ono Pharmaceutical Co LYSOPHOSPHATIDYL ACID RECEPTOR ANTAGONIST COMPOUNDS AND THEIR APPLICATIONS

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3070912D1 (en) * 1979-03-20 1985-09-05 Fisons Plc Pharmaceutical heterocyclic compounds, processes for their preparation and compositions containing them
US4474788A (en) * 1981-11-12 1984-10-02 Fisons Plc Anti-SRSA quinoline carboxylic acid derivatives
AU548450B2 (en) * 1983-08-08 1985-12-12 G.D. Searle & Co. Substituted dihydrobenzopyrans
CA1288107C (en) * 1983-12-27 1991-08-27 Yves Girard Leukotriene antagonists
US4565882A (en) * 1984-01-06 1986-01-21 G. D. Searle & Co. Substituted dihydrobenzopyran-2-carboxylates
US4546194A (en) * 1984-05-29 1985-10-08 G. D. Searle & Co. Substituted chromanon-2-yl alkanols and derivatives thereof
US4785004A (en) * 1985-12-23 1988-11-15 Ciba-Geigy Corporation Aromatic thioethers
US4889871A (en) * 1987-05-29 1989-12-26 G. D. Searle & Co. Alkoxy-substituted dihydrobenzopyran-2-carboxylate derivatives
EP0419411A3 (en) * 1989-09-19 1991-09-04 Ciba-Geigy Ag Additional alkanophenones

Also Published As

Publication number Publication date
HK192696A (en) 1996-10-25
HU210531A9 (en) 1995-04-28
NO171555C (en) 1993-03-31
ATE107639T1 (en) 1994-07-15
HU202852B (en) 1991-04-29
EP0335315A1 (en) 1989-10-04
CY1967A (en) 1997-07-04
FI94342B (en) 1995-05-15
JPH01299283A (en) 1989-12-04
FI891362A (en) 1989-09-30
KR0125933B1 (en) 1997-12-26
DK148989A (en) 1989-09-30
AU623383B2 (en) 1992-05-14
AU3225289A (en) 1989-10-12
JP2777183B2 (en) 1998-07-16
IE890935L (en) 1989-09-29
FI891362A0 (en) 1989-03-22
IL89713A0 (en) 1989-09-28
KR890014511A (en) 1989-10-24
PT90125B (en) 1994-10-31
NO891286D0 (en) 1989-03-28
FI94342C (en) 1995-08-25
EP0335315B1 (en) 1994-06-22
NO891286L (en) 1989-10-02
PT90125A (en) 1989-11-10
HUT49599A (en) 1989-10-30
NZ228477A (en) 1990-11-27
DK148989D0 (en) 1989-03-28
NO171555B (en) 1992-12-21
ES2056137T3 (en) 1994-10-01
DE58907920D1 (en) 1994-07-28
IE66248B1 (en) 1995-12-27
CA1340463C (en) 1999-03-23

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