ES2152539T3 - Imidazoles inhibidores de la lipoxigenasa. - Google Patents

Imidazoles inhibidores de la lipoxigenasa.

Info

Publication number
ES2152539T3
ES2152539T3 ES96923010T ES96923010T ES2152539T3 ES 2152539 T3 ES2152539 T3 ES 2152539T3 ES 96923010 T ES96923010 T ES 96923010T ES 96923010 T ES96923010 T ES 96923010T ES 2152539 T3 ES2152539 T3 ES 2152539T3
Authority
ES
Spain
Prior art keywords
halo
alkyl
pct
substituted
alkoxy
Prior art date
Legal status (The legal status 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 status listed.)
Expired - Lifetime
Application number
ES96923010T
Other languages
English (en)
Inventor
Takashi Mano
Rodney W Stevens
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Pfizer Inc
Original Assignee
Pfizer 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 Pfizer Inc filed Critical Pfizer Inc
Application granted granted Critical
Publication of ES2152539T3 publication Critical patent/ES2152539T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/08—Antiallergic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Pulmonology (AREA)
  • Immunology (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

LA PRESENTE INVENCION PROPONE UN COMPUESTO DE FORMULA (I) Y UNA SAL FARMACEUTICAMENTE ACEPTABLE DEL MISMO, DONDE AR ES FENILENO OPCIONALMENTE SUSTITUIDO CON HALO, HIDROXI, CIANO, AMINO, ALQUILO C 1 - C 4 , ALCOXI C 1 - C 4 , A LQUILTIO C 1 - C 4 , HALOALQUILO C 1 - C 4 O HALOALCOXI C 1 - C 4 ; X ES - A - X 1 - O - X SUP,1 - A -, DONDE A ES UN ENLACE DIRECTO O UN ALQUILENO C SUB,1 - C 4 , Y X 1 ES OXI, TIO, SULFINILO O SULFONILO; AR 1 ES FENILENO, PIRIDILENO O TIENILENO OPCIONALMENTE SUSTITUIDO CON HALO, HIDROXI, CIANO, NITRO, AMINO, ALQUILO C SUB,1 - C 4 , ALCOXI C 1 - C 4 , ALQUILTIO C 1 - C 4 , HALOALQUILO C 1 - C 4 , HALOALCOXI C SUB,1 - C 4 , ALQUILAMINO C 1 - C 4 O DI(ALQUIL C SUB,1 C 4 )AMINO; Y ES CN O CONR 1 R 2 DONDE R SUP,1 Y R 2 SON INDEPENDIENTEMENTE HIDROGENO O ALQUILO C SUB,1 C 4 ; Y R ES HIDROGENO O ALQUILO C 1 - C 6; W ES ALQUILENO C 2 - C 3 , UNO DE CUYOS ATOMOS DE CARBONO PUEDE SER REEMPLAZADO POR UN ATOMO DE OXIGENO. LA INVENCION PROPONE ADEMAS UNA COMPOSICION FARMACEUTICA PARA TRATAR ENFERMEDADES INFLAMATORIAS, ALERGIAS O ENFERMEDADES CARDIOVASCULARES O SIMILARES EN MAMIFEROS QUE INCLUYE UN COMPUESTO DE FORMULA (I) Y UN PORTADOR FARMACEUTICAMENTE ACEPTABLE.
ES96923010T 1995-09-18 1996-07-24 Imidazoles inhibidores de la lipoxigenasa. Expired - Lifetime ES2152539T3 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
IB9500767 1995-09-18
PCT/IB1996/000744 WO1997011079A1 (en) 1995-09-18 1996-07-24 Novel imidazole lipoxygenase inhibitors

Publications (1)

Publication Number Publication Date
ES2152539T3 true ES2152539T3 (es) 2001-02-01

Family

ID=11004367

Family Applications (1)

Application Number Title Priority Date Filing Date
ES96923010T Expired - Lifetime ES2152539T3 (es) 1995-09-18 1996-07-24 Imidazoles inhibidores de la lipoxigenasa.

Country Status (11)

Country Link
US (1) US6037355A (es)
EP (1) EP0863905B1 (es)
JP (1) JP3110049B2 (es)
AT (1) ATE197796T1 (es)
CA (1) CA2232267C (es)
DE (1) DE69611101T2 (es)
DK (1) DK0863905T3 (es)
ES (1) ES2152539T3 (es)
GR (1) GR3035279T3 (es)
PT (1) PT863905E (es)
WO (1) WO1997011079A1 (es)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6344563B1 (en) * 1999-08-31 2002-02-05 Timothy Norris Process for making 5-lipoxygenase inhibitors having varied heterocyclic ring systems
MX2009005526A (es) 2006-11-27 2009-06-05 Pfizer Prod Inc Analogos de pirazol.
EP3083577A4 (en) * 2013-12-19 2017-08-16 Archer Daniels Midland Co. Sulfonates of furan-2,5-dimethanol and (tetrahydrofuran-2,5-diyl)dimethanol and derivatives thereof

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IE911853A1 (en) * 1990-06-21 1992-01-01 Ici Plc Heterocyclene derivatives
EP0462830B1 (en) * 1990-06-21 1995-10-18 Zeneca Limited Cyclic ether derivatives
JPH09504775A (ja) * 1993-06-02 1997-05-13 ゼネカ・リミテッド 二環式エーテル誘導体および５−リポキシゲナーゼ阻害物質としてのそれらの使用
RU2126004C1 (ru) * 1993-06-14 1999-02-10 Пфайзер, Инк. Производные имидазола или их фармацевтически приемлемые соли
US5459271A (en) * 1993-07-20 1995-10-17 Merck Frosst Canada, Inc. Arylbicyclooctanes as inhibitors of leukotriene biosynthesis

Also Published As

Publication number Publication date
EP0863905B1 (en) 2000-11-29
DE69611101D1 (de) 2001-01-04
PT863905E (pt) 2001-03-30
MX9802103A (es) 1998-08-30
DK0863905T3 (da) 2001-01-02
JP3110049B2 (ja) 2000-11-20
ATE197796T1 (de) 2000-12-15
DE69611101T2 (de) 2001-04-05
CA2232267C (en) 2002-06-11
EP0863905A1 (en) 1998-09-16
WO1997011079A1 (en) 1997-03-27
US6037355A (en) 2000-03-14
CA2232267A1 (en) 1997-03-27
GR3035279T3 (en) 2001-04-30
JPH10511115A (ja) 1998-10-27

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