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MXPA03010583A - Derivados de pirimidina utiles como inhibidores de cox-2 selectivos. - Google Patents

Derivados de pirimidina utiles como inhibidores de cox-2 selectivos.

Info

Publication number
MXPA03010583A
MXPA03010583A MXPA03010583A MXPA03010583A MXPA03010583A MX PA03010583 A MXPA03010583 A MX PA03010583A MX PA03010583 A MXPA03010583 A MX PA03010583A MX PA03010583 A MXPA03010583 A MX PA03010583A MX PA03010583 A MXPA03010583 A MX PA03010583A
Authority
MX
Mexico
Prior art keywords
6alkyl
group
substituted
6alkoxy
formula
Prior art date
Application number
MXPA03010583A
Other languages
English (en)
Inventor
Naylor Alan
Original Assignee
Glaxo Group Ltd
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 Glaxo Group Ltd filed Critical Glaxo Group Ltd
Publication of MXPA03010583A publication Critical patent/MXPA03010583A/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/32One oxygen, sulfur or nitrogen atom
    • C07D239/34One oxygen atom
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • 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
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pain & Pain Management (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Rheumatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Saccharide Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

La presente invencion proporciona los compuestos de la formula (l), en donde: R1 es seleccionado del grupo que consiste de H, alquiloC1-6, alquiloC1-2 substituido de uno a cinco atomos de fluor, alqueniloC3-6, cicloalquiloC3-10alquiloC0-6, cicloalquilo puenteado por C4-12, A(CR4R5), y b(CR4R5)n; R2 es un alquiloC1-2 substituido de uno a cinco atomos de fluor; R3 es seleccionado del grupo que consiste de alquiloC1-6, NH2 y R7CONH; R4 y R5 son seleccionados independientemente de H o alquiloC1-6; A es un heteroarilo de 5- o 6- miembros no substituido o un arilo de 6-miembros no substituido, o un heteroarilo de 5- o 6-miembros o un arilo de 6-miembros substituido por uno o mas de R6; R6 es seleccionado del grupo que consiste de halogeno, alquiloC1-6, alquiloC1-6 substituido con uno o mas atomos de fluor, alcoxiC1-6, aicoxiC1-6 substituido con uno o mas de F, NH2SO2 y alquiloC1-6SO2; B es seleccionado del grupo que consiste de la formula (I) y (II) y en donde (IV) define el punto de adicion del anillo; R7 es seleccionado del grupo que consiste de H, alquiloC1-6 OCOalquiloC1-6 y alquiloC1-6 OCONHalquiloC1-6; y n es de 0 a 4. Los compuestos de la formula (I) son inhibidores potentes y selectivos de COX-2 y se utilizan en el tratamiento del dolor, fiebre e inflamacion de una variedad de condiciones y enfermedades.
MXPA03010583A 2001-05-25 2002-05-23 Derivados de pirimidina utiles como inhibidores de cox-2 selectivos. MXPA03010583A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB0112802.4A GB0112802D0 (en) 2001-05-25 2001-05-25 Pyrimidine derivatives
PCT/GB2002/002415 WO2002096885A1 (en) 2001-05-25 2002-05-23 Pyrimidine derivatives useful as selective cox-2 inhibitors

Publications (1)

Publication Number Publication Date
MXPA03010583A true MXPA03010583A (es) 2004-03-09

Family

ID=9915322

Family Applications (1)

Application Number Title Priority Date Filing Date
MXPA03010583A MXPA03010583A (es) 2001-05-25 2002-05-23 Derivados de pirimidina utiles como inhibidores de cox-2 selectivos.

Country Status (29)

Country Link
US (2) US7026327B2 (es)
EP (2) EP1493735B1 (es)
JP (1) JP4291688B2 (es)
KR (1) KR100889427B1 (es)
CN (1) CN1255387C (es)
AR (1) AR036028A1 (es)
AT (2) ATE412637T1 (es)
AU (1) AU2002302764B2 (es)
BR (1) BR0209787A (es)
CA (1) CA2448192A1 (es)
CO (1) CO5540311A2 (es)
CZ (1) CZ20033204A3 (es)
DE (2) DE60211149T2 (es)
DK (1) DK1390351T3 (es)
ES (2) ES2316918T3 (es)
GB (1) GB0112802D0 (es)
HK (1) HK1063311A1 (es)
HU (1) HUP0401280A3 (es)
IL (1) IL158799A0 (es)
MX (1) MXPA03010583A (es)
MY (1) MY130750A (es)
NO (1) NO326949B1 (es)
NZ (1) NZ529719A (es)
PL (1) PL366514A1 (es)
PT (1) PT1390351E (es)
SI (1) SI1390351T1 (es)
TW (1) TWI327140B (es)
WO (1) WO2002096885A1 (es)
ZA (1) ZA200308826B (es)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0021494D0 (en) 2000-09-01 2000-10-18 Glaxo Group Ltd Chemical comkpounds
GB0112810D0 (en) 2001-05-25 2001-07-18 Glaxo Group Ltd Pyrimidine derivatives
GB0112802D0 (en) 2001-05-25 2001-07-18 Glaxo Group Ltd Pyrimidine derivatives
ATE325115T1 (de) 2002-08-19 2006-06-15 Glaxo Group Ltd Pyrimidinderivate als selektive cox-2-inhibitoren
GB0221443D0 (en) 2002-09-16 2002-10-23 Glaxo Group Ltd Pyridine derivates
GB0227443D0 (en) * 2002-11-25 2002-12-31 Glaxo Group Ltd Pyrimidine derivatives
US20070270428A1 (en) * 2003-11-19 2007-11-22 James Hagan Use of Cyclooxygenase-2 Inhibitors for the Treatment of Depressive Disorders
JP2007511572A (ja) * 2003-11-19 2007-05-10 グラクソ グループ リミテッド 統合失調症治療のためのシクロオキシゲナーゼ−2選択的阻害剤の使用
EP4027993A4 (en) * 2019-09-13 2023-09-20 The Broad Institute Inc. CYCLO-OXYGENASE 2 INHIBITORS AND THEIR USES

Family Cites Families (32)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3149109A (en) 1962-02-20 1964-09-15 Searle & Co Certain 4-trifluoromethyl-2-(oxy/thio) pyrimidines
GB1121922A (en) * 1966-06-17 1968-07-31 Ici Ltd Pyrimidine derivatives
US5474995A (en) 1993-06-24 1995-12-12 Merck Frosst Canada, Inc. Phenyl heterocycles as cox-2 inhibitors
ES2141916T3 (es) 1993-11-30 2000-04-01 Searle & Co Pirazolil-bencenosulfonamidas sustituidas para el tratamiento de la inflamacion.
WO1996007641A1 (en) 1994-09-09 1996-03-14 Nippon Shinyaku Co., Ltd. Heterocyclic derivative and medicine
US5596008A (en) 1995-02-10 1997-01-21 G. D. Searle & Co. 3,4-Diaryl substituted pyridines for the treatment of inflammation
US6342510B1 (en) 1995-06-12 2002-01-29 G. D. Searle & Co. Treatment of inflammation and inflammation-related disorders with a combination of a cyclooxygenase-2 inhibitors and a leukotriene B4 receptor antagonist
US5700816A (en) 1995-06-12 1997-12-23 Isakson; Peter C. Treatment of inflammation and inflammation-related disorders with a combination of a cyclooxygenase-2 inhibitor and a leukotriene A4 hydrolase inhibitor
US6020343A (en) 1995-10-13 2000-02-01 Merck Frosst Canada, Inc. (Methylsulfonyl)phenyl-2-(5H)-furanones as COX-2 inhibitors
JPH09241161A (ja) 1996-03-08 1997-09-16 Nippon Shinyaku Co Ltd 医 薬
JPH09266197A (ja) * 1996-03-28 1997-10-07 Mitsubishi Electric Corp 半導体装置およびその製造方法
CZ292843B6 (cs) * 1996-07-18 2003-12-17 Merck Frosst Canada & Co. Derivát pyridinu a farmaceutický prostředek s jeho obsahem
IL154501A0 (en) 1996-10-15 2003-09-17 Searle & Co Use of cyclooxygenase-2 inhibitors for the manufacture of a medicament for the treatment and prevention of neoplasia
WO1998024782A2 (en) 1996-12-05 1998-06-11 Amgen Inc. Substituted pyrimidine compounds and their use
US6103737A (en) 1997-07-03 2000-08-15 Dupont Pharmaceuticals Company Aryl- and arylamino- substituted heterocycles as corticotropin releasing hormone antagonists
CA2303152A1 (en) * 1997-09-05 1999-03-18 Glaxo Group Limited 2,3-diaryl-pyrazolo[1,5-b]pyridazines derivatives, their preparation and their use as cyclooxygenase 2 (cox-2) inhibitors
US5972986A (en) 1997-10-14 1999-10-26 G.D. Searle & Co. Method of using cyclooxygenase-2 inhibitors in the treatment and prevention of neoplasia
US6306866B1 (en) 1998-03-06 2001-10-23 American Cyanamid Company Use of aryl-substituted pyrimidines as insecticidal and acaricidal agents
DE19909541A1 (de) 1998-03-06 1999-10-14 American Cyanamid Co Herbizide 2-Aryloxy- bzw. 2-Arylthio-6-arylpyrimidine
US6313072B1 (en) 1999-02-18 2001-11-06 American Cyanamid Company Herbicidal 2-aryloxy-or 2-arylthio-6-arylpyrimidines
EP1157025B1 (en) * 1999-02-27 2004-03-10 Glaxo Group Limited Pyrazolopyridines
GB9927844D0 (en) 1999-11-26 2000-01-26 Glaxo Group Ltd Chemical compounds
GB9930358D0 (en) * 1999-12-22 2000-02-09 Glaxo Group Ltd Process for the preparation of chemical compounds
GB0002336D0 (en) * 2000-02-01 2000-03-22 Glaxo Group Ltd Medicaments
GB0002312D0 (en) 2000-02-01 2000-03-22 Glaxo Group Ltd Medicaments
GB0003224D0 (en) 2000-02-11 2000-04-05 Glaxo Group Ltd Chemical compounds
GB0021494D0 (en) 2000-09-01 2000-10-18 Glaxo Group Ltd Chemical comkpounds
US6756498B2 (en) * 2001-04-27 2004-06-29 Smithkline Beecham Corporation Process for the preparation of chemical compounds
GB0112803D0 (en) 2001-05-25 2001-07-18 Glaxo Group Ltd Pyrimidine derivatives
GB0112810D0 (en) 2001-05-25 2001-07-18 Glaxo Group Ltd Pyrimidine derivatives
GB0112802D0 (en) 2001-05-25 2001-07-18 Glaxo Group Ltd Pyrimidine derivatives
US6861249B1 (en) * 2002-04-09 2005-03-01 David Kent Microbial spray for animal waste

Also Published As

Publication number Publication date
PT1390351E (pt) 2006-06-30
AU2002302764B2 (en) 2005-12-01
ES2316918T3 (es) 2009-04-16
IL158799A0 (en) 2004-05-12
NO20035206D0 (no) 2003-11-24
BR0209787A (pt) 2004-06-01
MY130750A (en) 2007-07-31
NO20035206L (no) 2003-11-24
HK1063311A1 (en) 2004-12-24
HUP0401280A3 (en) 2009-06-29
JP2005511485A (ja) 2005-04-28
DK1390351T3 (da) 2006-08-07
EP1390351A1 (en) 2004-02-25
US7026327B2 (en) 2006-04-11
JP4291688B2 (ja) 2009-07-08
EP1493735A1 (en) 2005-01-05
SI1390351T1 (sl) 2006-10-31
NZ529719A (en) 2006-02-24
CN1255387C (zh) 2006-05-10
WO2002096885A1 (en) 2002-12-05
DE60211149T2 (de) 2006-09-07
PL366514A1 (en) 2005-02-07
US20050032821A1 (en) 2005-02-10
CZ20033204A3 (en) 2004-03-17
DE60229669D1 (de) 2008-12-11
ATE412637T1 (de) 2008-11-15
ES2262809T3 (es) 2006-12-01
EP1493735B1 (en) 2008-10-29
CN1537104A (zh) 2004-10-13
ATE325103T1 (de) 2006-06-15
TWI327140B (en) 2010-07-11
HUP0401280A2 (hu) 2004-12-28
GB0112802D0 (en) 2001-07-18
DE60211149D1 (de) 2006-06-08
KR20040030629A (ko) 2004-04-09
ZA200308826B (en) 2005-02-14
NO326949B1 (no) 2009-03-16
KR100889427B1 (ko) 2009-03-23
US20050187235A1 (en) 2005-08-25
CA2448192A1 (en) 2002-12-05
CO5540311A2 (es) 2005-07-29
EP1390351B1 (en) 2006-05-03
AR036028A1 (es) 2004-08-04

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