PE20030712A1 - Indazolilpirrolotriazinas c-5 modificadas - Google Patents

Indazolilpirrolotriazinas c-5 modificadas

Info

Publication number
PE20030712A1
PE20030712A1 PE2002001102A PE2002001102A PE20030712A1 PE 20030712 A1 PE20030712 A1 PE 20030712A1 PE 2002001102 A PE2002001102 A PE 2002001102A PE 2002001102 A PE2002001102 A PE 2002001102A PE 20030712 A1 PE20030712 A1 PE 20030712A1
Authority
PE
Peru
Prior art keywords
indazol
triazin
heterocycle
benzyl
ilmetil
Prior art date
Application number
PE2002001102A
Other languages
English (en)
Inventor
Harold Mastalerz
James G Tarrant
Gregory D Vite
Guifen Zhang
Original Assignee
Bristol Myers Squibb Co
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 Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co
Publication of PE20030712A1 publication Critical patent/PE20030712A1/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic 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
    • C07D487/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic 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
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/009—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone characterised by the material treated
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/45—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements
    • C04B41/4584—Coating or impregnating of particulate or fibrous ceramic material
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2111/00—Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
    • C04B2111/00474—Uses not provided for elsewhere in C04B2111/00
    • C04B2111/00793—Uses not provided for elsewhere in C04B2111/00 as filters or diaphragms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Structural Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Materials Engineering (AREA)
  • General Chemical & Material Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Medicinal Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Inks, Pencil-Leads, Or Crayons (AREA)
  • Photoreceptors In Electrophotography (AREA)

Abstract

SE REFIERE A DERIVADOS DE INDAZOLILPIRROLOTRIAZINAS C-5 MODIFICADAS, DE FORMULA I SUS ENANTIOMEROS, DIASTEREOMEROS, SALES DONDE R ES SR2, SOR2, OR2, NR3R4; R1 ES ARILO, HETEROCICLO, ENTRE OTROS; R2 ES H, ALQUILO, ARILO, ARALQUILO, HETEROCICLO; R3 Y R4 SON H, ALQUILO, ARILO, HETEROCICLO; R2 Y R3 JUNTOS FORMAN UN ANILLO CARBOCICLO, HETEROCICLO. SON COMPUESTOS PREFERIDOS (5-[1,4]DIAZEPAN-1-ILMETIL-PIRROLO[2,1-f][1,2,4]TRIAZIN-4-IL)-[1-(3-FLUOR-BENCIL)-1H-INDAZOL-5-IL]-AMINA, [1-(3-FLUOR-BENCIL)-1H-INDAZOL-5-IL]-(5-IMIDAZOL-1-ILMETIL-PIRROLO[2,1-f][1,2,4]TRIAZIN-5-ILMETIL}-PIPERIDIN-3-CARBOXILICO, AMIDA DEL ACIDO 1-{4-[1-(3-FLUORO-BENCIL)-1H-INDAZOL-5-ILAMINO]-PIRROLO[2,1-f][1,2,4]TRIAZIN-5-ILMETIL}-PIPERIDIN-3-CARBOXILICO, ENTRE OTROS. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA. LOS COMPUESTOS MENCIONADOS INHIBEN LA ACTIVIDAD DE LA TIROSINA CINASA DE LOS RECEPTORES DEL FACTOR DE CRECIMIENTO TALES COMO HER1, HER2, HER4 Y SON UTILES COMO AGENTES ANTIPROLIFERATIVOS
PE2002001102A 2001-11-14 2002-11-14 Indazolilpirrolotriazinas c-5 modificadas PE20030712A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US33301401P 2001-11-14 2001-11-14

Publications (1)

Publication Number Publication Date
PE20030712A1 true PE20030712A1 (es) 2003-08-21

Family

ID=23300880

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2002001102A PE20030712A1 (es) 2001-11-14 2002-11-14 Indazolilpirrolotriazinas c-5 modificadas

Country Status (24)

Country Link
US (2) US6908916B2 (es)
EP (1) EP1446401B1 (es)
JP (1) JP4301440B2 (es)
KR (1) KR20050044441A (es)
CN (1) CN1615306A (es)
AR (1) AR037368A1 (es)
AT (1) ATE524462T1 (es)
BR (1) BR0214112A (es)
CA (1) CA2467068A1 (es)
ES (1) ES2370709T3 (es)
HR (1) HRP20040422A2 (es)
HU (1) HUP0402566A3 (es)
IL (1) IL161616A0 (es)
IS (1) IS7243A (es)
MX (1) MXPA04004492A (es)
NO (1) NO20041983L (es)
NZ (1) NZ533034A (es)
PE (1) PE20030712A1 (es)
PL (1) PL368909A1 (es)
RU (1) RU2004117549A (es)
TW (1) TW200300350A (es)
UY (1) UY27540A1 (es)
WO (1) WO2003042172A2 (es)
ZA (1) ZA200403694B (es)

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US6670357B2 (en) * 2000-11-17 2003-12-30 Bristol-Myers Squibb Company Methods of treating p38 kinase-associated conditions and pyrrolotriazine compounds useful as kinase inhibitors
US6867300B2 (en) 2000-11-17 2005-03-15 Bristol-Myers Squibb Company Methods for the preparation of pyrrolotriazine compounds useful as kinase inhibitors
TW200300350A (en) * 2001-11-14 2003-06-01 Bristol Myers Squibb Co C-5 modified indazolylpyrrolotriazines
DK1497019T3 (en) * 2002-04-23 2015-08-03 Bristol Myers Squibb Co PYRROLO-TRIAZINANILINE COMPOSITIONS USED AS KINase INHIBITORS
US7388009B2 (en) 2002-04-23 2008-06-17 Bristol-Myers Squibb Company Heteroaryl-substituted pyrrolo-triazine compounds useful as kinase inhibitors
EP1503996B1 (en) 2002-04-23 2008-12-24 Bristol-Myers Squibb Company Aryl ketone pyrrolo-triazine compounds useful as kinase inhibitors
TW200401638A (en) * 2002-06-20 2004-02-01 Bristol Myers Squibb Co Heterocyclic inhibitors of kinases
TWI329112B (en) * 2002-07-19 2010-08-21 Bristol Myers Squibb Co Novel inhibitors of kinases
ATE350383T1 (de) 2002-08-23 2007-01-15 Sloan Kettering Inst Cancer Synthese von epothilonen, zwischenprodukte dafür, analoga und deren verwendungen
US7649006B2 (en) 2002-08-23 2010-01-19 Sloan-Kettering Institute For Cancer Research Synthesis of epothilones, intermediates thereto and analogues thereof
TW200420565A (en) 2002-12-13 2004-10-16 Bristol Myers Squibb Co C-6 modified indazolylpyrrolotriazines
CN1771234A (zh) 2003-02-05 2006-05-10 布里斯托尔-迈尔斯斯奎布公司 吡咯并三嗪激酶抑制剂的制备方法
US7102001B2 (en) * 2003-12-12 2006-09-05 Bristol-Myers Squibb Company Process for preparing pyrrolotriazine
US20060014741A1 (en) * 2003-12-12 2006-01-19 Dimarco John D Synthetic process, and crystalline forms of a pyrrolotriazine compound
US7064203B2 (en) * 2003-12-29 2006-06-20 Bristol Myers Squibb Company Di-substituted pyrrolotriazine compounds
MY145634A (en) * 2003-12-29 2012-03-15 Bristol Myers Squibb Co Pyrrolotriazine compounds as kinase inhibitors
US7459562B2 (en) 2004-04-23 2008-12-02 Bristol-Myers Squibb Company Monocyclic heterocycles as kinase inhibitors
TW200538453A (en) 2004-04-26 2005-12-01 Bristol Myers Squibb Co Bicyclic heterocycles as kinase inhibitors
US7102002B2 (en) * 2004-06-16 2006-09-05 Bristol-Myers Squibb Company Pyrrolotriazine kinase inhibitors
US20050288290A1 (en) 2004-06-28 2005-12-29 Borzilleri Robert M Fused heterocyclic kinase inhibitors
US7432373B2 (en) 2004-06-28 2008-10-07 Bristol-Meyers Squibb Company Processes and intermediates useful for preparing fused heterocyclic kinase inhibitors
US7253167B2 (en) 2004-06-30 2007-08-07 Bristol-Myers Squibb Company Tricyclic-heteroaryl compounds useful as kinase inhibitors
TW200600513A (en) 2004-06-30 2006-01-01 Bristol Myers Squibb Co A method for preparing pyrrolotriazine compounds
US7102003B2 (en) * 2004-07-01 2006-09-05 Bristol-Myers Squibb Company Pyrrolotriazine compounds
US7504521B2 (en) 2004-08-05 2009-03-17 Bristol-Myers Squibb Co. Methods for the preparation of pyrrolotriazine compounds
TW200618803A (en) 2004-08-12 2006-06-16 Bristol Myers Squibb Co Process for preparing pyrrolotriazine aniline compounds useful as kinase inhibitors
US7151176B2 (en) 2004-10-21 2006-12-19 Bristol-Myers Squibb Company Pyrrolotriazine compounds
TW200635927A (en) * 2004-12-22 2006-10-16 Bristol Myers Squibb Co Synthetic process
WO2006104971A1 (en) 2005-03-28 2006-10-05 Bristol-Myers Squibb Company Atp competitive kinase inhibitors
US7534882B2 (en) 2005-04-06 2009-05-19 Bristol-Myers Squibb Company Method for preparing pyrrolotriazine compounds via in situ amination of pyrroles
US7547782B2 (en) 2005-09-30 2009-06-16 Bristol-Myers Squibb Company Met kinase inhibitors
US7514435B2 (en) * 2005-11-18 2009-04-07 Bristol-Myers Squibb Company Pyrrolotriazine kinase inhibitors
US7348325B2 (en) 2005-11-30 2008-03-25 Bristol-Myers Squibb Company Pyrrolotriazine kinase inhibitors
US8143393B2 (en) 2005-12-02 2012-03-27 Bayer Healthcare Llc Substituted 4-amino-pyrrolotriazine derivatives useful for treating hyper-proliferative disorders and diseases associated with angiogenesis
PE20070855A1 (es) * 2005-12-02 2007-10-14 Bayer Pharmaceuticals Corp Derivados de 4-amino-pirrolotriazina sustituida como inhibidores de quinasas
US8063208B2 (en) 2006-02-16 2011-11-22 Bristol-Myers Squibb Company Crystalline forms of (3R,4R)-4-amino-1-[[4-[(3-methoxyphenyl)amino]pyrrolo[2,1-f][1,2,4]triazin-5-yl]methyl]piperidin-3-ol
DE102006030479A1 (de) * 2006-07-01 2008-03-20 Merck Patent Gmbh Indazolderivate
US8071779B2 (en) 2006-12-18 2011-12-06 Inspire Pharmaceuticals, Inc. Cytoskeletal active rho kinase inhibitor compounds, composition and use
AR074830A1 (es) 2008-12-19 2011-02-16 Cephalon Inc Pirrolotriazinas como inhibidores de alk y jak2
JPWO2011013656A1 (ja) * 2009-07-28 2013-01-07 宇部興産株式会社 ピロロ［２，３−ｄ］ピリミジン誘導体
CN102627647A (zh) * 2012-03-20 2012-08-08 南京药石药物研发有限公司 4-氯-5-甲基-1H-吡咯并[2,1-f][1,2,4]三嗪的合成方法
WO2014115171A1 (en) * 2013-01-24 2014-07-31 Council Of Scientific & Industrial Research Triazine compounds and a process for preparation thereof
CN105979950A (zh) 2013-10-11 2016-09-28 百时美施贵宝公司 吡咯并三嗪激酶抑制剂
WO2015081783A1 (zh) * 2013-12-06 2015-06-11 江苏奥赛康药业股份有限公司 吡咯并[2,1-f][1,2,4]三嗪类衍生物及其制备方法和用途

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DE69628804T2 (de) 1995-12-08 2003-12-18 Pfizer Inc., New York Substitutierte heterozyclische Derivate als CRF Antagonisten
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TW200400034A (en) * 2002-05-20 2004-01-01 Bristol Myers Squibb Co Pyrazolo-pyrimidine aniline compounds useful as kinase inhibitors
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Also Published As

Publication number Publication date
US20030186983A1 (en) 2003-10-02
ATE524462T1 (de) 2011-09-15
NZ533034A (en) 2004-11-26
UY27540A1 (es) 2003-07-31
HUP0402566A2 (hu) 2005-03-29
MXPA04004492A (es) 2004-08-11
IL161616A0 (en) 2004-09-27
EP1446401B1 (en) 2011-09-14
NO20041983D0 (no) 2004-05-13
AR037368A1 (es) 2004-11-03
US6908916B2 (en) 2005-06-21
PL368909A1 (en) 2005-04-04
JP4301440B2 (ja) 2009-07-22
WO2003042172A2 (en) 2003-05-22
EP1446401A2 (en) 2004-08-18
CN1615306A (zh) 2005-05-11
JP2005509030A (ja) 2005-04-07
RU2004117549A (ru) 2006-01-10
HUP0402566A3 (en) 2009-01-28
TW200300350A (en) 2003-06-01
KR20050044441A (ko) 2005-05-12
NO20041983L (no) 2004-06-24
HRP20040422A2 (en) 2005-04-30
US20050209235A1 (en) 2005-09-22
BR0214112A (pt) 2004-09-14
ZA200403694B (en) 2006-06-28
ES2370709T3 (es) 2011-12-22
CA2467068A1 (en) 2003-05-22
IS7243A (is) 2004-04-30
EP1446401A4 (en) 2006-04-12
WO2003042172A3 (en) 2004-01-29

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