WO2007138472A3 - Dérivés de la triazolopyridazine - Google Patents

Dérivés de la triazolopyridazine Download PDF

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Publication number
WO2007138472A3
WO2007138472A3 PCT/IB2007/001446 IB2007001446W WO2007138472A3 WO 2007138472 A3 WO2007138472 A3 WO 2007138472A3 IB 2007001446 W IB2007001446 W IB 2007001446W WO 2007138472 A3 WO2007138472 A3 WO 2007138472A3
Authority
WO
WIPO (PCT)
Prior art keywords
compounds
formula
triazolopyridazine derivatives
relates
triazolopyridazine
Prior art date
Application number
PCT/IB2007/001446
Other languages
English (en)
Other versions
WO2007138472A2 (fr
Inventor
Hengmiao Cheng
Jingrong Jean Cui
Jacqui Elizabeth Hoffman
Lei Jia
Robert Steven Kania
Phuong Thi Quy Le
Mitchell David Nambu
Mason Alan Pairish
Hong Shen
Michelle Bich Tran-Dube
Original Assignee
Pfizer Prod Inc
Hengmiao Cheng
Jingrong Jean Cui
Jacqui Elizabeth Hoffman
Lei Jia
Robert Steven Kania
Phuong Thi Quy Le
Mitchell David Nambu
Mason Alan Pairish
Hong Shen
Michelle Bich Tran-Dube
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 Prod Inc, Hengmiao Cheng, Jingrong Jean Cui, Jacqui Elizabeth Hoffman, Lei Jia, Robert Steven Kania, Phuong Thi Quy Le, Mitchell David Nambu, Mason Alan Pairish, Hong Shen, Michelle Bich Tran-Dube filed Critical Pfizer Prod Inc
Priority to JP2009512702A priority Critical patent/JP2009538899A/ja
Priority to CA002651979A priority patent/CA2651979A1/fr
Priority to EP07734734A priority patent/EP2032578A2/fr
Publication of WO2007138472A2 publication Critical patent/WO2007138472A2/fr
Publication of WO2007138472A3 publication Critical patent/WO2007138472A3/fr

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
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Oncology (AREA)
  • Hematology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

La présente invention concerne des composés de formule (I) ou un de leurs sels pharmaceutiquement acceptable, dans laquelle R1, R2, R3 et R3' sont tels que définis ici. L'invention concerne également des compositions pharmaceutiques contenant les composés de formule (I) et des procédés de traitement des affections hyperprolifératives chez un mammifère par l'administration des composés de formule (I).
PCT/IB2007/001446 2006-05-30 2007-05-18 Dérivés de la triazolopyridazine WO2007138472A2 (fr)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP2009512702A JP2009538899A (ja) 2006-05-30 2007-05-18 トリアゾロピリダジン誘導体
CA002651979A CA2651979A1 (fr) 2006-05-30 2007-05-18 Derives de la triazolopyridazine
EP07734734A EP2032578A2 (fr) 2006-05-30 2007-05-18 Dérivés de la triazolopyridazine

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US80346906P 2006-05-30 2006-05-30
US60/803,469 2006-05-30

Publications (2)

Publication Number Publication Date
WO2007138472A2 WO2007138472A2 (fr) 2007-12-06
WO2007138472A3 true WO2007138472A3 (fr) 2008-02-07

Family

ID=38626862

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/IB2007/001446 WO2007138472A2 (fr) 2006-05-30 2007-05-18 Dérivés de la triazolopyridazine

Country Status (4)

Country Link
EP (1) EP2032578A2 (fr)
JP (1) JP2009538899A (fr)
CA (1) CA2651979A1 (fr)
WO (1) WO2007138472A2 (fr)

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US8198448B2 (en) 2006-07-14 2012-06-12 Amgen Inc. Fused heterocyclic derivatives and methods of use
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WO2009005675A1 (fr) 2007-06-28 2009-01-08 Abbott Laboratories Nouvelles triazolopyridazines
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FR2919870B1 (fr) * 2007-08-09 2014-05-16 Sanofi Aventis Nouveaux derives de 6-triazolopyridazine-sulfanyl benzothiazole et benzothiazole et benzimidazole, procede, compositions pharmaceutiques et nouvelle utilisation comme inhibiteurs de cmet
WO2009106577A1 (fr) 2008-02-28 2009-09-03 Novartis Ag Dérivés d’imidazo[1,2-b]pyridazine pour le traitement de maladies médiées par la tyrosine kinase c-met
US8324241B2 (en) 2008-04-11 2012-12-04 Bristol-Myers Squibb Company Triazolo compounds useful as DGAT1 inhibitors
WO2009126861A2 (fr) 2008-04-11 2009-10-15 Bristol-Myers Squibb Company Composés de triazolopyridine utiles en tant qu'inhibiteurs de dgat1
DE102008028905A1 (de) 2008-06-18 2009-12-24 Merck Patent Gmbh 3-(3-Pyrimidin-2-yl-benzyl)-[1,2,4]triazolo[4,3-b]pyridazinderivate
DE102008037790A1 (de) 2008-08-14 2010-02-18 Merck Patent Gmbh Bicyclische Triazolderivate
DE102008038222A1 (de) 2008-08-18 2010-02-25 Merck Patent Gmbh Indazol-5-carbonsäurehydrazid-derivate
DE102008038221A1 (de) 2008-08-18 2010-02-25 Merck Patent Gmbh 7-Azaindolderivate
DE102008038220A1 (de) 2008-08-18 2010-02-25 Merck Patent Gmbh Oxadiazolderivate
NZ592825A (en) * 2008-11-19 2013-01-25 Vertex Pharma A triazolothiadiazole inhibitor of c-met protein kinase
US8592448B2 (en) 2008-11-20 2013-11-26 OSI Pharmaceuticals, LLC Substituted pyrrolo[2,3-b]-pyridines and -pyrazines
DE102008063667A1 (de) 2008-12-18 2010-07-01 Merck Patent Gmbh 3-(3-Pyrimidin-2-yl-benzyl)-°[1,2,4]triazolo[4,3-b]pyrimidin-derivate
DE102008062825A1 (de) 2008-12-23 2010-06-24 Merck Patent Gmbh 3-(3-Pyrimidin-2-yl-benzyl)-[1,2,4]triazolo [4,3-b]pyridazin-derivate
FR2941950B1 (fr) * 2009-02-06 2011-04-01 Sanofi Aventis Derives de 6-(6-o-substitue-triazolopyridazine-sulfanyl) benzothiazoles et benzimidazoles : preparation, application comme medicaments et utilisation comme inhibiteurs de met.
FR2941951B1 (fr) * 2009-02-06 2011-04-01 Sanofi Aventis Derives de 6-(6-nh-substitue-triazolopyridazine-sulfanyl) benzothiazoles et benzimidazoles : preparation, application comme medicaments et utilisation comme inhibiteurs de met.
FR2941949B1 (fr) * 2009-02-06 2011-04-01 Sanofi Aventis Derives de 6-(6-o-cycloalkyl ou 6-nh-cycloalkyl- triazolopyridazine-sulfanyl)benzothiazoles et benzimidazoles preparation, application comme medicaments et utilisation comme inhibiteurs de met.
FR2941952B1 (fr) * 2009-02-06 2011-04-01 Sanofi Aventis Derives de 6-(6-substitue-triazolopyridazine-sulfanyl) 5-fluoro-benzothiazoles et 5-fluoro-benzimidazoles : preparation, application comme medicaments et utilisation comme inhibiteurs de met.
EA019647B1 (ru) * 2009-02-10 2014-05-30 Астразенека Аб ПРОИЗВОДНЫЕ ТРИАЗОЛО[4,3-b]ПИРИДАЗИНА И ИХ ПРИМЕНЕНИЕ ДЛЯ ЛЕЧЕНИЯ РАКА ПРЕДСТАТЕЛЬНОЙ ЖЕЛЕЗЫ
US8263776B2 (en) 2009-05-28 2012-09-11 Vertex Pharmaceuticals Incorporated Inhibitors of c-Met protein kinase
US8389526B2 (en) 2009-08-07 2013-03-05 Novartis Ag 3-heteroarylmethyl-imidazo[1,2-b]pyridazin-6-yl derivatives
MX2012001838A (es) 2009-08-12 2012-02-29 Novartis Ag Compuestos de hidrazona heterociclico y sus usos para tratar cancer e inflamacion.
IN2012DN01453A (fr) 2009-08-20 2015-06-05 Novartis Ag
PT3795573T (pt) 2009-12-31 2022-09-15 Hutchison Medipharma Ltd Certas triazolopirazinas, suas composições e seus métodos de utilização
AR081039A1 (es) 2010-05-14 2012-05-30 Osi Pharmaceuticals Llc Inhibidores biciclicos fusionados de quinasa
EP2569315A1 (fr) 2010-05-14 2013-03-20 OSI Pharmaceuticals, LLC Inhibiteurs de kinases bicycliques fusionnés
US20130315895A1 (en) 2010-07-01 2013-11-28 Takeda Pharmaceutical Company Limited COMBINATION OF A cMET INHIBITOR AND AN ANTIBODY TO HGF AND/OR cMET
PE20130525A1 (es) * 2010-07-02 2013-05-05 Gilead Sciences Inc Derivados de acido 2 quinolinil acetico como compuestos antivirales frente a vih
ES2634490T3 (es) 2010-07-02 2017-09-28 Gilead Sciences, Inc. Derivados de ácido napht-2-ylacetico para tratar el sida
AU2012245187B2 (en) 2011-04-21 2016-06-30 Gilead Sciences, Inc. Benzothiazole compounds and their pharmaceutical use
US20140088114A1 (en) 2011-05-16 2014-03-27 OSI Pharmaceuticals ,LLC Fused bicyclic kinase inhibitors
EP2755976B1 (fr) 2011-09-15 2018-07-18 Novartis AG 3-(quinolin-6-ylthio)-[1,2,4]triazolo[4,3-a]pyradines substituées en position 6 à activité tyrosine kinase
WO2013103738A1 (fr) 2012-01-04 2013-07-11 Gilead Sciences, Inc. Dérivés d'acide naphtalène acétique contre l'infection par le vih
WO2013103724A1 (fr) 2012-01-04 2013-07-11 Gilead Sciences, Inc. Dérivés d'acide 2-(tert-butoxy)-2-(7-méthylquinoléin-6-yl)acétique pour traiter le sida
CA2850881C (fr) 2012-04-20 2021-02-16 Gilead Sciences, Inc. Derives d'acide benzothiazol-6-yl acetique et leur utilisation dans le traitement d'une infection par le vih
CN104447867B (zh) * 2013-09-17 2017-12-26 江苏天士力帝益药业有限公司 一种噻吩并哌啶衍生物、制备方法及其应用
WO2015134854A2 (fr) * 2014-03-06 2015-09-11 Oyagen, Inc. Antagonistes à petites molécules obtenus par dimérisation de vif à titre d'agents anti-vih et pouvant être utilisés à titre d'agents thérapeutiques
PL224660B1 (pl) * 2014-07-23 2017-01-31 Inst Immunologii I Terapii Doświadczalnej Nowe analogi 1,2,4-triazoli i sposób otrzymywania analogów 1,2,4-triazoli
EP3229836B1 (fr) 2014-12-09 2019-11-13 Institut National de la Sante et de la Recherche Medicale (INSERM) Anticoprs monoclonaux contre 'axl'
WO2016135041A1 (fr) 2015-02-26 2016-09-01 INSERM (Institut National de la Santé et de la Recherche Médicale) Protéines de fusion et anticorps les contenant pour favoriser l'apoptose
CN108853108A (zh) * 2015-12-31 2018-11-23 北京浦润奥生物科技有限责任公司 化合物在制备用于治疗脑胶质瘤的药物中的用途
CN116969955B (zh) * 2023-09-25 2023-12-19 中国药科大学 一种[1,2,4]***[4,3-b]哒嗪类化合物及其制法与应用

Citations (5)

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Publication number Priority date Publication date Assignee Title
WO2002012236A1 (fr) * 2000-08-04 2002-02-14 Bayer Cropscience Ag Triazolopyrid(az)ines substituees en tant qu'agents de traitement des vegetaux (herbicides)
WO2004058769A2 (fr) * 2002-12-18 2004-07-15 Vertex Pharmaceuticals Incorporated Compositions utiles en tant qu'inhibiteurs des proteine kinases
EP1481977A1 (fr) * 2002-03-01 2004-12-01 Yamanouchi Pharmaceutical Co. Ltd. Compose heterocyclique azote
WO2007064797A2 (fr) * 2005-11-30 2007-06-07 Vertex Pharmaceuticals Incorporated Inhibiteurs de c-met et leurs utilisations
WO2007075567A1 (fr) * 2005-12-21 2007-07-05 Janssen Pharmaceutica, N.V. Triazolopyridazines en tant que modulateurs de la tyrosine kinase

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002012236A1 (fr) * 2000-08-04 2002-02-14 Bayer Cropscience Ag Triazolopyrid(az)ines substituees en tant qu'agents de traitement des vegetaux (herbicides)
EP1481977A1 (fr) * 2002-03-01 2004-12-01 Yamanouchi Pharmaceutical Co. Ltd. Compose heterocyclique azote
WO2004058769A2 (fr) * 2002-12-18 2004-07-15 Vertex Pharmaceuticals Incorporated Compositions utiles en tant qu'inhibiteurs des proteine kinases
WO2007064797A2 (fr) * 2005-11-30 2007-06-07 Vertex Pharmaceuticals Incorporated Inhibiteurs de c-met et leurs utilisations
WO2007075567A1 (fr) * 2005-12-21 2007-07-05 Janssen Pharmaceutica, N.V. Triazolopyridazines en tant que modulateurs de la tyrosine kinase

Non-Patent Citations (2)

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Title
CUCEK, KARMEN ET AL: "Synthesis of novel [1,2,4]triazolo[4,3-b]pyridazines", ARKIVOC (GAINESVILLE, FL, UNITED STATES) [ONLINE COMPUTER FILE] , (5), 79-86 CODEN: AGFUAR URL: HTTP://WWW.ARKAT-USA.ORG/ARK/JOURNAL/VOLUME2/PART3/TISLER/MT-161/MT- 161.PDF, 2001, XP002459200 *
KOSARY ET AL.: "Preparation of New[1,2,4]Triazolo[4,3-b]pyridazines", PHARMAZIE, vol. 38, no. 6, 1983, pages 369 - 371, XP001536587 *

Also Published As

Publication number Publication date
WO2007138472A2 (fr) 2007-12-06
CA2651979A1 (fr) 2007-12-06
JP2009538899A (ja) 2009-11-12
EP2032578A2 (fr) 2009-03-11

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