WO2007138472A3 - Dérivés de la triazolopyridazine - Google Patents
Dérivés de la triazolopyridazine Download PDFInfo
- 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
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).
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP07734734A EP2032578A2 (fr) | 2006-05-30 | 2007-05-18 | Dérivés de la triazolopyridazine |
CA002651979A CA2651979A1 (fr) | 2006-05-30 | 2007-05-18 | Derives de la triazolopyridazine |
JP2009512702A JP2009538899A (ja) | 2006-05-30 | 2007-05-18 | トリアゾロピリダジン誘導体 |
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) |
Families Citing this family (48)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
MX2008008277A (es) | 2005-12-21 | 2009-03-04 | Janssen Pharmaceutica Nv | Triazolopiridazinas como moduladores de tirosina cinasa. |
US8217177B2 (en) | 2006-07-14 | 2012-07-10 | Amgen Inc. | Fused heterocyclic derivatives and methods of use |
PE20080403A1 (es) * | 2006-07-14 | 2008-04-25 | Amgen Inc | Derivados heterociclicos fusionados y metodos de uso |
US8198448B2 (en) | 2006-07-14 | 2012-06-12 | Amgen Inc. | Fused heterocyclic derivatives and methods of use |
DK2081937T3 (da) * | 2006-10-23 | 2012-10-01 | Sgx Pharmaceuticals Inc | Triazolopyridazin-proteinkinasemodulatorer |
EP2170337A4 (fr) | 2007-06-28 | 2013-12-18 | Abbvie Inc | Nouvelles triazolopyridazines |
PA8792501A1 (es) * | 2007-08-09 | 2009-04-23 | Sanofi Aventis | Nuevos derivados de 6-triazolopiridacina-sulfanil benzotiazol y bencimidazol,su procedimiento de preparación,su aplicación como medicamentos,composiciones farmacéuticas y nueva utilización principalmente como inhibidores de met. |
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 |
KR20100128305A (ko) | 2008-02-28 | 2010-12-07 | 노파르티스 아게 | C-met 티로신 키나제 매개 질환의 치료를 위한 이미다조[1,2-b]피리다진 유도체 |
WO2009126861A2 (fr) | 2008-04-11 | 2009-10-15 | Bristol-Myers Squibb Company | Composés de triazolopyridine utiles en tant qu'inhibiteurs de dgat1 |
WO2009126624A1 (fr) | 2008-04-11 | 2009-10-15 | Bristol-Myers Squibb Company | Composés triazolos 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 |
CA2743000A1 (fr) * | 2008-11-19 | 2010-05-27 | Vertex Pharmaceuticals Incorporated | Inhibiteur a base de triazolothiadiazole de proteine kinase c-met |
WO2010059771A1 (fr) | 2008-11-20 | 2010-05-27 | Osi Pharmaceuticals, Inc. | Pyrrolo[2,3-b]-pyridines et pyrrolo[2,3-b]-pyrazines substituées |
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 |
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. |
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. |
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. |
KR20110113755A (ko) | 2009-02-10 | 2011-10-18 | 아스트라제네카 아베 | 트리아졸로 〔4,3-b〕 피리다진 유도체 및 전립샘암에 대한 이의 용도 |
CN102448969A (zh) * | 2009-05-28 | 2012-05-09 | 沃泰克斯药物股份有限公司 | C-met蛋白激酶抑制剂 |
US8389526B2 (en) | 2009-08-07 | 2013-03-05 | Novartis Ag | 3-heteroarylmethyl-imidazo[1,2-b]pyridazin-6-yl derivatives |
BR112012003262A8 (pt) | 2009-08-12 | 2016-05-17 | Novartis Ag | compostos de hidrazona heterocíclica e seus usos para tratar câncer e inflamação |
WO2011020861A1 (fr) | 2009-08-20 | 2011-02-24 | Novartis Ag | Composés d'oximes hétérocycliques |
PE20160588A1 (es) | 2009-12-31 | 2016-07-09 | Hutchison Medipharma Ltd | Compuestos de triazolopiridinas y triazolopirazinas inhibidores de c-met y composiciones de los mismos |
JP2013526570A (ja) | 2010-05-14 | 2013-06-24 | オーエスアイ・ファーマシューティカルズ,エルエルシー | 縮合二環式キナーゼ阻害剤 |
AR081039A1 (es) | 2010-05-14 | 2012-05-30 | Osi Pharmaceuticals Llc | Inhibidores biciclicos fusionados de quinasa |
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 |
EP2588455B1 (fr) * | 2010-07-02 | 2018-04-04 | Gilead Sciences, Inc. | Dérivés de l'acide 2-quinolinyl-acétique en tant que composés antiviraux hiv |
MA34397B1 (fr) | 2010-07-02 | 2013-07-03 | Gilead Sciences Inc | Dérivés d'acide napht-2-ylacétique dans le traitement du sida |
UA111841C2 (uk) | 2011-04-21 | 2016-06-24 | Гіліад Сайєнсіз, Інк. | Сполуки бензотіазолу та їх фармацевтичне застосування |
JP2014513724A (ja) | 2011-05-16 | 2014-06-05 | オーエスアイ・ファーマシューティカルズ,エルエルシー | 融合二環キナーゼ阻害剤 |
CA2848809A1 (fr) | 2011-09-15 | 2013-03-21 | Novartis Ag | 3-(quinolin-6-ylthio)-[1,2,4]triazolo[4,3-a]pyradines substituees en position 6 a activite tyrosine kinase |
US9376392B2 (en) | 2012-01-04 | 2016-06-28 | Gilead Sciences, Inc. | 2-(tert-butoxy)-2-(7-methylquinolin-6-yl) acetic acid derivatives for treating AIDS |
US9284323B2 (en) | 2012-01-04 | 2016-03-15 | Gilead Sciences, Inc. | Naphthalene acetic acid derivatives against HIV infection |
PE20141558A1 (es) | 2012-04-20 | 2014-11-06 | Gilead Sciences Inc | Derivados de acido benzotiazol-6-il acetico y su uso para tratar una infeccion por 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 |
US10398774B2 (en) | 2014-12-09 | 2019-09-03 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Human monoclonal antibodies against 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 |
CN106924260B (zh) * | 2015-12-31 | 2018-05-25 | 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]三唑[4,3-b]哒嗪类化合物及其制法与应用 |
Citations (5)
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 |
-
2007
- 2007-05-18 JP JP2009512702A patent/JP2009538899A/ja not_active Withdrawn
- 2007-05-18 WO PCT/IB2007/001446 patent/WO2007138472A2/fr active Application Filing
- 2007-05-18 EP EP07734734A patent/EP2032578A2/fr not_active Withdrawn
- 2007-05-18 CA CA002651979A patent/CA2651979A1/fr not_active Abandoned
Patent Citations (5)
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)
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 |
---|---|
JP2009538899A (ja) | 2009-11-12 |
CA2651979A1 (fr) | 2007-12-06 |
WO2007138472A2 (fr) | 2007-12-06 |
EP2032578A2 (fr) | 2009-03-11 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO2007138472A3 (fr) | Dérivés de la triazolopyridazine | |
RS20080533A (en) | Triazolopyrazine derivatives useful as anticancer agents | |
CA2510853A1 (fr) | Derives de pyrrolopyrimidine | |
WO2007061360A3 (fr) | Nouveau composes | |
WO2007020213A3 (fr) | Derives de thiazolylpiperidines | |
WO2009155121A3 (fr) | Inhibiteurs de la pi3 kinase | |
WO2005080352A3 (fr) | Derives de quinazoline et leur utilisation therapeutique | |
TW200728307A (en) | Novel spirochromanone derivatives | |
WO2008012635A3 (fr) | Dérivés d'amines utiles en tant qu'agents anticancéreux | |
WO2008001195A3 (fr) | Nouveaux procédés de synthèse d'inhibiteurs de dpp iv | |
WO2007112000A3 (fr) | Traitement de la douleur | |
TW200626158A (en) | Naphthaline derivatives | |
WO2005075425A3 (fr) | Derives de bisaryluree | |
WO2007135527A3 (fr) | Composés de benzimidazolyle | |
WO2006116733A3 (fr) | Inhibiteurs des proteines kinases | |
TW200722081A (en) | New therapeutic combinations for the treatment or prevention of depression | |
WO2006116148A3 (fr) | Traitement de l'abus de substances toxiques | |
WO2006077024A3 (fr) | Derives de 5-aminoindole | |
WO2007046867A3 (fr) | Derives de piperidine et leurs utilisations comme agents therapeutiques | |
WO2008006795A3 (fr) | Composés d'indole | |
TW200639156A (en) | New compounds | |
WO2006117211A3 (fr) | Derives d'uree, procedes pour leur fabrication et utilisations de ces derives | |
TW200716547A (en) | Piperidin-4-yl-amide derivatives | |
WO2003074529A3 (fr) | Derives indolyl-uree de thienopyridines utilises comme agents antiangiogeniques, et leurs methodes d'utilisation | |
WO2007131907A3 (fr) | Dérivés de 1h-indol-5-yl-pipérazin-1-yl-méthanone |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 07734734 Country of ref document: EP Kind code of ref document: A2 |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2651979 Country of ref document: CA |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2009512702 Country of ref document: JP |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2007734734 Country of ref document: EP |