TW201040187A - 6-(6-o-cycloalkyl-or 6-NH-cycloalkyl-triazolopyridazine-sulfanyl) benzothiazole and benzimidazole derivatives: preparation, and use as medicaments and as MET inhibitors - Google Patents

6-(6-o-cycloalkyl-or 6-NH-cycloalkyl-triazolopyridazine-sulfanyl) benzothiazole and benzimidazole derivatives: preparation, and use as medicaments and as MET inhibitors Download PDF

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Publication number
TW201040187A
TW201040187A TW099103558A TW99103558A TW201040187A TW 201040187 A TW201040187 A TW 201040187A TW 099103558 A TW099103558 A TW 099103558A TW 99103558 A TW99103558 A TW 99103558A TW 201040187 A TW201040187 A TW 201040187A
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group
triazolo
thio
formula
product
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TW099103558A
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Chinese (zh)
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Eric Bacque
Conception Nemecek
Antonio Ugolini
Sylvie Wentzler
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Sanofi Aventis
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic 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
    • C07D487/04Ortho-condensed systems
    • 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
    • A61K31/50Pyridazines; Hydrogenated pyridazines
    • A61K31/5025Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
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    • C07D277/60Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
    • C07D277/62Benzothiazoles
    • C07D277/68Benzothiazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
    • C07D277/82Nitrogen atoms
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links

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  • Oncology (AREA)
  • Dermatology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
TW099103558A 2009-02-06 2010-02-05 6-(6-o-cycloalkyl-or 6-NH-cycloalkyl-triazolopyridazine-sulfanyl) benzothiazole and benzimidazole derivatives: preparation, and use as medicaments and as MET inhibitors TW201040187A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR0900510A FR2941949B1 (fr) 2009-02-06 2009-02-06 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.

Publications (1)

Publication Number Publication Date
TW201040187A true TW201040187A (en) 2010-11-16

Family

ID=40863635

Family Applications (1)

Application Number Title Priority Date Filing Date
TW099103558A TW201040187A (en) 2009-02-06 2010-02-05 6-(6-o-cycloalkyl-or 6-NH-cycloalkyl-triazolopyridazine-sulfanyl) benzothiazole and benzimidazole derivatives: preparation, and use as medicaments and as MET inhibitors

Country Status (18)

Country Link
EP (1) EP2393790A1 (ko)
JP (1) JP2012517407A (ko)
KR (1) KR20110126660A (ko)
CN (1) CN102388029A (ko)
AR (1) AR075248A1 (ko)
AU (1) AU2010212231A1 (ko)
BR (1) BRPI1011354A2 (ko)
CA (1) CA2751525A1 (ko)
CO (1) CO6400222A2 (ko)
EA (1) EA201171010A1 (ko)
FR (1) FR2941949B1 (ko)
IL (1) IL214407A0 (ko)
MA (1) MA33102B1 (ko)
MX (1) MX2011008312A (ko)
SG (1) SG173558A1 (ko)
TW (1) TW201040187A (ko)
UY (1) UY32419A (ko)
WO (1) WO2010089506A1 (ko)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2848809A1 (en) 2011-09-15 2013-03-21 Novartis Ag 6-substituted 3-(quinolin-6-ylthio)-[1,2,4]triazolo[4,3-a]pyradines as c-met tyrosine kinase

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1298125A1 (en) 2001-09-26 2003-04-02 Aventis Pharma S.A. Substituted benzimidazole compounds and their use for the treatment of cancer
WO2007064797A2 (en) * 2005-11-30 2007-06-07 Vertex Pharmaceuticals Incorporated Inhibitors of c-met and uses thereof
CN101360748B (zh) * 2005-11-30 2012-05-30 沃泰克斯药物股份有限公司 c-MET抑制剂及其应用
PL1966214T3 (pl) * 2005-12-21 2017-04-28 Janssen Pharmaceutica N.V. Triazolopirydazyny jako modulatory kinazy tyrozynowej
JP2009538899A (ja) * 2006-05-30 2009-11-12 ファイザー・プロダクツ・インク トリアゾロピリダジン誘導体
PE20121506A1 (es) * 2006-07-14 2012-11-26 Amgen Inc Compuestos triazolopiridinas como inhibidores de c-met
BRPI0717320A2 (pt) * 2006-10-23 2013-10-22 Sgx Pharmaceuticals Inc Triazóis bicíclicos como moduladores de proteína cinase
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.

Also Published As

Publication number Publication date
SG173558A1 (en) 2011-09-29
EA201171010A1 (ru) 2012-03-30
BRPI1011354A2 (pt) 2019-09-24
WO2010089506A1 (fr) 2010-08-12
FR2941949B1 (fr) 2011-04-01
AU2010212231A1 (en) 2011-08-25
CA2751525A1 (fr) 2010-08-12
JP2012517407A (ja) 2012-08-02
MX2011008312A (es) 2011-11-02
CN102388029A (zh) 2012-03-21
MA33102B1 (fr) 2012-03-01
AR075248A1 (es) 2011-03-16
IL214407A0 (en) 2011-09-27
FR2941949A1 (fr) 2010-08-13
CO6400222A2 (es) 2012-03-15
KR20110126660A (ko) 2011-11-23
EP2393790A1 (fr) 2011-12-14
UY32419A (es) 2010-09-30

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