MA33107B1 - Derives de 6-(6-o-substitue-triazolopyridazine-sulfanyl) benzothiazoles et benzimidazoles : preparation, application comme medicaments et utilisation comme inhibiteurs de met - Google Patents

Derives de 6-(6-o-substitue-triazolopyridazine-sulfanyl) benzothiazoles et benzimidazoles : preparation, application comme medicaments et utilisation comme inhibiteurs de met

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Publication number
MA33107B1
MA33107B1 MA34152A MA34152A MA33107B1 MA 33107 B1 MA33107 B1 MA 33107B1 MA 34152 A MA34152 A MA 34152A MA 34152 A MA34152 A MA 34152A MA 33107 B1 MA33107 B1 MA 33107B1
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MA
Morocco
Prior art keywords
substituted
triazolopyridazine
benzothiazoles
sulfanyl
medicaments
Prior art date
Application number
MA34152A
Other languages
English (en)
Inventor
Dominique Damour
Conception Nemececk
Antonio Ugolini
Sylvie Wentzler
Eric Bacque
Original Assignee
Sanofi Sa
Abu Ghazaleh Intellectual Prop
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 Sanofi Sa, Abu Ghazaleh Intellectual Prop filed Critical Sanofi Sa
Publication of MA33107B1 publication Critical patent/MA33107B1/fr

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D277/00Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • 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
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
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    • CCHEMISTRY; METALLURGY
    • 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

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  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
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Abstract

L'INVENTION CONCERNE LES NOUVEAUX PRODUITS DE FORMULE (I): (I) DANS LAQUELLE (II) REPRÉSENTE UNE LIAISON SIMPLE OU DOUBLE; RA REPRÉSENTE -O-Z-RC AVEC Z SIMPLE LIAISON OU ALKYLÈNE ÉVENTUELLEMENT SUBSTITUÉ ET RC REPRÉSENTE CYCLOALKYLE, HÉTÉROCYCLOALKYLE, ARYLE OU HÉTÉROARYLE ÉVENTUELLEMENT SUBSTITUÉS; RB REPRÉSENTE H OU F; AVEC SI RB EST H, ALORS RC N'EST PAS CYCLOALKYLE QUAND Z EST SIMPLE LIAISON ET RC N'EST PAS HÉTÉROCYCLOALKYLE QUAND Z EST ALKYLÈNE; X REPRÉSENTE S, SO OU SO2, A REPRÉSENTE NH OU S; W REPRÉSENTE H, ALKYLE, CYCLOALKYLE OU COR AVEC R REPRÉSENTE CYCLOALKYLE; ALKYLE; ALCOXY; O- PHÉNYLE; -O-(CH2)N-PHÉNYLE AVEC N= 1 À 4; OU NR1 R2 AVEC R1 REPRÉSENTE H OU ALK ET R2 REPRÉSENTE H, CYCLOALKYLE OU ALKYLE; OU BIEN R1, R2 FORMENT AVEC N UN CYCLE RENFERMANT ÉVENTUELLEMENT O, S, N ET/OU NH; TOUS CES RADICAUX ÉTANT ÉVENTUELLEMENT SUBSTITUÉS; CES PRODUITS ÉTANT SOUS TOUTES LES FORMES ISOMÈRES ET LES SELS, À TITRE DE MÉDICAMENTS NOTAMMENT COMME INHIBITEURS DE MET.
MA34152A 2009-02-06 2010-02-04 Derives de 6-(6-o-substitue-triazolopyridazine-sulfanyl) benzothiazoles et benzimidazoles : preparation, application comme medicaments et utilisation comme inhibiteurs de met MA33107B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR0900512A FR2941950B1 (fr) 2009-02-06 2009-02-06 Derives de 6-(6-o-substitue-triazolopyridazine-sulfanyl) benzothiazoles et benzimidazoles : preparation, application comme medicaments et utilisation comme inhibiteurs de met.
PCT/FR2010/050178 WO2010089507A1 (fr) 2009-02-06 2010-02-04 Derives de 6-(6-o-substitue-triazolopyridazine-sulfanyl) benzothiazoles et benzimidazoles : preparation, application comme medicaments et utilisation comme inhibiteurs de met

Publications (1)

Publication Number Publication Date
MA33107B1 true MA33107B1 (fr) 2012-03-01

Family

ID=40872767

Family Applications (1)

Application Number Title Priority Date Filing Date
MA34152A MA33107B1 (fr) 2009-02-06 2010-02-04 Derives de 6-(6-o-substitue-triazolopyridazine-sulfanyl) benzothiazoles et benzimidazoles : preparation, application comme medicaments et utilisation comme inhibiteurs de met

Country Status (19)

Country Link
EP (1) EP2393791A1 (fr)
JP (1) JP2012517408A (fr)
KR (1) KR20110132560A (fr)
CN (1) CN102378759A (fr)
AR (1) AR075249A1 (fr)
AU (1) AU2010212232A1 (fr)
BR (1) BRPI1008232A2 (fr)
CA (1) CA2750875A1 (fr)
CL (1) CL2011001879A1 (fr)
CO (1) CO6400223A2 (fr)
EA (1) EA201171011A1 (fr)
FR (1) FR2941950B1 (fr)
IL (1) IL214406A0 (fr)
MA (1) MA33107B1 (fr)
MX (1) MX2011008319A (fr)
SG (1) SG173559A1 (fr)
TW (1) TW201031670A (fr)
UY (1) UY32420A (fr)
WO (1) WO2010089507A1 (fr)

Families Citing this family (18)

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Publication number Priority date Publication date Assignee Title
EA026655B1 (ru) 2011-09-15 2017-05-31 Новартис Аг 6-ЗАМЕЩЕННЫЕ 3-(ХИНОЛИН-6-ИЛТИО)[1,2,4]ТРИАЗОЛО[4,3-a]ПИРИДИНЫ В КАЧЕСТВЕ ИНГИБИТОРОВ c-MET ТИРОЗИНКИНАЗЫ
US9586963B2 (en) * 2011-09-27 2017-03-07 Genfit Derivatives of 6-substituted triazolopyridazines as Rev-Erb agonists
GB201321745D0 (en) * 2013-12-09 2014-01-22 Ucb Pharma Sa Therapeutic agents
EP4687905A1 (fr) 2023-03-30 2026-02-11 Revolution Medicines, Inc. Compositions pour induire une hydrolyse de ras gtp et leurs utilisations
AU2024265078A1 (en) 2023-05-04 2025-12-11 Revolution Medicines, Inc. Combination therapy for a ras related disease or disorder
IL326136A (en) 2023-08-07 2026-03-01 Revolution Medicines Inc RMC-6291 for use in the treatment of a disease or disorder associated with the RAS protein
US20250154171A1 (en) 2023-10-12 2025-05-15 Revolution Medicines, Inc. Ras inhibitors
WO2025171296A1 (fr) 2024-02-09 2025-08-14 Revolution Medicines, Inc. Inhibiteurs de ras
WO2025240847A1 (fr) 2024-05-17 2025-11-20 Revolution Medicines, Inc. Inhibiteurs de ras
US20250375445A1 (en) 2024-06-07 2025-12-11 Revolution Medicines, Inc. Methods of treating a ras protein-related disease or disorder
WO2025265060A1 (fr) 2024-06-21 2025-12-26 Revolution Medicines, Inc. Compositions thérapeutiques et procédés de gestion d'effets liés au traitement
WO2026006747A1 (fr) 2024-06-28 2026-01-02 Revolution Medicines, Inc. Inhibiteurs de ras
WO2026015825A1 (fr) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Utilisation d'un inhibiteur de ras pour traiter le cancer du pancréas
WO2026015796A1 (fr) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Méthodes de traitement d'une maladie ou d'un trouble lié à ras
WO2026015801A1 (fr) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Méthodes de traitement d'une maladie ou d'un trouble liés à ras
WO2026015790A1 (fr) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Méthodes de traitement d'une maladie ou d'un trouble lié à ras
WO2026050446A1 (fr) 2024-08-29 2026-03-05 Revolution Medicines, Inc. Inhibiteurs de ras
WO2026072904A2 (fr) 2024-09-26 2026-04-02 Revolution Medicines, Inc. Compositions et méthodes de traitement du cancer du poumon

Family Cites Families (7)

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Publication number Priority date Publication date Assignee Title
EP1298125A1 (fr) 2001-09-26 2003-04-02 Aventis Pharma S.A. Benzimidazoles substitués et leur usage comme traitement du cancer
KR20080080584A (ko) * 2005-11-30 2008-09-04 버텍스 파마슈티칼스 인코포레이티드 c-Met의 억제제 및 이의 용도
HUE030390T2 (en) * 2005-12-21 2017-05-29 Janssen Pharmaceutica Nv Triazolopyridazines as tyrosine kinase modulators
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
PE20080403A1 (es) * 2006-07-14 2008-04-25 Amgen Inc Derivados heterociclicos fusionados y metodos de uso
AU2007309149C1 (en) * 2006-10-23 2013-04-04 Sgx Pharmaceuticals, Inc. Bicyclic triazoles as protein kinase modulators
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
WO2010089507A1 (fr) 2010-08-12
UY32420A (es) 2010-09-30
EA201171011A1 (ru) 2012-03-30
IL214406A0 (en) 2011-09-27
FR2941950A1 (fr) 2010-08-13
MX2011008319A (es) 2012-01-25
CA2750875A1 (fr) 2010-08-12
AR075249A1 (es) 2011-03-16
BRPI1008232A2 (pt) 2016-03-08
CN102378759A (zh) 2012-03-14
EP2393791A1 (fr) 2011-12-14
FR2941950B1 (fr) 2011-04-01
CO6400223A2 (es) 2012-03-15
JP2012517408A (ja) 2012-08-02
TW201031670A (en) 2010-09-01
AU2010212232A1 (en) 2011-08-25
SG173559A1 (en) 2011-09-29
CL2011001879A1 (es) 2012-01-06
KR20110132560A (ko) 2011-12-08

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