EA201171010A1 - Derivatives of 6- (6-O-Cycloalkyl- or 6-NH-Cycloalkyltriazolephenyl) Benzenothiazols and Benzimidazols: A METHOD OF OBTAINING, APPLICATION IN THE QUALITY OF DRUGS CORRECTIVE CORRELS CORRELS CORRELS CORRELING CORRELS CORRELING CORRELE-CORRECTIONS - Google Patents

Derivatives of 6- (6-O-Cycloalkyl- or 6-NH-Cycloalkyltriazolephenyl) Benzenothiazols and Benzimidazols: A METHOD OF OBTAINING, APPLICATION IN THE QUALITY OF DRUGS CORRECTIVE CORRELS CORRELS CORRELS CORRELING CORRELS CORRELING CORRELE-CORRECTIONS

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Publication number
EA201171010A1
EA201171010A1 EA201171010A EA201171010A EA201171010A1 EA 201171010 A1 EA201171010 A1 EA 201171010A1 EA 201171010 A EA201171010 A EA 201171010A EA 201171010 A EA201171010 A EA 201171010A EA 201171010 A1 EA201171010 A1 EA 201171010A1
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EA
Eurasian Patent Office
Prior art keywords
correls
correling
cycloalkyl
cycloalkyltriazolephenyl
correle
Prior art date
Application number
EA201171010A
Other languages
Russian (ru)
Inventor
Эрик Бак
Консепсьон Немесек
Антонио Юголини
Сильви Венслер
Батист Ронан
Доминик Дамур
Original Assignee
Санофи
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Publication date
Application filed by Санофи filed Critical Санофи
Publication of EA201171010A1 publication Critical patent/EA201171010A1/en

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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
    • 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
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61P17/06Antipsoriatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P21/00Drugs for disorders of the muscular or neuromuscular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P3/00Drugs for disorders of the metabolism
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    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P35/00Antineoplastic agents
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    • A61P35/00Antineoplastic agents
    • A61P35/04Antineoplastic agents specific for metastasis
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    • A61P37/00Drugs for immunological or allergic disorders
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    • A61P37/08Antiallergic agents
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
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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
    • CCHEMISTRY; METALLURGY
    • 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

Abstract

Изобретение относится к новым соединениям формулы (I), в которойозначает простую или двойную связь; Ra означает -O-циклоалкил или -NH-циклоалкил; Х означает S, SO или SO; А означает NH или S; W означает Н, алкил или COR, где R означает циклоалкил; алкил; алкокси; O-фенил; -O-(CH)-фенил, где n=1-4; или NR1R2, где R1 означает Н или алкил и R2 означает Н, циклоалкил, гетероциклоалкил или алкил; или R1, R2 образуют вместе с N цикл, необязательно содержащий О, S, N и/или NH; причем все эти радикалы необязательно замещены; эти соединения, находящиеся во всех изомерных формах и в виде солей, используются в качестве лекарственных средств, в частности в качестве ингибиторов MET.The invention relates to new compounds of formula (I), in which means a single or double bond; Ra is —O-cycloalkyl or —NH-cycloalkyl; X is S, SO or SO; A is NH or S; W is H, alkyl or COR, where R is cycloalkyl; alkyl; alkoxy; O-phenyl; -O- (CH) -phenyl, where n = 1-4; or NR1R2, where R1 is H or alkyl and R2 is H, cycloalkyl, heterocycloalkyl or alkyl; or R1, R2 form together with N a ring optionally containing O, S, N and / or NH; moreover, all of these radicals are optionally substituted; these compounds, found in all isomeric forms and in the form of salts, are used as medicines, in particular as MET inhibitors.

EA201171010A 2009-02-06 2010-02-04 Derivatives of 6- (6-O-Cycloalkyl- or 6-NH-Cycloalkyltriazolephenyl) Benzenothiazols and Benzimidazols: A METHOD OF OBTAINING, APPLICATION IN THE QUALITY OF DRUGS CORRECTIVE CORRELS CORRELS CORRELS CORRELING CORRELS CORRELING CORRELE-CORRECTIONS EA201171010A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR0900510A FR2941949B1 (en) 2009-02-06 2009-02-06 DERIVATIVES OF 6- (6-O-CYCLOALKYL OR 6-NH-CYCLOALKYL-TRIAZOLOPYRIDAZINE-SULFANYL) BENZOTHIAZOLES AND BENZIMIDAZOLES PREPARATION, APPLICATION AS MEDICAMENTS AND USE AS INHIBITORS OF MET.
PCT/FR2010/050177 WO2010089506A1 (en) 2009-02-06 2010-02-04 Derivatives of 6-(6-o-cycloalkyl or 6-nh-cycloalkyl-triazolopyridazine-sulfanyl) benzothiazoles and benzimidazoles, preparation thereof, use thereof as drugs, and use thereof as met inhibitors

Publications (1)

Publication Number Publication Date
EA201171010A1 true EA201171010A1 (en) 2012-03-30

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
EA201171010A EA201171010A1 (en) 2009-02-06 2010-02-04 Derivatives of 6- (6-O-Cycloalkyl- or 6-NH-Cycloalkyltriazolephenyl) Benzenothiazols and Benzimidazols: A METHOD OF OBTAINING, APPLICATION IN THE QUALITY OF DRUGS CORRECTIVE CORRELS CORRELS CORRELS CORRELING CORRELS CORRELING CORRELE-CORRECTIONS

Country Status (18)

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

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013038362A1 (en) 2011-09-15 2013-03-21 Novartis Ag 6 - substituted 3 - (quinolin- 6 - ylthio) - [1,2,4] triazolo [4, 3 -a] pyradines as 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
ZA200804681B (en) * 2005-11-30 2009-11-25 Vertex Pharma Inc Inhibitors of C-Met and uses thereof
EP1963329B1 (en) * 2005-11-30 2013-01-23 Vertex Pharmaceuticals Incorporated Inhibitors of c-met and uses thereof
ME02736B (en) * 2005-12-21 2017-10-20 Janssen Pharmaceutica Nv Triazolopyridazines as tyrosine kinase modulators
EP2032578A2 (en) * 2006-05-30 2009-03-11 Pfizer Products Incorporated Triazolopyridazine derivatives
PE20121506A1 (en) * 2006-07-14 2012-11-26 Amgen Inc TRIAZOLOPYRIDINE COMPOUNDS AS C-MET INHIBITORS
CA2667428A1 (en) * 2006-10-23 2008-05-02 Sgx Pharmaceuticals, Inc. Bicyclic triazoles as protein kinase modulators
PA8792501A1 (en) * 2007-08-09 2009-04-23 Sanofi Aventis NEW DERIVATIVES OF 6-TRIAZOLOPIRIDACINA-SULFANIL BENZOTIAZOL AND BENCIMIDAZOL, ITS PREPARATION PROCEDURE, ITS APPLICATION AS MEDICATIONS, PHARMACEUTICAL COMPOSITIONS AND NEW MAIN USE AS MET INHIBITORS.

Also Published As

Publication number Publication date
BRPI1011354A2 (en) 2019-09-24
AR075248A1 (en) 2011-03-16
KR20110126660A (en) 2011-11-23
CN102388029A (en) 2012-03-21
SG173558A1 (en) 2011-09-29
MX2011008312A (en) 2011-11-02
EP2393790A1 (en) 2011-12-14
JP2012517407A (en) 2012-08-02
FR2941949A1 (en) 2010-08-13
CO6400222A2 (en) 2012-03-15
CA2751525A1 (en) 2010-08-12
IL214407A0 (en) 2011-09-27
AU2010212231A1 (en) 2011-08-25
WO2010089506A1 (en) 2010-08-12
FR2941949B1 (en) 2011-04-01
TW201040187A (en) 2010-11-16
UY32419A (en) 2010-09-30
MA33102B1 (en) 2012-03-01

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