PE20110819A1 - Compuestos de carbazol carboxamida utiles como inhibidores de cinasa - Google Patents

Compuestos de carbazol carboxamida utiles como inhibidores de cinasa

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Publication number
PE20110819A1
PE20110819A1 PE2011001234A PE2011001234A PE20110819A1 PE 20110819 A1 PE20110819 A1 PE 20110819A1 PE 2011001234 A PE2011001234 A PE 2011001234A PE 2011001234 A PE2011001234 A PE 2011001234A PE 20110819 A1 PE20110819 A1 PE 20110819A1
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PE
Peru
Prior art keywords
carbazol
carboxamide
methylpiperazin
carbonyl
kinase inhibitors
Prior art date
Application number
PE2011001234A
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English (en)
Inventor
Qingjie Liu
Douglas G Batt
George V Delucca
Andrew J Tebben
Qing Shi
Original Assignee
Bristol Myers Squibb Co
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Publication date
Application filed by Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co
Publication of PE20110819A1 publication Critical patent/PE20110819A1/es

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    • C07D209/56Ring systems containing three or more rings
    • C07D209/80[b, c]- or [b, d]-condensed
    • C07D209/82Carbazoles; Hydrogenated carbazoles
    • C07D209/88Carbazoles; Hydrogenated carbazoles 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 to carbon atoms of the ring system
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    • 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
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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    • A61P37/02Immunomodulators
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    • C07D487/04Ortho-condensed systems

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
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  • Plural Heterocyclic Compounds (AREA)
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Abstract

SE REFIERE A COMPUESTOS DERIVADOS DE CARBAZOL CARBOXAMIDA DE FORMULA (I) DONDE LAS LINEAS DISCONTINUAS SON UN ENLACE SIMPLE O DOBLE; A ES HALO, CARBOCICLO(C3-C10) SUSTITUIDO CON 0-3 B, ARILO(C6-C10) SUSTITUIDO CON 0-3 B, ENTRE OTROS, EN DONDE B ES HALOGENO, CN, NITRO, -C(=O)O-, ENTRE OTROS; UNO DE D1 Y D2 ES D Y EL OTRO ES H O HALO, EN DONDE D ES HALOGENO, CH=N-OH, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: 4-BROMO-7-(4-METILPIPERAZIN-1-CARBONIL)-9H-CARBAZOL-1-CARBOXAMIDA; 4-(5-AMINONAFTALEN-1-IL)-7-(4-METILPIPERAZIN-1-CARBONIL)-9H-CARBAZOL-1-CARBOXAMIDA; 4-(7-FLUORO-1H-INDOL-6-IL)-7-(4-METILPIPERAZIN-1-CARBONIL)-9H-CARBAZOL-1-CARBOXAMIDA; ENTRE OTROS. TAMBIEN SE REFIERE A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE CINASA INCLUYENDO LA MODULACION DE TIROSINA CINASA DE BRUTON (Btk) SIENDO UTILES EN EL TRATAMIENTO DE LUPUS ERITEMATOSO SISTEMICO, ARTRITIS REUMATOIDE, ESCLEROSIS MULTIPLE, RECHAZO DE TRASPLANTE
PE2011001234A 2008-12-19 2009-12-17 Compuestos de carbazol carboxamida utiles como inhibidores de cinasa PE20110819A1 (es)

Applications Claiming Priority (1)

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US13904708P 2008-12-19 2008-12-19

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PE20110819A1 true PE20110819A1 (es) 2011-11-02

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US (2) US8084620B2 (es)
EP (1) EP2391602B1 (es)
JP (1) JP5487214B2 (es)
KR (1) KR20110098827A (es)
CN (1) CN102325753B (es)
AR (1) AR074812A1 (es)
AU (1) AU2009335821A1 (es)
BR (1) BRPI0922565A2 (es)
CA (1) CA2747670A1 (es)
CL (1) CL2011001516A1 (es)
CO (1) CO6390055A2 (es)
EA (1) EA019041B1 (es)
ES (1) ES2443948T3 (es)
IL (1) IL213185A0 (es)
MX (1) MX2011006171A (es)
NZ (1) NZ593096A (es)
PE (1) PE20110819A1 (es)
SG (1) SG171815A1 (es)
TN (1) TN2011000274A1 (es)
TW (1) TW201028401A (es)
WO (1) WO2010080481A1 (es)
ZA (1) ZA201104469B (es)

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