ES2153809T1 - Inhibicion de la cinasa de raf por uso de difenil-ureas sustituidas simetrica y asimetricamente. - Google Patents

Inhibicion de la cinasa de raf por uso de difenil-ureas sustituidas simetrica y asimetricamente.

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Publication number
ES2153809T1
ES2153809T1 ES98963809T ES98963809T ES2153809T1 ES 2153809 T1 ES2153809 T1 ES 2153809T1 ES 98963809 T ES98963809 T ES 98963809T ES 98963809 T ES98963809 T ES 98963809T ES 2153809 T1 ES2153809 T1 ES 2153809T1
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Spain
Prior art keywords
optionally substituted
alkyl
halogen
alkoxy
until reaching
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ES98963809T
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English (en)
Other versions
ES2153809T3 (es
Inventor
Scott Miller
Martin Osterhout
Jacques Dumas
Uday Khire
Timothy Bruno Lowinger
Bernd Riedl
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Bayer AG
Bayer Corp
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Bayer AG
Bayer Corp
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Publication of ES2153809T3 publication Critical patent/ES2153809T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Separation Of Suspended Particles By Flocculating Agents (AREA)

Abstract

Un compuesto de fórmula I: **fórmula I** en la que A es **fórmula II** R3, R4, R5 y R6 son, cada uno independientemente, H, halógeno, NO2, alquilo C1-10, opcionalmente sustituido con halógeno hasta llegar a perhaloalquilo, alcoxi C1-10, opcionalmente sustituido con halógeno hasta llegar a perhaloalcoxi, arilo C6-12, opcionalmente sustituido con alquilo C1-10 ó alcoxi C1-10, ó heteroarilo C5-12, opcionalmente sustituido con alquilo C1-10 ó alcoxi C1-10, y uno de los R3-R6 puede ser -X-Y; o dos R3-R 6 adyacentes pueden ser en común un anillo de arilo o heteroarilo con 5-12 átomos, opcionalmente sustituido con alquilo C1-10, alcoxi C1-10, cicloaquilo C3-10, alquenilo C2-10, alcanoílo C1-10, arilo C6-12, heteroarilo C5-12; arilalquilo C6-12, alquilarilo C6-12, halógeno; NR1 R1 ; -NO2; -CF3; -COOR1 ; -NHCOR 1 ; -CN; -CONR1 R1 ; -SO2R2 ; -SOR2 ; -SR2 ; en que R1 es H o alquilo C1-10 y R2 es alquilo C1-10, opcionalmente sustituido con halógeno hasta llegar a perhalo, estando el -S(O2)- opcionalmente incorporado en el anillo de arilo o heteroarilo; R4'',R5'' y R6'' son independientemente H, halógeno, alquilo C1-C10, opcionalmente sustituido con halógeno hasta llegar a perhaloalquilo, **fórmula III** alcoxi C1-C10 opcionalmente sustituido con halógeno hasta llegar a perhaloalcoxi o -X-Y, y uno cualquiera de los R4'', R5'' ó R6'' es -X-Y, o dos radicales adyacentes de R4 0, R 5 0 y R 6 0 en común son un anillo heteroarilo con 5-12 átomos, opcionalmente sustituido con alquilo C1-10, alcoxiC1-10, cicloalquilo C3-10, alquenilo C2-10, alcanoílo C1-10, arilo C6-12, heteroarilo C5-12 o arilalquilo C6-12; R6 0 es adicionalmente -NHCOR 1 , -NR 1 COR 1 ó NO2; R1 es alquilo C1-10 opcionalmente sustituido con halógeno hasta llegar a perhalo; R3 0 es H, halógeno, alquilo C1-C10, opcionalmente sustituido con halógeno hasta llegar a perhaloalquilo, alcoxi C1-C10, opcionalmente sustituido con halógeno hasta llegar a perhaloalcoxi; X es-CH2-, -S-, -N(CH3)-, -NHC(O)-, -CH2-S-, -S-CH2-, -C(O)- o -O-; y X es adicionalmente un enlace simple cuando Y es piridilo; e Y es fenilo, piridilo, naftilo, piridona, pirazina, pirimidina, benzodioxano, benzopiridina o benzotiazol, cada uno opcionalmente sustituido con alquilo C1-10, alcoxi C1-10, halógeno, OH, -SCH3, NO2 o, cuando Y es fenilo, con **fórmula IV** o una de sus sales farmacéuticamente aceptables, con la condición de que si X es -O- o -S-, R3'' y R6'' son H, e Y es fenilo sin sustituir con OH, entonces R6 ha de ser alcoxi.
ES98963809T 1997-12-22 1998-12-22 Inhibicion de la cinasa raf por uso de difnil-ureas sustituidas simetrica y asimetricamente. Expired - Lifetime ES2153809T3 (es)

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