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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
Authority
ES
Spain
Prior art keywords
optionally substituted
alkyl
halogen
alkoxy
until reaching
Prior art date
Legal status (The legal status 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 status listed.)
Granted
Application number
ES98963809T
Other languages
English (en)
Other versions
ES2153809T3 (es
Inventor
Scott Miller
Martin Osterhout
Jacques Dumas
Uday Khire
Timothy Bruno Lowinger
Bernd Riedl
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bayer AG
Bayer Corp
Original Assignee
Bayer AG
Bayer Corp
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Application filed by Bayer AG, Bayer Corp filed Critical Bayer AG
Publication of ES2153809T1 publication Critical patent/ES2153809T1/es
Application granted granted Critical
Publication of ES2153809T3 publication Critical patent/ES2153809T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
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  • Preparation Of Compounds By Using Micro-Organisms (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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AU763024B2 (en) 2003-07-10
DE69829412D1 (de) 2005-04-21
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HUP0004437A3 (en) 2002-10-28
ATE291011T1 (de) 2005-04-15
EP1049664A1 (en) 2000-11-08
IL136690A (en) 2006-12-31
CZ20002351A3 (cs) 2000-12-13
SK286564B6 (sk) 2009-01-07
RU2247109C2 (ru) 2005-02-27
BG64594B1 (bg) 2005-08-31
TR200002616T2 (tr) 2000-11-21
NO329181B1 (no) 2010-09-06
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ES2153809T3 (es) 2005-07-16
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