Heteroaryl amines as glycogen synthase kinase 3beta...

C - Chemistry – Metallurgy – 07 – D

Patent

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C07D 403/12 (2006.01) A61K 31/435 (2006.01) A61K 31/50 (2006.01) A61K 31/505 (2006.01) A61P 3/10 (2006.01) C07D 213/53 (2006.01) C07D 213/74 (2006.01) C07D 239/42 (2006.01) C07D 239/48 (2006.01) C07D 401/04 (2006.01) C07D 401/12 (2006.01) C07D 403/04 (2006.01) C07D 405/12 (2006.01) C07D 409/12 (2006.01) C07D 417/12 (2006.01)

Patent

CA 2463822

This invention concerns a compound of formula (I), a N-oxide, a pharmaceutically acceptable addition salt, a quaternary amine and a stereochemically isomeric form thereof, wherein ring A is a 6-membered heterocycle; R1 is hydrogen; aryl; formyl; C1-6alkylcarbonyl; optionally substituted C1-6alkyl; C1-6alkyloxycarbonyl; optionally substituted C1- 6alkyloxy C1-6alkylcarbonyl; X is a direct bond or a linker atom or group; Z is a direct bond or a linker atom or group; R2 is hydrogen, C1-10alkyl, C2- 10alkenyl, C2-10alkynyl, a carbocycle or a heterocycle, each of said groups may optionally be substituted; R3 is hydrogen; hydroxy; halo; optionally substituted C1-6alkyl or C1-6alkenyl or C2-6alkynyl; C1-6alkyloxy; C1- 6alkylthio; C1-6alkyloxycarbonyl; C1-6alkylcarbonyloxy; carboxyl; cyano; nitro; amino; mono- or di(C1-6alkyl)amino; polyhaloC1-6alkyl; polyhaloC1- 6alkyloxy; polyhaloC1-6alkylthio; R21; R21-C1-6alkyl; R21-O-; R21-S-; R21- C(=0)-; R21-S(=0)p-; R7-S =O R7-S(=O)p-NH-; R21-S(=O)p-NH-; R7-C(=0)-; - NHC(=0)H; -C(=O)NHNH2; R7-C(=O)-NH-; R21-C(=O)-NH-; -C(=NH)R7; -C(=NH)R21; R~ is an optionally substituted heterocycle provided that -X-R2 and/or R3 is other than hydrogen;their use, pharmaceutical compositions comprising them and processes for their preparation.

L'invention concerne un composé de formule (I), un <I>N</I>-oxyde, un sel d'addition pharmaceutiquement acceptable, une amine quaternaire et une forme stéréochimiquement isomère correspondante. Dans ladite formule, la chaîne A est un hétérocycle à 6 chaînons; R?1¿ est hydrogène; aryle; formyle; alkylcarbonyle C¿1-6?; alkyle C¿1-6? éventuellement substitué; alkyloxycarbonyle C¿1-6?; alkyloxy C¿1-6? alkylcarbonyle C¿1-6? éventuellement substitué; X est une liaison directe ou un atome ou un groupe de liaison; Z est une liaison directe ou un atome ou un groupe de liaison; R?2¿ est hydrogène; alkyle C¿1-10?; alcényle C¿2-10; ?alkynyle C¿2-10?; un carbocycle ou un hétérocycle, chacun de ces groupes pouvant être éventuellement substitué; R?3¿ est hydrogène; hydroxy; halo; alkyle C¿1-6? éventuellement substitué ou alcényle C¿2-6? ou alkynyle C¿2-6?; alkyloxy C¿1-6?; alkylthio C¿1-6?; alkyloxycarbonyle C¿1-6?; alkylcarbonyloxy C¿1-6?; carboxyle; cyano; nitro; amino; mono ou di (alkyle C¿1-6?)amino; polyhaloalkyle C¿1-6?; polyhaloalkyloxy C¿1-6?; polyhaloalkylthio C¿1-6?; R?21¿; R?21¿- alkyle C¿1-6?; R?21¿-O-; R?21¿-S-; R?21¿-C(=0)-; R?21¿-S(=0)¿p?-; R?7¿-S(=0)¿p?-; R?7¿-S(=0)¿p?-NH; R?21¿-S(=0)¿p?-NH-; R?7¿-C(=0)-; -NHC(=O)H; -C(=O)NHNH¿2?; R?7¿-C(=0)-NH-;¿ ?R?21¿-C(=0)-NH-; -C(=NH)R?7¿; -C(=NH)R?21¿; R?4¿ est un hétérocycle éventuellement substitué à condition que -X-R?2 ¿et/ou R?3¿ soient autres qu'hydrogène. L'invention concerne également l'utilisation d'un tel composé, des compositions pharmaceutiques à base de ce type de composé, et des procédés d'élaboration correspondants.

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