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TRIAZOLOPYRIMIDINE DERIVATIVES AS GLYCOGEN SYNTHASE KINASE 3 INHIBITORS

机译:三唑嘧啶衍生物作为糖原合成酶激酶3抑制剂

摘要

This invention concerns a compound of formula; ;a N-oxide, a pharmaceutically acceptable addition salt, a quaternary amine and a stereochemically isomeric form thereof, wherein ring A represents phenyl, pyridyl, pyrimidinyl, pyridazinyl or pyrazinyl; R1 represents hydrogen; aryl; formyl; C1-6alkylcarbonyl; C1-6alkyl; C1-6alkyloxycarbonyl; C1-6alkyl substituted with formyl, C1-6alkylcarbonyl, C1-6alkyloxycarbonyl or C1-6alkylcarbonyloxy; X represents a direct bond; —(CH2)n3— or —(CH2)n4—X1a—X1b—; R2 represents an optionally substituted cyclic system; provided that N,3-diphenyl-3H-1,2,3-triazolo[4,5-d]pyrimidin-5-amine is not included; their use, pharmaceutical compositions comprising them and processes for their preparation.
机译:本发明涉及式的化合物。 N-氧化物,药学上可接受的加成盐,季胺及其立体化学异构形式,其中环A代表苯基,吡啶基,嘧啶基,哒嗪基或吡嗪基; R 1 代表氢;芳基甲酰基C 1-6 烷基羰基; C 1-6 烷基; C 1-6 烷氧基羰基;被甲酰基,C 1-6 烷基羰基,C 1-6 烷氧基羰基或C 1-6 <取代的C 1-6 烷基/ Sub>烷基羰基氧基; X代表直接键; -(CH 2 n3 -或-(CH 2 n4 -X 1a —X 1b -; R 2 表示一个可选取代的环系统;但不包括N,3-二苯基-3H-1,2,3-三唑并[4,5-d]嘧啶-5-胺;它们的用途,包含它们的药物组合物及其制备方法。

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