首页> 外国专利> DERIVATIVES OF 4-AMINO-6-PHENYLPYRROLO2,3PYRIMIDINE POSSESSING INHIBITORY EFFECT ON TYROSINE KINASE ACTIVITY, THEIR USING AND METHODS FOR THEIR PREPARING (VARIANTS)

DERIVATIVES OF 4-AMINO-6-PHENYLPYRROLO2,3PYRIMIDINE POSSESSING INHIBITORY EFFECT ON TYROSINE KINASE ACTIVITY, THEIR USING AND METHODS FOR THEIR PREPARING (VARIANTS)

机译:4-氨基-6-苯并吡咯并[2,3]嘧啶对酪氨酸激酶活性的抑制作用及其用途和制备方法(变体)

摘要

FIELD: organic chemistry, medicine, oncology, biochemistry, pharmacy.;SUBSTANCE: invention relates to novel compounds of the formula (I): or their pharmaceutically acceptable salts possessing the inhibitory effect on activity of tyrosine kinase. Proposed compounds can be used in treatment of proliferative disease, such as tumor. In the formula (I) each R1 and R2 means independently of one another hydrogen atom, methyl, ethyl, isopropyl, hydroxyethyl, piperidine-1-ylmethylcarbonyl, pyrrolidine-1-ylmethylcarbonyl, morpholine-4-ylmethylcarbonyl, 4-methylpiperazine-1-ylmethylcarbonyl, N,N-dimethylaminomethylcarbonyl, 4-ethylpiperazine-1-ylmethylcarbonyl, piperidine-1-ylethylcarbonyl, N,N-diethylaminoethylcarbonyl, N,N-dimethylaminopropylcarbonyl, 2-pyridylcarbonyl, tetrahydropyrane-4-yl, morpholine-4-ylethyl, N,N-diethylaminoethyl, tert.-butyl; or R1 and R2 in common with nitrogen atom to which they are bound form 4-ethylpiperazine-1-yl, pyrrolidine-1-yl, 4-methylpiperazine-1-yl, piperidine-1-yl, morpholine-4-yl, 3,5-dimethylpiperazine-1-yl; R3 is chosen from 3-chloro-4-fluorophenyl, phenyl, 4-benzyloxyphenyl, 3-hydroxy-4-methylphenyl, 3-hydroxy-4-methoxyphenyl, 4-chlorophenyl, 3-chlorophenyl, 2-chlorophenyl, 2,5-dichlorophenyl, 3-methoxyphenyl, benzo[1,3]dioxol-5-yl, 6-methoxypyridine-3-yl, 2-methoxypyridine-4-yl, pyridine-2(1H)-one-5-yl, pyridine-2(1H)-one-4-yl, 3-methoxyphenyl, 3-methylphenyl, pyridine-2(1H)_one-4-yl; G means -CH2-; Q means -NH-; X absents or means -CH(CH3)-, -CH2- under condition that if X absents then R3 is bound by ring carbon atom. Also, invention relates to variants of methods for synthesis of compounds of the formula (I), preparing a pharmaceutical composition and using compounds proposed.;EFFECT: valuable medicinal and biochemical properties of compounds and pharmaceutical composition, improved method for synthesis and preparing.;13 cl, 147 ex
机译:技术领域:本发明涉及式(I)的新型化合物:<图像文件=“ 00000002.GIF” he =“ 38” imgContent =“ undefined” imgFormat =“ GIF“ wi =” 93“ />或其药学上可接受的盐对酪氨酸激酶的活性具有抑制作用。所提出的化合物可以用于治疗增生性疾病,例如肿瘤。在式(I)中,每个R 1 和R 2 均彼此独立地表示氢原子,甲基,乙基,异丙基,羟乙基,哌啶-1-基甲基羰基,吡咯烷- 1-基甲基羰基,吗啉-4-基甲基羰基,4-甲基哌嗪-1-基甲基羰基,N,N-二甲基氨基甲基羰基,4-乙基哌嗪-1-基甲基羰基,哌啶-1-基乙基羰基,N,N-二乙基氨基乙基羰基,N,N-二甲基氨基丙基羰基, 2-吡啶基羰基,四氢吡喃-4-基,吗啉-4-基乙基,N,N-二乙基氨基乙基,叔丁基;或R 1 和R 2 与它们所键合的氮原子共同形成4-乙基哌嗪-1-基,吡咯烷-1-基,4-甲基哌嗪-1 -基,哌啶-1-基,吗啉-4-基,3,5-二甲基哌嗪-1-基; R 3 选自3-氯-4-氟苯基,苯基,4-苄氧基苯基,3-羟基-4-甲基苯基,3-羟基-4-甲氧基苯基,4-氯苯基,3-氯苯基, 2-氯苯基,2,5-二氯苯基,3-甲氧基苯基,苯并[1,3]二恶基-5-基,6-甲氧基吡啶-3-基,2-甲氧基吡啶-4-基,吡啶-2(1H)- -5-基,吡啶-2(1H)-一-4-基,3-甲氧基苯基,3-甲基苯基,吡啶-2(1H)_一-4-基; G表示-CH 2 -; Q表示-NH-; X不存在或表示-CH(CH 3 )-,-CH 2 -的条件是:如果X不存在,则R 3 被环约束碳原子。本发明还涉及合成式(I)化合物,制备药物组合物和使用所提出的化合物的方法的变体。效果:化合物和药物组合物的有价值的药物和生化性质,改进的合成和制备方法。 13 cl,147 ex

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