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2-AMINOALKYLTHIENO2,3-DPYRIMIDINES, METHOD FOR THEIR PREPARING, MEDICINAL AGENT AND METHOD FOR ITS PREPARING

机译:2-氨基烷基噻吩并[2,3-D]嘧啶类及其制备方法,药物制剂及其制备方法

摘要

FIELD: organic chemistry, medicine, biochemistry, pharmacy.;SUBSTANCE: invention relates to 2-aminomethylthieno[2,3-d]pyrimidines of the general formula (I): wherein R1 and R2 in common with C-atoms with which they are bound form 5-7-membered monounsubstituted cycloalkenyl ring; R3 and R4 are similar or different and represent independently of one another (C1-C8)-alkoxy-group or halogen atom; R5 and R6 can be similar or different and represent independently of one another hydrogen atom, linear or branched (C1-C8)-alkyl group that can be substituted with one or more hydroxyl, (C1-C8)-alkoxy-group, amine, mono-(C1-C8-alkyl)-amine or di-(C1-C8-alkyl)-amine groups, or in common with nitrogen atom to which they are bound form a heterocyclic ring that comprises optionally one or more additional nitrogen atoms and substituted with one or more hydroxyl, (C1-C8)-alkoxy- or (C1-C8)-alkylol groups. Compounds elicit the inhibitory effect with respect to activity of phosphodiesterase V and can be used in treatment of cardiovascular system states and in disturbance in the potency injury. Also, invention describes a medicinal preparation based on compounds said, a method for its preparing and a method for preparing compounds.;EFFECT: improved preparing method, valuable medicinal and biochemical properties of compounds.;6 cl, 1 tbl, 16 ex
机译:技术领域:本发明涉及通式(I)的2-氨基甲基噻吩并[2,3-d]嘧啶:<图像文件=“ 00000002.GIF” he =“ 43” imgContent =“ undefined” imgFormat =“ GIF” wi =“ 83” />其中R 1 和R 2 与以5形式结合的C原子相同-7元单未取代的环烯基环; R 3 和R 4 相似或不同,彼此独立表示(C 1 -C 8 ) -烷氧基或卤素原子; R 5 和R 6 可以相同或不同,并且彼此独立地表示直链或支链的氢原子(C 1 -C 8 )-烷基,(C 1 -C 8 )-烷氧基,胺基,单- (C 1 -C 8 -烷基)-胺或二-(C 1 -C 8 -烷基)-胺基团,或与它们所键合的氮原子共同形成杂环,该杂环可包含一个或多个其他氮原子,并被一个或多个羟基((C 1 -C < Sub> 8 )-烷氧基-或(C 1 -C 8 )-烷氧基。化合物引起关于磷酸二酯酶V活性的抑制作用,并且可以用于治疗心血管系统状态和用于效力损伤中。此外,本发明还描述了基于所述化合物的药物制剂,其制备方法和化合物的制备方法。效果:改进的制备方法,化合物的有价值的药物和生化特性。6 cl,1 tbl,16 ex

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