首页> 外国专利> SUBSTITUTED DERIVATIVES OF DIAMINO-1,3,5-TRIASINE, PHARMACEUTIC COMPOSITION, METHOD OF OBTAINING PHARMACEUTIC COMPOSITION AND METHOD OF OBTAINING SUBSTITUTED DERIVATIVES OF DIAMINO-1,3,5-TRIASINE

SUBSTITUTED DERIVATIVES OF DIAMINO-1,3,5-TRIASINE, PHARMACEUTIC COMPOSITION, METHOD OF OBTAINING PHARMACEUTIC COMPOSITION AND METHOD OF OBTAINING SUBSTITUTED DERIVATIVES OF DIAMINO-1,3,5-TRIASINE

机译:DIAMINO-1,3,5-三胺的替代衍生物,药物成分,获得药物成分的方法以及获得DIAMINO-1,3,5-三胺的替代衍生物的方法

摘要

This invention concerns the compounds of formula CHEM the pharmaceutically acceptable acid addition salts and the stereochemically isomeric forms thereof, wherein R1 and R2 are each independently selected from hydrogen; hydroxy; amino; optionally substituted C1-6alkyl; C1-6alkyloxy; C1-6alkylcarbonyl; C1-6alkyloxycarbonyl; Ar1; mono- or di(C1-6alkyl)amino; mono- or di(C1-6alkyl)aminocarbonyl; dihydro-2(3H)-furanone; or R1 and R2 taken together may form pyrrolidinyl, piperidinyl, morpholinyl, azido or mono- or di(C1-6alkyl)aminoC1-4alkylidene; R3 is hydrogen, Ar1, C1-6alkylcarbonyl, C1-6alkyl, C1-6alkyloxycarbonyl, C1-6alkyl substituted with C1-6alkyloxycarbonyl; and R4, R5, R6, R7 and R8 are each independently selected from hydrogen, halo, C1-6alkyl, C1-6alkyloxy, cyano, aminocarbonyl, nitro, amino, trihalomethyl or trihalomethyloxy; L is optionally substituted C1-10alkyl; C3-10alkenyl; C3-10alkynyl; C3-7cycloalkyl; Ar1 is optionally substituted phenyl; for the manufacture of a medicine for the treatment of subjects suffering from HIV (Human Immunodeficiency Virus) infection. It further relates to new compounds being a subgroup of the compounds of formula (I), their preparation and compositions comprising them.
机译:本发明涉及式的化合物及其药学上可接受的酸加成盐及其立体化学异构形式,其中R 1和R 2各自独立地选自氢;羟基氨基任选取代的C 1-6烷基; C 1-6烷氧基; C 1-6烷基羰基; C 1-6烷氧基羰基; Ar <1>;单或二(C 1-6烷基)氨基;单或二(C 1-6烷基)氨基羰基;二氢-2(3H)-呋喃酮;或者R 1和R 2一起可以形成吡咯烷基,哌啶基,吗啉基,叠氮基或单或二(C 1-6烷基)氨基C 1-4亚烷基; R 3为氢,Ar 1,C 1-6烷基羰基,C 1-6烷基,C 1-6烷氧基羰基,被C 1-6烷氧基羰基取代的C 1-6烷基; R 4,R 5,R 6,R 7和R 8各自独立地选自氢,卤素,C 1-6烷基,C 1-6烷氧基,氰基,氨基羰基,硝基,氨基,三卤甲基或三卤甲氧基; L为任选取代的C 1-10烷基; C3-10烯基; C3-10炔基; C3-7环烷基; Ar 1是任选取代的苯基;制造用于治疗患有HIV(人类免疫缺陷病毒)感染的受试者的药物。它还涉及作为式(I)化合物的子集的新化合物,其制备和包含它们的组合物。

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