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Bilaterally substituted tricyclic compounds for the treatment of human immunodeficiency virus type 1 (HIV-1) infection and other diseases

机译:双向取代的三环化合物,用于治疗1型人类免疫缺陷病毒(HIV-1)感染和其他疾病

摘要

Compound of Formula (I) ** Formula ** or a pharmaceutical salt, ester, solvate or hydrate thereof. wherein A, B and C are benzene, R1 and R2 are in bilateral disubstitution 1,3 with respect to each other in benzene A and in meta relative to the carbon atom of A bonded to benzene B; and are independently selected from optionally substituted aminomethyl, aminoethyl, and aminopropyl; R3 and R4 are in bilateral disubstitution 1,3 with respect to each other in benzene B and in ortho relative to the carbon atom of B bonded to benzene A; and are independently selected from hydrogen, (C1-C6) alkylamide, (C1-C6) alkyl ester, hydroxyalkyl (C1-C6), halo (C1-C6) alkyl, (C1-C6) alkoxyalkyl, (C1-C8) alkyl , with the proviso that at least one of R3 and R4 is not hydrogen; R5 and R6 are in bilateral disubstitution 1,3 with respect to each other in benzene C and in ortho relative to the carbon atom of C bonded to benzene B; and are independently selected from optionally substituted aminomethyl, aminoethyl, and aminopropyl; R7 and R8 are independently selected from hydrogen, halogen, hydroxyl, (C1-C10) alkoxy, (C1-C10) alkylamine, (C1-C10) alkylguanidine, (C1-C10) alkylamide, (C1-C10) alkyl ester, hydroxyalkyl (C1-C10), alkoxyalkyl (C1-C10), haloalkyl (C1-C10), alkyl (C1-C10), aryl alkoxy and aryl ester
机译:式(I)** ** **的化合物或其药用盐,酯,溶剂化物或水合物。其中A,B和C为苯,R1和R2在苯A中相对于彼此的双键结构为1,3,且相对于与苯B键合的A的碳原子为间位。且独立地选自任选取代的氨甲基,氨乙基和氨丙基; R3和R4在苯B中相对于彼此和在相对于与苯A键合的B的碳原子邻位的情况下为双键性1,3。并且独立地选自氢,(C1-C6)烷基酰胺,(C1-C6)烷基酯,羟烷基(C1-C6),卤素(C1-C6)烷基,(C1-C6)烷氧基烷基,(C1-C8)烷基,条件是R3和R4中至少一个不是氢; R5和R6在苯C中相对于彼此键合为1,3,并且相对于与苯B键合的C的碳原子为邻位;且独立地选自任选取代的氨甲基,氨乙基和氨丙基; R7和R8独立地选自氢,卤素,羟基,(C1-C10)烷氧基,(C1-C10)烷基胺,(C1-C10)烷基胍,(C1-C10)烷基酰胺,(C1-C10)烷基酯,羟烷基(C1-C10),烷氧基烷基(C1-C10),卤代烷基(C1-C10),烷基(C1-C10),芳基烷氧基和芳基酯

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