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Indole and 2,3-dihydroindole derivatives useful for inhibiting serotonin reuptake and antagonism of 5-HT1a receptors

机译:吲哚和2,3-二氢吲哚衍生物可用于抑制5-HT1a受体的5-羟色胺再摄取和拮抗作用

摘要

An indole or 2,3-dihydro-indole derivative of formula (I), its enantiomers or mixtures thereof, or an acid addition salt thereof, wherein: X is -O-, -S-, or -CR4R5-; Y is -CR6R7-, -CR6R7-CR8R9-, or -CR6=CR7-; or X and Y together form a group -CR4=CR5-, or -CR4=CR5-CR6R7-; Z is-O-, or -S-; W is N, C, or CH; A is a group selected from a group of formula (II), (III) and (IV) wherein the dotted lines mean an optional bond; R1, R2, R3, R12, R13, R14, R15, R16 and R17 are each independently selected from hydrogen, halogen, trifluoromethyl, alkyl, alkenyl, alkynyl, cycloalkyl, alkoxy, hydroxy, formyl, acyl, amino, alkylamino, dialkylamino, acylamino, alkoxycarbonylamino, aminocarbonylamino, alkylaminocarbonylamino, dialkylaminocarbonylamino, nitro and cyano; R4, R5, R6, R7, R8 and R9 are each independently selected form hydrogen and alkyl; R11 is selected from hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, aryl, arylalkyl, acyl and formyl. The compounds are useful for the treatment of diseases that respond to serotonin reuptake and antagonism of 5-HT1A receptors.
机译:式(I)的吲哚或2,3-二氢吲哚衍生物,其对映异构体或其混合物或其酸加成盐,其中:X为-O-,-S-或-CR 4 R 5-; Y是-CR6R7-,-CR6R7-CR8R9-或-CR6 = CR7-; X或Y一起形成基团-CR4 = CR5-,或-CR4 = CR5-CR6R7-; Z为-O-或-S-; W是N,C或CH; A是选自式(II),(III)和(IV)的组的基团,其中虚线表示任选的键; R1,R2,R3,R12,R13,R14,R15,R16和R17各自独立地选自氢,卤素,三氟甲基,烷基,烯基,炔基,环烷基,烷氧基,羟基,甲酰基,酰基,氨基,烷基氨基,二烷基氨基,酰基氨基,烷氧基羰基氨基,氨基羰基氨基,烷基氨基羰基氨基,二烷基氨基羰基氨基,硝基和氰基; R4,R5,R6,R7,R8和R9各自独立地选自氢和烷基; R11选自氢,烷基,烯基,炔基,环烷基,芳基,芳基烷基,酰基和甲酰基。该化合物可用于治疗对5-羟色胺再摄取和5-HT1A受体拮抗有反应的疾病。

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