首页> 外国专利> Beta-adrenergic blocking indole derivs. - prepd. e.g. by reacting (2,3)-epoxy-propoxy cpds. with amines

Beta-adrenergic blocking indole derivs. - prepd. e.g. by reacting (2,3)-epoxy-propoxy cpds. with amines

机译:β-肾上腺素阻断吲哚衍生。 -准备例如通过使(2,3)-环氧-丙氧基cpds反应与胺

摘要

Indole derivs of formula (I) and their salts are new. In (I) A is alkylene; B is S or a direct bond; R1 is opt. branched lower alkyl; R2 is alkyl hydroxyalkyl, alkoxyalkyl or pivoloyloxymethyl; and R3 is lower alkyl, hydroxyalkyl, pivaloyloxymethyl, alkoxyalkyl, alkoxycarbonyl, or a group -CONR4 R5 in which R4 and R5 are H or lower alkyl. (I) can therefore be used for the treatment or prophylaxis of cardiovascular disorders. Specific cpds. (I) include 4-(2-hydroxy-3-tert-butylaminopropoxy)-2-ethoxycarbonyl-6-methyli- ndole. In an example, this is prepd. by reacting 1.7 g 4-(2,3-epoxypropoxy)-2-ethoxycarbonyl-6-methylindole 3 days at room temp. with 25 ml. tert-butylamine.
机译:式(I)的吲哚衍生物及其盐是新的。在(I)中,A为亚烷基; B是S或直接键; R1是可选的。支链低级烷基; R 2为烷基羟烷基,烷氧基烷基或亚吡咯酰氧基甲基; R3为低级烷基,羟烷基,新戊酰氧基甲基,烷氧基烷基,烷氧基羰基或基团-CONR4 R5,其中R4和R5为H或低级烷基。 (I)因此可以用于治疗或预防心血管疾病。特定的cpds。 (I)包括4-(2-羟基-3-叔丁基氨基丙氧基)-2-乙氧基羰基-6-甲基吲哚。在一个示例中,这是准备的。使1.7g 4-(2,3-环氧丙氧基)-2-乙氧基羰基-6-甲基吲哚在室温下反应3天。 25毫升叔丁胺。

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