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Basic substituted 1,4 - benzo dioxanes and their pharmacologically not toxic acid-addition salts and method for their preparation and pharmaceutical compositions containing these compounds

机译:碱性取代的1,4-苯并二恶烷及其药理学上无毒的酸加成盐及其制备方法和含有这些化合物的药物组合物

摘要

1388325 Derivatives of benzo-1,4-dioxan MANUFACTURE DE PRODUITS PHARMACEUTIQUES A CHRISTIAENS SA 25 Sept 1973 [26 Sept 1972] 44435/72 Heading C2C The invention comprises compounds of formula and their acid addition salts, wherein n= 1 or 2, X is O: or H 2 , A is Ph or 2-pyridyl, and either R 1 is C 1-4 alkyl and R 2 is H or C 1-4 alkyl, or NR 1 R 2 forms a heterocyclic ring. In examples, these compounds are prepared (where Z is benzo-1,4-dioxan-2-yl) by (a) reacting the chloroalkyl compound with HNR 1 R 2 ; (b) reacting the arylaminomethyl compound ZCH 2 NHA (made from the sulphonate ZCH 2 O 3 SMe and ANH 2 ) with or (c) reducing the amides (X=O:) to the amines (X=H 2 ). Therapeutic compositions for oral or parenteral administration comprise compounds of the above formula, which have antiarrhythmic activity and are not depressants for the myocardial function.
机译:1388325苯并-1,4-二恶烷的衍生物药品制造商SA 1973年9月25日[1972年9月26日]标题C2C本发明包括下式的化合物及其酸加成盐,其中n = 1或2,X是O:或H 2,A是Ph或2-吡啶基,并且R 1是C 1-4烷基并且R 2是H或C 1-4烷基,或NR 1 R 2形成杂环。在实例中,通过(a)使氯代烷基化合物与HNR 1 R 2反应,制备这些化合物(其中Z为苯并-1,4-二恶烷-2-基)。 (b)使芳基氨基甲基化合物ZCH 2 NHA(由磺酸盐ZCH 2 O 3 SMe和ANH 2制成)与或(c)将酰胺(X = O :)还原为胺(X = H 2)。口服或肠胃外给药的治疗组合物包含上式的化合物,其具有抗心律不齐的活性并且不是心肌功能的抑制剂。

著录项

  • 公开/公告号DE000002347757C3

    专利类型

  • 公开/公告日1977-02-10

    原文格式PDF

  • 申请/专利权人

    申请/专利号DE2347757A

  • 发明设计人

    申请日1973-09-22

  • 分类号C07D319/16;C07D405/00;A61K31/35;

  • 国家 DE

  • 入库时间 2022-08-23 00:10:12

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