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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
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
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.
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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。
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