首页> 外国专利> method for the preparation of a pharmaceutical preparation with local anaesthetic effect - a dialkylamino - 2, 6 - butyroxylidide and / or the pharmaceutical acceptable salt thereof contains.and the application of this method obtained formed pharmaceutical preparations and method for preparing dialkylamino - 2.6 - butyroxilididen and the pharmaceutical acceptable salts thereof.

method for the preparation of a pharmaceutical preparation with local anaesthetic effect - a dialkylamino - 2, 6 - butyroxylidide and / or the pharmaceutical acceptable salt thereof contains.and the application of this method obtained formed pharmaceutical preparations and method for preparing dialkylamino - 2.6 - butyroxilididen and the pharmaceutical acceptable salts thereof.

机译:的具有局麻作用的药物制剂的制备方法-二烷基氨基-2,6-丁氧基乙氧基化物和/或其药学上可接受的盐。该方法的应用获得了形成的药物制剂和二烷基氨基的制备方法-2.6-丁腈和其药学上可接受的盐。

摘要

1369259 Xylidine derivatives ASTRA PHARMACEUTICAL PRODUCTS Inc 21 Dec 1971 [22 Dec 1970 19 July 1971] 59377/71 Heading C2C Novel xylidine derivatives of the Formula I wherein RSP1/SP is ethyl, propyl, or butyl; RSP2/SP and RSP3/SP each are methyl, ethyl, propyl or butyl or RSP2/SP and RSP3/SP together is tetramethylene; the total sum of carbon atoms in RSP1/SP, RSP2/SP and RSP3/SP being at least six; and pharmaceutically acceptable acid addition salts thereof are prepared by reacting the appropriate 2-alkyl-2-bromo-(or iodo)-2SP1/SP,6SP1/SP- acetoxylides with amines of the formula H-NRSP2/SPRSP3/SP, or with amines of the formula RSP2/SPNH 2 , and reacting the thus obtained 2-alkyl- 2-alkylamino-2SP1/SP,6SP1/SP-acetozylidides, with alkylating agents. The racemic compounds thus obtained may be resolved by treatment with l- and d-tartaric acid. 2 - Alkyl - 2 - iodo - 2SP1/SP,6SP1/SP- acetoxylidides are obtained by reacting potassium iodide with the corresponding 2 - alkyl - 2 - bromo - 2SP1/SP,6SP1/SP- acetoxylidides, resulting from the reaction between the appropriate acid chloride and 2,6-xylidine. 2-Bromobutyryl chloride is obtained by reacting 2-bromobutyric acid with thionyl chloride. Pharmaceutical compositions, suitable for parenteral or topical administration, contain the above novel compounds or pharmaceutically acceptable acid addition salts thereof in association with pharmaceutically acceptable carriers. The compounds possess local anaesthetic activity.
机译:1369259二甲苯基衍生物ASTRA PHARMACEUTICAL PRODUCTS Inc. 1971年12月21日[1970年12月22日1971年7月19日]标题C2C其中R 1 为乙基,丙基或丁基的式I的新颖二甲苯基衍生物; R 2 和R 3 分别为甲基,乙基,丙基或丁基,或者R 2 和R 3 一起为四亚甲基R 1 ,R 2 和R 3 中碳原子的总和至少为6;及其药学上可接受的酸加成盐是通过使适当的2-烷基-2-溴-(或碘)-2 1 ,6 1 -乙酰氧基化物与式H-NR 2 R 3 ,或与式R 2 NH 2的胺反应,使所得的2-烷基- 2-烷基氨基-2 1 ,6 1 -乙酰唑基,具有烷基化剂。如此获得的外消旋化合物可以通过用1-酒石酸和d-酒石酸处理而拆分。通过使碘化钾与相应的2-烷基-2-溴-2 反应获得2-烷基-2-碘-2 1 ,6 1 -乙酰氧基1 ,6 1 -乙酰氧基利德化合物,是由适当的酰氯和2,6-二甲苯胺之间的反应产生的。通过使2-溴丁酸与亚硫酰氯反应获得2-溴丁酰氯。适用于肠胃外或局部给药的药物组合物包含上述新型化合物或其药学上可接受的酸加成盐以及药学上可接受的载体。该化合物具有局部麻醉活性。

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