首页> 外国专利> PREPARATION OF PLUS-3R-N-MONOMETHYLAMINO-4C-PHENYL-4T-ETHOXYCARBONYL-CYCLOHEXENE-1 ITS L- OR D-0,0-DIBENZOYL-TARTRATE

PREPARATION OF PLUS-3R-N-MONOMETHYLAMINO-4C-PHENYL-4T-ETHOXYCARBONYL-CYCLOHEXENE-1 ITS L- OR D-0,0-DIBENZOYL-TARTRATE

机译:制备%PLUS <-3R-N-甲酰胺基-4C-苯基-4T-乙氧基羰基-环己烯-%1 <其L-或D-0,0-二苯甲酰酒石酸酯

摘要

1344960 (+) - 3r - N - monomethylamino- 4c - phenyl 4t - ethoxycarbonylcyclohex - 1 - ene WARNER-LAMBERT CO 26 June 1972 [30 June 1971] 29846/72 Heading C2C The novel title compound and acid addition salts thereof such as the hydrochloride and the D- or L-o,o-dibenzoyltartrates are prepared by resolution of the receamic compound with an optically active o,o-dibenzoyltartaric acid or by monodemethylation of (+)-3r-N-dimethylamino - 4c - phenyl - 4t - ethoxycarbonylcyclohex- 1-ene by bromination in a chlorinated hydrocarbon at - 15‹ to 20‹ C. followed by treatment with water. Pharmaceutical compositions in conventional forms for oral, rectal or parenteral administration and having analgesic activity comprise the above novel compound or a salt thereof and a carrier or diluent.
机译:1344960(+)-3r-N-单甲基氨基-4c-苯基4t-乙氧羰基环己基-1-烯WARNER-LAMBERT CO 1972年6月26日[1971年6月30日] 29846/72标题C2C新的标题化合物及其酸加成盐,例如盐酸盐和D-或L,o-二苯甲酰酒石酸酯是通过用光学活性的o,o-二苯甲酰酒石酸拆分残余化合物或通过(+)-3r-N-二甲基氨基-4c-苯基-4t-乙氧基羰基环己基的单去甲基化制备的-在-15℃至20℃下在氯化烃中溴化1-烯,然后用水处理。用于口服,直肠或肠胃外给药并具有镇痛活性的常规形式的药物组合物包含上述新型化合物或其盐和载体或稀释剂。

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