首页> 外国专利> analogifremgangsmåde to manufacture of trans - 2,10 - dichloro - 6 - ethoxycarbonyl - 12 methyl - 12h dibenzo (d, g) (1,3) dioxocin, possibly in combination with the cis - isomer.

analogifremgangsmåde to manufacture of trans - 2,10 - dichloro - 6 - ethoxycarbonyl - 12 methyl - 12h dibenzo (d, g) (1,3) dioxocin, possibly in combination with the cis - isomer.

机译:以反式2,2-二氯-6-乙氧羰基-12甲基-12h二苯并(d,g)(1,3)二恶英制造,可能与顺式异构体组合使用。

摘要

1414886 2,10-Dichloro-12-methyl-12H-dibenzo(d,g)(1,3)dioxocines EGYT GYOGYSZERVEGYESZETI GYAR 25 Sept 1973 [18 Dec 1972] 44793/73 Heading C2C Novel 2,10-dichloro-12-methyl-12H-dibenzo- (d,g)(1,3)dioxocines of the general formula wherein R is a hydroxy, C 1-4 alkoxy or C 1-4 alkylamino group, and, when R is a hydroxy group, base addition salts thereof are prepared by reacting 1,1-bis-(2-hydroxy-5-chlorophenyl)- ethane with a compound of the general formula Cl 2 CH-COR in the presence of a base and a polar solvent, followed optionally by one or more of the following steps: (a) esterification of a resulting free acid; (b) salification of a resulting free acid; (c) conversion of a resulting acid or ester into the corresponding C 1-4 alkylamide; (d) hydrolysis of a resulting ester or amide to give the corresponding free acid (or a base addition salt thereof); (e) conversion of a resulting ester into another C 1-4 alkyl ester by metathesis; (f) conversion of a resulting salt to the free acid by treatment with an acid; and (g) separation of a resulting mixture of cis- and trans-isomers into the pure isomers. Pharmaceutical compositions having serum cholesterol, triglyceride and free lipoid reducing and liver-protecting activity comprise, as active ingredient, a 2,10-dichloro-12-methyl-12H-dibenzo(d,g)(1,3)dioxocine of the first general formula above, or, when R is a hydroxy group, a pharmaceutically acceptable base addition salt thereof, together with a carrier, binder and/or auxiliary substance usable in the pharmaceutical industry.
机译:1414886 2,10-二氯-12-甲基-12H-二苯并(d,g)(1,3)二恶英酮EGYT GYOGYSZERVEGYESZETI GYAR 1973年9月25日[1972年12月18日] 44793/73标题C2C Novel 2,10-dichloro-12-通式的甲基-12H-二苯并-(d,g)(1,3)二氧杂环辛酮,其中R为羟基,C 1-4烷氧基或C 1-4烷基氨基,且当R为羟基时,为碱通过在碱和极性溶剂存在下使1,1-双-(2-羟基-5-氯苯基)乙烷与通式Cl 2 CH-COR的化合物反应,然后任选地通过以下一个或多个步骤:(a)酯化所得的游离酸; (b)产生的游离酸的盐化; (c)将所得的酸或酯转化为相应的C 1-4烷基酰胺; (d)水解所得的酯或酰胺,得到相应的游离酸(或其碱加成盐); (e)通过复分解将所得的酯转化为另一种C 1-4烷基酯; (f)通过用酸处理将所得盐转化为游离酸; (g)将所得的顺式和反式异构体混合物分离成纯的异构体。具有血清胆固醇,甘油三酸酯和游离脂质减少和肝脏保护活性的药物组合物包含作为活性成分的第一种的2,10-二氯-12-甲基-12H-二苯并(d,g)(1,3)二氧辛酸通式,或当R为羟基时,其药学上可接受的碱加成盐,以及可用于制药工业的载体,粘合剂和/或辅助物质。

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