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Design and Synthesis of Estrogen Derivative

机译:雌激素衍生物的设计与合成

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摘要

In this study, an estrogen derivative was synthesized. The first stage involves the synthesis of 17-(2-amino-ethylimino)-13-methyl-7,8,9,11,12,13.14.15,16,17-decahydro-6H-cyclopenta[a]phenanthren-3-ol (3) by the reaction of estrone with ethylenediamine using boric acid as catalyst. The second stage was achieved by reaction of compound 3 with chloroacetyl chloride in presence of triethylamine to form N-{2-[(3-chloro-2-oxo-cyclobutyl)-(3-hydroxy-13-methyl-7,8.9,l 1.12,13,14,15.16,17-decahydro-6H-cyclopentafa]phenanthren-17-yl)-amino]ethylcarbamic chloride (5). The third stage was achieved by reaction of compound 5 with thiourea to form 2-[(2-amino-ethyl)-(3-hydroxy-13-methyl-7,8,9,11,12,13,14.15,16-17-decahydro-6H-cyclopenta[a]phenanthren-17-yl)amino]-4-chloro-cyclobutanone (7) in methanol. The structures of compounds obtained were confirmed by spectroscopically.
机译:在这项研究中,合成了雌激素衍生物。第一阶段涉及17-(2-氨基-乙基亚氨基)-13-甲基-7,8,9,11,12,13.14.15,16,17-十氢-6H-环戊[a]菲蒽3的合成-雌二醇(3),通过使用硼酸作为催化剂,使雌酮与乙二胺反应。第二阶段是在三乙胺存在下,化合物3与氯乙酰氯反应形成N- {2-[(3-氯-2-氧代-环丁基)-(3-羟基-13-甲基-7,8.9, l 1.12,13,14,15.16,17-十氢-6H-环戊五]菲蒽-17-基)-氨基]乙基氨基甲酸氯(5)。第三阶段是通过化合物5与硫脲反应形成2-[((2-氨基-乙基))-(3-羟基-13-甲基-7,8,9,11,12,13,14.15,16-在甲醇中的17-十氢-6H-环戊[a]菲基-17(基)氨基] -4-氯-环丁酮(7)。所得化合物的结构通过光谱确认。

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