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首页> 外文期刊>Synthetic Communications >Simple and Convenient Synthesis of 21-Thioalkylether Derivatives of Methyl 16-Prednisolone Carboxylates
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Simple and Convenient Synthesis of 21-Thioalkylether Derivatives of Methyl 16-Prednisolone Carboxylates

机译:16泼尼松龙羧酸甲酯的21-硫代烷基醚衍生物的简便合成

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The antedrug approach for corticosteroids has been described as a fundamentally sound approach for the development of safer anti-inflammatory and antiasthmatic therapy.However,the derivatization of prednisolone and its congeners have been considered to be major pitfalls,because their syntheses are complicated by the presence of numerous carboxylate esters and hydroxyl functions in the steroid nucleus.A simple and direct synthesis of 21-thioalkylether derivatives of methyl 16-prednisolonecarboxylates is described.The 21-mesylate of the methyl 16-prednisolonecarboxylate and 9-fluoro-17-dehydro methyl 16-prednisolonecarboxy-late were reacted with Na-thioalkoxides to furnish the desired thioethers in good yields.A previously published method for the methanolysis of 16-cyanoprednisolone to methylcarboxylate has been reexamined,and the conditions are explained clearly.The reaction conditions for all these reactions were critical.
机译:皮质类固醇的前药治疗方法被认为是开发更安全的抗炎和抗哮喘疗法的根本方法。但是,泼尼松龙及其同类物的衍生化被认为是一个重大陷阱,因为它们的合成由于存在而变得复杂类固醇核中许多羧酸酯和羟基官能团的描述。描述了16-泼尼松龙羧酸甲酯的21-硫代烷基醚衍生物的简单直接合成.16-泼尼松龙羧酸甲酯和9-氟-17-脱氢甲基16的21-甲磺酸酯。 -泼尼松龙羧酸酯与Na-硫代醇盐反应可提供所需收率的硫醚。重新检查了先前发表的将16-氰基间苯二酚甲醇化为甲基羧酸酯的方法,并明确说明了条件。所有这些反应的反应条件至关重要。

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