首页> 外文期刊>Green chemistry >One-pot synthesis of tetrahydro-pyrrolobenzodiazepines and tetrahydro-pyrrolobenzodiazepinones through sequential 1,3-dipolar cycloaddition/N-alkylation (N-acylation)/Staudinger/aza-Wittig reactions
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One-pot synthesis of tetrahydro-pyrrolobenzodiazepines and tetrahydro-pyrrolobenzodiazepinones through sequential 1,3-dipolar cycloaddition/N-alkylation (N-acylation)/Staudinger/aza-Wittig reactions

机译:通过顺序1,3-偶极环加入/ N-烷基化/苯甲酸盐/富兰酮(N-酰化)/ Staudinger / Aza-Wittig反应,单罐合成四氢 - 吡咯唑二氧基酮和四氢 - 吡咯唑二氧嘧啶

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摘要

A new synthetic method for diastereoselective synthesis of tetrahydro-pyrrolo[1,2-d][1,4]benzodiazepines and tetrahydro-pyrrolo[1,2-d][1,4]diazepinones is developed which involves 1,3-dipolar cycloaddition, N-alkylation or N-acylation and Staudinger/aza-Wittig reactions. This one-pot and three-step synthesis of four components gave two different heterocyclic scaffolds. Green chemistry metrics analysis of the reaction process provided favorable results.
机译:开发了一种新的用于反对 - 吡咯醇合成四氢吡咯的合成方法[1,4] [1,4] [1,2] [1,2-D] [1,2-D] [1,2-D] [1,4]二氮杂藻。涉及1,3-偶像 环加成,N-烷基化或N-酰化和富豪/ AZA-Wittig反应。 该一罐和四步合成的四个组分给出了两种不同的杂环支架。 反应过程的绿色化学度量分析提供了有利的结果。

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