A Simple Synthesis of Polyfunctionalized 4-Aminopyrazolidin-3-ones as ‘Aza-deoxa’ Analogs of<scp>D</scp>-Cycloserine
作者:Ana Novak、Matej Štefanič、Uroš Grošelj、Martina Hrast、Marta Kasunič、Stanislav Gobec、Branko Stanovnik、Jurij Svete
DOI:10.1002/hlca.201300169
日期:2014.2
A simple five‐step synthesis of fully substituted (4RS,5RS)‐4‐aminopyrazolidin‐3‐ones as analogs of D‐cycloserine was developed. It comprises a two‐step preparation of 5‐substituted (4RS,5RS)‐4‐(benzyloxycarbonylamino)pyrazolidin‐3‐ones, reductive alkylation at N(1), alkylation of the amidic N(2) with alkyl halides, and simultaneous hydrogenolytic deprotection/reductive alkylation of the primary NH2
开发了一种简单的五步合成方法,将D-环丝氨酸类似物完全取代(4 RS,5 RS)-4-氨基吡唑啉-3-酮。它包括5取代(4 RS,5 RS)-4-(苄氧基羰基氨基)吡唑烷丁-3-酮的两步制备,在N(1)上的还原烷基化,在酰胺N(2)上用烷基卤化物进行烷基化,并同时进行NH 2伯基的氢解脱保护/还原烷基化反应。通过合成,仅需使用两种常见试剂(醛(或酮)和烷基卤化物)即可轻松实现吡唑烷丁-3-酮核的逐步功能化。通过NMR光谱和X射线衍射阐明了产物的结构。