综述与进展

核苷类前药ProTides的不对称合成:磷手性中心的构建

  • 刘祎辰 ,
  • 程杰飞 ,
  • 洪然
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  • a 中国科学院上海有机化学研究所分子合成卓越中心 天然产物有机合成化学重点实验室 上海 200032;
    b 上海中医药大学 创新中药研究院 上海 201203;
    c 中国科学院大学 北京 100049

收稿日期: 2020-05-13

  修回日期: 2020-06-11

  网络出版日期: 2020-06-19

基金资助

中国科学院前沿科学重点研究(No.QYZDY-SSW-SLH026)、中国科学院战略性先导科技专项(No.XDB20000000)资助项目.

Asymmetric Synthesis of Prodrug Nucleotides (ProTides): Construction of the P-Stereogenic Centers

  • Liu Yichen ,
  • Cheng Jiefei ,
  • Hong Ran
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  • a CAS Key Laboratory of Synthetic Chemistry of Natural Substances, Center for Excellence in Molecular Synthesis, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032;
    b Innovation Research Institute of Traditional Chinese Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai 201203;
    c University of Chinese Academy of Sciences, Beijing 100049

Received date: 2020-05-13

  Revised date: 2020-06-11

  Online published: 2020-06-19

Supported by

Project supported by the Key Research Program of Frontier Sciences (No. QYZDY-SSW-SLH026); the Strategic Priority Research Program of the Chinese Academy of Sciences (No. XDB20000000).

摘要

抗病毒药物瑞德西韦正处于临床试验阶段,以验证其对新型冠状病毒的疗效.瑞德西韦是一类结构特殊的前药(prodrug),原先由吉利德公司开发用于埃博拉病的治疗.ProTide (prodrug nucleotide)技术是McGuigan等发展的一种前药设计策略,在抗病毒、抗肿瘤等药物的开发中具有广泛应用.ProTide分子中五价磷原子的手性对药物活性的影响显著.因此,此类结构的高效不对称合成引起了学术界和工业界的广泛兴趣.归纳了近年来ProTide立体选择性偶联方法的新进展,分两类分别进行综述,即使用光学纯P(V)前体的反应和使用消旋的P(V)前体的反应.包括(动态)动力学拆分在内的多种策略被用于构建此类磷手性中心,其中一些合成方法可实现千克规模的制备.还总结了光学纯磷酰胺前体的不对称合成方法.此外,对一些代表性的ProTide试验药物的临床表现,也做了简要讨论.

本文引用格式

刘祎辰 , 程杰飞 , 洪然 . 核苷类前药ProTides的不对称合成:磷手性中心的构建[J]. 有机化学, 2020 , 40(10) : 3237 -3248 . DOI: 10.6023/cjoc202005030

Abstract

As an antivirus drug, remdesivir is currently in clinical studies for the treatment of COVID-19. Remdesivir is a prodrug originally developed by Gilead for the treatment of Ebola. The prodrug nucleotide (ProTide) technology is a prodrug-designing strategy developed by McGuigan and co-workers, in which a phosphoramidate side-chain is covalently attached to the hydroxy group of a drug molecule in order to enhance the cell permeability and metabolic activation efficiency. This approach has proved to be very successful in the identification of nucleoside analogues with antiviral or antitumor activities. It is also adapted in the application of non-nucleoside agents, such as neurodegeneration therapeutics, further demonstrating its usefulness in drug discovery. The chirality of the pentavalent phosphorous plays a significant role in the bioactivity of a ProTide molecule. Therefore, the efficient synthesis of such chemical scaffold in a highly enantioselective manner is very desirable and has intrigued great interests from both academia and pharmaceutical industry. In this review, based on the reactions employing optically pure P(V) precursors or P-racemic P(V) precursors, the recent advances on the stereoselective assembly of ProTide compounds are summarized. Various innovative strategies, including (dynamic) kinetic resolutions, were implemented to construct the vital P-stereogenic center with high regio- and stereo-selectivity. It is notable that several methods could be performed at kilogram scale, which are highlighted to showcase their practical values in the process chemistry. The asymmetric synthesis of enantiopure phosphoramidate precursors is illustrated in detail which will be informative for future drug development. Moreover, the clinical performance of some investigational ProTide drugs is also briefly discussed.

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