Modular continuous flow synthesis of zidovudine (AZT): a two-stage integrated process enabling safe azidation and enhanced sustainability in HIV drug manufacturing

IF 2.9 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Yan Chen, Rongkun Jiang, Fang Zhao, Yufang Xu, Xuhong Qian and Weiping Zhu
{"title":"Modular continuous flow synthesis of zidovudine (AZT): a two-stage integrated process enabling safe azidation and enhanced sustainability in HIV drug manufacturing","authors":"Yan Chen, Rongkun Jiang, Fang Zhao, Yufang Xu, Xuhong Qian and Weiping Zhu","doi":"10.1039/D5RE00370A","DOIUrl":null,"url":null,"abstract":"<p >AIDS is one of the deadliest global epidemics. Zidovudine (<strong>AZT</strong>), the first FDA-approved HIV treatment, is a key component of antiretroviral therapy. The current industrial synthesis of <strong>AZT</strong> exhibits several drawbacks: low selectivity of hydroxyl protection, hazardous azidation, and prolonged reaction times/extended processing durations, contributing to suboptimal efficiency, safety hazards, and environmental burden. To address these limitations, we developed a modular continuous flow process for the synthesis of <strong>AZT</strong>. We actively addressed the solvent and reagent compatibility issues and balanced the yield of integrated reactions. This process integrated hydroxyl protection and cyclization in module A, followed by azidation and hydroxyl deprotection in module B, with seamless filtration connecting the two modules. The integrated platform achieves a 69% overall yield across four transformations, reducing the batch time of 2550 minutes to a residence time of 108 minutes. Compared to traditional batch processes, the continuous flow system enhances the selectivity of hydroxyl protection, enables safer handling of azidation reactions, significantly reduces the <em>E</em>-factor from 375 to 210 while increasing the space–time yield (STY) to 17.39 g L<small><sup>−1</sup></small> h<small><sup>−1</sup></small>, resulting in a 289-fold performance gain over the batch process.</p>","PeriodicalId":101,"journal":{"name":"Reaction Chemistry & Engineering","volume":" 3","pages":" 665-673"},"PeriodicalIF":2.9000,"publicationDate":"2025-11-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Reaction Chemistry & Engineering","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2026/re/d5re00370a","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

AIDS is one of the deadliest global epidemics. Zidovudine (AZT), the first FDA-approved HIV treatment, is a key component of antiretroviral therapy. The current industrial synthesis of AZT exhibits several drawbacks: low selectivity of hydroxyl protection, hazardous azidation, and prolonged reaction times/extended processing durations, contributing to suboptimal efficiency, safety hazards, and environmental burden. To address these limitations, we developed a modular continuous flow process for the synthesis of AZT. We actively addressed the solvent and reagent compatibility issues and balanced the yield of integrated reactions. This process integrated hydroxyl protection and cyclization in module A, followed by azidation and hydroxyl deprotection in module B, with seamless filtration connecting the two modules. The integrated platform achieves a 69% overall yield across four transformations, reducing the batch time of 2550 minutes to a residence time of 108 minutes. Compared to traditional batch processes, the continuous flow system enhances the selectivity of hydroxyl protection, enables safer handling of azidation reactions, significantly reduces the E-factor from 375 to 210 while increasing the space–time yield (STY) to 17.39 g L−1 h−1, resulting in a 289-fold performance gain over the batch process.

Abstract Image

齐多夫定(AZT)的模块化连续流合成:一个两阶段的综合过程,使安全叠氮化和增强艾滋病毒药物生产的可持续性
艾滋病是全球最致命的流行病之一。齐多夫定(AZT)是fda批准的首个HIV治疗药物,是抗逆转录病毒治疗的关键组成部分。目前AZT的工业合成有几个缺点:羟基保护选择性低,叠氮化危险,反应时间长/处理时间长,导致效率不佳,安全隐患和环境负担。为了解决这些限制,我们开发了一种模块化的连续流工艺来合成AZT。我们积极解决了溶剂和试剂的相容性问题,平衡了综合反应的产率。该工艺在模块A中集成了羟基保护和环化,在模块B中集成了叠氮化和羟基去保护,两个模块之间通过无缝过滤连接。集成平台通过四次转换实现了69%的总收率,将2550分钟的批处理时间减少到108分钟的停留时间。与传统的间歇式工艺相比,连续流系统提高了羟基保护的选择性,使叠氮化反应的处理更加安全,将e因子从375降低到210,同时将时空产率(STY)提高到17.39 g L−1 h−1,从而使性能比间歇式工艺提高289倍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Reaction Chemistry & Engineering
Reaction Chemistry & Engineering Chemistry-Chemistry (miscellaneous)
CiteScore
6.60
自引率
7.70%
发文量
227
期刊介绍: Reaction Chemistry & Engineering is a new journal reporting cutting edge research into all aspects of making molecules for the benefit of fundamental research, applied processes and wider society. From fundamental, molecular-level chemistry to large scale chemical production, Reaction Chemistry & Engineering brings together communities of chemists and chemical engineers working to ensure the crucial role of reaction chemistry in today’s world.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书