Optimized synthesis of anti-COVID-19 drugs aided by retrosynthesis software

被引:0
|
作者
Qi, Wentao [1 ]
Zhai, Dong [1 ]
Song, Danna [1 ]
Liu, Chengcheng [1 ]
Yang, Junxia [1 ]
Sun, Lei [1 ]
Li, Youyong [2 ]
Li, Xingwei [1 ]
Deng, Weiqiao [1 ]
机构
[1] Shandong Univ, Inst Mol Sci & Engn, Inst Frontier & Interdisciplinary Sci, Qingdao 266237, Peoples R China
[2] Soochow Univ, Inst Funct Nano & Soft Mat FUNSOM, Jiangsu Key Lab Carbon Based Funct Mat & Devices, Suzhou 215123, Peoples R China
来源
RSC MEDICINAL CHEMISTRY | 2023年 / 14卷 / 07期
基金
国家重点研发计划;
关键词
FAVIPIRAVIR T-705; COMPUTER; DESIGN; ROUTE;
D O I
10.1039/d2md00444e
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Considering the millions of COVID-19 patients worldwide, a global critical challenge of low-cost and efficient anti-COVID-19 drug production has emerged. Favipiravir is one of the potential anti-COVID-19 drugs, but its original synthetic route with 7 harsh steps gives a low product yield (0.8%) and has a high cost ($68 per g). Herein, we demonstrated a low-cost and efficient synthesis route for favipiravir designed using improved retrosynthesis software, which involves only 3 steps under safe and near-ambient air conditions. A yield of 32% and cost of $1.54 per g were achieved by this synthetic route. We also used the same strategy to optimize the synthesis of sabizabulin. We anticipate that these synthetic routes will contribute to the prevention and treatment of COVID-19.
引用
收藏
页码:1254 / 1259
页数:7
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