药品
2019年冠状病毒病(COVID-19)
冠状病毒
过程开发
药物开发
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
候选药物
病毒学
制造工艺
2019-20冠状病毒爆发
医学
药理学
纳米技术
生化工程
材料科学
工艺工程
工程类
传染病(医学专业)
内科学
复合材料
疾病
爆发
作者
Jeremy D. Mason,Jan Spink,Mahesh Pallerla,Zhenhua Wu,Rajeev Kumar Singh,Aravind Babu Pulipaka,Jia‐Bao Liu,Marvin M. Vega,Xu Wang,Michael J. Sofia,Ganapati REDDY PAMULAPATI
标识
DOI:10.1021/acs.oprd.4c00528
摘要
A scalable process for manufacturing of the anticoronavirus clinical candidate AB-343 has been developed. The lactam-containing subunit of the molecule was prepared using a novel synthetic route involving a nitro-Michael reaction and a rhodium-catalyzed nitro group hydrogenation followed by in situ translactamization sequence as a key transformation. The drug substance was assembled via sequential amide coupling and deprotection reactions, followed by a final dehydration of a primary amide to the corresponding nitrile using T3P. AB-343 drug substance was successfully manufactured on a multikilogram scale using this route, which was suitable for supporting IND-enabling studies and Phase I clinical development.
科研通智能强力驱动
Strongly Powered by AbleSci AI