Process Development toward a Key Fragment of the PCSK9 Inhibitor Enlicitide Decanoate

IF 3.1 3区 化学 Q2 CHEMISTRY, APPLIED
Kai-Jiong Xiao*, Yonggang Chen, Yingju Xu, Gao Shang, Lushi Tan, Fangzhou Xie, Chengqian Xiao, Yongpeng Yuan, Baoqiang Wan, Guiquan Liu and Jingjun Yin, 
{"title":"Process Development toward a Key Fragment of the PCSK9 Inhibitor Enlicitide Decanoate","authors":"Kai-Jiong Xiao*,&nbsp;Yonggang Chen,&nbsp;Yingju Xu,&nbsp;Gao Shang,&nbsp;Lushi Tan,&nbsp;Fangzhou Xie,&nbsp;Chengqian Xiao,&nbsp;Yongpeng Yuan,&nbsp;Baoqiang Wan,&nbsp;Guiquan Liu and Jingjun Yin,&nbsp;","doi":"10.1021/acs.oprd.4c0050410.1021/acs.oprd.4c00504","DOIUrl":null,"url":null,"abstract":"<p >Here we report the development of a large-scale manufacturing process for the synthesis of the Northern Fragment of enlicitide decanoate (MK-0616), an orally bioavailable inhibitor of proprotein convertase subtilisin/kexin type 9 (PCSK9). The key topics covered are (1) process development for the selective tryptophan allylation; (2) development of the one-pot process for two consecutive peptide coupling reactions; (3) process development for the one-pot cleavage of two <i>N</i>-<i>tert</i>-butyloxycarbonyl (<i>N</i>-Boc) groups and a <i>tert</i>-butyl ester; and (4) process development of the magnesium chloride (MgCl<sub>2</sub>)-mediated selective macrolactamization. This optimized process was demonstrated to produce the key fragment at &gt;150 kg scale per batch in the synthesis of enlicitide.</p>","PeriodicalId":55,"journal":{"name":"Organic Process Research & Development","volume":"29 4","pages":"1083–1092 1083–1092"},"PeriodicalIF":3.1000,"publicationDate":"2025-04-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic Process Research & Development","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.oprd.4c00504","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
引用次数: 0

Abstract

Here we report the development of a large-scale manufacturing process for the synthesis of the Northern Fragment of enlicitide decanoate (MK-0616), an orally bioavailable inhibitor of proprotein convertase subtilisin/kexin type 9 (PCSK9). The key topics covered are (1) process development for the selective tryptophan allylation; (2) development of the one-pot process for two consecutive peptide coupling reactions; (3) process development for the one-pot cleavage of two N-tert-butyloxycarbonyl (N-Boc) groups and a tert-butyl ester; and (4) process development of the magnesium chloride (MgCl2)-mediated selective macrolactamization. This optimized process was demonstrated to produce the key fragment at >150 kg scale per batch in the synthesis of enlicitide.

Abstract Image

在此,我们报告了用于合成癸酸恩替卡韦北片段(MK-0616)的大规模生产工艺的开发情况,MK-0616 是一种口服生物活性抑制剂,可用于抑制 9 型丙脯氨酸转化酶亚基酶/kexin (PCSK9)。主要内容包括:(1) 选择性色氨酸烯丙基化的工艺开发;(2) 两个连续肽偶联反应的单锅工艺开发;(3) 两个 N-叔丁氧羰基(N-Boc)和一个叔丁基酯的单锅裂解工艺开发;以及 (4) 氯化镁(MgCl2)介导的选择性大内酰胺化工艺开发。在合成烯丙内酯的过程中,这一优化工艺已被证明能够以每批 150 千克的规模生产出关键片段。
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
CiteScore
6.90
自引率
14.70%
发文量
251
审稿时长
2 months
期刊介绍: The journal Organic Process Research & Development serves as a communication tool between industrial chemists and chemists working in universities and research institutes. As such, it reports original work from the broad field of industrial process chemistry but also presents academic results that are relevant, or potentially relevant, to industrial applications. Process chemistry is the science that enables the safe, environmentally benign and ultimately economical manufacturing of organic compounds that are required in larger amounts to help address the needs of society. Consequently, the Journal encompasses every aspect of organic chemistry, including all aspects of catalysis, synthetic methodology development and synthetic strategy exploration, but also includes aspects from analytical and solid-state chemistry and chemical engineering, such as work-up tools,process safety, or flow-chemistry. The goal of development and optimization of chemical reactions and processes is their transfer to a larger scale; original work describing such studies and the actual implementation on scale is highly relevant to the journal. However, studies on new developments from either industry, research institutes or academia that have not yet been demonstrated on scale, but where an industrial utility can be expected and where the study has addressed important prerequisites for a scale-up and has given confidence into the reliability and practicality of the chemistry, also serve the mission of OPR&D as a communication tool between the different contributors to the field.
×
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:481959085
Book学术官方微信