Process Development toward the Continuous Manufacturing of Baloxavir Marboxil

IF 3.5 3区 化学 Q2 CHEMISTRY, APPLIED Organic Process Research & Development Pub Date : 2025-03-10 DOI:10.1021/acs.oprd.4c00517
Keith S. Barbato, Qinglin Su, Youhua Li, Anjana Ramnath, Wei Wu, Chuntian Hu, Stephen C. Born, Paul Hermant, Paul Stonestreet, Michael Berg, Bayan Takizawa, Salvatore Mascia
{"title":"Process Development toward the Continuous Manufacturing of Baloxavir Marboxil","authors":"Keith S. Barbato, Qinglin Su, Youhua Li, Anjana Ramnath, Wei Wu, Chuntian Hu, Stephen C. Born, Paul Hermant, Paul Stonestreet, Michael Berg, Bayan Takizawa, Salvatore Mascia","doi":"10.1021/acs.oprd.4c00517","DOIUrl":null,"url":null,"abstract":"We report the initial studies toward the continuous processing of Baloxavir Marboxil, the active pharmaceutical ingredient (API) of Roche’s commercial product Xofluza. The motivation behind this effort is to transition to integrated continuous manufacturing (ICM) as a platform to create an agile and on-demand supply chain capability for a drug that has highly variable market demand. The work described herein includes an improved late-stage synthetic route to Baloxavir Marboxil that (1) reduced a four-step synthesis down to two steps, (2) identified key diastereomeric crystallization conditions to reach required material specifications, and (3) removed the use of <i>N,N</i>-dimethylacetamide in exchange for a more environmentally benign solvent mixture of acetonitrile and water. After a full revision of the two-step synthetic route in batch mode, key unit operations were translated to continuous mode to evaluate their performance. Collectively, this work eliminated 16 unit operations, significantly simplified the process, and is projected to reduce the lead time from 12 months to several days using ICM.","PeriodicalId":55,"journal":{"name":"Organic Process Research & Development","volume":"203 1","pages":""},"PeriodicalIF":3.5000,"publicationDate":"2025-03-10","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://doi.org/10.1021/acs.oprd.4c00517","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

We report the initial studies toward the continuous processing of Baloxavir Marboxil, the active pharmaceutical ingredient (API) of Roche’s commercial product Xofluza. The motivation behind this effort is to transition to integrated continuous manufacturing (ICM) as a platform to create an agile and on-demand supply chain capability for a drug that has highly variable market demand. The work described herein includes an improved late-stage synthetic route to Baloxavir Marboxil that (1) reduced a four-step synthesis down to two steps, (2) identified key diastereomeric crystallization conditions to reach required material specifications, and (3) removed the use of N,N-dimethylacetamide in exchange for a more environmentally benign solvent mixture of acetonitrile and water. After a full revision of the two-step synthetic route in batch mode, key unit operations were translated to continuous mode to evaluate their performance. Collectively, this work eliminated 16 unit operations, significantly simplified the process, and is projected to reduce the lead time from 12 months to several days using ICM.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
巴洛昔韦马博西连续生产工艺的开发
我们报告了罗氏商业产品Xofluza的活性药物成分(API) Baloxavir Marboxil连续加工的初步研究。这一努力背后的动机是过渡到集成连续制造(ICM)作为一个平台,为具有高度可变市场需求的药物创建敏捷和按需供应链能力。本文所述的工作包括改进巴洛昔韦马博西的后期合成路线,该路线(1)将四步合成减少到两步,(2)确定了达到所需材料规格的关键非对异构体结晶条件,以及(3)不再使用N,N-二甲基乙酰胺,取而代之的是更环保的乙腈和水的溶剂混合物。在批量模式下对两步合成路线进行全面修正后,将关键单元操作转换为连续模式以评估其性能。总的来说,这项工作减少了16个单元作业,大大简化了流程,并且预计使用ICM将把交货时间从12个月缩短到几天。
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 去求助
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.
期刊最新文献
First Method for Trace-Level Quantification of the Potential Genotoxic Impurity Bis(neopentyl glycolato)diboron Using GC–MS Development of a Claisen Condensation in Flow toward the Synthesis of MK-7845 Generalized Digital Framework for the Sustainable Recovery of Active Pharmaceutical Ingredients from Solid Drug Formulations Reductive Transformations with Sodium Borohydride and Their Applications Bayesian Optimization and Kinetic Modeling for Continuous-Flow Synthesis of 4-(Chloromethyl)-2,2-dimethyl-1,3-dioxolane Directed by Computational Fluid Dynamics
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1