Thermally Hazardous 1,3-Dioxolane Coupling Reaction Required for a Pharmaceutical Candidate Starting Material, Made Safer by Employing Process Safety Data as Key Design of Experiments Output Variables

IF 3.5 3区 化学 Q2 CHEMISTRY, APPLIED Organic Process Research & Development Pub Date : 2025-03-10 DOI:10.1021/acs.oprd.4c00519
James Clarke, Duncan Farr, Jimmy Wang, Heather Ingram, Caroline Chapman, Harriet Field, Christopher P. Breen, Eva M. Gulotty, Sara Mason, Grace Russell, Oliver Williams, Shruti Kumta, Jerry Britto, Li-Jen Ping
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Abstract

The optimization of a ruthenium-catalyzed catechol, terminal-alkyne coupling reaction to form a key benzodioxolane intermediate toward Lotiglipron is described. This transformation required the use of 3-butyn-2-ol, a valuable yet thermally hazardous reagent. Manual reaction condition optimization delivered a good yield but a poor process safety profile. Further reaction understanding was gained by performing a design of experiments (DoE) screening of relevant reaction conditions while using differential scanning calorimetry output data as well as productivity optimization parameters to strike a balance of process safety and chemical yield. To the best of our knowledge, this work represents the first report of using process safety data as DoE output to guide safe reaction condition selection. Finally, the optimal conditions were demonstrated in a lab-scale flow reactor with good translation of results from the batch reaction.

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采用工艺安全数据作为实验输出变量的关键设计,使候选药物起始原料所需的热危险1,3-二恶烷偶联反应更安全
研究了钌催化的邻苯二酚端炔偶联反应生成洛替格列酮的苯并二氧唑烷关键中间体的优化过程。这种转化需要使用3-丁-2-醇,这是一种有价值但热危险的试剂。手动反应条件优化提供了良好的产率,但工艺安全性差。通过对相关反应条件进行实验设计(DoE)筛选,同时使用差示扫描量热输出数据和生产率优化参数,以达到工艺安全和化学产率的平衡,进一步了解了反应。据我们所知,这项工作代表了使用过程安全数据作为DoE输出来指导安全反应条件选择的第一份报告。最后,在实验室规模的流动反应器中验证了最佳条件,并对间歇式反应的结果进行了很好的转化。
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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.
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