Guareschi-Thorpe反应合成S1P受体1激动剂

IF 3.5 3区 化学 Q2 CHEMISTRY, APPLIED
Gunther Schmidt, Martin H. Bolli, Cyrille Lescop, Stefan Abele*
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引用次数: 5

摘要

通过两个关键中间体的后期收敛偶联,实际合成了S1P受体1激动剂ACT-334441(1)。第一个中间体是2-环戊基-6-甲氧基异烟酸,其骨架由1-环戊基乙烷、草酸乙酯和氰乙酸酯在Guareschi-Thorpe反应中以42%的收率经过5步合成。第二种是手性中间体,是由对映异构纯(R)-异丙基甘油(R)-索酮)和3-乙基-4-羟基-5-甲基苯并腈在一锅反应中以71%的收率合成的酚醚。整个序列包含18个化学步骤和10个分离的中间产物。所有原料都很便宜,并且可以大量获得,反应条件与标准的中试工厂设备相匹配,并且该路线可重复性地为临床研究提供3-20公斤纯度和产量极高的1。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Practical Synthesis of a S1P Receptor 1 Agonist via a Guareschi–Thorpe Reaction

Practical Synthesis of a S1P Receptor 1 Agonist via a Guareschi–Thorpe Reaction

A practical synthesis of S1P receptor 1 agonist ACT-334441 (1) through late-stage convergent coupling of two key intermediates is described. The first intermediate is 2-cyclopentyl-6-methoxyisonicotinic acid whose skeleton was built from 1-cyclopentylethanone, ethyl oxalate, and cyanoacetate in a Guareschi–Thorpe reaction in 42% yield over five steps. The second, chiral intermediate, is a phenol ether derived from enantiomerically pure (R)-isopropylidene glycerol ((R)-solketal) and 3-ethyl-4-hydroxy-5-methylbenzonitrile in 71% yield in a one-pot reaction. The overall sequence entails 18 chemical steps with 10 isolated intermediates. All raw materials are cheap and readily available in bulk quantities, the reaction conditions match with standard pilot plant equipment, and the route reproducibly afforded 3–20 kg of 1 in excellent purity and yield for clinical studies.

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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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