Department of Chemistry & Pharmaceutical Sciences, Amsterdam Institute of Molecular & Life Sciences (AIMMS), Vrije Universiteit Amsterdam, De Boelelaan 1108, 1081 HZ Amsterdam, The Netherlands.
Department of Chemistry, The University of Manchester, Manchester Institute of Biotechnology, 131 Princess Street, Manchester M1 7DN, United Kingdom.
J Org Chem. 2023 Sep 1;88(17):12565-12571. doi: 10.1021/acs.joc.3c01274. Epub 2023 Aug 22.
In the wake of the Covid-19 pandemic, it has become clear that global access to efficacious antiviral drugs will be critical to combat future outbreaks of SARS-CoV-2 or related viruses. The orally available SARS-CoV-2 main protease inhibitor nirmatrelvir has proven an effective treatment option for Covid-19, especially in compromised patients. We report a new synthesis of nirmatrelvir featuring a highly enantioselective biocatalytic desymmetrization (>99% ee) and a highly diastereoselective multicomponent reaction (>25:1 dr) as the key steps. Our route avoids the use of transition metals and peptide coupling reagents, resulting in an overall highly efficient and atom-economic process.
在 COVID-19 大流行之后,很明显,全球获得有效的抗病毒药物对于应对未来 SARS-CoV-2 或相关病毒的爆发将至关重要。可口服的 SARS-CoV-2 主蛋白酶抑制剂奈玛特韦已被证明是 COVID-19 的一种有效治疗选择,特别是对有并发症的患者。我们报告了一种新的奈玛特韦合成方法,其中包括高度对映选择性的生物催化去对称化(>99%ee)和高度非对映选择性的多组分反应(>25:1 dr)作为关键步骤。我们的路线避免了使用过渡金属和肽偶联试剂,从而实现了整体高效和原子经济性的过程。