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Multicomponent Synthesis of the SARS-CoV-2 Main Protease Inhibitor Nirmatrelvir

[Image: see text] 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 tre...

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Detalles Bibliográficos
Autores principales: Preschel, H. Daniel, Otte, Ruben T., Zhuo, Ying, Ruscoe, Rebecca E., Burke, Ashleigh J., Kellerhals, Rachel, Horst, Brendan, Hennig, Sven, Janssen, Elwin, Green, Anthony P., Turner, Nicholas J., Ruijter, Eelco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10476182/
https://www.ncbi.nlm.nih.gov/pubmed/37607396
http://dx.doi.org/10.1021/acs.joc.3c01274
Descripción
Sumario:[Image: see text] 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.