A sustainable, efficient, and potentially cost-effective approach to the antimalarial drug candidate MMV688533

A 6-step synthesis of the antimalarial drug candidate MMV688533 is reported. Key transformations carried out under aqueous micellar conditions include two Sonogashira couplings and amide bond formation. Compared with the first-generation manufacturing process reported by Sanofi, the current route fe...

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Detalles Bibliográficos
Autores principales: Kavthe, Rahul D., Iyer, Karthik S., Caravez, Juan C., Lipshutz, Bruce H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Chemistry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10266478/
https://www.ncbi.nlm.nih.gov/pubmed/37325157
http://dx.doi.org/10.1039/d3sc01699d
Descripción
Sumario:A 6-step synthesis of the antimalarial drug candidate MMV688533 is reported. Key transformations carried out under aqueous micellar conditions include two Sonogashira couplings and amide bond formation. Compared with the first-generation manufacturing process reported by Sanofi, the current route features ppm levels of palladium loading, less material input, less organic solvent, and no traditional amide coupling reagents. The overall yield is improved ten-fold, from 6.4% to 67%.

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