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Synthesis and Characterization of 5-MeO-DMT Succinate for Clinical Use

[Image: see text] To support clinical use, a multigram-scale process has been developed to provide 5-MeO-DMT, a psychedelic natural product found in the parotid gland secretions of the toad, Incilius alvarius. Several synthetic routes were initially explored, and the selected process featured an opt...

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Detalles Bibliográficos
Autores principales: Sherwood, Alexander M., Claveau, Romain, Lancelotta, Rafael, Kaylo, Kristi W., Lenoch, Kelsey
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7745443/
https://www.ncbi.nlm.nih.gov/pubmed/33344861
http://dx.doi.org/10.1021/acsomega.0c05099
Descripción
Sumario:[Image: see text] To support clinical use, a multigram-scale process has been developed to provide 5-MeO-DMT, a psychedelic natural product found in the parotid gland secretions of the toad, Incilius alvarius. Several synthetic routes were initially explored, and the selected process featured an optimized Fischer indole reaction to 5-MeO-DMT freebase in high-yield, from which the 1:1 succinate salt was produced to provide 136 g of crystalline active pharmaceutical ingredient (API) with 99.86% peak area by high-performance liquid chromatography (HPLC) and a net yield of 49%. The report provides in-process monitoring, validated analytical methods, impurity formation and removal, and solid-state characterization of the API essential for subsequent clinical development.