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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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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
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author Sherwood, Alexander M.
Claveau, Romain
Lancelotta, Rafael
Kaylo, Kristi W.
Lenoch, Kelsey
author_facet Sherwood, Alexander M.
Claveau, Romain
Lancelotta, Rafael
Kaylo, Kristi W.
Lenoch, Kelsey
author_sort Sherwood, Alexander M.
collection PubMed
description [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.
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spelling pubmed-77454432020-12-18 Synthesis and Characterization of 5-MeO-DMT Succinate for Clinical Use Sherwood, Alexander M. Claveau, Romain Lancelotta, Rafael Kaylo, Kristi W. Lenoch, Kelsey ACS Omega [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. American Chemical Society 2020-12-02 /pmc/articles/PMC7745443/ /pubmed/33344861 http://dx.doi.org/10.1021/acsomega.0c05099 Text en © 2020 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes.
spellingShingle Sherwood, Alexander M.
Claveau, Romain
Lancelotta, Rafael
Kaylo, Kristi W.
Lenoch, Kelsey
Synthesis and Characterization of 5-MeO-DMT Succinate for Clinical Use
title Synthesis and Characterization of 5-MeO-DMT Succinate for Clinical Use
title_full Synthesis and Characterization of 5-MeO-DMT Succinate for Clinical Use
title_fullStr Synthesis and Characterization of 5-MeO-DMT Succinate for Clinical Use
title_full_unstemmed Synthesis and Characterization of 5-MeO-DMT Succinate for Clinical Use
title_short Synthesis and Characterization of 5-MeO-DMT Succinate for Clinical Use
title_sort synthesis and characterization of 5-meo-dmt succinate for clinical use
url 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
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