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Direct Phosphorylation of Psilocin Enables Optimized cGMP Kilogram-Scale Manufacture of Psilocybin
[Image: see text] A second-generation kilogram-scale synthesis of the psychedelic tryptamine psilocybin has been developed. The synthesis was designed to address several challenges first encountered with the scale-up of previously described literature procedures, which were not optimized for providi...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7364850/ https://www.ncbi.nlm.nih.gov/pubmed/32685866 http://dx.doi.org/10.1021/acsomega.0c02387 |
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author | Kargbo, Robert B. Sherwood, Alexander Walker, Andrew Cozzi, Nicholas V. Dagger, Raymond E. Sable, Jessica O’Hern, Kelsey Kaylo, Kristi Patterson, Tura Tarpley, Gary Meisenheimer, Poncho |
author_facet | Kargbo, Robert B. Sherwood, Alexander Walker, Andrew Cozzi, Nicholas V. Dagger, Raymond E. Sable, Jessica O’Hern, Kelsey Kaylo, Kristi Patterson, Tura Tarpley, Gary Meisenheimer, Poncho |
author_sort | Kargbo, Robert B. |
collection | PubMed |
description | [Image: see text] A second-generation kilogram-scale synthesis of the psychedelic tryptamine psilocybin has been developed. The synthesis was designed to address several challenges first encountered with the scale-up of previously described literature procedures, which were not optimized for providing consistent yield and purity of products, atom economy, or being run in pilot plant-scale reactors. These challenges were addressed and circumvented with the design of the second-generation route, which featured an optimized cGMP large-scale Speeter–Anthony tryptamine synthesis to the intermediate psilocin with improved in-process control and impurity removal over the three steps. Psilocin was subsequently phosphorylated directly with phosphorous oxychloride for the first time, avoiding a tedious and poor atom economy benzyl-protecting group strategy common to all previously described methods for producing psilocybin. In this report, the challenges encountered in a 100 g scale first-generation literature-based synthesis are highlighted, followed by a detailed description of the newly developed second-generation synthesis to provide over one kilogram of high-purity psilocybin under cGMP. |
format | Online Article Text |
id | pubmed-7364850 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-73648502020-07-17 Direct Phosphorylation of Psilocin Enables Optimized cGMP Kilogram-Scale Manufacture of Psilocybin Kargbo, Robert B. Sherwood, Alexander Walker, Andrew Cozzi, Nicholas V. Dagger, Raymond E. Sable, Jessica O’Hern, Kelsey Kaylo, Kristi Patterson, Tura Tarpley, Gary Meisenheimer, Poncho ACS Omega [Image: see text] A second-generation kilogram-scale synthesis of the psychedelic tryptamine psilocybin has been developed. The synthesis was designed to address several challenges first encountered with the scale-up of previously described literature procedures, which were not optimized for providing consistent yield and purity of products, atom economy, or being run in pilot plant-scale reactors. These challenges were addressed and circumvented with the design of the second-generation route, which featured an optimized cGMP large-scale Speeter–Anthony tryptamine synthesis to the intermediate psilocin with improved in-process control and impurity removal over the three steps. Psilocin was subsequently phosphorylated directly with phosphorous oxychloride for the first time, avoiding a tedious and poor atom economy benzyl-protecting group strategy common to all previously described methods for producing psilocybin. In this report, the challenges encountered in a 100 g scale first-generation literature-based synthesis are highlighted, followed by a detailed description of the newly developed second-generation synthesis to provide over one kilogram of high-purity psilocybin under cGMP. American Chemical Society 2020-07-01 /pmc/articles/PMC7364850/ /pubmed/32685866 http://dx.doi.org/10.1021/acsomega.0c02387 Text en Copyright © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Kargbo, Robert B. Sherwood, Alexander Walker, Andrew Cozzi, Nicholas V. Dagger, Raymond E. Sable, Jessica O’Hern, Kelsey Kaylo, Kristi Patterson, Tura Tarpley, Gary Meisenheimer, Poncho Direct Phosphorylation of Psilocin Enables Optimized cGMP Kilogram-Scale Manufacture of Psilocybin |
title | Direct Phosphorylation of Psilocin Enables Optimized
cGMP Kilogram-Scale Manufacture of Psilocybin |
title_full | Direct Phosphorylation of Psilocin Enables Optimized
cGMP Kilogram-Scale Manufacture of Psilocybin |
title_fullStr | Direct Phosphorylation of Psilocin Enables Optimized
cGMP Kilogram-Scale Manufacture of Psilocybin |
title_full_unstemmed | Direct Phosphorylation of Psilocin Enables Optimized
cGMP Kilogram-Scale Manufacture of Psilocybin |
title_short | Direct Phosphorylation of Psilocin Enables Optimized
cGMP Kilogram-Scale Manufacture of Psilocybin |
title_sort | direct phosphorylation of psilocin enables optimized
cgmp kilogram-scale manufacture of psilocybin |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7364850/ https://www.ncbi.nlm.nih.gov/pubmed/32685866 http://dx.doi.org/10.1021/acsomega.0c02387 |
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