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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
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.
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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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