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Flow Synthesis of L-α-Glycerylphosphorylcholine: Studies on Synthetic Routes Applicable to a Flow Reactor and Optimization of Reaction Conditions

L-α-Glycerylphosphorylcholine (L-α-GPC) has mainly been produced by two methods: extraction from plants rich in phosphatidylcholine and chemical synthesis. However, production through extraction involves difficult processes, such as fermentation, extractions and ripening, and conventional chemical s...

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Autores principales: Park, Jihun, Lee, Seungjae, Kim, Gyungtak, Malpani, Yashwardhan R., Park, Boyoung Y., Hwang, Ye-Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9692846/
https://www.ncbi.nlm.nih.gov/pubmed/36432671
http://dx.doi.org/10.3390/pharmaceutics14112480
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author Park, Jihun
Lee, Seungjae
Kim, Gyungtak
Malpani, Yashwardhan R.
Park, Boyoung Y.
Hwang, Ye-Jin
author_facet Park, Jihun
Lee, Seungjae
Kim, Gyungtak
Malpani, Yashwardhan R.
Park, Boyoung Y.
Hwang, Ye-Jin
author_sort Park, Jihun
collection PubMed
description L-α-Glycerylphosphorylcholine (L-α-GPC) has mainly been produced by two methods: extraction from plants rich in phosphatidylcholine and chemical synthesis. However, production through extraction involves difficult processes, such as fermentation, extractions and ripening, and conventional chemical synthesis methods with high-cost reactants and a batch reactor. These methods are not ideal for large-quantity production. Thus, it is important to develop a simple production method of L-α-GPC, which is suitable for mass production without the need for expensive reactants. Here, we studied synthetic L-α-GPC methods that are applicable to a flow synthesis system, which can provide selectivity, reproducibility, scalability, and a high yield in short reaction time using inexpensive starting materials. We developed a two-step synthetic route to produce L-α-GPC, including the synthesis of phosphoryl choline using choline chloride and phosphoryl oxychloride (POCl(3)) as a first step and synthesis of L-α-GPC by reacting phosphoryl choline with (R)-([Formula: see text])-3-chloro-1,2-propanediol (CPD) as a second step under basic conditions. Both steps were separately performed in a customized flow reactor, and reaction conditions were optimized. Finally, phosphoryl choline and L-α-GPC, the products first and second reactions, were successfully synthesized with high conversion yields of 97% and 79%, respectively.
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spelling pubmed-96928462022-11-26 Flow Synthesis of L-α-Glycerylphosphorylcholine: Studies on Synthetic Routes Applicable to a Flow Reactor and Optimization of Reaction Conditions Park, Jihun Lee, Seungjae Kim, Gyungtak Malpani, Yashwardhan R. Park, Boyoung Y. Hwang, Ye-Jin Pharmaceutics Article L-α-Glycerylphosphorylcholine (L-α-GPC) has mainly been produced by two methods: extraction from plants rich in phosphatidylcholine and chemical synthesis. However, production through extraction involves difficult processes, such as fermentation, extractions and ripening, and conventional chemical synthesis methods with high-cost reactants and a batch reactor. These methods are not ideal for large-quantity production. Thus, it is important to develop a simple production method of L-α-GPC, which is suitable for mass production without the need for expensive reactants. Here, we studied synthetic L-α-GPC methods that are applicable to a flow synthesis system, which can provide selectivity, reproducibility, scalability, and a high yield in short reaction time using inexpensive starting materials. We developed a two-step synthetic route to produce L-α-GPC, including the synthesis of phosphoryl choline using choline chloride and phosphoryl oxychloride (POCl(3)) as a first step and synthesis of L-α-GPC by reacting phosphoryl choline with (R)-([Formula: see text])-3-chloro-1,2-propanediol (CPD) as a second step under basic conditions. Both steps were separately performed in a customized flow reactor, and reaction conditions were optimized. Finally, phosphoryl choline and L-α-GPC, the products first and second reactions, were successfully synthesized with high conversion yields of 97% and 79%, respectively. MDPI 2022-11-16 /pmc/articles/PMC9692846/ /pubmed/36432671 http://dx.doi.org/10.3390/pharmaceutics14112480 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Park, Jihun
Lee, Seungjae
Kim, Gyungtak
Malpani, Yashwardhan R.
Park, Boyoung Y.
Hwang, Ye-Jin
Flow Synthesis of L-α-Glycerylphosphorylcholine: Studies on Synthetic Routes Applicable to a Flow Reactor and Optimization of Reaction Conditions
title Flow Synthesis of L-α-Glycerylphosphorylcholine: Studies on Synthetic Routes Applicable to a Flow Reactor and Optimization of Reaction Conditions
title_full Flow Synthesis of L-α-Glycerylphosphorylcholine: Studies on Synthetic Routes Applicable to a Flow Reactor and Optimization of Reaction Conditions
title_fullStr Flow Synthesis of L-α-Glycerylphosphorylcholine: Studies on Synthetic Routes Applicable to a Flow Reactor and Optimization of Reaction Conditions
title_full_unstemmed Flow Synthesis of L-α-Glycerylphosphorylcholine: Studies on Synthetic Routes Applicable to a Flow Reactor and Optimization of Reaction Conditions
title_short Flow Synthesis of L-α-Glycerylphosphorylcholine: Studies on Synthetic Routes Applicable to a Flow Reactor and Optimization of Reaction Conditions
title_sort flow synthesis of l-α-glycerylphosphorylcholine: studies on synthetic routes applicable to a flow reactor and optimization of reaction conditions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9692846/
https://www.ncbi.nlm.nih.gov/pubmed/36432671
http://dx.doi.org/10.3390/pharmaceutics14112480
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