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Methyl Mercapturate Synthesis: An Efficient, Convenient and Simple Method

A safe and simple method for methyl S-arylmercapturate synthesis is described. Thirteen such compounds, to be used afterwards in metabolism studies, have been obtained with yields ranging from 71 to 99.6%. These compounds were obtained using a sulfa-Michael addition and synthesized by adding the cor...

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Detalles Bibliográficos
Autores principales: Cossec, Benoît, Cosnier, Frédéric, Burgart, Manuella
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245067/
https://www.ncbi.nlm.nih.gov/pubmed/18830162
http://dx.doi.org/10.3390/molecules13102394
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author Cossec, Benoît
Cosnier, Frédéric
Burgart, Manuella
author_facet Cossec, Benoît
Cosnier, Frédéric
Burgart, Manuella
author_sort Cossec, Benoît
collection PubMed
description A safe and simple method for methyl S-arylmercapturate synthesis is described. Thirteen such compounds, to be used afterwards in metabolism studies, have been obtained with yields ranging from 71 to 99.6%. These compounds were obtained using a sulfa-Michael addition and synthesized by adding the corresponding thiophenols to a mixture composed of methyl 2-acetamidoacrylate (MAA), potassium carbonate and a phase transfer catalyst, Aliquat 336. MAA, the initial synthon, was itself isolated in quasi quantitative yield following a fully described synthesis.
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spelling pubmed-62450672018-11-30 Methyl Mercapturate Synthesis: An Efficient, Convenient and Simple Method Cossec, Benoît Cosnier, Frédéric Burgart, Manuella Molecules Article A safe and simple method for methyl S-arylmercapturate synthesis is described. Thirteen such compounds, to be used afterwards in metabolism studies, have been obtained with yields ranging from 71 to 99.6%. These compounds were obtained using a sulfa-Michael addition and synthesized by adding the corresponding thiophenols to a mixture composed of methyl 2-acetamidoacrylate (MAA), potassium carbonate and a phase transfer catalyst, Aliquat 336. MAA, the initial synthon, was itself isolated in quasi quantitative yield following a fully described synthesis. MDPI 2008-10-01 /pmc/articles/PMC6245067/ /pubmed/18830162 http://dx.doi.org/10.3390/molecules13102394 Text en © 2008 by the authors. Licensee Molecular Diversity Preservation International, Basel, Switzerland. This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Cossec, Benoît
Cosnier, Frédéric
Burgart, Manuella
Methyl Mercapturate Synthesis: An Efficient, Convenient and Simple Method
title Methyl Mercapturate Synthesis: An Efficient, Convenient and Simple Method
title_full Methyl Mercapturate Synthesis: An Efficient, Convenient and Simple Method
title_fullStr Methyl Mercapturate Synthesis: An Efficient, Convenient and Simple Method
title_full_unstemmed Methyl Mercapturate Synthesis: An Efficient, Convenient and Simple Method
title_short Methyl Mercapturate Synthesis: An Efficient, Convenient and Simple Method
title_sort methyl mercapturate synthesis: an efficient, convenient and simple method
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245067/
https://www.ncbi.nlm.nih.gov/pubmed/18830162
http://dx.doi.org/10.3390/molecules13102394
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