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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2008
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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. |
format | Online Article Text |
id | pubmed-6245067 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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