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A Mild and Facile One-Pot Synthesis of N-Methyl-3-Acyl-Pyrroles
N-Methyl-3-acylpyrroles were synthesized via a multicomponent reaction of dimethylacetylene dicarboxylate (DMAD), N-methylhydroxylamine and acylchlorides in the presence of KHCO(3). For comparison both conventional and microwave protocols were examined in this procedure. The reaction is clean and gi...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263317/ https://www.ncbi.nlm.nih.gov/pubmed/20657459 http://dx.doi.org/10.3390/molecules15052972 |
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author | Valizadeh, Hassan Fakhari, Ashraf |
author_facet | Valizadeh, Hassan Fakhari, Ashraf |
author_sort | Valizadeh, Hassan |
collection | PubMed |
description | N-Methyl-3-acylpyrroles were synthesized via a multicomponent reaction of dimethylacetylene dicarboxylate (DMAD), N-methylhydroxylamine and acylchlorides in the presence of KHCO(3). For comparison both conventional and microwave protocols were examined in this procedure. The reaction is clean and gives the products in good to excellent yields under conventional heating conditions at 40 ºC in anhydrous dichloromethane. |
format | Online Article Text |
id | pubmed-6263317 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62633172019-01-02 A Mild and Facile One-Pot Synthesis of N-Methyl-3-Acyl-Pyrroles Valizadeh, Hassan Fakhari, Ashraf Molecules Article N-Methyl-3-acylpyrroles were synthesized via a multicomponent reaction of dimethylacetylene dicarboxylate (DMAD), N-methylhydroxylamine and acylchlorides in the presence of KHCO(3). For comparison both conventional and microwave protocols were examined in this procedure. The reaction is clean and gives the products in good to excellent yields under conventional heating conditions at 40 ºC in anhydrous dichloromethane. MDPI 2010-04-27 /pmc/articles/PMC6263317/ /pubmed/20657459 http://dx.doi.org/10.3390/molecules15052972 Text en © 2010 by the authors; licensee MDPI, 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 Valizadeh, Hassan Fakhari, Ashraf A Mild and Facile One-Pot Synthesis of N-Methyl-3-Acyl-Pyrroles |
title | A Mild and Facile One-Pot Synthesis of N-Methyl-3-Acyl-Pyrroles |
title_full | A Mild and Facile One-Pot Synthesis of N-Methyl-3-Acyl-Pyrroles |
title_fullStr | A Mild and Facile One-Pot Synthesis of N-Methyl-3-Acyl-Pyrroles |
title_full_unstemmed | A Mild and Facile One-Pot Synthesis of N-Methyl-3-Acyl-Pyrroles |
title_short | A Mild and Facile One-Pot Synthesis of N-Methyl-3-Acyl-Pyrroles |
title_sort | mild and facile one-pot synthesis of n-methyl-3-acyl-pyrroles |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263317/ https://www.ncbi.nlm.nih.gov/pubmed/20657459 http://dx.doi.org/10.3390/molecules15052972 |
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