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Regioselective Synthesis of New 2-(E)-Cyano(thiazolidin-2-ylidene)thiazoles
Cyclocondensation of 2-[bis(methylthio)methylene]malononitrile (1) and cysteamine (2) afforded 2-(thiazolidin-2-ylidene)malononitrile (3). This compound on treatment with NaSH gave the corresponding thioamide derivative 4a in a regioselective manner on the basis of its single crystal X-ray diffracti...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6255026/ https://www.ncbi.nlm.nih.gov/pubmed/20032863 http://dx.doi.org/10.3390/molecules14114849 |
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author | Bakavoli, Mehdi Beyzaie, Hamid Rahimizadeh, Mohammad Eshghi, Hossein Takjoo, Reza |
author_facet | Bakavoli, Mehdi Beyzaie, Hamid Rahimizadeh, Mohammad Eshghi, Hossein Takjoo, Reza |
author_sort | Bakavoli, Mehdi |
collection | PubMed |
description | Cyclocondensation of 2-[bis(methylthio)methylene]malononitrile (1) and cysteamine (2) afforded 2-(thiazolidin-2-ylidene)malononitrile (3). This compound on treatment with NaSH gave the corresponding thioamide derivative 4a in a regioselective manner on the basis of its single crystal X-ray diffraction analysis. Reaction of this compound with several α-bromocarbonyl compounds gave new 2-(E)-cyano(thiazolidin-2-ylidene)thiazoles 5a-g. |
format | Online Article Text |
id | pubmed-6255026 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Molecular Diversity Preservation International |
record_format | MEDLINE/PubMed |
spelling | pubmed-62550262018-11-30 Regioselective Synthesis of New 2-(E)-Cyano(thiazolidin-2-ylidene)thiazoles Bakavoli, Mehdi Beyzaie, Hamid Rahimizadeh, Mohammad Eshghi, Hossein Takjoo, Reza Molecules Article Cyclocondensation of 2-[bis(methylthio)methylene]malononitrile (1) and cysteamine (2) afforded 2-(thiazolidin-2-ylidene)malononitrile (3). This compound on treatment with NaSH gave the corresponding thioamide derivative 4a in a regioselective manner on the basis of its single crystal X-ray diffraction analysis. Reaction of this compound with several α-bromocarbonyl compounds gave new 2-(E)-cyano(thiazolidin-2-ylidene)thiazoles 5a-g. Molecular Diversity Preservation International 2009-11-25 /pmc/articles/PMC6255026/ /pubmed/20032863 http://dx.doi.org/10.3390/molecules14114849 Text en © 2009 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 Bakavoli, Mehdi Beyzaie, Hamid Rahimizadeh, Mohammad Eshghi, Hossein Takjoo, Reza Regioselective Synthesis of New 2-(E)-Cyano(thiazolidin-2-ylidene)thiazoles |
title | Regioselective Synthesis of New 2-(E)-Cyano(thiazolidin-2-ylidene)thiazoles |
title_full | Regioselective Synthesis of New 2-(E)-Cyano(thiazolidin-2-ylidene)thiazoles |
title_fullStr | Regioselective Synthesis of New 2-(E)-Cyano(thiazolidin-2-ylidene)thiazoles |
title_full_unstemmed | Regioselective Synthesis of New 2-(E)-Cyano(thiazolidin-2-ylidene)thiazoles |
title_short | Regioselective Synthesis of New 2-(E)-Cyano(thiazolidin-2-ylidene)thiazoles |
title_sort | regioselective synthesis of new 2-(e)-cyano(thiazolidin-2-ylidene)thiazoles |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6255026/ https://www.ncbi.nlm.nih.gov/pubmed/20032863 http://dx.doi.org/10.3390/molecules14114849 |
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