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Ultrasound Promoted Synthesis of Bis(substituted pyrazol-4-ylcarbonyl)-Substituted Thioureas

A series of novel bis(substituted pyrazol-4-ylcarbonyl)-substituted thioureas have been synthesized by the reactions of substituted pyrazol-4-ylcarbonyl isothiocyanates with different diamines under ultrasound irradiation and classical heating method at 20-25 °C. In general, substantial improvement...

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Detalles Bibliográficos
Autores principales: Xiao, Li, Liu, Chen-Jiang, Li, Yan-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254392/
https://www.ncbi.nlm.nih.gov/pubmed/19384273
http://dx.doi.org/10.3390/molecules14041423
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author Xiao, Li
Liu, Chen-Jiang
Li, Yan-Ping
author_facet Xiao, Li
Liu, Chen-Jiang
Li, Yan-Ping
author_sort Xiao, Li
collection PubMed
description A series of novel bis(substituted pyrazol-4-ylcarbonyl)-substituted thioureas have been synthesized by the reactions of substituted pyrazol-4-ylcarbonyl isothiocyanates with different diamines under ultrasound irradiation and classical heating method at 20-25 °C. In general, substantial improvement in rates and modest yields increases were observed when reactions were carried out under sonication, compared with the classical heating method. The structures of these compounds have been elucidated by elemental and spectral (IR, (1)H-NMR) analysis.
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spelling pubmed-62543922018-11-30 Ultrasound Promoted Synthesis of Bis(substituted pyrazol-4-ylcarbonyl)-Substituted Thioureas Xiao, Li Liu, Chen-Jiang Li, Yan-Ping Molecules Communication A series of novel bis(substituted pyrazol-4-ylcarbonyl)-substituted thioureas have been synthesized by the reactions of substituted pyrazol-4-ylcarbonyl isothiocyanates with different diamines under ultrasound irradiation and classical heating method at 20-25 °C. In general, substantial improvement in rates and modest yields increases were observed when reactions were carried out under sonication, compared with the classical heating method. The structures of these compounds have been elucidated by elemental and spectral (IR, (1)H-NMR) analysis. Molecular Diversity Preservation International (MDPI) 2009-03-31 /pmc/articles/PMC6254392/ /pubmed/19384273 http://dx.doi.org/10.3390/molecules14041423 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 Communication
Xiao, Li
Liu, Chen-Jiang
Li, Yan-Ping
Ultrasound Promoted Synthesis of Bis(substituted pyrazol-4-ylcarbonyl)-Substituted Thioureas
title Ultrasound Promoted Synthesis of Bis(substituted pyrazol-4-ylcarbonyl)-Substituted Thioureas
title_full Ultrasound Promoted Synthesis of Bis(substituted pyrazol-4-ylcarbonyl)-Substituted Thioureas
title_fullStr Ultrasound Promoted Synthesis of Bis(substituted pyrazol-4-ylcarbonyl)-Substituted Thioureas
title_full_unstemmed Ultrasound Promoted Synthesis of Bis(substituted pyrazol-4-ylcarbonyl)-Substituted Thioureas
title_short Ultrasound Promoted Synthesis of Bis(substituted pyrazol-4-ylcarbonyl)-Substituted Thioureas
title_sort ultrasound promoted synthesis of bis(substituted pyrazol-4-ylcarbonyl)-substituted thioureas
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254392/
https://www.ncbi.nlm.nih.gov/pubmed/19384273
http://dx.doi.org/10.3390/molecules14041423
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