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Synthesis of Some Novel Pyrazolo[1,5-a]pyrimidine Derivatives and Their Application as Disperse Dyes

A series of novel monoazo-disperse dyes containing pyrazolo[1,5-a]pyrimidine structures were synthesized starting with the coupling reaction between ethyl cyanoacetate and 4-hydroxybenzenediazonium chloride, followed by treatment of the resulting hydrazone product with hydrazine hydrate. The pyrazol...

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Autores principales: Al-Etaibi, Alya M., Al-Awadi, Nouria A., El-Apasery, Morsy A., Ibrahim, Maher R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264419/
https://www.ncbi.nlm.nih.gov/pubmed/21697775
http://dx.doi.org/10.3390/molecules16065182
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author Al-Etaibi, Alya M.
Al-Awadi, Nouria A.
El-Apasery, Morsy A.
Ibrahim, Maher R.
author_facet Al-Etaibi, Alya M.
Al-Awadi, Nouria A.
El-Apasery, Morsy A.
Ibrahim, Maher R.
author_sort Al-Etaibi, Alya M.
collection PubMed
description A series of novel monoazo-disperse dyes containing pyrazolo[1,5-a]pyrimidine structures were synthesized starting with the coupling reaction between ethyl cyanoacetate and 4-hydroxybenzenediazonium chloride, followed by treatment of the resulting hydrazone product with hydrazine hydrate. The pyrazolohydrazone 6 is then treated with either 2,4-pentandione and enaminonitrile or aryl-substituted enaminoketones to give the target pyrazolo[1,5-a]pyrimidine dyes 7 and 15a-d. Structural assignments to the dyes were made using NMR spectroscopic methods. A new high temperature method, using microwave heating, was employed to apply these dyes to polyester fibers. Most of the dyed fabrics tested displayed moderate light fastness and excellent washing fastness properties.
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spelling pubmed-62644192018-12-10 Synthesis of Some Novel Pyrazolo[1,5-a]pyrimidine Derivatives and Their Application as Disperse Dyes Al-Etaibi, Alya M. Al-Awadi, Nouria A. El-Apasery, Morsy A. Ibrahim, Maher R. Molecules Article A series of novel monoazo-disperse dyes containing pyrazolo[1,5-a]pyrimidine structures were synthesized starting with the coupling reaction between ethyl cyanoacetate and 4-hydroxybenzenediazonium chloride, followed by treatment of the resulting hydrazone product with hydrazine hydrate. The pyrazolohydrazone 6 is then treated with either 2,4-pentandione and enaminonitrile or aryl-substituted enaminoketones to give the target pyrazolo[1,5-a]pyrimidine dyes 7 and 15a-d. Structural assignments to the dyes were made using NMR spectroscopic methods. A new high temperature method, using microwave heating, was employed to apply these dyes to polyester fibers. Most of the dyed fabrics tested displayed moderate light fastness and excellent washing fastness properties. MDPI 2011-06-22 /pmc/articles/PMC6264419/ /pubmed/21697775 http://dx.doi.org/10.3390/molecules16065182 Text en © 2011 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
Al-Etaibi, Alya M.
Al-Awadi, Nouria A.
El-Apasery, Morsy A.
Ibrahim, Maher R.
Synthesis of Some Novel Pyrazolo[1,5-a]pyrimidine Derivatives and Their Application as Disperse Dyes
title Synthesis of Some Novel Pyrazolo[1,5-a]pyrimidine Derivatives and Their Application as Disperse Dyes
title_full Synthesis of Some Novel Pyrazolo[1,5-a]pyrimidine Derivatives and Their Application as Disperse Dyes
title_fullStr Synthesis of Some Novel Pyrazolo[1,5-a]pyrimidine Derivatives and Their Application as Disperse Dyes
title_full_unstemmed Synthesis of Some Novel Pyrazolo[1,5-a]pyrimidine Derivatives and Their Application as Disperse Dyes
title_short Synthesis of Some Novel Pyrazolo[1,5-a]pyrimidine Derivatives and Their Application as Disperse Dyes
title_sort synthesis of some novel pyrazolo[1,5-a]pyrimidine derivatives and their application as disperse dyes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264419/
https://www.ncbi.nlm.nih.gov/pubmed/21697775
http://dx.doi.org/10.3390/molecules16065182
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