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One-pot synthesis of 1,3,5-triazine-2,4-dithione derivatives via three-component reactions

A catalyst-free one-pot synthetic methodology was developed for the preparation of 1,3,5-triazine-2,4-dithione derivatives through three-component reactions of arylaldehydes, thiourea, and orthoformates. The procedure tolerated a diverse range of arylaldehydes and orthoformates and provided a rapid...

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Autores principales: Kang, Gui-Feng, Zhang, Gang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7323627/
https://www.ncbi.nlm.nih.gov/pubmed/32647546
http://dx.doi.org/10.3762/bjoc.16.120
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author Kang, Gui-Feng
Zhang, Gang
author_facet Kang, Gui-Feng
Zhang, Gang
author_sort Kang, Gui-Feng
collection PubMed
description A catalyst-free one-pot synthetic methodology was developed for the preparation of 1,3,5-triazine-2,4-dithione derivatives through three-component reactions of arylaldehydes, thiourea, and orthoformates. The procedure tolerated a diverse range of arylaldehydes and orthoformates and provided a rapid entry to a variety of 4-aryl-6-(alkylthio)-3,4-dihydro-1,3,5-triazine-2(1H)-thiones (29 examples). The synthetic strategy relies on the dual role of thiourea in the cyclization with the aldehydes and the alkylation via an intermediate imidate formation. The structures of 1,3,5-triazine-2,4-dithione derivatives were characterized by spectroscopic techniques as well as by single crystal X-ray diffraction.
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spelling pubmed-73236272020-07-08 One-pot synthesis of 1,3,5-triazine-2,4-dithione derivatives via three-component reactions Kang, Gui-Feng Zhang, Gang Beilstein J Org Chem Full Research Paper A catalyst-free one-pot synthetic methodology was developed for the preparation of 1,3,5-triazine-2,4-dithione derivatives through three-component reactions of arylaldehydes, thiourea, and orthoformates. The procedure tolerated a diverse range of arylaldehydes and orthoformates and provided a rapid entry to a variety of 4-aryl-6-(alkylthio)-3,4-dihydro-1,3,5-triazine-2(1H)-thiones (29 examples). The synthetic strategy relies on the dual role of thiourea in the cyclization with the aldehydes and the alkylation via an intermediate imidate formation. The structures of 1,3,5-triazine-2,4-dithione derivatives were characterized by spectroscopic techniques as well as by single crystal X-ray diffraction. Beilstein-Institut 2020-06-24 /pmc/articles/PMC7323627/ /pubmed/32647546 http://dx.doi.org/10.3762/bjoc.16.120 Text en Copyright © 2020, Kang and Zhang https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Kang, Gui-Feng
Zhang, Gang
One-pot synthesis of 1,3,5-triazine-2,4-dithione derivatives via three-component reactions
title One-pot synthesis of 1,3,5-triazine-2,4-dithione derivatives via three-component reactions
title_full One-pot synthesis of 1,3,5-triazine-2,4-dithione derivatives via three-component reactions
title_fullStr One-pot synthesis of 1,3,5-triazine-2,4-dithione derivatives via three-component reactions
title_full_unstemmed One-pot synthesis of 1,3,5-triazine-2,4-dithione derivatives via three-component reactions
title_short One-pot synthesis of 1,3,5-triazine-2,4-dithione derivatives via three-component reactions
title_sort one-pot synthesis of 1,3,5-triazine-2,4-dithione derivatives via three-component reactions
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7323627/
https://www.ncbi.nlm.nih.gov/pubmed/32647546
http://dx.doi.org/10.3762/bjoc.16.120
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