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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2020
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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. |
format | Online Article Text |
id | pubmed-7323627 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
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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