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General Method of Synthesis of 5-(Het)arylamino-1,2,3-triazoles via Buchwald–Hartwig Reaction of 5-Amino- or 5-Halo-1,2,3-triazoles
An efficient access to the novel 5-(het)arylamino-1,2,3-triazole derivatives has been developed. The method is based on Buchwald–Hartwig cross-coupling reaction of 5-Amino or 5-Halo-1,2,3-triazoles with (het)aryl halides and amines, respectively. As result, it was found that palladium complex [(THP-...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8949195/ https://www.ncbi.nlm.nih.gov/pubmed/35335361 http://dx.doi.org/10.3390/molecules27061999 |
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author | Gribanov, Pavel S. Philippova, Anna N. Topchiy, Maxim A. Minaeva, Lidiya I. Asachenko, Andrey F. Osipov, Sergey N. |
author_facet | Gribanov, Pavel S. Philippova, Anna N. Topchiy, Maxim A. Minaeva, Lidiya I. Asachenko, Andrey F. Osipov, Sergey N. |
author_sort | Gribanov, Pavel S. |
collection | PubMed |
description | An efficient access to the novel 5-(het)arylamino-1,2,3-triazole derivatives has been developed. The method is based on Buchwald–Hartwig cross-coupling reaction of 5-Amino or 5-Halo-1,2,3-triazoles with (het)aryl halides and amines, respectively. As result, it was found that palladium complex [(THP-Dipp)Pd(cinn)Cl] bearing expanded-ring N-heterocyclic carbene ligand is the most active catalyst for the process to afford the target molecules in high yields. |
format | Online Article Text |
id | pubmed-8949195 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-89491952022-03-26 General Method of Synthesis of 5-(Het)arylamino-1,2,3-triazoles via Buchwald–Hartwig Reaction of 5-Amino- or 5-Halo-1,2,3-triazoles Gribanov, Pavel S. Philippova, Anna N. Topchiy, Maxim A. Minaeva, Lidiya I. Asachenko, Andrey F. Osipov, Sergey N. Molecules Article An efficient access to the novel 5-(het)arylamino-1,2,3-triazole derivatives has been developed. The method is based on Buchwald–Hartwig cross-coupling reaction of 5-Amino or 5-Halo-1,2,3-triazoles with (het)aryl halides and amines, respectively. As result, it was found that palladium complex [(THP-Dipp)Pd(cinn)Cl] bearing expanded-ring N-heterocyclic carbene ligand is the most active catalyst for the process to afford the target molecules in high yields. MDPI 2022-03-20 /pmc/articles/PMC8949195/ /pubmed/35335361 http://dx.doi.org/10.3390/molecules27061999 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Gribanov, Pavel S. Philippova, Anna N. Topchiy, Maxim A. Minaeva, Lidiya I. Asachenko, Andrey F. Osipov, Sergey N. General Method of Synthesis of 5-(Het)arylamino-1,2,3-triazoles via Buchwald–Hartwig Reaction of 5-Amino- or 5-Halo-1,2,3-triazoles |
title | General Method of Synthesis of 5-(Het)arylamino-1,2,3-triazoles via Buchwald–Hartwig Reaction of 5-Amino- or 5-Halo-1,2,3-triazoles |
title_full | General Method of Synthesis of 5-(Het)arylamino-1,2,3-triazoles via Buchwald–Hartwig Reaction of 5-Amino- or 5-Halo-1,2,3-triazoles |
title_fullStr | General Method of Synthesis of 5-(Het)arylamino-1,2,3-triazoles via Buchwald–Hartwig Reaction of 5-Amino- or 5-Halo-1,2,3-triazoles |
title_full_unstemmed | General Method of Synthesis of 5-(Het)arylamino-1,2,3-triazoles via Buchwald–Hartwig Reaction of 5-Amino- or 5-Halo-1,2,3-triazoles |
title_short | General Method of Synthesis of 5-(Het)arylamino-1,2,3-triazoles via Buchwald–Hartwig Reaction of 5-Amino- or 5-Halo-1,2,3-triazoles |
title_sort | general method of synthesis of 5-(het)arylamino-1,2,3-triazoles via buchwald–hartwig reaction of 5-amino- or 5-halo-1,2,3-triazoles |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8949195/ https://www.ncbi.nlm.nih.gov/pubmed/35335361 http://dx.doi.org/10.3390/molecules27061999 |
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