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A Simple and Easily Implemented Method for the Regioselective Introduction of Deuterium into Azolo[1,5-a]pyrimidines Molecules
A method for the technically easy-to-implement synthesis of deuterium-labeled pyrazolo[1,5-a]pyrimidines and 1,2,4-triazolo[1,5-a]pyrimidines have been developed. The regioselectivity of such transformations has been shown. (1)H NMR and mass spectrometric methods have proved the quantitative nature...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10054722/ https://www.ncbi.nlm.nih.gov/pubmed/36985841 http://dx.doi.org/10.3390/molecules28062869 |
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author | Danagulyan, Gevorg G. Panosyan, Henrik A. Gharibyan, Vache K. Hasratyan, Ani H. |
author_facet | Danagulyan, Gevorg G. Panosyan, Henrik A. Gharibyan, Vache K. Hasratyan, Ani H. |
author_sort | Danagulyan, Gevorg G. |
collection | PubMed |
description | A method for the technically easy-to-implement synthesis of deuterium-labeled pyrazolo[1,5-a]pyrimidines and 1,2,4-triazolo[1,5-a]pyrimidines have been developed. The regioselectivity of such transformations has been shown. (1)H NMR and mass spectrometric methods have proved the quantitative nature of such transformations and the kinetics of deuterium exchange has been studied. Spectrally, at different temperatures (+30 °C, −10 °C and −15 °C), the kinetics of the process was studied both in CD(3)OD and in deuterated alkali. |
format | Online Article Text |
id | pubmed-10054722 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-100547222023-03-30 A Simple and Easily Implemented Method for the Regioselective Introduction of Deuterium into Azolo[1,5-a]pyrimidines Molecules Danagulyan, Gevorg G. Panosyan, Henrik A. Gharibyan, Vache K. Hasratyan, Ani H. Molecules Article A method for the technically easy-to-implement synthesis of deuterium-labeled pyrazolo[1,5-a]pyrimidines and 1,2,4-triazolo[1,5-a]pyrimidines have been developed. The regioselectivity of such transformations has been shown. (1)H NMR and mass spectrometric methods have proved the quantitative nature of such transformations and the kinetics of deuterium exchange has been studied. Spectrally, at different temperatures (+30 °C, −10 °C and −15 °C), the kinetics of the process was studied both in CD(3)OD and in deuterated alkali. MDPI 2023-03-22 /pmc/articles/PMC10054722/ /pubmed/36985841 http://dx.doi.org/10.3390/molecules28062869 Text en © 2023 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 Danagulyan, Gevorg G. Panosyan, Henrik A. Gharibyan, Vache K. Hasratyan, Ani H. A Simple and Easily Implemented Method for the Regioselective Introduction of Deuterium into Azolo[1,5-a]pyrimidines Molecules |
title | A Simple and Easily Implemented Method for the Regioselective Introduction of Deuterium into Azolo[1,5-a]pyrimidines Molecules |
title_full | A Simple and Easily Implemented Method for the Regioselective Introduction of Deuterium into Azolo[1,5-a]pyrimidines Molecules |
title_fullStr | A Simple and Easily Implemented Method for the Regioselective Introduction of Deuterium into Azolo[1,5-a]pyrimidines Molecules |
title_full_unstemmed | A Simple and Easily Implemented Method for the Regioselective Introduction of Deuterium into Azolo[1,5-a]pyrimidines Molecules |
title_short | A Simple and Easily Implemented Method for the Regioselective Introduction of Deuterium into Azolo[1,5-a]pyrimidines Molecules |
title_sort | simple and easily implemented method for the regioselective introduction of deuterium into azolo[1,5-a]pyrimidines molecules |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10054722/ https://www.ncbi.nlm.nih.gov/pubmed/36985841 http://dx.doi.org/10.3390/molecules28062869 |
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