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SNH Amidation of 5-Nitroisoquinoline: Access to Nitro- and Nitroso Derivatives of Amides and Ureas on the Basis of Isoquinoline
For the first time, amides and ureas based on both 5-nitroisoquinoline and 5-nitrosoisoquinoline were obtained by direct nucleophilic substitution of hydrogen in the 5-nitroisoquinoline molecule. In the case of urea and monosubstituted ureas, only 5-nitrosoisoquinoline-6-amine is formed under anhydr...
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/PMC9694180/ https://www.ncbi.nlm.nih.gov/pubmed/36431962 http://dx.doi.org/10.3390/molecules27227862 |
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author | Avakyan, Elena K. Borovleva, Anastasia A. Pobedinskaya, Diana Yu. Demidov, Oleg P. Ermolenko, Artem P. Larin, Alexander N. Borovlev, Ivan V. |
author_facet | Avakyan, Elena K. Borovleva, Anastasia A. Pobedinskaya, Diana Yu. Demidov, Oleg P. Ermolenko, Artem P. Larin, Alexander N. Borovlev, Ivan V. |
author_sort | Avakyan, Elena K. |
collection | PubMed |
description | For the first time, amides and ureas based on both 5-nitroisoquinoline and 5-nitrosoisoquinoline were obtained by direct nucleophilic substitution of hydrogen in the 5-nitroisoquinoline molecule. In the case of urea and monosubstituted ureas, only 5-nitrosoisoquinoline-6-amine is formed under anhydrous conditions. |
format | Online Article Text |
id | pubmed-9694180 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96941802022-11-26 SNH Amidation of 5-Nitroisoquinoline: Access to Nitro- and Nitroso Derivatives of Amides and Ureas on the Basis of Isoquinoline Avakyan, Elena K. Borovleva, Anastasia A. Pobedinskaya, Diana Yu. Demidov, Oleg P. Ermolenko, Artem P. Larin, Alexander N. Borovlev, Ivan V. Molecules Article For the first time, amides and ureas based on both 5-nitroisoquinoline and 5-nitrosoisoquinoline were obtained by direct nucleophilic substitution of hydrogen in the 5-nitroisoquinoline molecule. In the case of urea and monosubstituted ureas, only 5-nitrosoisoquinoline-6-amine is formed under anhydrous conditions. MDPI 2022-11-14 /pmc/articles/PMC9694180/ /pubmed/36431962 http://dx.doi.org/10.3390/molecules27227862 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 Avakyan, Elena K. Borovleva, Anastasia A. Pobedinskaya, Diana Yu. Demidov, Oleg P. Ermolenko, Artem P. Larin, Alexander N. Borovlev, Ivan V. SNH Amidation of 5-Nitroisoquinoline: Access to Nitro- and Nitroso Derivatives of Amides and Ureas on the Basis of Isoquinoline |
title | SNH Amidation of 5-Nitroisoquinoline: Access to Nitro- and Nitroso Derivatives of Amides and Ureas on the Basis of Isoquinoline |
title_full | SNH Amidation of 5-Nitroisoquinoline: Access to Nitro- and Nitroso Derivatives of Amides and Ureas on the Basis of Isoquinoline |
title_fullStr | SNH Amidation of 5-Nitroisoquinoline: Access to Nitro- and Nitroso Derivatives of Amides and Ureas on the Basis of Isoquinoline |
title_full_unstemmed | SNH Amidation of 5-Nitroisoquinoline: Access to Nitro- and Nitroso Derivatives of Amides and Ureas on the Basis of Isoquinoline |
title_short | SNH Amidation of 5-Nitroisoquinoline: Access to Nitro- and Nitroso Derivatives of Amides and Ureas on the Basis of Isoquinoline |
title_sort | snh amidation of 5-nitroisoquinoline: access to nitro- and nitroso derivatives of amides and ureas on the basis of isoquinoline |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9694180/ https://www.ncbi.nlm.nih.gov/pubmed/36431962 http://dx.doi.org/10.3390/molecules27227862 |
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