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Malononitrile-activated synthesis and anti-cholinesterase activity of styrylquinoxalin-2(1H)-ones
Herein, we report a base-free malononitrile activated condensation of 3-methylquinoxaline-2(1H)-one (3MQ) 1 with aryl aldehydes 3a–3ad for synthesis of styrylquinoxalin-2(1H)-ones (SQs) 4a–4ad with excellent yields. In this reaction, malononitrile activates the aldehyde via Knoevenagel condensation...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9052867/ https://www.ncbi.nlm.nih.gov/pubmed/35493659 http://dx.doi.org/10.1039/d0ra02816a |
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author | Mahajan, Sheena Slathia, Nancy Nuthakki, Vijay K. Bharate, Sandip B. Kapoor, Kamal K. |
author_facet | Mahajan, Sheena Slathia, Nancy Nuthakki, Vijay K. Bharate, Sandip B. Kapoor, Kamal K. |
author_sort | Mahajan, Sheena |
collection | PubMed |
description | Herein, we report a base-free malononitrile activated condensation of 3-methylquinoxaline-2(1H)-one (3MQ) 1 with aryl aldehydes 3a–3ad for synthesis of styrylquinoxalin-2(1H)-ones (SQs) 4a–4ad with excellent yields. In this reaction, malononitrile activates the aldehyde via Knoevenagel condensation towards reaction with 3MQ 1 and gets liberated during the course of reaction to yield the desired SQs 4a–4ad. The SQs were evaluated for in vitro cholinesterase inhibition and 4n was found to display a mixed type of inhibition of AChE, which was supported by molecular modelling studies. This study has led to the discovery of a new chemotype for cholinesterase inhibition which might be useful in finding a remedy for Alzheimer's disease. |
format | Online Article Text |
id | pubmed-9052867 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90528672022-04-29 Malononitrile-activated synthesis and anti-cholinesterase activity of styrylquinoxalin-2(1H)-ones Mahajan, Sheena Slathia, Nancy Nuthakki, Vijay K. Bharate, Sandip B. Kapoor, Kamal K. RSC Adv Chemistry Herein, we report a base-free malononitrile activated condensation of 3-methylquinoxaline-2(1H)-one (3MQ) 1 with aryl aldehydes 3a–3ad for synthesis of styrylquinoxalin-2(1H)-ones (SQs) 4a–4ad with excellent yields. In this reaction, malononitrile activates the aldehyde via Knoevenagel condensation towards reaction with 3MQ 1 and gets liberated during the course of reaction to yield the desired SQs 4a–4ad. The SQs were evaluated for in vitro cholinesterase inhibition and 4n was found to display a mixed type of inhibition of AChE, which was supported by molecular modelling studies. This study has led to the discovery of a new chemotype for cholinesterase inhibition which might be useful in finding a remedy for Alzheimer's disease. The Royal Society of Chemistry 2020-04-21 /pmc/articles/PMC9052867/ /pubmed/35493659 http://dx.doi.org/10.1039/d0ra02816a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Mahajan, Sheena Slathia, Nancy Nuthakki, Vijay K. Bharate, Sandip B. Kapoor, Kamal K. Malononitrile-activated synthesis and anti-cholinesterase activity of styrylquinoxalin-2(1H)-ones |
title | Malononitrile-activated synthesis and anti-cholinesterase activity of styrylquinoxalin-2(1H)-ones |
title_full | Malononitrile-activated synthesis and anti-cholinesterase activity of styrylquinoxalin-2(1H)-ones |
title_fullStr | Malononitrile-activated synthesis and anti-cholinesterase activity of styrylquinoxalin-2(1H)-ones |
title_full_unstemmed | Malononitrile-activated synthesis and anti-cholinesterase activity of styrylquinoxalin-2(1H)-ones |
title_short | Malononitrile-activated synthesis and anti-cholinesterase activity of styrylquinoxalin-2(1H)-ones |
title_sort | malononitrile-activated synthesis and anti-cholinesterase activity of styrylquinoxalin-2(1h)-ones |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9052867/ https://www.ncbi.nlm.nih.gov/pubmed/35493659 http://dx.doi.org/10.1039/d0ra02816a |
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