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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...

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Detalles Bibliográficos
Autores principales: Mahajan, Sheena, Slathia, Nancy, Nuthakki, Vijay K., Bharate, Sandip B., Kapoor, Kamal K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
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.
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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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