Herein, we report a base-free malononitrile activated condensation of 3-methylquinoxaline-2(1)-one (3MQ) 1 with aryl aldehydes 3a-3ad for synthesis of styrylquinoxalin-2(1)-ones (SQs) 4a-4ad with excellent yields. In this reaction, malononitrile activates the aldehyde 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 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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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9052867 | PMC |
http://dx.doi.org/10.1039/d0ra02816a | DOI Listing |
Herein, we report a base-free malononitrile activated condensation of 3-methylquinoxaline-2(1)-one (3MQ) 1 with aryl aldehydes 3a-3ad for synthesis of styrylquinoxalin-2(1)-ones (SQs) 4a-4ad with excellent yields. In this reaction, malononitrile activates the aldehyde 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 cholinesterase inhibition and 4n was found to display a mixed type of inhibition of AChE, which was supported by molecular modelling studies.
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