Malononitrile-activated synthesis and anti-cholinesterase activity of styrylquinoxalin-2(1)-ones
Herein, we report a base-free malononitrile activated condensation of 3-methylquinoxaline-2(1 H )-one (3MQ) 1 with aryl aldehydes 3a-3ad for synthesis of styrylquinoxalin-2(1 H )-ones (SQs) 4a-4ad with excellent yields. In this reaction, malononitrile activates the aldehyde via Knoevenagel condensat...
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Veröffentlicht in: | RSC advances 2020-04, Vol.1 (27), p.15966-15975 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Herein, we report a base-free malononitrile activated condensation of 3-methylquinoxaline-2(1
H
)-one (3MQ)
1
with aryl aldehydes
3a-3ad
for synthesis of styrylquinoxalin-2(1
H
)-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.
SQs displaying anti-Alzheimer activity is serendipitous. Malononitrile as a handle to facilitate nucleophilic attack has been applied for the first time for the easy access of SQs. |
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ISSN: | 2046-2069 2046-2069 |
DOI: | 10.1039/d0ra02816a |