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Ultrasound-assisted-one-pot synthesis and antiplasmodium evaluation of 3-substituted-isoindolin-1-ones
As the attempts to control malaria through chemotherapy strategies are restricted, we have prepared a small library of 3-substituted-isoindolinones from ( Z )-3-benzylideneisobenzofuran-1(3 H )-ones in one-pot fashion under ultrasound irradiation. The one-pot reaction was scalable and efficiently pr...
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Published in: | RSC advances 2023-09, Vol.13 (37), p.25959-25967 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | As the attempts to control malaria through chemotherapy strategies are restricted, we have prepared a small library of 3-substituted-isoindolinones from (
Z
)-3-benzylideneisobenzofuran-1(3
H
)-ones in one-pot fashion under ultrasound irradiation. The one-pot reaction was scalable and efficiently produced the desired products (
1a-m
) in high yields in a short reaction time. Evaluation of their
in vitro
antiplasmodium assay against the 3D7 (chloroquine-sensitive) and FCR3 (chloroquine-resistant) strains of
Plasmodium falciparum
demonstrated that they displayed moderate to strong antiplasmodium activities (the IC
50
values ranging from 4.21-34.80 μM) and low resistance indices. The
in silico
prediction of ADME and physicochemical properties showed that the synthesized compounds met the drug-likeliness requirements and featured low toxicity effects. Based on the evaluation of the antiplasmodium profiles, 3-substituted-isoindolinone derivatives of
1a
,
1d
,
1h
, and
1l
may become potential antiplasmodium candidates.
A library of 3-substituted-isoindolin-1-ones has been synthesized from 3-alkylidenephtalides and primary amines through one-pot reaction under ultrasonic irradiation. Four isoindolin-1-ones have great potential to be antiplasmodium candidates. |
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ISSN: | 2046-2069 2046-2069 |
DOI: | 10.1039/d3ra02829a |