Journal
SYNLETT
Volume 25, Issue 9, Pages 1257-1262Publisher
GEORG THIEME VERLAG KG
DOI: 10.1055/s-0033-1341108
Keywords
5-arylidene-2-imino-4-thiazolidinone; thiourea; microwave irradiation; multicomponent reaction; Knoevenagel condensation
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A concise approach for the preparation of 5-arylidene-2-imino-4-thiazolidinone derivatives is described. Structurally diverse amines, isothiocyanates, aldehydes, and chloroacetyl chloride were combined under microwave irradiation to afford new 5-arylidene-2-imino-4-thiazolidinone derivatives. The one-pot synthesis involves the in situ formation of a thiourea followed by reaction with chloroacetyl chloride and an aldehyde to generate the target compounds.
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