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Synthesis of Some New Functionalized Bis-thiazolidin-5-one and Bis-thiazolidin-4-one Derivatives

DOI: 10.5923/j.chemistry.20120205.06

Keywords: Thiocarbamoyl,chloroacetyl chloride,bis-thiazolidin-5(and 4-)-ones,Japp-Klingmann reaction

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Abstract:

A series of bis-thiazolidin-5-one and bis-thiazolidin-4-one derivatives 3and5 was prepared by the treatment of highly functional thiocarbamoyl intermediates 2 and 4 with chloroacetyl chloride and chloroacetic acid, respectively. Treatment of the bis-thiocarbamoyl derivative 4a with diazotized sulphanilic acid affected acetyl cleavage to afford the corresponding arylhydrazono-thiocarbamoyl derivative 6.The title compounds bis-thiazolidin-5-one and bis-thiazolidin-4-one derivatives showed high reactivity towards azo coupling reaction with diazotized sulphanilic acid and Knoevenagel reaction with 4-isopropylbenzaldehyde.

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