Reaction of thiocarboxanilide derivatives of 2-phenylimino-3-phenyl-4-thiazolidinone and 1,3-diphenyl-2-thioxo-4-imidazolone with hydrazonoyl halides and active chloromethylene compounds
Hamdi M. Hassaneen, Omar A. Miqdad, Nada M. Abunada, Ahmad A. Fares
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DOI: 10.4236/ns.2011.33026   PDF    HTML     7,157 Downloads   14,134 Views   Citations

Abstract

The potassium salts of thiocarboxanilide of 2- phenylimino-3-phenyl-4-thiazolidinone and 1,3- diphenyl-2-thioxo-4-imidazolone react with hydrazonoyl halides in N,N-dimethylformamide to afford the corresponding 1,3,4-thiadiazoline derivatives. 2-Phenylimino-3-phenyl-4-thiazolidinone reacts with active chloromethylene compounds in N,N-dimethylformamide to give the corresponding thiazolylidenethiazolidin-4-one derivatives. The new compounds were characterized using IR, 1H NMR, 13C NMR and mass spectra.

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Hassaneen, H. , Miqdad, O. , Abunada, N. and Fares, A. (2011) Reaction of thiocarboxanilide derivatives of 2-phenylimino-3-phenyl-4-thiazolidinone and 1,3-diphenyl-2-thioxo-4-imidazolone with hydrazonoyl halides and active chloromethylene compounds. Natural Science, 3, 199-207. doi: 10.4236/ns.2011.33026.

Conflicts of Interest

The authors declare no conflicts of interest.

References

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