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Molecules  2001 

One-Pot Quinazolin-4-ylidenethiourea Synthesis via N-(2-Cyanophenyl)benzimidoyl isothiocyanate

DOI: 10.3390/60700574

Keywords: N-(2-cyanophenyl)benzimidoyl isothicyanate, 1, 1-disubstituted-3-(2-phenyl- 3H-quinazolin-4-ylidene)thioureas, intramolecular cycloaddition, 1, 1-disubstituted-3-[(2- cyanophenylimino)phenylmethyl]thioureas, quinazolines

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Abstract:

1,1-Disubstituted-3-(2-phenyl-3H-quinazolin-4-ylidene)thioureas (8) were synthesized in a one pot reaction of N-(2-cyanophenyl)benzimidoyl isothicyanate (3) with secondary amines. The products underwent transamination reactions. Compounds 8a-8g were identified by FTIR, 1H-NMR, 13C-NMR, mass spectroscopy and X-ray crystallography.

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