%0 Journal Article
%T One-Pot Quinazolin-4-ylidenethiourea Synthesis via N-(2-Cyanophenyl)benzimidoyl isothiocyanate
%A Walid M. Fathalla
%A Michal £¿ajan
%A Jarom¨ªr Marek
%A Pavel Pazdera
%J Molecules
%D 2001
%I MDPI AG
%R 10.3390/60700574
%X 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.
%K N-(2-cyanophenyl)benzimidoyl isothicyanate
%K 1
%K 1-disubstituted-3-(2-phenyl- 3H-quinazolin-4-ylidene)thioureas
%K intramolecular cycloaddition
%K 1
%K 1-disubstituted-3-[(2- cyanophenylimino)phenylmethyl]thioureas
%K quinazolines
%U http://www.mdpi.com/1420-3049/6/7/574