One-Pot Quinazolin-4-ylidenethiourea Synthesis via N-(2-Cyanophenyl)benzimidoyl isothiocyanate
Authors | |
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Year of publication | 2001 |
Type | Article in Periodical |
Magazine / Source | Molecules |
MU Faculty or unit | |
Citation | |
Field | Organic chemistry |
Keywords | N-(2-cyanophenyl)benzimidoyl isothicyanate; quinazolines; thioureas |
Description | 1,1-Disubstituted-3-(2-phenyl-3H-quinazolin-4-ylidene)thioureas were synthesized in a one pot reaction of N-(2-cyanophenyl)benzimidoyl isothicyanate with secondary amines. The products underwent trans-amination reactions. Products were identified by FTIR, 1 H-NMR, 13 C NMR, mass spectroscopy and X-ray crystallography. |
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