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