One-Pot Quinazolin-4-yl-thiourea Synthesis via N-(2-Cyano-phenyl)benzimidoyl isothiocyanate
| Autoři | |
|---|---|
| Rok publikování | 2001 |
| Druh | Článek v odborném periodiku |
| Časopis / Zdroj | Molecules |
| Fakulta / Pracoviště MU | |
| Citace | |
| Obor | Organická chemie |
| Klíčová slova | 1-(2-phenylquinazolin-4-yl)-3-substituted thioureas; quinazolines; thioureas; benzimidoyl isothiocyanates |
| Popis | 1-substituted-3-(2-phenylquinazolin-4-yl) thioureas were produced by an intramolecular cycloaddition reaction of 1-substitued-3-[(2-cyanophenylimino)phenyl-methyl]thioureas. These compounds in turn were prepared by a domino reaction of N-(2-cyanophenyl)benzimidoyl isothiocyanate with primary amines. The structures of products were confirmed by FTIR, 1 H-NMR, 13 C-NMR, mass spectroscopy and X-ray crystallography. |
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