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SYNTHESIS OF NEW 1-SUBSTITUTED 4-(2-PHENYLQUINAZOLIN-4-YL)- AND 4-(2-PHENYLQUINAZOLIN-4-YLIDENE) THIOSEMICARBAZIDES
Authors | |
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Year of publication | 2008 |
Type | Article in Periodical |
Magazine / Source | Chemistry of Heterocyclic Compounds |
MU Faculty or unit | |
Citation | |
Field | Organic chemistry |
Keywords | quinazoline; thiosemicarbazide; domino reaction; hydrogen bond interaction |
Description | Two new 1-substituted 4-(2-phenylquinazolin-4-yl)- and 4-(2-phenylquinazolin-4-ylidene) thio-semicarbazides were formed by a multistep domino reaction of imidoyl isothiocyanate derivative with 1,1-di-R-hydrazine in acetone solution. Application of hydrazine hydrate under the same reaction conditions afforded 4-(2-phenylquinazolin-4(3H)-ylidene)-2-(propen-2-yl)-1-(propan-2-ylidene) thio-semicarbazide via a six-step triple-component domino reaction. |
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