Abstract:A preparative method for the synthesis of 2 alkyl 1,2,4 benzotriazin 3(2H ) ones 3 was developed. The method involves treatment with sodium cyanate of 2 alkylbenzotetrazinium tetrafluoroborates, which exist in solutions in equilibrium with o (alkylazo)aryldiazonium tetrafluoroborates. Reduction of compounds 3 with zinc in acetic acid afforded 2 alkyl 1,4 dihydro 1,2,4 benzotriazin 3(2H ) ones.
Synthesis of 2-Alkyl-1,2,4-benzotriazin-3(2H)-ones and 2-Alkyl-1,4-dihydro-1,2,4-benzotriazin-3(2H)-ones-[via reaction of tetrazinium salts (I) with sodium cyanate]. -(LIPILIN*, D. L.; CHURAKOV, A. M.; STRELENKO, Y. A.; TARTAKOVSKY, V. A.; Russ.
Synthesis of 2-Alkyl-1,2,4-benzotriazin-3(2H)-ones and 2-Alkyl-1,4-dihydro-1,2,4-benzotriazin-3(2H)-ones-[via reaction of tetrazinium salts (I) with sodium cyanate]. -(LIPILIN*, D. L.; CHURAKOV, A. M.; STRELENKO, Y. A.; TARTAKOVSKY, V. A.; Russ.
Construction of non-aromatic 1,2,3,6-tetrahydro-1,2,3,4-tetrazines through [4 + 2] cycloaddition of α-halogeno hydrazones with azodicarboxylic acid derivatives.
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