6-Methyl-3-phenyl-l,2,4-triazine-4-oxide

The condensation of amidrazone with isonitrosoacetophenone occurs via formation of the hydrazone 136. The elimination of the ammonia molecule from intermediate 136 yields 3-methyl-6-phenyl-l,2,4-triazine 4-oxide 137 (71LA12). 

Acid hydrolysis of 3-methyl-6-phenyl-l,2,4-triazine 4-oxide (827) yields 4-phenyl-1,2,3-triazole through an acyclic intermediate (828) (Scheme 168) <89AHC(46)73>. 1,2,4-Triazine 2-oxides (829) undergo rearrangement in basic conditions (Equation (80)) to form 4-substituted 2//-1,2,3-triazoles <89AHC(46)73>. l-(2-Nitrophenyl)-5-aryltetrazoles (830) and l-aryl-5-(2-nitrophenyl)tetrazoles are converted into 2-arylbenzotriazoles (831) by refluxing in nitrobenzene (Equation (81)) <81AJC69l>. 

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See also in sourсe #XX -- [ , ]

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