120617-41-6

Upstream product

• 116471-24-0 6-methyl-3-(1-methylhydrazino)-5-oxo-4-thriphenylphosphoranylideneamino-4,5-dihydro<1,2,4>triazine 
• 100-52-7 benzaldehyde 

Downstream Products

• 120617-48-3 7-Allylamino-3,8-dimethyl-8H-[1,2,4]triazolo[5,1-c][1,2,4]triazin-4-one 
• 100-47-0 benzonitrile 
• 120617-43-8 7-Ethylamino-3,8-dimethyl-8H-[1,2,4]triazolo[5,1-c][1,2,4]triazin-4-one 
• 120617-45-0 7-Isopropylamino-3,8-dimethyl-8H-[1,2,4]triazolo[5,1-c][1,2,4]triazin-4-one 
• 120617-47-2 7-Benzylamino-3,8-dimethyl-8H-[1,2,4]triazolo[5,1-c][1,2,4]triazin-4-one 
• 120617-42-7 7-methylamino-3,8-dimethyl-4-oxo<1,2,4>triazolo<5,1-c><1,2,4>triazine 
• 120617-46-1 7-Cyclohexylamino-3,8-dimethyl-8H-[1,2,4]triazolo[5,1-c][1,2,4]triazin-4-one 
• 120617-44-9 3,8-Dimethyl-7-propylamino-8H-[1,2,4]triazolo[5,1-c][1,2,4]triazin-4-one 

Relevant academic research and scientific papers

Iminophosphorane-mediated Synthesis of Fused Triazines: Preparation of Triazolotriazine and Triazinotetrazine Derivatives

A number of triazolotriazine and triazinotetrazine derivatives have been prepared. 3-(2-Benzylidene-1-methylhydrazino)-6-methyl-5-oxo-4-triphenylphosphoranylideneamino-4,5-dihydro-1,2,4-triazine (3), available from the iminophosphorane (2) and benzaldehyde, reacts with aliphatic isocyanates at room temperature to give the corresponding 8H-triazolotriazinones (6)-(12).On the other hand, iminophosphorane (2) reacts with acyl chlorides at room temperature to give 3-(2-acyl-1-methylhydrazino)-6-methyl-5-oxo-4-triphenylphosphoranylideneamino-4,5-dihydro-1,2,4-triazines (13)-(15), which react with isocyanates at room temperature to give 2H-triazinotetrazines (17)-(24).