750588-07-9

Upstream product

• 333-20-0 potassium thioacyanate 
• 94011-79-7 3-chloro-5,6-diphenylpyridazine-4-carbonitrile 

Downstream Products

• 750588-28-4 5-imino-5,6,7,8-tetrahydro-6-(4-methoxyphenyl)-3,4-diphenylpyrimido[4,5-c]pyridazine-7-thione 
• 750588-26-2 5-imino-5,6,7,8-tetrahydro-3,4,6-triphenylpyrimido[4,5-c]pyridazine-7-thione 
• 750588-10-4 5,6-dihydro-7-[2-(methylphenylmethylene)hydrazino]-5-imino-3,4,6-triphenylpyrimido[4,5-c]pyridazine 
• 750588-17-1 5,6-dihydro-7-ethoxymethylenehydrazono-5-imino-3,4,6-triphenyl-8H-pyrimido[4,5-c]pyridazine 
• 750588-38-6 7-benzylidenehydrazino-5,6-dihydro-5-imino-3,4,6-triphenylpyrimido[4,5-c]pyridazine 
• 750588-14-8 4,5-dihydro-5-imino-4,6,7-triphenyl-s-triazolo[3',4':2,3]pyrimido[4,5-c]pyridazine-1(2H)-thione 
• 750588-34-2 5,6-dihydro-7-hydrazino-5-imino-3,4,6-triphenylpyrimido[4,5-c]pyridazine 

Relevant academic research and scientific papers

Synthesis and Reactions of Novel Pyrimido[4,5-c]pyridazine and s-Triazolo[3',4':2,3]pyrimido[4,5-c]pyridazine Derivatives

The reaction of 3-chloro-5,6-diphenylpyridazine-4-carbonitrile with potassium thiocyanate gave the corresponding isothiocyanate derivative. This was reacted with aromatic amines in ethanol to afford pyrimido[4,5-c]pyridazine derivatives. The reaction of the latter compounds with hydrazine hydrate led to the formation of 6-hydrazino derivatives. One hydrazino compound was reacted with a variety of reagents to produce other new pyrimidopyridazines as well as a number of s-triazolo derivatives.