1482-35-5

Upstream product

• 826-85-7 1-phenylpyrazol-5-amine 
• 119-36-8 methyl salicylate 
• 84939-74-2 5-chloroacetylamino-4-carbethoxy-1-phenylpyrazole 
• 16078-71-0 ethyl 5-amino-1-phenyl-1H-pyrazole-4-carboxylate 
• 84939-52-6 N-metil-N-(1-fenil-4-carbetossi-pirazol-5-yl)cloroacetammide 

Downstream Products

• 83451-32-5 N-Methyl(1-phenylpyrazol-5-yl)-2-carbomethoxybenzamide 
• 83451-34-7 N-Methyl-(1-phenylpyrazol-5-yl)-2-carboxybenzamide 
• 83451-36-9 10-Methyl-1-phenyl-1,10-dihydro-1,2,10-triaza-benzo[f]azulene-4,9-dione 
• 122127-66-6 1,4,5,5a,6,7,10,11,11a,13-decahydro-5a,6,10,13-tetramethyl-4-methylene-1,9-diphenyl-5,12:10,12-dimethano-12H-pyrazolo<3,4-b>pyrazolo<4',3':6,7>azepino<2,3-f>azocine 

Relevant academic research and scientific papers

Synthesis of pyrazolo[3,4-e][1,4]diazepine-4,7-diones with central nervous system activity

The synthesis of 1-phenyl-5,8-dimethyl-1,4,5,6,7,8-hexahydro-pyrazolo[3,4-e][1,4] diazepin-4,7-dione and of 1-phenyl-3,5,8-trimethyl-1,4,5,6,7,8-hexahydro-pyrazolo[3,4-e] [1,4]diazepin-4,7-dione is described. These compounds exhibit activity on CNS in animals.

Studies on the Synthesis of Heterocyclic Compounds. Part VI. The Action of Methyl Salicylate on Some 5-Aminopyrazoles

Some 1-phenyl-3-R-5-aminopyrazoles reacted with methyl salicylate to give N-(1-phenyl-3-R-pyrazol-5-yl)-2-methoxybenzamides (3a,b,c), 1-phenyl-2-methyl-3-R-salicyloilimino-3-pyrazolines (4a,b,c) together with 1-phenyl-3-R-5-methylamino pyrazoles (5a,b,c).The structures of the new compounds 3 and 4 were determined on the basis of analytical and spectroscopic data as well as on the acid hydrolysis products.