75263-95-5

Usage

InChI:InChI=1/C18H14N4O/c23-18-16-11-20-22(15-9-5-2-6-10-15)17(16)19-13-21(18)12-14-7-3-1-4-8-14/h1-11,13H,12H2

Upstream product

• 21314-17-0 1-phenyl-1,5-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one 
• 100-39-0 benzyl bromide 
• 16078-71-0 ethyl 5-amino-1-phenyl-1H-pyrazole-4-carboxylate 
• 122-51-0 orthoformic acid triethyl ester 
• 100-46-9 benzylamine 
• 102129-13-5 N,N-Dimethyl-N'-(4-carboethoxy-1-phenylpyrazol-5-yl)formamidine hydrochloride 

Relevant academic research and scientific papers

Synthesis of some new pyrazolo[3,4-d]pyrimidine derivatives of expected anticancer and radioprotective activity

On the account of the reported anticancer activity of pyrazolo[3,4-d]pyrimidines, a new series of pyrazolo[3,4-d]pyrimidine derivatives were synthesized and tested for in-vitro anticancer activity against Ehrlich Ascites Carcinoma (EAC) cell line. Moreove

The one-pot conversion of pyrimidinone derivatives into substituted pyrimidines using diphenylphosphinic chloride under a mild condition

Pyrimidinone derivatives reacted with diphenylphosphinic chloride followed by addition of nucleophiles to afford substituted pyrimidine derivatives at a mild temperature (20-66°C).