165401-50-3

Upstream product

• 139057-03-7 3-pentane-2,4-dione 
• 532-55-8 Benzoyl isothiocyanate 
• 165401-46-7 1-amino-1-morpholino-1-butene-3-one 

Downstream Products

• 339584-48-4 5-acetyl-4-methylsulfanyl-6-morpholino-2-phenylpyrimidine 
• 1415972-99-4 3-methyl-4-morpholino-6-phenyl-1H-pyrazolo[3,4-d]pyrimidine 
• 1415973-08-8 1,3-dimethyl-4-morpholino-6-phenyl-1H-pyrazolo[3,4-d]pyrimidine 
• 165401-59-2 5-acetyl-6-benzylamino-2-phenyl-3H-pyrimidine-4-thione 
• 165401-56-9 5-acetyl-6-morpholino-2-phenylpyrimidine-4(3H)-thione 

Relevant academic research and scientific papers

Synthesis of 4-aminopyrazolo[3,4-d]pyrimidine derivatives from 5-acetyl-6-amino-4-methylsulfanyl- or 5-acetyl-6-amino-4- methylsulfonylpyrimidines

Diacetyl ketene N,S-acetal was used for the synthesis of 5-acetyl-6-amino-4-methylsulfanylpyrimidines substituted at the exocyclic nitrogen atom, which were further oxidized with m-chloroperbenzoic acid to the corresponding methylsulfonylpyrimidines. Reac

Synthesis of functionalized pyrimidine-4-thiones and derivatives of pyridopirimidine-5-one from monoacylketene aminals

Monoacylketene aminals containing an unsubstituted NH2 group react as C-nucleophiles with benzoyl isothiocyanate to give the corresponding thioamides which ubdergo cyclization by sodium methoxide in methanol to afford 6-R-amino-5-acetyl-2-phenyl-3H-pyrimi