165401-48-9

Upstream product

• 122603-83-2 2-acetyl-1-amino-1-benzoylaminoethene 
• 532-55-8 Benzoyl isothiocyanate 

Downstream Products

• 165401-52-5 5-acetyl-6-benzoylamino-2-phenyl-3H-pyrimidine-4-thione 
• 172951-26-7 5-acetyl-6-amino-4-methylsulfanyl-2-phenylpyrimidine 
• 1415973-12-4 4-amino-1,3-dimethyl-6-phenyl-1H-pyrazolo[3,4-d]pyrimidine 
• 1415973-03-3 4-amino-3-methyl-6-phenyl-1H-pyrazolo[3,4-d]pyrimidine 
• 1415973-16-8 5-acetyl-6-amino-4-methylsulfonyl-2-phenylpyrimidine 
• 1415973-35-1 C₁₃H₁₅N₅S 
• 1415973-37-3 C₂₆H₂₆N₈S₂ 
• 611-74-5 N,N-dimethylbenzamide 
• 165401-60-5 5-acetyl-6-benzoylamino-4-methylthio-2-phenylpyrimidine 

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