1044749-16-7

Upstream product

• 609-12-1 ethyl 2-bromoisovalerate 
• 75279-55-9 6-chloro-2-fluorophenylacetonitrile 
• 1242134-29-7 2-{[(allylsulfanyl)methyl]sulfanyl}-6-(6-chloro-2-fluorobenzyl)-5-isopropylpyrimidin-4(3H)-one 
• 1044749-11-2 ethyl 4-(2-Chloro-6-fluorophenyl)-3-oxo-2-iso-propylbutanoate 
• 17356-08-0 thiourea 

Downstream Products

• 1044748-90-4 C₂₂H₂₀ClFN₂O₂S 
• 1044748-91-5 C₂₂H₁₉ClF₂N₂O₂S 
• 1044748-92-6 C₂₃H₂₂ClFN₂O₃S 
• 1262963-59-6 2-(methylsulfanyl)-6-(2-fluoro-6-chlorobenzyl)-5-isopropylpyrimidin-4(3H)-one 
• 1242134-29-7 2-{[(allylsulfanyl)methyl]sulfanyl}-6-(6-chloro-2-fluorobenzyl)-5-isopropylpyrimidin-4(3H)-one 

Relevant academic research and scientific papers

The specific character of the reaction of derivatives of 2-thioxo-2,3-dihydropyrimidin-4(1H)-one with iodomethane and alkyl chloromethyl sulfides

The alkylation of 5-alkyl-6-(2,6-dihalobenzyl)-2-thioxo-2,3- dihydropyrimidin-4(1H)-ones with MeI, AllSCH2Cl, and MeSCH 2Cl in the K2CO3-DMF, NaOMe-MeOH, and KOH-EtOH systems was investigated. A hypothetical mec

Synthesis of new derivatives of 5-alkyl-6-(2,6-dihalobenzyl)-2- (methylsulfanyl)pyrimidin-4(3H)-one and the features of their oxidation

The synthesis and features of the regioselective S-monomethylation of new 5-alkyl-6-(arylmethyl)-2-thioxo-2,3-dihydropyrimidin-4(1H)-ones were investigated, and also the character of the oxidative degradation of these compounds when treated with the syste

5-alkyl-6-benzyl-2-(2-oxo-2-phenylethylsulfanyl)pyrimidin-4(3H)-ones, a series of anti-HIV-1 agents of the dihydro-alkoxy-benzyl-oxopyrimidine family with peculiar structure - Activity relationship profile

A series of dihydro-alkylthio-benzyl-oxopyrimidines (S-DABOs) bearing a 2-aryl-2-oxoethylsulfanyl chain at pyrimidine C2, an alkyl group at C5, and a 2,6-dichloro-, 2-chloro-6-fluoro-, and 2,6-difluoro-benzyl substitution at C6 (oxophenethyl-S-DABOs, 6-8)