103594-68-9

Upstream product

• 38353-06-9 5-bromo-1H-pyrimidin-2-one 
• 100-39-0 benzyl bromide 

Downstream Products

• 1609637-83-3 C₂₉H₃₄N₂O₂Si 
• 1609637-84-4 C₂₉H₃₄N₂O₂Si 
• 1609637-85-5 (±)-1-benzyl-4-(3-hydroxyphenyl)-5-phenyl-3,4-dihydropyrimidine-2(1H)-one 
• 122476-84-0 1-benzyl-5-phenylpyrimidin-2(1H)-one 
• 103594-80-5 1-benzyl-5-bromo-4-phenylpyrimidin-2(1H)-one 
• 103594-72-5 1-benzyl-5-bromo-3,4-dihydro-4-phenylpyrimidin-2(1H)-one 
• 107377-18-4 1-benzyl-5-bromo-3,4-dihydropyrimidin-2(1H)-one 
• 155056-17-0 1-benzyl-5-(5-tert-butyldimethylsilyloxymethyl-2-furyl)pyrimidin-2(1H)-one 

Relevant academic research and scientific papers

Structure Investigations on Products from the Reaction of Organocopper, Organolithium and Organomagnesium Reagents with 2(1H)-Pyrimidinones

Alkyl- and arylcuprates and alkyl- and aryllithium and -magnesium reagents form 3,4- or/and 3,6-adducts with 1-benzyl-2(1H)pyrimidinones.The effect of 5-halo substituents on the reactivity and regioselectivity is reported.Structure analyses were made by NMR spectroscopy.Dehydrogenation gives the conjugated, substituted pyrimidinines.X-Ray crystallographic data for 1-benzyl-5-chloro-4-phenyl-2(1H)-pyrimidinone and its regioisomer 1-benzyl-5-chloro-6-phenyl-2(1H)-pyrimidinone are discussed.