88045-77-6

Upstream product

• 54326-16-8 5-chloropyrimidin-2-one 
• 3587-60-8 Benzyloxymethyl chloride 
• 52132-66-8 Benzyl-methylthiomethylether 
• 42748-90-3 5-chloro-2(1H)-PYRIMIDONE hydrochloride 
• 20194-18-7 sodium phenyl-methanolate 

Downstream Products

• 103594-76-9 1-benzyloxymethyl-5-chloro-4-(4-chlorophenyl)-3,4-dihydropyrimidin-2(1H)-one 
• 103594-77-0 1-benzyloxymethyl-5-chloro-3,4-dihydro-4-(4-methoxyphenyl)pyrimidin-2(1H)-one 
• 103594-75-8 1-benzyloxymethyl-5-chloro-3,4-dihydro-4-phenylpyrimidin-2(1H)-one 
• 101946-70-7 1-benzyloxymethyl-5-chloro-3,4-dihydro-4-phenylethynylpyrimidin-2(1H)-one 
• 101946-75-2 1-benzyloxymethyl-5-chloro-3,6-dihydro-6-ethynylpyrimidin-2(1H)-one 
• 101946-71-8 1-benzyloxymethyl-3,6-dihydro-6-phenylethynyl-2(1H)-pyrimidinone 
• 103594-85-0 1-benzyloxymethyl-5-chloro-4-(4-methoxyphenyl)pyrimidin-2(1H)-one 
• 103594-84-9 1-benzyloxymethyl-5-chloro-4-(4-chlorophenyl)pyrimidin-2(1H)-one 
• 103594-83-8 1-benzyloxymethyl-5-chloro-4-phenylpyrimidin-2(1H)-one 
• 101946-76-3 1-benzyloxymethyl-5-chloro-4-phenylethynylpyrimidin-2(1H)-one 

Relevant academic research and scientific papers

Sulfonic and Phosphonic Acids Formed by Bisulfite and Phosphite Adduct Formation with Pyrimidinones

By analogy with carbonyl compounds, ?-electron deficient 2-pyrimidinones form adducts with sodium bisulfite and phosphite esters.Both the 3,4- and 3,6-bisulfite adducts were found.The 3,4-isomer was often predominant and was obtained isomerically pure by selective precipitation from an aqueous solution.The adduct formation is reversible in aqueous solution.The adduct was also readily cleaved by trifluoroacetic acid.With tris(trimethylsilyl) phosphite, regiospecific formation of the 3,4-adduct was observed.The corresponding 3,4-dihydro-4-phosphonic acid was prepared by methanol cleavage of the silyl ester function.

2-Stannyloxypyrimidines in Regioselective Alkylation Reactions

2(1H)-Pyrimidinones are readily O-stannylated by reaction with bis(tributyltin)oxide.The stannylated products are converted into 1-alkyl-2(1H)-pyrimidinones on treatment with alkylating agents.With palladium(0) catalysis, allyl acetate becomes a specific

Substituted pyrimidin-2-ones and the salts thereof

Compounds of the general formula: STR1 wherein X represents halogen or trifluoromethyl; R1 and R2, independently represent hydrogen or lower alkyl; R3, R4 and R5, which may be the same or different, each represent hydrogen, lower alkyl, lower alkenyl, lower alkynyl, lower alkanoyl, lower alkenoyl, C7-16 aralkyl or C6-10 aryl or a 5-9 membered unsaturated or aromatic heterocyclic ring; one or both of R4 and R5 may also represent aroyl groups; Z represents an oxygen atom or a sulfur atom or oxide thereof or a group NR6 (wherein R6 is as defined for R hereinafter or represents the group COR7 in which R7 represents hydrogen or optionally substituted aryl, heterocyclic, aralkyl, lower alkyl or lower alkoxy group; and R represents a C6-10 carbocyclic aromatic group or a heterocyclic group containing a 5-9 membered unsaturated or aromatic heterocyclic ring which ring contains one or more heteroatoms selected from O, N and S and optionally carries a fused ring which carbocyclic or heterocyclic group may carry one or more C1-4 alkyl or phenyl groups said groups being optionally substituted; and where acid or basic groups are present, the salts thereof are useful in combating abnormal cell proliferation. The compounds of the invention are prepared by inter alia alkylation, ring closure and oxidation.