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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 980177Generated: October 26, 2026

5-Chloro-2(1H)-pyrimidinone → 5-Chloro-1-(4-methylthiophenacyl)pyrimidin-2-one

https://huagongshe.com/reaction/980177

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-2(1H)-pyrimidinoneHCID 108578—
Reactant2-Bromo-4'-methylthioacetophenoneHCID 18368152—
SolventEthanolHCID 702—
SolventTriethylamineHCID 8471—
Product5-Chloro-1-(4-methylthiophenacyl)pyrimidin-2-oneHCID 5379127163.3%

Reaction Steps

A suspension of 5-chloropyrimidin-2-one (312 mg) and 2-bromo-4'-methylthioacetophenone (525 mg) in triethylamine (1 ml) and ethanol (20 ml) was stirred at ambient temperature for 2.25 hours. The resulting suspension was concentrated at reduced pressure then diluted with water (50 ml). The collected precipitate was crystallised from acetone to give the title pyrimidinone (404 mg,); m.p. 192°-197°, λmaxEtOH 229 nm (ε 14450), 312 nm (ε 21470), λinf 239.5 nm (ε 9930).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04636509
Source datasetuspto-grants-1987_01
ORD IDord-bf3f0cab3246439a8dc2f70650dcfbf8
Source noteuspto-grants-1987_01