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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 980178Generated: October 30, 2026

5-Chloro-2(1H)-pyrimidinone → HCID 12795544, compound

https://huagongshe.com/reaction/980178

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-2(1H)-pyrimidinoneHCID 108578—
Reactant2-Bromo-4'-(methylsulfonyl)acetophenoneHCID 735823—
SolventEthanolHCID 702—
SolventTriethylamineHCID 8471—
ProductHCID 12795544HCID 1279554423.9%

Reaction Steps

A suspension of 5-chloropyrimidin-2-one (411 mg) and 2-bromo-4'-methylsulphonyl acetophenone (835 mg) in triethylamine (1 ml) and ethanol (20 ml) was stirred at ambient temperature for one hour. The resulting suspension was concentrated at reduced pressure then diluted with water (100 ml). The collected precipitate was crystallised from acetone, then from ethanol to give the title pyrimidinone (235 mg); m.p. 257°-258°; λmaxEtOH 242 nm (ε 23650), 286 nm (ε 1950), 334 nm (ε 1680), λinf 293 nm (ε 1850).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04636509
Source datasetuspto-grants-1987_01
ORD IDord-7a6d1f99eee74fb7a664901b55d1f4f9
Source noteuspto-grants-1987_01