Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1906158Generated: October 31, 2026

5-Chloro-2(1H)-pyrimidinone → HCID 12791252, compound

https://huagongshe.com/reaction/1906158

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-2(1H)-pyrimidinoneHCID 108578—
Reactant2-bromo-1-(1H-indol-3-yl)ethanoneHCID 11310936—
SolventEthanolHCID 702—
SolventTriethylamineHCID 8471—
ProductHCID 12791252HCID 1279125257.4%

Reaction Steps

A mixture of 5-chloropyrimidin-2-one (522 mg) and 3-bromoacetylindole (1.19 g) in triethylamine (0.84 ml) and ethanol (25 ml) was stirred at room temperature. After 1.5 h the mixture was heated to 55° C. After a further 1.5 h the mixture was cooled and the resulting precipitate collected and washed with cold ethanol. Recrystallisation twice from ethyl acetate and once from ethanol gave the title pyrimidinone (660 mg), m.p. 228°-229° C., λmax (EtOH) 240 nm (ε 16,370) 300.5 nm (ε 13,090).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04650800
Source datasetuspto-grants-1987_03
ORD IDord-ab83a1a35df74ae5b92aa9bbb23a3478
Source noteuspto-grants-1987_03