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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280086Generated: October 30, 2026

3-Bromo-1-phenylpropane-1,2-dione → [6-Ethyl-5-methyl-7-(methylthio)imidazo[1,2-a]pyrimidin-2-yl]phenylmethanone

https://huagongshe.com/reaction/280086

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-1-phenylpropane-1,2-dioneHCID 12568911—
Reactant5-Ethyl-4-methyl-6-(methylsulfanyl)pyrimidin-2-amineHCID 13301101—
SolventDiethyl EtherHCID 3283—
Product[6-Ethyl-5-methyl-7-(methylthio)imidazo[1,2-a]pyrimidin-2-yl]phenylmethanoneHCID 1004114254.4%

Reaction Steps

A stirred suspension of 4.5 g of 5-ethyl-4-methyl-6-methylthio-2-pyrimidinamine in 28 ml of ether was treated with 5.5 g of 3-bromo-1-phenylpropane-1,2-dione to obtain a yellow solution. After standing two days at room temperature, the crystallized pyrimidinium salt was filtered off, washed with ether and heated for one hour in refluxing ethanol. The solution was evaporated to dryness under reduced pressure and the residue was shaken with a mixture of chloroform and aqueous potassium carbonate. The organic layer was washed, dried over MgSO4 and evaporated to dryness under reduced pressure. Trituration of the residue with ethanol and filtration yielded 4.1 g (53% yield) of [6-ethyl-5-methyl-7-(methylthio)imidazo[1,2-a]pyrimidin-2-yl]phenylmethanone after recrystallization from methanol in the form of a buff solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04588720
Source datasetuspto-grants-1986_05
ORD IDord-cf2285667ba045208d7a43659acab45f
Source noteuspto-grants-1986_05