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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509527Generated: October 31, 2026

2-Amino-1-[3-ethoxy-2,3-dioxo-1-(2-phenylethyl)propyl]pyridinium bromide → Ethyl 3-(2-phenylethyl)imidazo[1,2-a]pyridine-2-carboxylate

https://huagongshe.com/reaction/1509527

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-1-[3-ethoxy-2,3-dioxo-1-(2-phenylethyl)propyl]pyridinium bromideHCID 86642209—
SolventEthanolHCID 702—
ProductEthyl 3-(2-phenylethyl)imidazo[1,2-a]pyridine-2-carboxylateHCID 5835569493.3%

Reaction Steps

To a solution of ethyl 3-bromo-2-oxo-5-phenylpentanoate (1.9 g) in THF (10 ml) was added 2-aminopyridine (600 mg) at room temperature, and the reaction mixture was heated under reflux for 15 hr. The precipitated crystals were collected by filtration, washed with THF to give 2-amino-1-[3-ethoxy-2,3-dioxo-1-(2-phenylethyl)propyl]pyridinium bromide (1.36 g). 2-Amino-1-[3-ethoxy-2,3-dioxo-1-(2-phenylethyl)propyl]pyridinium bromide (1.36 g) was dissolved in ethanol (10 ml), and the mixture was refluxed under heating for 3 hr. The reaction mixture was concentrated, and dissolved in dichloromethane. The solution was washed successively with aqueous sodium bicarbonate and saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was recrystallized from ethyl acetate-diethyl ether to give the object product (950 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221836B2
Source datasetuspto-grants-2015_12
ORD IDord-ed8040e3efa241e39fb28cc8d47f8b13
Source noteuspto-grants-2015_12