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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2169007Generated: November 1, 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/2169007

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 numberUS09045436B2
Source datasetuspto-grants-2015_06
ORD IDord-f6ff2660fdf549e697e388c99df968e2
Source noteuspto-grants-2015_06