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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440470Generated: October 30, 2026

Ethyl bromopyruvate → 2,8-Diethyl imidazo[1,2-a]pyridine-2,8-dicarboxylate

https://huagongshe.com/reaction/1440470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromopyruvateHCID 66144—
ReactantEthyl 2-aminopyridine-3-carboxylateHCID 12433260—
SolventMethyl Ethyl KetoneHCID 6569—
Product2,8-Diethyl imidazo[1,2-a]pyridine-2,8-dicarboxylateHCID 1898385226.7%

Reaction Steps

A mixture of ethyl bromopyruvate (2.3 g, 10.2 m mol and ethyl 2-aminonicotinate (1.7 g, 10 m mol) in methyl ethyl ketone (17 ml) was refluxed for 5 hours. After completion of the reaction, the mixture was cooled to room temperature and distilled under reduced pressure to remove the solvent. The residue to which saturated sodium hydrogen carbonate aqueous solution (50 ml) was added was extracted with chloroform (100 ml×3). The extract was washed with water, dried over MgSO4 and concentrated under reduced pressure. The concentrate was purified by silica gel column chromatography (eluent: ethyl acetate) to give the object compound (0.7 g, yield 26.7%) as crystals. m.p. 97° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05498774
Source datasetuspto-grants-1996_03
ORD IDord-117e9f0b65764745badc6d7273b6fe6c
Source noteuspto-grants-1996_03