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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158846Generated: November 1, 2026

1,2-Dimethoxyethane → ethyl imidazo[1,2-a]pyrazine-2-carboxylate

https://huagongshe.com/reaction/1158846

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantEthyl bromopyruvateHCID 66144—
ReactantAminopyrazineHCID 78747—
SolventEthanolHCID 702—
Productethyl imidazo[1,2-a]pyrazine-2-carboxylateHCID 11845418—

Reaction Conditions

Temperature0 °C

Reaction Steps

Ethyl bromopyruvate (62.9 g) was added to the DME (258 mL) solution of 2-aminopyrazine (24.8 g) at room temperature and stirred for 2.5 h. The reaction mixture was cooled to 0° C. and stirred for 30 min to afford a pale brown precipitate. The precipitate was filtered and washed with Et2O to give pale brown crystals. The suspension of the precipitate (66.1 g) in EtOH (1.29 L) was heated at reflux temperature to turn to clear solution. After refluxing for 2 h, the reaction mixture was concentrated under reduced pressure, then mixed with CHCl3 and saturated NaHCO3aq. The mixture was filtered through a pad of Celite and the separated organic layer was dried (MgSO4) and filtered. The filtrate was concentrated under reduced pressure. The residue was applied to silica gel column chromatography, then the column was eluted with CHCl3-MeOH (99/1˜97/3), and collected fractions were concentrated under reduced pressure followed by recrystallization from CHCl3-Et2O. The titled compound was obtained as pale pink crystals. Yield: 10.9 g, 22%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812014B2
Source datasetuspto-grants-2010_10
ORD IDord-207cdd867f024854a5874aa969de9d32
Source noteuspto-grants-2010_10