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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086172Generated: November 1, 2026

Ethyl 4-chloroacetoacetate → HCID 14207605, compound

https://huagongshe.com/reaction/1086172

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-chloroacetoacetateHCID 69484—
Reactant5-Bromo-N~3~-methylpyrazine-2,3-diamineHCID 12198520—
SolventDimethylformamideHCID 6228—
ProductHCID 14207605HCID 1420760530%

Reaction Steps

2.03 g (10 mmol) of 2-amino-5-bromo-3-methylaminopyrazine are dissolved in 5 ml of dimethylformamide (DMF). A solution of 1.645 g(10 mmol) of ethyl (chloroacetyl)acetate in 5 ml of DMF is added dropwise with stirring. The mixture is maintained with stirring and under gentle reflux for 3 hours. The DMF is then evaporated off under reduced pressure and the residue, dissolved in 50 ml of anhydrous ethanol, is brought to reflux for one hour. After removal of the solvent, the residue is taken up with water, alkalinized and extracted with dichloromethane. After dehydration over anhydrous calcium chloride, the solvent is evaporated off under reduced pressure. The crude product is purified by chromatography on a silica column (eluant=dichloromethane to which 5% of methanol has been added). 0.4 g (Yld=30%) of ethyl 6-bromo-8-methylaminoimidazo[1,2-a]pyrazine-2-acetate (m.p. 104° C.) is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05028605
Source datasetuspto-grants-1991_07
ORD IDord-79cce7a7c39949959beb7fa26d3256e6
Source noteuspto-grants-1991_07