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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206332Generated: October 25, 2026

Ethyl 4-chloroacetoacetate → Ethyl 2-(6,8-dimethylimidazo[1,2-a]pyrazin-2-yl)acetate

https://huagongshe.com/reaction/2206332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-chloroacetoacetateHCID 69484—
Reactant2-Amino-3,5-dimethylpyrazineHCID 2774764—
SolventEthanolHCID 702—
ProductEthyl 2-(6,8-dimethylimidazo[1,2-a]pyrazin-2-yl)acetateHCID 8965713287.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

A 75 mL pressure vessel was charged with ethyl 4-chloro-3-oxo-butyrate (4 g, 24.4 mmol), 3,5-dimethylpyrazin-2-amine (3 g, 24.4 mmol) and 200 proof ethanol (24 mL). After stirring at 100° C. in an oil bath for 16 hours, the reaction mixture was concentrated, diluted with dichloromethane and a saturated sodium bicarbonate solution. The organic layer was separated and the aqueous layer was extracted with dichloromethane twice. The combined organic layers were dried over anhydrous sodium sulfate, filtered, concentrated, and purified on silica gel. Elution with a gradient mixture of dichloromethane and methanol yielded ethyl 2-(6,8-dimethylimidazo[1,2-a]pyrazin-2-yl)acetate as a light brown solid (5 g). MS m/z 234 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371336B2
Source datasetuspto-grants-2016_06
ORD IDord-e52cce5288d7459ab66ec5f1a1a4f47a
Source noteuspto-grants-2016_06