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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 4-chloroacetoacetate | HCID 69484 | — |
| Reactant | 2-Amino-3,5-dimethylpyrazine | HCID 2774764 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 2-(6,8-dimethylimidazo[1,2-a]pyrazin-2-yl)acetate | HCID 89657132 | 87.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09371336B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-e52cce5288d7459ab66ec5f1a1a4f47a |
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| Source note | uspto-grants-2016_06 |
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