HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570178Generated: October 30, 2026
Water → Ethyl 6-(trifluoromethyl)imidazo[1,2-a]pyrazine-2-carboxylate
https://huagongshe.com/reaction/570178
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl bromopyruvate | HCID 66144 | — |
| Reactant | 5-(Trifluoromethyl)pyrazin-2-amine | HCID 13341115 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | Ethyl 6-(trifluoromethyl)imidazo[1,2-a]pyrazine-2-carboxylate | HCID 67516905 | — |
Reaction Steps
To a solution of 2-amino-5-(trifluoromethyl)pyrazine (500 mg, 3.07 mmol) in 1,2-dimethoxyethane (10 mL) was added dropwise ethyl bromopyruvate (0.5 mL, 4.0 mmol). The reaction mixture was warmed to 60° C. for 72 hours. The reaction mixture was then cooled to room temperature, and water was added (10 mL) to precipitate a solid. The suspension was stirred for 10 minutes, filtered, and the isolated solid was washed with water to afford the desired ester which was used in the next step without further drying. 1H NMR (CDCl3) δ 9.22 (s, 1H), 8.59 (s, 1H), 8.39 (s, 1H), 4.50 (q, 2H), 1.47 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09023850B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-64538f5d37134e94bbfbf800a18ef048 |
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| Source note | uspto-grants-2015_05 |
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