HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086172Generated: November 1, 2026
Ethyl 4-chloroacetoacetate → HCID 14207605, compound
https://huagongshe.com/reaction/1086172
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 4-chloroacetoacetate | HCID 69484 | — |
| Reactant | 5-Bromo-N~3~-methylpyrazine-2,3-diamine | HCID 12198520 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 14207605 | HCID 14207605 | 30% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05028605 |
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| Source dataset | uspto-grants-1991_07 |
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| ORD ID | ord-79cce7a7c39949959beb7fa26d3256e6 |
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| Source note | uspto-grants-1991_07 |
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