HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 240337Generated: October 29, 2026
Water → Ethyl 4-methyl-3-oxoquinoxaline-2-carboxylate
https://huagongshe.com/reaction/240337
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 3-hydroxyquinoxaline-2-carboxylate | HCID 248643 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 4-methyl-3-oxoquinoxaline-2-carboxylate | HCID 252209 | 71% |
Reaction Steps
4.0 g (18.3 mmol) of ethyl 2-oxo-1,2-dihydroquinoxaline-3-carboxylate was dissolved in N,N-dimethylformamide (100 mL), and under a nitrogen stream, 0.81 g (20.3 mmol) of 60% sodium hydride (oily) was added thereto, while maintaining the liquid temperature in the range of 5° C. to 10° C. After stirring the mixture for one hour at room temperature, 3.9 g (27.5 mmol) of iodomethane was added dropwise to the reaction solution. The mixture was stirred for a day at room temperature, and then the reaction mixture was poured into water, and extracted with ethyl acetate. The organic layer was washed with water and a saturated aqueous solution of sodium chloride, and dried over anhydrous sodium sulfate. The inorganic matter was separated by filtration, and then the solvent was distilled off under reduced pressure. The residue thus obtained was purified by silica gel chromatography (developing solvent: ethyl acetate:hexane=3:2), to obtain 3.0 g (yield: 71%) of ethyl 1-methyl-2-oxo-1,2-dihydroquinoxaline-3-carboxylate as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08648075B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-8248e52247a3496e908757fe88a9ae37 |
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| Source note | uspto-grants-2014_02 |
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