HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 343802Generated: October 31, 2026
Potassium Carbonate → HCID 53812208, compound
https://huagongshe.com/reaction/343802
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl bromoacetate | HCID 60984 | — |
| Reactant | HCID 53906871 | HCID 53906871 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 53812208 | HCID 53812208 | 48.2% |
Reaction Steps
A mixture of N-(7-chloro-2,3-dimethoxy-6-methylquinoxalin-5-yl)methanesulphonamide (694 mg, 2.09 mmol), potassium carbonate (347 mg, 2.51 mmol) and acetone (21 ml) was heated at reflux for 10 minutes and was then allowed to cool to room temperature. Methyl bromoacetate (396 μl, 640 mg, 4.19 mmol) was added and the mixture was heated at reflux for 18 hours. The mixture was allowed to cool to room temperature and was concentrated under reduced pressure. The residue was dissolved in dichloromethane and washed twice with water and then brine and then dried (MgSO4) and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel eluting with dichloromethane to give N-(7-chloro-2,3-dimethoxy-6-methylquinoxalin-5-yl)-N-(methoxycarbonylmethyl)methanesulphonamide as a white solid (407 mg, 48%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05863917 |
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| Source dataset | uspto-grants-1999_01 |
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| ORD ID | ord-8ee385b7e848465ea69f248b08709d3b |
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| Source note | uspto-grants-1999_01 |
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