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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038471Generated: November 3, 2026

Methyl iodide → 7-Bromo-8-hydroxymethyl-1,3,3-trimethyl-3,4-dihydro-1H-quinoxalin-2-one

https://huagongshe.com/reaction/1038471

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantEthyl AcetateHCID 8857—
ReactantCarbonate IonHCID 19660—
Reactant7-Bromo-8-hydroxymethyl-3,3-dimethyl-3,4-dihydro-1H-quinoxalin-2-oneHCID 57672000—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product7-Bromo-8-hydroxymethyl-1,3,3-trimethyl-3,4-dihydro-1H-quinoxalin-2-oneHCID 5767195169.1%

Reaction Steps

A mixture of 7-bromo-8-hydroxymethyl-3,3-dimethyl-3,4-dihydro-1H-quinoxalin-2-one (Reference Compound No. 5, 62.7 mg, 0.220 mmol), methyl iodide (68.6% L, 1.10 mmol), and cessium carbonate (180 mg, 0.552 mmol) was suspended in anhydrous N,N-dimethylformamide (1 mL) and stirred at room temperature for 2.5 hours. Ethyl acetate (10 mL) and water (10 mL) were added to the reaction mixture and partitioned. The organic layer was washed with saturated brine (10 mL), dried over anhydrous magnesium sulfate, and then the solvent was removed under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give the titled reference compound (45.5 mg) as an orange amorphous product. (Yield 69%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08551991B2
Source datasetuspto-grants-2013_10
ORD IDord-afcf6b6f6c5047529d47ee2be3928cf4
Source noteuspto-grants-2013_10