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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1458561Generated: October 31, 2026

Chloroacetonitrile → HCID 22097030, compound

https://huagongshe.com/reaction/1458561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetonitrileHCID 7856—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 54321377HCID 54321377—
SolventAcetoneHCID 180—
ProductHCID 22097030HCID 2209703054%

Reaction Steps

Chloroacetonitrile (233 μl, 279 mg, 3,69 mmol) was added to a refluxing mixture of N-(6,7-dichloro-2,3-dimethoxyquinoxalin-5-yl)methane-sulphonamide (from Preparation 3, 1.00 g, 2.84 mmol) and potassium carbonate (0.47 g, 3.41 mmol) in acetone (50 ml) under nitrogen. The mixture was refluxed for 18 h and was then allowed to cool, and was partitioned between ethyl acetate (500 ml) and water (500 ml). The organic phase was dried (MgSO4) and concentrated under reduced pressure. The residue was purified by flash chromatography (eluting with 0-100% ethyl acetate in hexane and then 5% methanol in dichloromethane) to give N-(6,7-dichloro-2,3-dimethoxyquinoxalin-5-yl)-N-(cyanomethyl) methanesulphonamide as an off-white solid (600 mg, 54%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05852016
Source datasetuspto-grants-1998_12
ORD IDord-14f6b7edb2cc4a298d26aa83bd8b6c29
Source noteuspto-grants-1998_12