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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957110Generated: October 31, 2026

Imidazole → 6,7Dichloro-2,3-dimethoxy-5-(1-imidazol-1-ylethyl)quinoxaline

https://huagongshe.com/reaction/1957110

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantPotassium CarbonateHCID 11430—
Reactant5-(1-Chloroethyl)-6,7-dichloro-2,3-dimethoxyquinoxalineHCID 19068870—
SolventDimethylformamideHCID 6228—
Product6,7Dichloro-2,3-dimethoxy-5-(1-imidazol-1-ylethyl)quinoxalineHCID 1906890558%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 5-(1-chloroethyl)-6,7dichloro-2,3-dimethoxyquinoxaline (95 mg, 0.295 mmol), imidazole (22 mg, 0.325 mmol), anhydrous potassium carbonate (45 mg, 0.325 mmol) in dry dimethylformamide (10 mL) was heated under nitrogen at 100° C. for 6 hours, cooled, and partitioned between brine and three portions of ethyl acetate. The combined organic solutions were dried (MgSO4) and concentrated under reduced pressure. The residue was purified by flash column chromatography (gradient elution with dichloromethane:mehanol) to give 6,7dichloro-2,3-dimethoxy-5-(1-imidazol-1-ylethyl)quinoxaline (60 mg, 58%); as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05783572
Source datasetuspto-grants-1998_07
ORD IDord-3192c6fc49e14bf090c3436935f87c28
Source noteuspto-grants-1998_07