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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086208Generated: October 26, 2026

Imidazole → 5-(1H-imidazol-1-ylmethyl)quinoxaline

https://huagongshe.com/reaction/1086208

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactant5-(Bromomethyl)quinoxalineHCID 10149129—
SolventAcetonitrileHCID 6342—
Product5-(1H-imidazol-1-ylmethyl)quinoxalineHCID 1987586020.5%

Reaction Steps

A mixture of 15.5 parts of 5-(bromomethyl)quinoxaline, 23.5 parts of 1H-imidazole and 160 parts of acetonitrile was stirred for 1.5 hours at reflux temperature. The reaction mixture was evaporated and the residue was taken up in water. The product was extracted three times with 65 parts of dichloromethane. The combined extracts were dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of dichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from a mixture of 2-propanone and 2,2'-oxybispropane. The product was filtered off and dried, yielding 3 parts (20.5%) of 5-(1H-imidazol-1-yl-methyl)quinoxaline; mp. 121.2° C. (comp. 41).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05028606
Source datasetuspto-grants-1991_07
ORD IDord-406ef8768fcd4994b8601f349bb6c14b
Source noteuspto-grants-1991_07