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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 43045Generated: October 26, 2026

5-Bromo-8-(3,5-dimethoxy-phenyl)-quinoxaline → 8-(3,5-Dimethoxy-phenyl)-quinoxaline-5-carbonitrile

https://huagongshe.com/reaction/43045

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-8-(3,5-dimethoxy-phenyl)-quinoxalineHCID 59292825—
ReactantHCID 178418546HCID 178418546—
SolventEthyl AcetateHCID 8857—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product8-(3,5-Dimethoxy-phenyl)-quinoxaline-5-carbonitrileHCID 59292884—

Reaction Conditions

Temperature180 °C

Reaction Steps

A mixture of 5-bromo-8-(3,5-dimethoxy-phenyl)-quinoxaline (Step 1.4) (4.54 g, 13.2 mmol) and CuCN (1.54 g, 17.1 mmol, 1.3 equiv) in NMP (50 mL) was stirred for 2 h at 180° C., under an argon atmosphere. The reaction mixture was allowed to cool to rt, diluted with EtOAc (10% aqueous solution of ethylenediamine) (150 mL), and filtered to afford 1.19 g (batch 1) of the title compound as a yellow solid. The filtrate was extracted with DCM. The organic phase was washed with H2O and brine, dried (Na2SO4), filtered and concentrated. The residue was triturated in EtOAc to provide 2.31 g (batch 2) of the title compound: ESI-MS: 292.1 [M+H]+; tR=4.53 min (System 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536175B2
Source datasetuspto-grants-2013_09
ORD IDord-772ab5a6080a4b2ab56013fb6350e3ff
Source noteuspto-grants-2013_09