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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2391839Generated: October 28, 2026

5-Bromo-8-(2-fluoro-3,5-dimethoxy-phenyl)-quinoxaline → 8-(2-Fluoro-3,5-dimethoxy-phenyl)-quinoxaline-5-carbonitrile

https://huagongshe.com/reaction/2391839

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-8-(2-fluoro-3,5-dimethoxy-phenyl)-quinoxalineHCID 59292961—
ReactantHCID 178418546HCID 178418546—
SolventDichloromethaneHCID 6344—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product8-(2-Fluoro-3,5-dimethoxy-phenyl)-quinoxaline-5-carbonitrileHCID 5929291762%

Reaction Conditions

Temperature160 °C

Reaction Steps

A mixture of 5-bromo-8-(2-fluoro-3,5-dimethoxy-phenyl)-quinoxaline (Step 94.3) (3.09 g, 8.5 mmol) and CuCN (918 mg, 10.2 mmol, 1.2 equiv) in NMP (30 mL) was stirred for 6.5 h at 160° C., under an argon atmosphere. The reaction mixture was allowed to cool to rt, diluted with DCM/(10% aqueous solution of ethylenediamine) (200 mL, v/v 1:1), filtered through celite and the filtrate extracted with DCM. The organic phase was washed with H2O and brine, dried (Na2SO4), filtered and concentrated. The residue was triturated in DCM to provide 1.63 g of the title compound as a white solid: ESI-MS: 310.1 [M+H]+; tR=4.41 min (System 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273882B2
Source datasetuspto-grants-2012_09
ORD IDord-f84b40bc38434407aa6d69b8013dbd23
Source noteuspto-grants-2012_09