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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 43124Generated: October 27, 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/43124

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 numberUS08536175B2
Source datasetuspto-grants-2013_09
ORD IDord-0e7e73df431241a3a348dc0932f0e7fd
Source noteuspto-grants-2013_09