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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189802Generated: October 27, 2026

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

https://huagongshe.com/reaction/1189802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSelectfluorHCID 2724933—
Reactant5-Bromo-8-(3,5-dimethoxy-phenyl)-quinoxalineHCID 59292825—
SolventAcetonitrileHCID 6342—
Product5-Bromo-8-(2-fluoro-3,5-dimethoxy-phenyl)-quinoxalineHCID 59292961—

Reaction Steps

SelectFluor (20.5 g, 58 mmol, 2 equiv) was added portionwise to a solution of 5-bromo-8-(3,5-dimethoxy-phenyl)-quinoxaline (Step 1.4) (10 g, 29 mmol) in CH3CN (300 mL) at rt. The reaction mixture was stirred at rt for 0.5 h, quenched by addition of H2O and concentrated to remove CH3CN. The resulting mixture was diluted with EtOAc/H2O and filtered to provide a white solid (batch 1). The filtrate was extracted with EtOAc. The organic phase was washed with H2O and brine, dried (Na2SO4), filtered and concentrated to afford batch 2. The two batches were combined and purified by silica gel MPLC (Hex/EtOAc, 7:3) to afford a sample of 5-bromo-8-(2-fluoro-3,5-dimethoxy-phenyl)-quinoxaline (Step 94.3) and a sample of the title compound which was further purified by trituration in EtOAc to provide 2.28 g of a white solid. Title compound: ESI-MS: 381.0/382.9 [M+H]+; tR=4.92 min (System 1); TLC: Rf=0.26 (Hex/EtOAc, 7:3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674099B2
Source datasetuspto-grants-2014_03
ORD IDord-b5c3f4db100246ad936ae1c5b2c5814b
Source noteuspto-grants-2014_03