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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181861Generated: November 4, 2026

Ethyl Acetate → 7-Bromo-2-ethyl-3-nitropyrazolo[1,5-a]pyridine

https://huagongshe.com/reaction/1181861

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantNitronium tetrafluoroborateHCID 11073463—
Reactant7-Bromo-2-ethylpyrazolo[1,5-a]pyridineHCID 21984510—
SolventAcetonitrileHCID 6342—
Product7-Bromo-2-ethyl-3-nitropyrazolo[1,5-a]pyridineHCID 2198448150.8%

Reaction Steps

After dissolving 7-bromo-2-ethylpyrazolo[1,5-a]pyridine (1.1 g) in acetonitrile (20 mL), nitronium tetrafluoroborate (1.3 g) was added while stirring on ice, and stirring was continued for 30 minutes. The reaction mixture was added to ice water, extraction was performed with ethyl acetate and the extract was washed with water and brine. After drying over anhydrous magnesium sulfate and filtration, the solvent was concentrated under reduced pressure, the residue was purified by silica gel column chromatography, and the title compound (670 mg) was obtained from the n-hexane:ethyl acetate (10:1) fraction as yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07285666B2
Source datasetuspto-grants-2007_10
ORD IDord-cacdbe8ed7f64283a8fe1d7f61b18cf7
Source noteuspto-grants-2007_10