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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2253361Generated: November 3, 2026

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

https://huagongshe.com/reaction/2253361

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

To a solution of 7-bromo-2-ethylpyrazolo[1,5-a]pyridine (1.1 g) dissolved in acetonitrile (20 mL) was added nitronium tetrafluoroborate (1.3 g) was added thereto while cooling with ice, and the reaction mixture was stirred for 30 minutes. The reaction mixture was then added to ice water, extraction was performed with ethyl acetate, and the organic extract was washed with water and brine. The obtained organic extract was dried over anhydrous magnesium sulfate and filtered, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography and the title compound (670 mg) was obtained as yellow crystals from the n-hexane:ethyl acetate (10:1) fraction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07323569B2
Source datasetuspto-grants-2008_01
ORD IDord-c7e536c6103d48c7a34fbad2ab0e6c53
Source noteuspto-grants-2008_01