Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181867Generated: October 25, 2026

Water → 7-Bromo-2-ethyl-4-methoxy-3-nitropyrazolo[1,5-a]pyridine

https://huagongshe.com/reaction/1181867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantNitronium tetrafluoroborateHCID 11073463—
Reactant7-Bromo-2-ethyl-4-methoxypyrazolo[1,5-a]pyridineHCID 21984567—
SolventAcetonitrileHCID 6342—
Product7-Bromo-2-ethyl-4-methoxy-3-nitropyrazolo[1,5-a]pyridineHCID 2198453447.9%

Reaction Steps

After adding nitronium tetrafluoroborate (176 mg) to a solution of 7-bromo-2-ethyl-4-methoxypyrazolo[1,5-a]pyridine (282 mg) in acetonitrile (20 mL) at 0° C., the mixture was stirred for 20 minutes. Upon completion of the reaction, water was added, extraction was performed with ethyl acetate, the extract was washed with saturated aqueous sodium hydrogencarbonate and brine and dried over magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was subjected to silica gel column chromatography (20 g), and the title compound (159 mg) was obtained from the n-hexane:ethyl acetate (3:1) fraction as yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07285666B2
Source datasetuspto-grants-2007_10
ORD IDord-220f2eafe03a453b95ad88976bb0a231
Source noteuspto-grants-2007_10