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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2253362Generated: October 26, 2026

Ethanol → 7-Bromo-2-ethylpyrazolo[1,5-a]pyridine-3-amine

https://huagongshe.com/reaction/2253362

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantWaterHCID 962—
Reactant7-Bromo-2-ethyl-3-nitropyrazolo[1,5-a]pyridineHCID 21984481—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
Product7-Bromo-2-ethylpyrazolo[1,5-a]pyridine-3-amineHCID 2108411173.3%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a suspension of 7-bromo-2-ethyl-3-nitropyrazolo[1,5-a]pyridine (1.78 g) in a mixed solution of ethanol (100 mL), water (50 mL) and acetic acid (10 mL) was added zinc powder (1.78 g) at room temperature and the reaction mixture was stirred for 1 hour at 65° C. The reaction mixture was filtered through celite to remove insoluble residue and the filtrate was evaporated under reduced pressure. Water was added to the obtained residue and extraction was performed with ethyl acetate, and after washing the organic extract with water, saturated aqueous sodium bicarbonate and brine, the 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 (60 g) and the title compound (1.16 g) was obtained as a dark green oil from the ethyl acetate:n-hexane (4:1) fraction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07323569B2
Source datasetuspto-grants-2008_01
ORD IDord-dc12276073cd482ebf2d83c5a53e4395
Source noteuspto-grants-2008_01