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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864984Generated: October 26, 2026

Water → 7-(2,4-Dichlorophenyl)-2-ethylpyrazolo[1,5-a]pyridine

https://huagongshe.com/reaction/1864984

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
Reactant2,4-Dichlorophenylboric acidHCID 21984477—
Reactant7-Bromo-2-ethylpyrazolo[1,5-a]pyridineHCID 21984510—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product7-(2,4-Dichlorophenyl)-2-ethylpyrazolo[1,5-a]pyridineHCID 2198463597.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

After dissolving 7-bromo-2-ethylpyrazolo[1,5-a]pyridine (300 mg) in ethanol (2 mL) and toluene (4 mL), 2,4-dichlorophenylboric acid (508 mg), tetrakis(triphenylphosphine)palladium(0) complex (154 mg) and 2M aqueous sodium carbonate (1.33 mL) were added and the mixture was heated and stirred at 80° C. for 3 hours under a nitrogen stream. Water was added to the reaction mixture, extraction was performed with ethyl acetate and the organic layer washed with 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 (380 mg) was obtained from the n-hexane:ethyl acetate (100:1) fraction as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625925B2
Source datasetuspto-grants-2009_12
ORD IDord-9ebccb9cd1444728a1c2ac38f400d908
Source noteuspto-grants-2009_12