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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864983Generated: November 1, 2026

Water → 7-Bromo-2-ethylpyrazolo[1,5-a]pyridine

https://huagongshe.com/reaction/1864983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,2-Dibromo-1,1,2,2-tetrachloroethaneHCID 69426—
Reactant2-Ethylpyrazolo[1,5-a]pyridineHCID 16116261—
ReactantHCID 178418244HCID 178418244—
SolventTetrahydrofuranHCID 8028—
Product7-Bromo-2-ethylpyrazolo[1,5-a]pyridineHCID 2198451073.1%

Reaction Steps

After dissolving 2-ethylpyrazolo[1,5-a]pyridine (80 mg) in tetrahydrofuran (1 mL), an n-butyllithiumhexane solution (1.6 M; 0.58 mL) was added dropwise at −78° C. under a nitrogen stream, and the mixture was stirred for 30 minutes. A solution of 1,2-dibromo-1,1,2,2-tetrachloroethane (196 mg) in tetrahydrofuran (0.5 mL) was added to the reaction mixture, and stirring was continued for 30 minutes. The temperature was increased to room temperature, water was added, extraction was performed with ethyl acetate and the organic layer 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 (90 mg) was obtained from the n-hexane:ethyl acetate (20:1) fraction as a light brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625925B2
Source datasetuspto-grants-2009_12
ORD IDord-4b7d28bf5f6a47adb6f9eb0cc93f6659
Source noteuspto-grants-2009_12