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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864995Generated: October 31, 2026

1,2-Dibromo-1,1,2,2-tetrachloroethane → 7-Bromo-2-methoxypyrazolo[1,5-a]pyridine

https://huagongshe.com/reaction/1864995

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-Dibromo-1,1,2,2-tetrachloroethaneHCID 69426—
Reactant2-Methoxypyrazolo[1,5-a]pyridineHCID 12284427—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product7-Bromo-2-methoxypyrazolo[1,5-a]pyridineHCID 2198465864.8%

Reaction Steps

A solution of 2-methoxypyrazolo[1,5-a]pyridine (7.15 g) [CAS No. 59942-88-0] in tetrahydrofuran (140 mL) was cooled to −78° C. under a nitrogen stream, and then a solution of n-butyllithium in hexane (1.6 M; 46 mL) was added dropwise and the mixture was stirred for 30 minutes. A solution of 1,2-dibromo-1,1,2,2-tetrachloroethane (18.9 g) in tetrahydrofuran (30 mL) was added dropwise at −78° C., and stirring was continued for 1 hour. After increasing the temperature of the reaction mixture to room temperature and adding water, extraction was performed with ethyl acetate and the extract washed with brine. After drying the obtained organic layer over anhydrous magnesium sulfate and filtering it, the solvent was concentrated under reduced pressure, the residue was purified by silica gel column chromatography, and the title compound (7.1 g) was obtained from the n-hexane:ethyl acetate (50:1) fraction as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625925B2
Source datasetuspto-grants-2009_12
ORD IDord-7dbea4d48bdb499c8814e3c641078ac5
Source noteuspto-grants-2009_12