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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 347826Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/347826

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt1,2-Dibromo-1,1,2,2-tetrachloroethaneHCID 69426—
Edukt2-Ethylpyrazolo[1,5-a]pyridineHCID 16116261—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt7-Bromo-2-ethylpyrazolo[1,5-a]pyridineHCID 2198451073,1%

Reaktionsschritte

To a solution of 2-ethylpyrazolo[1,5-a]pyridine (80 mg) dissolved in tetrahydrofuran (1 mL) was added n-butyllithium (1.6M hexane solution: 0.58 mL) dropwise at −78° C. under a nitrogen stream, and the reaction mixture was further stirred for 30 minutes at the same temperature. A solution of 1,2-dibromo-1,1,2,2-tetrachloroethane (196 mg) in tetrahydrofuran (0.5 mL) was added dropwise to the reaction mixture, and stirring was continued for 30 minutes. After raising the temperature to room temperature and adding water to the reaction mixture, extraction was performed with ethyl acetate and the organic extract was washed with water and brine. The obtained organic extract was dried over anhydrous magnesium sulfate and filtered, the solvent was evaporated under reduced pressure, the residue was purified by silica gel column chromatography and the title compound (90 mg) was obtained as a light brown oil from the n-hexane:ethyl acetate (20:1) fraction.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07176216B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-a846a0dc936f4d218d91c63c6b3c0bc5
Quellennotizuspto-grants-2007_02