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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1864991Erstellt: 26. Oktober 2026

1,2-Dibromoethane → 7-Bromo-2-ethyl-4-methoxypyrazolo[1,5-a]pyridine

https://huagongshe.com/reaction/1864991

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-DibromoethaneHCID 7839—
EduktAmmonium ChlorideHCID 25517—
Edukt2-Ethyl-4-methoxypyrazolo[1,5-a]pyridineHCID 21984578—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt7-Bromo-2-ethyl-4-methoxypyrazolo[1,5-a]pyridineHCID 21984567—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

n-Butyllithium (1.31 mL) was slowly added dropwise to a solution of 2-ethyl-4-methoxypyrazolo[1,5-a]pyridine (303 mg) in tetrahydrofuran (15 mL) at −78° C. After stirring the mixture at −78° C. for 1 hour, 1,2-dibromoethane (0.18 mL) was added and stirring was continued for 1 hour. Saturated aqueous ammonium chloride was added, extraction was performed with ethyl acetate, the extract washed with brine and dried over magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was subjected to silica gel column chromatography (20 g), and the title compound (282 mg) was obtained from the n-hexane:ethyl acetate (5:1) fraction as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07625925B2
Quelldatensatzuspto-grants-2009_12
ORD IDord-36c761d88e6d4f768136cecaec694884
Quellennotizuspto-grants-2009_12