Reaktion #9285

Reaktionsgleichung

ammonium chloride

n-Butyllithium

2-ethyl-4-methoxypyrazolo[1,5-a]pyridine

1,2-dibromoethane

→

title compound

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

Lösungsmittel

tetrahydrofuran

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.STIRRINGstirring
2. 2
   workup.WAITwas continued for 1 hour
3. 3
   Extraktionextraction
4. 4
   Waschenthe extract was washed with brine
5. 5
   Trocknendried over magnesium sulfate
6. 6
   workup.DISTILLATIONthe solvent was distilled off under reduced pressure

Vorschrift

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 was 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.

Quelle