Reacción #9285

ord-b182e6e6acd04d0da1ff082f2af748a0

Ecuación de reacción

[Cl-].[NH4+]
ammonium chloride
[Li][CH2]CCC
n-Butyllithium
CCc1cc2c(OC)cccn2n1
2-ethyl-4-methoxypyrazolo[1,5-a]pyridine
BrCCBr
1,2-dibromoethane
CCc1cc2c(OC)ccc(Br)n2n1
title compound
CCc1cc2c(OC)ccc(Br)n2n1
7-Bromo-2-ethyl-4-methoxypyrazolo[1,5-a]pyridine

Disolventes

Condiciones de reacción

Temperatura
-78°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

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

Procedimiento

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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07091215B2uspto-grants-2006_08