Reacción #9599
ord-02f3772b166949dc9620d2ef20591eba
Ecuación de reacción
Reactantes
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1OtroA thick walled glass tube, equipped with magnetic stir-bar
- 2OtroThe tube was purged with nitrogen
- 3Otrosealed
- 4Temperaturato cool
- 5Concentraciónconcentrated under reduced pressure
- 6OtroThe solid residue was partitioned between dichloromethane and water
- 7workup.ADDITIONthe mixture was adjusted to pH 12 with the addition of 10% aqueous sodium hydroxide
- 8OtroThe organic layer was separated
- 9Otropurified by flash chromatography on silica gel (
- 10Lavadoeluting with chloroform
- 11Otromethanol in a gradient from 100:0 to 90:10) followed by recrystallization from acetonitrile
Procedimiento
A thick walled glass tube, equipped with magnetic stir-bar, was charged with toluene (20 mL/g), palladium (II) acetate (0.1 equivalents), tri-ortho-tolylphosphine (0.3 equivalents), triethylamine (3.0 equivalents), 2-vinylpyridine (1.0 equivalent), and 7-bromo-2-ethoxymethyl-1-(3-methoxypropyl)-1H-imidazo[4,5-c]quinolin-4-amine (1.0 eq.). The tube was purged with nitrogen and sealed. The reaction mixture was heated at 120° C. for 24–48 hours. The reaction mixture was allowed to cool and then concentrated under reduced pressure. The solid residue was partitioned between dichloromethane and water, and the mixture was adjusted to pH 12 with the addition of 10% aqueous sodium hydroxide. The organic layer was separated and purified by flash chromatography on silica gel (eluting with chloroform:methanol in a gradient from 100:0 to 90:10) followed by recrystallization from acetonitrile to provide (E)-2-ethoxymethyl-1-(3-methoxypropyl)-7-(2-pyridin-2-ylvinyl)-1H-imidazo[4,5-c]quinolin-4-amine as an off-white solid.