Reacción #9599

ord-02f3772b166949dc9620d2ef20591eba

Ecuación de reacción

Cc1ccccc1P(c1ccccc1C)c1ccccc1C
tri-ortho-tolylphosphine
CCN(CC)CC
triethylamine
C=Cc1ccccn1
2-vinylpyridine
CCOCc1nc2c(N)nc3cc(Br)ccc3c2n1CCCOC
7-bromo-2-ethoxymethyl-1-(3-methoxypropyl)-1H-imidazo[4,5-c]quinolin-4-amine
CCOCc1nc2c(N)nc3cc(/C=C/c4ccccn4)ccc3c2n1CCCOC
(E)-2-ethoxymethyl-1-(3-methoxypropyl)-7-(2-pyridin-2-ylvinyl)-1H-imidazo[4,5-c]quinolin-4-amine

Disolventes

Condiciones de reacción

Temperatura
120°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroA thick walled glass tube, equipped with magnetic stir-bar
  2. 2
    OtroThe tube was purged with nitrogen
  3. 3
    Otrosealed
  4. 4
    Temperaturato cool
  5. 5
    Concentraciónconcentrated under reduced pressure
  6. 6
    OtroThe solid residue was partitioned between dichloromethane and water
  7. 7
    workup.ADDITIONthe mixture was adjusted to pH 12 with the addition of 10% aqueous sodium hydroxide
  8. 8
    OtroThe organic layer was separated
  9. 9
    Otropurified by flash chromatography on silica gel (
  10. 10
    Lavadoeluting with chloroform
  11. 11
    Otromethanol 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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07091214B2uspto-grants-2006_08