Réaction #502097

ord-168cdef8280448c485a0f1aa1909b388

Équation de réaction

[BH4-].[Na+]
sodium borohydride
O=Cc1ccc(-c2ccc3nc(-c4ccc(Cl)cc4)cn3c2)o1
5-[2-(4-chlorophenyl)imidazo[1,2-a]pyridin-6-yl]furan-2-carbaldehyde
OCc1ccc(-c2ccc3nc(-c4ccc(Cl)cc4)cn3c2)o1
compound
Rendement 37.3%
OCc1ccc(-c2ccc3nc(-c4ccc(Cl)cc4)cn3c2)o1
{5-[2-(4-Chlorophenyl)imidazo[1,2-a]pyridin-6-yl]furan-2-yl}methanol
Rendement 37.3%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autrethe solvent is then evaporated off under reduced pressure
  2. 2
    AutreThe organic phase is separated
  3. 3
    Séchagedried over sodium sulphate
  4. 4
    Concentrationconcentrated under reduced pressure

Mode opératoire

122 mg of sodium borohydride are added, in small portions, to 104 mg of 5-[2-(4-chlorophenyl)imidazo[1,2-a]pyridin-6-yl]furan-2-carbaldehyde dissolved in 20 ml of methanol. The mixture is subsequently stirred at ambient temperature for 2 hours, and the solvent is then evaporated off under reduced pressure. The residue is taken up between dichloromethane and water. The organic phase is separated, dried over sodium sulphate and concentrated under reduced pressure. 39 mg of compound are obtained.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08088765B2uspto-grants-2012_01