Reacción #502097

ord-168cdef8280448c485a0f1aa1909b388

Ecuación de reacción

[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
Rendimiento 37.3%
OCc1ccc(-c2ccc3nc(-c4ccc(Cl)cc4)cn3c2)o1
{5-[2-(4-Chlorophenyl)imidazo[1,2-a]pyridin-6-yl]furan-2-yl}methanol
Rendimiento 37.3%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrothe solvent is then evaporated off under reduced pressure
  2. 2
    OtroThe organic phase is separated
  3. 3
    Secadodried over sodium sulphate
  4. 4
    Concentraciónconcentrated under reduced pressure

Procedimiento

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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08088765B2uspto-grants-2012_01