Reacción #1897

ord-b73af90813ea458ca97a1404afcbed16

Ecuación de reacción

Nc1ccc(Br)cc1-c1cccnc1C(=O)c1ncccc1-c1cc(Br)ccc1N
2-amino-5-bromophenyl-2-pyridylketone
CO
methanol
[BH4-].[Na+]
sodium borohydride
Nc1ccc(Br)cc1C(O)c1ccccn1
2-amino-5-bromo-α-(2-pyridyl)benzyl alcohol

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe solvent methanol was evaporated off under reduced pressure
  2. 2
    workup.ADDITIONThe residue was treated with an aqueous solution of hydrochloric acid
  3. 3
    Extracciónextracted with ethyl acetate
  4. 4
    LavadoThe ethyl acetate layer was washed with water
  5. 5
    Secadodried over anhydrous magnesium sulfate
  6. 6
    Concentraciónconcentrated under reduced pressure
  7. 7
    OtroThe residue was purified by silica gel column chromatography (eluent, hexane:ethyl acetate=2:1)

Procedimiento

In 100 ml of methanol was dissolved 10 g of 2-amino-5-bromophenyl-2-pyridylketone. To the solution was added 1.7 g of sodium borohydride and stirred for 30 minutes. The solvent methanol was evaporated off under reduced pressure. The residue was treated with an aqueous solution of hydrochloric acid. The decomposed residue was then neutralized with 200 ml of a sodium bicarbonate aqueous solution, and extracted with ethyl acetate. The ethyl acetate layer was washed with water, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent, hexane:ethyl acetate=2:1) to give 2-amino-5-bromo-α-(2-pyridyl)benzyl alcohol (9.0 g) as prisms, m.p. 104°-105° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05726306uspto-grants-1998_03