Reaction #1897

ord-b73af90813ea458ca97a1404afcbed16

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

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

Procedure

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05726306uspto-grants-1998_03