Reaction #2329058

ord-082236599bb4446c8f6f692dcc34b403

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    ExtractionThe reaction solution was extracted twice with ethyl acetate/water
  2. 2
    DryingThe organic phases were dried over magnesium sulfate
  3. 3
    Concentrationconcentrated
  4. 4
    OtherThis gave the product of molecular weight 463.51 (C26H26F1N3O4)

Procedure

199 mg of hydroxylammonium hydrochloride were added to a solution of 200 mg of 4-[3-[3-(4-fluorophenyl)-3-hydroxypropyl]-2-(4-methoxyphenyl)-4-oxoazetidin-1-yl]benzonitrile (8) and 0.45 ml of triethylamin in 15 ml of isopropanol. The mixture was stirred at room temperature for 12 h. The reaction solution was extracted twice with ethyl acetate/water. The organic phases were dried over magnesium sulfate and concentrated. This gave the product of molecular weight 463.51 (C26H26F1N3O4); MS (ESI): 464.19 (M+H+).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07671047B2uspto-grants-2010_03