Reaction #2329056

ord-75e9cf667067418cacb83f161e0910ba

Reaction equation

Cl.[NH3+]O
hydroxylammonium hydrochloride
N#Cc1ccccc1C1C(CCC(O)c2ccc(F)cc2)C(=O)N1c1ccc(F)cc1
{1-(4-fluorophenyl)-3-[3-(4-fluorophenyl)-3-hydroxypropyl]-4-oxoazetidin-2-yl}benzonitrile
CCN(CC)CC
triethylamine
N=C(NO)c1ccc(C2C(CCC(O)c3ccc(F)cc3)C(=O)N2c2ccc(F)cc2)cc1
4-{1-(4-Fluorophenyl)-3-[3-(4-fluorophenyl)-3-hydroxypropyl]-4-oxoazetidin-2-yl}-N-hydroxybenzamidine

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 451.48 (C25H23F2N3O3)

Procedure

199 mg of hydroxylammonium hydrochloride were added to a solution of 200 mg of {1-(4-fluorophenyl)-3-[3-(4-fluorophenyl)-3-hydroxypropyl]-4-oxoazetidin-2-yl}benzonitrile and 0.45 ml of triethylamine in 15 ml of isopropanol, and 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 451.48 (C25H23F2N3O3); MS (ESI): 452.10 (M+H+).

Source

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