Reaktion #1715382

ord-adcdf9b314904d5e8e488b79e72133bf

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeTo a 100 ml flask was
  2. 2
    Sonstigewas removed

Vorschrift

To a 100 ml flask was (S)-tert-butyl 3-(4-chlorophenyl)-1-oxo-1-(3-(pyridin-4-yl)isoxazol-5-ylamino)propan-2-ylcarbamate TFA salt 3.1.B (200 mg, 0.54 mmole), 10 ml of CH2Cl2, and 10 ml of TFA. The reaction was stirred at room temperature for 4 hours at which time the solvent was removed to give (S)-2-amino-3-(4-chlorophenyl)-N-(3-(pyridin-4-yl)isoxazol-5-yl)propanamide TFA salt 3.1.C as a light yellow solid (250 mg, 100% yield).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08785468B2uspto-grants-2014_07