Réaction #10170

ord-0300c97a88a5417abebd157852f56576

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Extractionthe reaction mixture was extracted with ethyl acetate
  2. 2
    LavageThe combined organic extracts were washed with water and brine
  3. 3
    Séchagedried (sodium sulfate)
  4. 4
    Concentrationconcentrated
  5. 5
    Autreto give the crude product
  6. 6
    AutreThis was purified by silica gel chromatography

Mode opératoire

(±)-Trans-1-amino-3-oxabicyclo[3.1.0]hexan-2-one (128 mg, 1.13 mmol) was mixed with 3,3,3-trifluoropropionic acid in 2.3 mL of N,N-dimethylformamide. Hydroxybenzotriazole (17.4 mg, 0.11 mmol) was added followed by 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (282 mg, 1.47 mmol). The pH of the reaction mixture was adjusted to 8.5 with triethylamine and the mixture was allowed to stir at ambient temperature for 2 hours. Water was then added and the reaction mixture was extracted with ethyl acetate. The combined organic extracts were washed with water and brine, then dried (sodium sulfate) and concentrated to give the crude product. This was purified by silica gel chromatography to afford 120 mg (45%) of 3,3,3-trifluoro-N-[(±)-trans-2-oxo-3-oxabicyclo[3.1.0]hex-1-yl]-propanamide.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07091380B2uspto-grants-2006_08