Reacción #10170

ord-0300c97a88a5417abebd157852f56576

Ecuación de reacción

CCN=C=NCCCN(C)C
1-ethyl-3-(3-dimethylaminopropyl)carbodiimide
N[C@@]12C[C@H]1COC2=O
(±)-Trans-1-amino-3-oxabicyclo[3.1.0]hexan-2-one
O=C(O)CC(F)(F)F
3,3,3-trifluoropropionic acid
Oc1cccc2[nH]nnc12
Hydroxybenzotriazole
O=C(CC(F)(F)F)N[C@@]12C[C@H]1COC2=O
3,3,3-trifluoro-N-[(±)-trans-2-oxo-3-oxabicyclo[3.1.0]hex-1-yl]-propanamide
Rendimiento 45.0%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Extracciónthe reaction mixture was extracted with ethyl acetate
  2. 2
    LavadoThe combined organic extracts were washed with water and brine
  3. 3
    Secadodried (sodium sulfate)
  4. 4
    Concentraciónconcentrated
  5. 5
    Otroto give the crude product
  6. 6
    OtroThis was purified by silica gel chromatography

Procedimiento

(±)-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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07091380B2uspto-grants-2006_08