Reacción #77808

ord-166dbfddd38c4b35b4a216d8319fea93

Condiciones de reacción

Temperatura
30°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaunder cooling with ice
  2. 2
    workup.STIRRINGwas stirred further for 2 hours at 30° C
  3. 3
    workup.DISTILLATIONSolvent was distilled off under reduced pressure, and 25% aqueous ammonia
  4. 4
    workup.ADDITIONwas added to the residue, which
  5. 5
    Extracciónwas extracted with ethyl acetate
  6. 6
    LavadoThe organic layer was washed with water and saturated brine in sequence
  7. 7
    Secadodried over anhydrous sodium sulfate
  8. 8
    workup.DISTILLATIONSolvent was distilled off under reduced pressure
  9. 9
    Otrothe residue obtained
  10. 10
    Otrowas crystallized from hexane
  11. 11
    Filtraciónethyl acetate=1:1, and then the crystals were collected by filtration

Procedimiento

To a solution of 2.26 g of 5-amino-2-methoxy-N-(4-trifluoromethylbenzyl)benzamide in 27 ml of acetone and 11 ml of methanol were added 5.6 ml of 47% solution of hydrobromic acid, 540 mg of sodium nitrite and 2 ml of water under cooling with ice, and the mixture was stirred for 10 minutes. To the reaction mixture were added 3.00 g of acrylamide, and, after heated to 30° C., 135 mg of cupric oxide were added little by little, and the mixture was stirred further for 2 hours at 30° C. Solvent was distilled off under reduced pressure, and 25% aqueous ammonia was added to the residue, which was extracted with ethyl acetate. The organic layer was washed with water and saturated brine in sequence and dried over anhydrous sodium sulfate. Solvent was distilled off under reduced pressure, the residue obtained was crystallized from hexane:ethyl acetate=1:1, and then the crystals were collected by filtration to obtain 1.55 g of 5-(2-bromo-2-carbamoylethyl)-2-methoxy-N-(4-trifluoromethylbenzyl)benzamide as colorless crystals.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06706763B1uspto-grants-2004_03