Reacción #4276

ord-0bc03ba9e5e2470fbc42b20b354ea151

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroAfter solvent-removal
  2. 2
    Otropartitioning
  3. 3
    Otroseparation
  4. 4
    Lavadowashing
  5. 5
    Otrodrying
  6. 6
    Concentraciónconcentrating
  7. 7
    Otrothe analytical product was obtained via chromatography on silica gel (ethyl acetate-hexane elution, 3:7 v/v)

Procedimiento

According to the method of Example 5, 1-methyl-2-chloromethyl-5-(2'-fluorophenyl)-2,3-dihydro-1H-1,4-benzodiazepine (200 mg, 0.66 mmole) and m-trifluoromethyl aniline (319 mg, 1.97 mmole) were combined in 2 ml of dry N,N-dimethylformamide, and potassium carbonate (273 mg, 1.97 mmole) and sodium iodide (198 mg, 1.32 mmole) were added to this mixture (which was heated at 65° C. for 18 hours). After solvent-removal, partitioning, separation, washing, drying and concentrating, the analytical product was obtained via chromatography on silica gel (ethyl acetate-hexane elution, 3:7 v/v) and was shown to be 96% pure by HPLC.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04724237uspto-grants-1988_02