Reacción #1785954

ord-3fa4578bc3c549c8814f6d87e2bbdbd0

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.DISSOLUTIONwere then dissolved
  2. 2
    Temperaturaunder heat
  3. 3
    OtroCrystals so precipitated
  4. 4
    Filtraciónwere collected by filtration
  5. 5
    Otrodried

Procedimiento

(R)-(−)-2-[3-[3-(1-tert-Butylcarbonylmethyl-2-oxo-5-c yclohexyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepin-3-yl)urei do]phenyl]-2-methylpropionic acid (158 mg) and N,N′-dibenzylethylenediamine (67 mg) were added to acetonitrile (2 mL), and were then dissolved under heat. The reaction mixture was allowed to stand. Crystals so precipitated were collected by filtration and dried, whereby the title compound (200 mg) was obtained. Yield: 89%.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06344452B1uspto-grants-2002_02