Reacción #1785954
ord-3fa4578bc3c549c8814f6d87e2bbdbd0
Ecuación de reacción
Reactantes
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1workup.DISSOLUTIONwere then dissolved
- 2Temperaturaunder heat
- 3OtroCrystals so precipitated
- 4Filtraciónwere collected by filtration
- 5Otrodried
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%.