Reacción #170707

ord-6c2e55e5135a4bbda15edba2497a37f4

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    ConcentraciónThis reaction solution was concentrated
  2. 2
    workup.ADDITIONn-hexane (4 ml) was added
  3. 3
    workup.STIRRINGthe mixture was stirred
  4. 4
    FiltraciónThe insoluble substance was collected by filtration
  5. 5
    Lavadowashed with n-hexane
  6. 6
    Otrodried under reduced pressure

Procedimiento

To a solution of [(R)-2-tert-butoxycarbonylamino-2-[1-phenyl-5-(3-propylphenyl)-1H-pyrazol-3-ylcarbamoyl]ethyl]carbamic acid tert-butyl ester (328 mg) in 1,4-dioxane (3 ml) was added a 4M solution of hydrogen chloride in 1,4-dioxane (3 ml) at room temperature, and the mixture was stirred for 2 hours. This reaction solution was concentrated, and then n-hexane (4 ml) was added thereto, and the mixture was stirred. The insoluble substance was collected by filtration, washed with n-hexane, and dried under reduced pressure to give the titled compound (181 mg).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08846746B2uspto-grants-2014_09