Reacción #11561

ord-b337c3f6b67740aa913be31c3193b3a0

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe solvent was evaporated under reduced pressure from the reaction mixture
  2. 2
    Filtraciónthe precipitated crystals were filtered off with ethyl acetate

Procedimiento

Methyl iodide (90 μl, 1.5 mmol) was added to a solution of 1-[2-(1-adamantyl)ethyl]-1-pentyl-3-[3-(4-pyridyl)propyl]urea (Compound No. 1-1) (0.30 g, 0.73 mmol) in acetone (1.5 ml) at room temperature, and the mixture was stirred overnight. The solvent was evaporated under reduced pressure from the reaction mixture, and the precipitated crystals were filtered off with ethyl acetate to give 389 mg (96%) of the titled compound.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07098226B2uspto-grants-2006_08