Reacción #8136

ord-acc6327e872d44b5954e4f6a3294ed3c

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.DISTILLATIONThe solvent was distilled off under reduced pressure, and toluene
  2. 2
    workup.ADDITIONwas added further
  3. 3
    TemperaturaThe residue was heated at 190 to 200° C. for 30 minutes under a nitrogen atmosphere

Procedimiento

Trifluoroacetic acid (21 mL) was added to 2-cyclopropylmethyl-4-[2,2-di(tert-butoxycarbonyl)ethyl]-6-(3-fluoro-4-methoxyphenyl)-2H-pyridazin-3-one (1.39 g, 2.77 mmol), and the mixture was stirred at room temperature for 30 minutes. The solvent was distilled off under reduced pressure, and toluene was added further, followed by azeotropic boiling. The residue was heated at 190 to 200° C. for 30 minutes under a nitrogen atmosphere to yield the title compound as a pale brown powder (yield: 907 mg, 94.7%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07087606B2uspto-grants-2006_08