Reacción #2000293

ord-85de4847ebec470081e2330141a64a29

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaat reflux for 4 h
  2. 2
    workup.ADDITIONit was poured on ice
  3. 3
    ExtracciónThe aqueous solution was extracted three times with dichloromethane
  4. 4
    SecadoThe combined organic layers were dried with magnesium sulfate
  5. 5
    Otroevaporated

Procedimiento

2.6 g (12.0 mmol) of 7-chloro-6-fluoro-isoquinoline 2-oxide (5) were heated in 40 ml of POCl3 at reflux for 4 h. After the mixture has cooled down to room temperature, it was poured on ice. The aqueous solution was extracted three times with dichloromethane. The combined organic layers were dried with magnesium sulfate and evaporated to yield 2.91 g of the title compound, which was used without further purification. Rt=2.34 min (Method A). Detected mass: 216.0/218.0 (M+H+).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08609691B2uspto-grants-2013_12