Reacción #411056

ord-1e17ee0626d943439926e7915051c237

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.STIRRINGthe mixture was stirred at 80° C. for 8 hours
  2. 2
    FiltraciónThe crude mixture was then filtered
  3. 3
    Concentraciónthe filtrate was concentrated under reduced pressure
  4. 4
    Lavadothe solution was washed once with 1 N sodium hydroxide solution and twice with water
  5. 5
    OtroThe organic phases were dried
  6. 6
    Concentraciónconcentrated under reduced pressure
  7. 7
    OtroThe crude product was purified by flash chromatography on a silica gel column, dichloromethane/methanol (19.8/0.2) Yield: 4.15 g (87% of theory)

Procedimiento

2.59 g (19.0 mmol) of potassium carbonate were added at 60° C. to a suspension of 3.0 g (12.0 mmol) of 7-benzyl-3-methylxanthine (prepared according to Example 1a) in 50 ml of dimethylformamide and the mixture was stirred at this temperature for one hour. 2.69 g (15.0 mmol) of 4-chlorophenoxymethyl chloride were then added dropwise and the mixture was stirred at 80° C. for 8 hours. The crude mixture was then filtered, the filtrate was concentrated under reduced pressure, the residue was taken up in dichloromethane, and the solution was washed once with 1 N sodium hydroxide solution and twice with water. The organic phases were dried using magnesium sulfate and concentrated under reduced pressure. The crude product was purified by flash chromatography on a silica gel column, dichloromethane/methanol (19.8/0.2) Yield: 4.15 g (87% of theory); melting point: 96° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06214992B1uspto-grants-2001_04