Reacción #463607

ord-88f5d475501241098154bbe215df8e61

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroAfter completion of the reaction
  2. 2
    workup.DISTILLATIONthe solvent was distilled off under reduced pressure
  3. 3
    workup.ADDITIONthe residue was treated with methylene chloride-saturated aqueous sodium hydrogen carbonate solution
  4. 4
    SecadoThe methylene chloride layer was dried over sodium sulfate
  5. 5
    Concentraciónconcentrated under reduced pressure

Procedimiento

In 4 ml of methylene chloride-pyridine (2:1) was dissolved 150 mg (0.25 mmol) of 1,2-O-dioleylglycerol. Then, 1 ml of a solution of 150 mg (0.75 mmol) (2-dimethylaminoethyl)sulfamoyl chloride in methylene chloride was added and the reaction was carried out at ambient temperature for 2 hours. After completion of the reaction, the solvent was distilled off under reduced pressure and the residue was treated with methylene chloride-saturated aqueous sodium hydrogen carbonate solution. The methylene chloride layer was dried over sodium sulfate and concentrated under reduced pressure. The residue was subjected to column chromatography (silica gel/methylene chloride-methanol) to provide 34 mg (18%) of the title compound of the invention.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06020317uspto-grants-2000_02