Réaction #3733

ord-fe8f501adbbe4ac2972456200d435247

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températurewas refluxed for 9 hours
  2. 2
    ExtractionThe reaction mixture was then extracted with water (4×30 ml)
  3. 3
    Séchagethe organic layer dried over anhydrous sodium sulphate
  4. 4
    Autrethe solvent removed in vacuo
  5. 5
    AutreThe residue was recrystallised from ethanol

Mode opératoire

1,3-Di-n-butyl-8-bromo xanthine (2 g, 0.0029 mol) was dissolved in toluene (50 ml). After addition of piperidine (5 g, 0.0058 mol) the mixture was refluxed for 9 hours. The reaction mixture was then extracted with water (4×30 ml), the organic layer dried over anhydrous sodium sulphate and the solvent removed in vacuo. The residue was recrystallised from ethanol to give the title product, yield 0.4 g (20%), m.pt. 221° C.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05734051uspto-grants-1998_03