Réaction #69574

ord-325932623b9542d1bf4f0f3d99938ca3

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe layers were separated
  2. 2
    Extractionthe aqueous layer was then re-extracted with DCM (75 ml)
  3. 3
    Lavagewashed with saturated brine solution (100 ml)
  4. 4
    AutreThe organic layers were then separated
  5. 5
    Séchagedried (MgSO4)
  6. 6
    Concentrationconcentrated to dryness

Mode opératoire

To a solution of 1,1-dimethylethyl (3R)-3-methyl-1-piperazinecarboxylate (1.5 g, 7.49 mmol, supplier Aldrich) in DCM (30 ml) was added DIPEA (1.962 ml, 11.23 mmol) and then portionwise addition of 4-(trifluoromethyl)benzenesulfonyl chloride (2.2 g, 8.99 mmol) at room temperature. The resultant mixture was stirred under an atmosphere of Ar for 2 hours before addition of 1M HCl solution (75 ml) and DCM (75 ml). The layers were separated and the aqueous layer was then re-extracted with DCM (75 ml), the organic layers were combined and washed with saturated brine solution (100 ml). The organic layers were then separated, dried (MgSO4) and concentrated to dryness giving the title compound (3.39 g).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08530478B2uspto-grants-2013_09