Reaktion #505455

ord-57273fd18cb041e9a2d7e04530dec9cf

Reaktionsgleichung

C[C@@H]1CN(C(=O)OC(C)(C)C)CCN1
1,1-dimethylethyl(3R)-3-methyl-1-piperazinecarboxylate
CCN(C(C)C)C(C)C
DIPEA
Cl
HCl
O=S(=O)(Cl)c1ccc(C(F)(F)F)cc1
4-(trifluoromethyl)benzenesulfonyl chloride
C[C@@H]1CN(C(=O)OC(C)(C)C)CCN1S(=O)(=O)c1ccc(C(F)(F)F)cc1
title compound
Ausbeute 110.8%
C[C@@H]1CN(C(=O)OC(C)(C)C)CCN1S(=O)(=O)c1ccc(C(F)(F)F)cc1
1,1-Dimethylethyl(3R)-3-methyl-4-{[4-(trifluoromethyl)phenyl]sulfonyl}-1-piperazinecarboxylate
Ausbeute 110.8%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe layers were separated
  2. 2
    Extraktionthe aqueous layer was then re-extracted with DCM (75 ml)
  3. 3
    Waschenwashed with saturated brine solution (100 ml)
  4. 4
    SonstigeThe organic layers were then separated
  5. 5
    Trocknendried (MgSO4)
  6. 6
    Einengenconcentrated to dryness

Vorschrift

To a solution of 1,1-dimethylethyl(3R)-3-methyl-1-piperazinecarboxylate (1.50 g, 7.49 mmol) in DCM (30 ml) was added DIPEA (1.96 ml, 11.2 mmol) and then portionwise addition of 4-(trifluoromethyl)benzenesulfonyl chloride (2.20 g, 8.99 mmol) at rt. The resultant mixture was stirred under an atmosphere of argon for 2 hours before addition of 1M aq. 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).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08093249B2uspto-grants-2012_01