Reaktion #41823

ord-4a9435fcea3d419e8d97eb77a8f43fff

Reaktionsgleichung

CC(C)N1CCN(C(=O)c2ccc(C=O)cc2)CC1
4-(4-isopropyl-piperazine-1-carbonyl)-benzaldehyde
O=S([O-])O.[Na+]
NaHSO3
CC(C)N1CCN(C(=O)c2ccc(C(O)S(=O)(=O)[O-])cc2)CC1.[Na+]
title compound
CC(C)N1CCN(C(=O)c2ccc(C(O)S(=O)(=O)[O-])cc2)CC1.[Na+]
Hydroxy-[4-(4-isopropyl-piperazine-1-carbonyl)-phenyl]-methanesulfonic acid sodium salt

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturcooled to 0° C.
  2. 2
    workup.STIRRINGstirred for 3 h
  3. 3
    workup.STIRRINGto aid stirring
  4. 4
    SonstigeA precipitate formed
  5. 5
    Filtrationwas collected by suction filtration through a glass frit
  6. 6
    Filtrationwith filter paper
  7. 7
    WaschenThe filter cake was washed with hexane (1×50 mL)
  8. 8
    Sonstigedried under vacuum for 16 h

Vorschrift

A solution of 4-(4-isopropyl-piperazine-1-carbonyl)-benzaldehyde (20.0 g, 76.9 mmol) in EtOH (200 mL) was stirred at room temperature for 15 min. To the resulting solution was added a solution of NaHSO3 (9.6 g) in H2O (25 mL), dropwise over 30 min. The resulting suspension was stirred at room temperature for 2 h, then cooled to 0° C. and stirred for 3 h, adding EtOH periodically (total 200 mL) to aid stirring. A precipitate formed and was collected by suction filtration through a glass frit lined with filter paper. The filter cake was washed with hexane (1×50 mL), and dried under vacuum for 16 h to yield the title compound as a white solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07728129B2uspto-grants-2010_06