Reaktion #499165

ord-f157c392102844b2aaa45fa45e18f4a5

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe reaction was then heated
  2. 2
    Temperaturto reflux overnight
  3. 3
    Einengenconcentrated in vacuo
  4. 4
    workup.DISSOLUTIONThe residue was dissolved in methylene chloride
  5. 5
    Waschenwashed with aqueous ammonium chloride (NH4Cl) and saturated brine
  6. 6
    Trocknendried with MgSO4
  7. 7
    SonstigePurification

Vorschrift

Sodium hydride (930 mg, 23.3 mmol of 60% oil dispersion) was washed with hexanes under a nitrogen atmosphere and suspended in 100 mL of anhydrous THF. Thiomorpholin-3-one (1.0 g, 8.55 mmol) was added, followed immediately by 2-(4-methylpiperazin-1-yl)-benzaldehyde (1.58 g., 7.75 mmol). The reaction was then heated to reflux overnight, cooled to room temperature and concentrated in vacuo. The residue was dissolved in methylene chloride and washed with aqueous ammonium chloride (NH4Cl) and saturated brine and then dried with MgSO4. Purification using flash chromatography gave 2-{hydroxy-[2-(4-methylpiperazin-1-yl)phenyl]-methyl}-thiomorpholin-3-one as a white solid, m.p. 137-139° C. Mass spectrum 322 (M+1).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06562813B2uspto-grants-2003_05