Reaktion #1169477

ord-51a8de4eecfb44648a9644ea571af97f

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionextracted with ethyl acetate
  2. 2
    WaschenThe organic layer is washed with water and saturated brine
  3. 3
    Trocknendried over anhydrous sodium sulfate
  4. 4
    Sonstigeevaporated
  5. 5
    Sonstigeto remove the solvent
  6. 6
    SonstigeThe oily residue is purified by silica gel column chromatography (solvent; chloroform/ethyl acetate=100:1)
  7. 7
    Sonstigeevaporated
  8. 8
    Sonstigeto remove the solvent
  9. 9
    SonstigeThe resulting crude crystals are recrystallized from methylene chloride/isopropyl ether

Vorschrift

To a suspension of sodium hydride (65 mg) in dimethylacetamide (0.5 ml) and tetrahydrofuran (0.5 ml) is added dropwise a solution of 4-(2-hydroxy-1,1-dimethylethyl)-N-{6-[2-hydroxyethoxy]-5-(4-methylphenyl)pyrimidin-4-yl}benzenesulfonamide (135 mg) in dimethylacetamide (2 ml) and THF (2 ml) solution over period of 5 minutes at room temperature, and thereto is added 5-bromo-2-chloropyrimidine (399 mg). The mixture is stirred at room temperature for 6 days. The reaction mixture is acidified with cold diluted hydrochloric acid, and extracted with ethyl acetate. The organic layer is washed with water and saturated brine, dried over anhydrous sodium sulfate, and evaporated to remove the solvent. The oily residue is purified by silica gel column chromatography (solvent; chloroform/ethyl acetate=100:1), and evaporated to remove the solvent. The resulting crude crystals are recrystallized from methylene chloride/isopropyl ether to give 4-[2-(5-bromopyrimidin-2-yloxy)-l, 1 -dimethylethyl]-N-{6-[2-(5-bromopyrimidin-2-yloxy)ethoxy]-5-(4-methylphenyl)pyrimidin-4-yl}benzenesulfonamide (77 mg) as colorless crystals.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05589478uspto-grants-1996_12