Reaktion #413877

ord-6f2990b5f65f4b19840d9479b169ccbc

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Filtrationfiltered
  2. 2
    Sonstigeevaporated under reduced pressure
  3. 3
    Sonstigethe residue was recrystallized from isopropyl ether and again from CH3CN

Vorschrift

A solution of 512 mg of p-(benzyloxy)-N-[5-(p-chlorophenyl)-6-(2-hydroxyethoxy)-4-pyrimidinyl]benzene-sulfonamide in 30 ml of glacial acetic acid was treated with 2 ml of 4N HCl in dioxane and 100 mg of 10% palladium-carbon. The mixture was hydrogenated while stirring, thereafter the solution was suction filtered, evaporated under reduced pressure and the residue was recrystallized from isopropyl ether and again from CH3CN. There was obtained N-[5-(p-chlorophenyl)-4-pyrimidinyl]-p-hydroxybenzenesulfonamide, melting point 231°-232° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05270313uspto-grants-1993_12