Reaktion #1671402

ord-24ef3d1360fc4b5c975404b4cf988ee5

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    FiltrationThe catalyst was filtered off
  2. 2
    Einengenthe filtrate was concentrated
  3. 3
    workup.DISSOLUTIONthe residue was dissolved in 10 ml of 1N NaOH
  4. 4
    Filtrationfiltered
  5. 5
    SonstigeThe precipitate which separated slowly
  6. 6
    Filtrationwas filtered off under suction
  7. 7
    Waschenrinsed
  8. 8
    Sonstigedried in a high vacuum

Vorschrift

0.5 g (0.0014 mol) of 4-amino-N-(2-bromo-6-methylamino-pyridin-4-yl)-benzenesulfonamide was dissolved in 25 ml of ethanol, treated with 0.05 g of Pd/C and hydrogenated with hydrogen gas under normal pressure for 1 hour. The catalyst was filtered off, the filtrate was concentrated and the residue was dissolved in 10 ml of 1N NaOH, filtered and the filtrate was then adjusted pH 8 by means of 1N HCl. The precipitate which separated slowly was filtered off under suction, rinsed and dried in a high vacuum. There was obtained 0.22 g (57%) of 4-amino-N-(2-methylamino-pyridin-4-yl)-benzenesulfonamide as white crystals; m.p.: >261° C. (dec).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05932599uspto-grants-1999_08