Reaktion #698010

ord-fcf419b0a0a14b5f9f88f05a992ec703

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturat reflux for 2 hours
  2. 2
    Extraktionextracted with ethyl acetate
  3. 3
    Trocknenthe organic phase was dried over sodium sulfate
  4. 4
    SonstigeAfter removal of the solvent the residue
  5. 5
    workup.DISSOLUTIONwas dissolved in 4 ml of methanol
  6. 6
    workup.ADDITIONtreated with 3 ml of 2M HCl
  7. 7
    workup.ADDITIONAfter the addition of 7-8 ml of ethyl acetate the product
  8. 8
    Sonstigeseparated out slowly
  9. 9
    FiltrationIt was filtered off
  10. 10
    Sonstigedried in a vacuum

Vorschrift

0.113 g (0.00026 mol) of N-[3-(4-acetylamino-phenyl-sulfonylamino)-5-(acetyl-methyl-amino)-phenyl]-N-methyl-acetamide was dissolved in 10 ml of 1N NaOH and boiled at reflux for 2 hours. The mixture was neutralized with 1N HCl, extracted with ethyl acetate and the organic phase was dried over sodium sulfate. After removal of the solvent the residue was dissolved in 4 ml of methanol and treated with 3 ml of 2M HCl. After the addition of 7-8 ml of ethyl acetate the product separated out slowly. It was filtered off and dried in a vacuum. There was obtained 0.085 g (74%) of 4-amino-N-(3,5-bis-methylamino-phenyl)-benzenesulfonamide hydrochloride (1:2.6) as a pink coloured amorphous solid. MS (ISN): me/e=305 (C14H17N4O2S-).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05998665uspto-grants-1999_12