Reaktion #473853

ord-8c2640f99fa3477ebee11044a0edcec4

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturthe mixture refluxed for 24 hours
  2. 2
    TemperaturAfter cooling
  3. 3
    Einengenthe reaction was concentrated
  4. 4
    Filtrationthe precipitate was filtered off
  5. 5
    Filtrationfiltered
  6. 6
    Sonstigedried

Vorschrift

2-[(4-(imidazol-1-yl)-phenyl]-3-benzyloxy-6-acetamido-4H-1-benzopyran-4-one (7 g; 15.5 mmol) was suspended in ethanol (250 mL), HCl 4N (16 mL; 62 mmol) was added and the mixture refluxed for 24 hours. After cooling, the reaction was concentrated and the precipitate was filtered off. The crude was suspended in diisopropyl ether, filtered and dried to give the titled compound as light yellow solid. 1H-NMR (d6-DMSO): 9.91 (s, 1H); 8.44 (d, 1H); 8.22 (d, 2H); 7.90 (d, 3H); 7.78 (d, 2H); 7.33 (d, 1H); 7.32 (m, 6H); 5.16 (s, 2H); MS (EI) 410 (M+1), 319 (M-91).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08372866B2uspto-grants-2013_02