Reacción #219193

ord-cd7f843aafde4cfd83dbff3f9bb88a2e

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaat reflux for two hours
  2. 2
    ExtracciónExtraction with ethyl acetate
  3. 3
    Secadodrying over sodium sulphate
  4. 4
    Filtraciónfiltering
  5. 5
    Otroevaporation of the resulting filtrate to dryness

Procedimiento

A solution of 4-[1-(4-acetaminophenacyl)-1H-benzimidazol-2-yl]-furazan-3-yl-N-(2-cyanoethyl)-amine (0.061 g) in aqueous hydrochloric acid (5 ml, HCl conc.) is heated at reflux for two hours. The mixture is diluted with water and neutralized by addition of sodium bicarbonate. Extraction with ethyl acetate, drying over sodium sulphate, filtering and evaporation of the resulting filtrate to dryness gives the title compound in pure form, m.p. 174-177° C. 1H-NMR (400 MHz, d6-DMSO): 12.40 (s, 1H); 7.84 (m, 4H); 7.38 (m, 3H); 6.65 (m, 2H); 6.28 (S, 2H); 6.17 (s, 2H); 3.57 (m, 2H); 2.66 (t, 2H).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07385061B2uspto-grants-2008_06