Réaction #851

ord-83e2d9b7b08846c09e3e4e23f2dc9784

Équation de réaction

Nc1ccc(NC(=O)c2ccc(N)cc2)cc1
4,4'-Diaminobenzanilide
S=C=NCc1ccccc1
benzylisothiocyanate
O=C(Nc1ccc(NC(=S)NCc2ccccc2)cc1)c1ccc(NC(=S)NCc2ccccc2)cc1
colorless crystal
Rendement 43.4%
O=C(Nc1ccc(NC(=S)NCc2ccccc2)cc1)c1ccc(NC(=S)NCc2ccccc2)cc1
4,4'-di(benzylthiocarbamoylamino)benzanilide
Rendement 43.4%

Solvants

Conditions de réaction

Température
55°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureAfter cooling
  2. 2
    Filtrationthe reaction mixture was filtered
  3. 3
    Lavagewashed with acetone/n-hexane

Mode opératoire

4,4'-Diaminobenzanilide (0.568 g, 2.5 mM) was dissolved in 20 ml of acetone, and 2 equivalents of benzylisothiocyanate (0.746 g, 5 mM) was added. The mixture was stirred at 55° C. for 10 minutes. After cooling, the reaction mixture was filtered, and washed with acetone/n-hexane to obtain 0.57 g (43.4% yield) of a colorless crystal of compound A-16.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05723075uspto-grants-1998_03