Réaction #3355

ord-c2c072d6e317473092782f2fc460da4e

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe compound was prepared
  2. 2
    AutreThe crude product was purified on a silica gel column
  3. 3
    Concentrationconcentrated in vacuo
  4. 4
    Autrethe solid was crystallized from ethanol/water (1:1 v/v)

Mode opératoire

The compound was prepared according to the general method of Preparation 9 using 2,2'-dithiobisbenzoyl chloride (3.0 g, 8.0 mmol) in 30 mL of dichloromethane and 4-[(acetylamino) sulfonyl]aniline (5.6 g, 26.0 mmol) in 100 mL of pyridine. The crude product was purified on a silica gel column using chloroform/methanol (1:1 v/v) as the mobile phase. The pure fractions were pooled, concentrated in vacuo, and the solid was crystallized from ethanol/water (1:1 v/v) to yield 0.5 g of the title compound, mp 180°-182° C.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05733921uspto-grants-1998_03