Réaction #63762

ord-95f22f69963446b3a4ee940056743b5e

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autreat an internal temperature of 40°
  2. 2
    Autresubseguently evaporated in vacuo
  3. 3
    AutreThe residue is crystallized from tert.butyl methyl ether/ether

Mode opératoire

3.53 g of 2-[[(3,5-dimethyl-2-pyridyl)methyl]sulphinyl]-5 -(trifluoromethyl)benzimidazole are dissolved in 50 ml of tetrahydrofuran and treated with 0.77 g of cysteamine. 40 ml of 3N hydrochloric acid are added thereto at an internal temperature of 40°. The mixture is stirred at 40° overnight and subseguently evaporated in vacuo. The residue is crystallized from tert.butyl methyl ether/ether. There is obtained 2-[[(2-aminoethyl)dithio]methyl]-3,5-dimethyl-1 -[5-(trifluoromethyl)-2-benzimidazolyl]pyridinium chloride of melting point 115°-120°.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US04766133uspto-grants-1988_08