Réaction #83346

ord-08c795c675d44ec988099b77cf02e9b6

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autrecondensed
  2. 2
    Autrepurified by HPLC over silica gel
  3. 3
    Lavageeluted with 25-30% ethyl acetate/hexane

Mode opératoire

2-Chloro-6-methoxyquinoline (52.0 mmoles, 10.0 g), 4-aminothiophenol (52.0 mmoles, 6.5 g) and dimethylaminopyridine (52.0 mmoles, 6.3 g) were stirred for 16 hr in 250 ml ethanol. The reaction was condensed and purified by HPLC over silica gel eluted with 25-30% ethyl acetate/hexane to yield 2-(4-aminophenylthio)-6-methoxyquinoline. 8.5 g, 58% product. Mass spec (FD) 282. Calculated for C16H14N2OS: C, 68.06; H, 5.00, N, 9.92. Found: C, 68.04; H, 4.97; N, 10.02.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05624937uspto-grants-1997_04