Réaction #4926

ord-9d16c145823b4fd287c4a6545f748c2d

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    FiltrationThe resulting solution was filtered
  2. 2
    Concentrationconcentrated
  3. 3
    workup.DISSOLUTIONThe residue was dissolved in isopropyl alcohol
  4. 4
    workup.ADDITIONa few drops of ethereal hydrogen chloride were added
  5. 5
    AutreThe hydrochloride salt crystals were recrystallized
  6. 6
    workup.DISSOLUTIONby dissolving in ethyl alcohol
  7. 7
    Autreabove 200° C.

Mode opératoire

To a solution of 0.5 g (0.002 mole) of 2-(2-chloroethyl)-2,3-dihydro-4-methylpyrido[4,3-f][1,4]-oxazepine-5(4H)-thione in 20 ml of ethyl alcohol was added 2 ml of 40% aqueous dimethylamine. The mixture was heated in a steel bomb to 100° C. for 14 hr. The resulting solution was filtered and concentrated. The residue was dissolved in isopropyl alcohol and a few drops of ethereal hydrogen chloride were added. The hydrochloride salt crystals were recrystallized by dissolving in ethyl alcohol and boiling while replacing the ethyl alcohol with isopropyl alcohol. The yield of product was 0.3 g (47%), m.p.: decomp. above 200° C.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US04727152uspto-grants-1988_02