Reaktion #431875

ord-51fd0243d6b04062a1810d51847ac00e

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturthe whole is heated
  2. 2
    Temperaturunder reflux for 10 hours
  3. 3
    TemperaturAfter cooling
  4. 4
    Sonstigedecanting
  5. 5
    workup.ADDITIONether is added
  6. 6
    Filtrationafter filtering

Vorschrift

5 g of 3-(5-methyloxazol-2-yl)-pyridine prepared as indicated in Chimica Therap 4, 437 (1973) is dissolved in 50 cm3 of ethanol, 3 cm3 of iodomethane is added and the whole is heated under reflux for 10 hours. After cooling and decanting, ether is added, and after filtering, 8.68 g of product is obtained. M.p.=147°-148° C., after crystallization from ethanol.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05053416uspto-grants-1991_10