Reaktion #215200

ord-746b25b0ff0343ab96d3cfe18e29f42f

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeAfter completion of the reaction
  2. 2
    workup.ADDITIONthe mixture was poured into ice-cold water
  3. 3
    Filtrationthe precipitated crystals were filtered off
  4. 4
    Sonstigerecrystallized from a mixture of ethanol and water

Vorschrift

To a mixture of 6 g of 6-(5-methyl-3-oxo-2,3,4,5-tetrahydropyridazin-6-yl)-1,4,4-trimethyl-1,2,3,4-tetrahydroquinolin-2-one and 60 ml of dimethylformamide was added 1.8 g of sodium hdyride. After 30 minutes, 4.6 g of butyl bromide was added to the mixture and the whole mixture was stirred for one hour. After completion of the reaction, the mixture was poured into ice-cold water and the precipitated crystals were filtered off and recrystallized from a mixture of ethanol and water to give 5.2 g of 6-(2-butyl-5-methyl-3-oxo-2,3,4,5-tetrahydropyridazin-6-yl)-1,4,4-trimethyl-1,2,3,4-tetrahydroquinolin-2-one, melting at 137°-139° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04258185uspto-grants-1981_03