Reaktion #95791

ord-22be1726fadb4acbaeeae2c9b2d8fc0c

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturheated
  2. 2
    Temperaturunder reflux for 0.5 hour
  3. 3
    TemperaturAfter cooling
  4. 4
    Filtrationthe separated material is filtered off under suction
  5. 5
    Sonstigerecrystallised from ethanol

Vorschrift

4.1 g of ethyl α-amino-1,3,4,5-tetrahydro-5-oxo-2H-1,4-benzodiazepin-2-ylidene-acetate are dissolved in 25 ml of ethyl acetate, treated with 3.1 ml (18.1 mmol) of N,N-dimethylformamide diethyl acetal and heated to boiling under reflux for 0.5 hour. After cooling, the separated material is filtered off under suction and recrystallised from ethanol. After chromatography of the mother liquor, there is obtained a second portion of ethyl 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate of the same purity; melting point 166°-168° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04346033uspto-grants-1982_08