Reacción #95595

ord-3e3aa5f130f14bf1a33e3cd58dbcc0c4

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaheated
  2. 2
    Temperaturaunder reflux for 0.5 hour
  3. 3
    TemperaturaAfter cooling
  4. 4
    Filtraciónthe separated material is filtered off under suction
  5. 5
    Otrorecrystallised from ethanol

Procedimiento

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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04346030uspto-grants-1982_08