反応 #95595

ord-3e3aa5f130f14bf1a33e3cd58dbcc0c4

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度heated
  2. 2
    温度under reflux for 0.5 hour
  3. 3
    温度After cooling
  4. 4
    ろ過the separated material is filtered off under suction
  5. 5
    その他recrystallised from ethanol

実験手順

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.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US04346030uspto-grants-1982_08