反応 #3683

ord-02ea72ab16be477a9f0a58c1ebfcfb1d

反応方程式

c1ccc2c(c1)Cn1nccc1CN2
5,10-dihydro-4H-pyrazolo[5,1-c][1,4]benzodiazepine
Cc1ccc(F)cc1C(=O)Nc1ccc(C(=O)Cl)c(Cl)c1
4-[(5-fluoro-2-methylbenzoyl)amino]-2-chlorobenzoyl chloride
CCN(C(C)C)C(C)C
diisopropylethylamine
Cc1ccc(F)cc1C(=O)Nc1ccc(C(=O)N2Cc3ccnn3Cc3ccccc32)c(Cl)c1
N-[4-(4H-Pyrazolo[5,1-c][1,4]benzodiazepin-5(10H)-ylcarbonyl)-3-chlorophenyl]-5-fluoro-2-methylbenzamide

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    洗浄The mixture is washed with H2 O, 1N HCl, H2O, 1M NaHCO3, brine
  2. 2
    乾燥dried (Na2SO4)
  3. 3
    洗浄the filter cake washed with dichloromethane
  4. 4
    濃縮The filtrate is concentrated
  5. 5
    その他the solid crystallized from ethyl acetate
  6. 6
    その他to give crystals, m.p. 137°-140° C.

実験手順

A mixture of 0.185 g of 5,10-dihydro-4H-pyrazolo[5,1-c][1,4]benzodiazepine, 0.391 g of 4-[(5-fluoro-2-methylbenzoyl)amino]-2-chlorobenzoyl chloride and 0.158 g of diisopropylethylamine in 10 ml of dichloromethane is stirred at room temperature overnight. The mixture is washed with H2 O, 1N HCl, H2O, 1M NaHCO3, brine and dried (Na2SO4). The solution is passed through a thin pad of hydrous magnesium silicate and the filter cake washed with dichloromethane. The filtrate is again passed through a thin pad of hydrous magnesium silicate. The filtrate is concentrated and the solid crystallized from ethyl acetate to give crystals, m.p. 137°-140° C.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05733905uspto-grants-1998_03