反応 #3683
ord-02ea72ab16be477a9f0a58c1ebfcfb1d
反応方程式
5,10-dihydro-4H-pyrazolo[5,1-c][1,4]benzodiazepine
4-[(5-fluoro-2-methylbenzoyl)amino]-2-chlorobenzoyl chloride
diisopropylethylamine
→
N-[4-(4H-Pyrazolo[5,1-c][1,4]benzodiazepin-5(10H)-ylcarbonyl)-3-chlorophenyl]-5-fluoro-2-methylbenzamide
反応物
試薬
なし
反応条件
詳細条件
See reaction.notes.procedure_details.
後処理
- 1洗浄The mixture is washed with H2 O, 1N HCl, H2O, 1M NaHCO3, brine
- 2乾燥dried (Na2SO4)
- 3洗浄the filter cake washed with dichloromethane
- 4濃縮The filtrate is concentrated
- 5その他the solid crystallized from ethyl acetate
- 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.