反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- 110 °C
PROCEDURE
实验过程
A mixture of 0.16 g of 10-[(6-chloro-3-pyridinyl)carbonyl]-10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepine, 0.5 ml of benzylamine and 0.2 ml of N,N'-dimethylpropyleneurea is stirred and heated at 110° C. for 7 hours. After cooling to room temperature, the mixture is washed with hexane (3 times 10 ml). The residue is dissolved in water and made alkaline with 1N NaOH. The suspension is washed with H2O and extracted with ethyl acetate. The organic extract is washed with brine, dried (Na2SO4) and filtered through a thin pad of hydrous magnesium silicate. The filtrate is evaporated and the residue triturated with diethyl ether-hexane to give 0.20 g of white solid; mass spectrum (CI) 395 (M+H).
WORKUP
后处理
- temperatureAfter cooling to room temperature
- washthe mixture is washed with hexane (3 times 10 ml)
- dissolutionThe residue is dissolved in water
- washThe suspension is washed with H2O
- extractionextracted with ethyl acetate
- extractionThe organic extract
- washis washed with brine
- dry with materialdried (Na2SO4)
- filtrationfiltered through a thin pad of hydrous magnesium silicate
- customThe filtrate is evaporated
- customthe residue triturated with diethyl ether-hexane