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
- 100 °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, 40 mg of pyridine and 2 ml of 2-methylpropylamine is stirred and heated at 100° C. in a sealed vessel for 1 hour. To the mixture is added 0.2 ml of N,N-dimethylpropyleneurea and the mixture is heated at 110° C. for 7 hours. The volatiles are removed under vacuum and 10 ml of 0.5N NaOH is added to the residue. The mixture is filtered and the solid washed with water and then hexane. The solid is dissolved in ethyl acetate and the solution washed with 0.5N NaOH, brine and dried (Na2SO4). The solution is filtered through a thin pad of hydrous magnesium silicate and the filtrate concentrated to dryness. The residue is triturated with diisopropylether-hexane to give 0.18 g of white solid; mass spectrum (CI) 361 (M+H).
WORKUP
后处理
- temperaturethe mixture is heated at 110° C. for 7 hours
- customThe volatiles are removed under vacuum and 10 ml of 0.5N NaOH
- additionis added to the residue
- filtrationThe mixture is filtered
- washthe solid washed with water
- dissolutionThe solid is dissolved in ethyl acetate
- washthe solution washed with 0.5N NaOH, brine
- dry with materialdried (Na2SO4)
- filtrationThe solution is filtered through a thin pad of hydrous magnesium silicate
- concentrationthe filtrate concentrated to dryness
- customThe residue is triturated with diisopropylether-hexane