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
- 75 °C
PROCEDURE
实验过程
To a 250 ml round-bottomed flask equipped with N2 inlet were added N-tert-butyl-2-[3-bromo-2-oxo-5-phenyl-2,3,4,5-tetrahydro-1H-(1)benzazepin-1-yl]ethanoic acid amide, (8.317 g, 19.37 mmoles), 90 ml dimethylformamide (DMF), and sodium azide (5.25 g, 80 mmoles, under nitrogen), and the mixture was heated at 75° C. for 20 hours with stirring. The reaction mixture was then cooled and distributed between water and ethyl acetate, separated, and the aqueous phase was again extracted. The combined extracts were washed with water three times, with bicarbonate solution once, and then dried with brine and sodium sulfate and filtered and evaporated, leaving a gummy residue, 8.58 g (100%), containing some solvent.
WORKUP
后处理
- customTo a 250 ml round-bottomed flask equipped with N2 inlet
- temperatureThe reaction mixture was then cooled
- customseparated
- extractionthe aqueous phase was again extracted
- washThe combined extracts were washed with water three times, with bicarbonate solution once
- dry with materialdried with brine and sodium sulfate
- filtrationfiltered
- customevaporated
- customleaving a gummy residue, 8.58 g (100%)
- additioncontaining some solvent