HRID263480

反应详情

EQUATION

反应方程式

HRID 263480 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

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

  1. customTo a 250 ml round-bottomed flask equipped with N2 inlet
  2. temperatureThe reaction mixture was then cooled
  3. customseparated
  4. extractionthe aqueous phase was again extracted
  5. washThe combined extracts were washed with water three times, with bicarbonate solution once
  6. dry with materialdried with brine and sodium sulfate
  7. filtrationfiltered
  8. customevaporated
  9. customleaving a gummy residue, 8.58 g (100%)
  10. additioncontaining some solvent