HRID388046

反应详情

EQUATION

反应方程式

HRID 388046 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

tert-Butyl 4-(((4-(4-amino-3-fluorophenoxy)-6-cyano-7-quinolyl)oxy)methyl)-1-piperidinecarboxylate (523 mg), pyridine (0.17 ml) and tetrahydrofuran (10 ml) were stirred while cooling on ice, and then phenyl chloroformate was added dropwise. Immediately after completion of the dropwise addition, the cooling bath was removed and the mixture was returned to room temperature. After 15 minutes of stirring, water and ethyl acetate were added for extraction. Silica gel was added to the extract and the solvent was distilled off under reduced pressure for adsorption. The reaction solution-adsorbed silica gel was purified by column chromatography (hexane:ethyl acetate=1:1, followed by 1:2, ethyl acetate) in a dry column packed with silica gel, to obtain 490 mg of a yellow powder.

WORKUP

后处理

  1. temperaturewhile cooling on ice
  2. additionImmediately after completion of the dropwise addition
  3. customthe cooling bath was removed
  4. customwas returned to room temperature
  5. additionwater and ethyl acetate were added for extraction
  6. additionSilica gel was added to the
  7. extractionextract
  8. distillationthe solvent was distilled off under reduced pressure for adsorption
  9. customThe reaction solution-adsorbed silica gel
  10. customwas purified by column chromatography (hexane:ethyl acetate=1:1, followed by 1:2, ethyl acetate) in a dry column