HRID1882961

反应详情

EQUATION

反应方程式

HRID 1882961 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
70 °C

PROCEDURE

实验过程

A solution containing 2-(1-Boc-piperidin-4-yl-methylidene)amino-N-(5-chloropyridin-2-yl)-5-fluorobenzamide from above (6.0 g, 13 mmol) and borane trimethylamine complex (2.9 g, 39 mmol) in glacial acetic acid (100 mL) was heated at 70° C. for 24 h. The solution was allowed to cool to room temperature; then the solvent was removed in vacuo, and the residue was partitioned between dichloromethane (200 mL) and water (100 mL). The biphasic mixture was treated with 2 N NaOH until neutral; then the organic layer was separated and the aqueous layer was washed again with dichloromethane (100 mL). The combined organic layers were washed with brine (100 mL), dried with MgSO4, and filtered. The filtrate was concentrated in vacuo to give 5.85 g (97%) of the title compound as an orange foam which was used directly in the next step without further purification.

WORKUP

后处理

  1. temperatureto cool to room temperature
  2. customthen the solvent was removed in vacuo
  3. customthe residue was partitioned between dichloromethane (200 mL) and water (100 mL)
  4. additionThe biphasic mixture was treated with 2 N NaOH until neutral
  5. customthen the organic layer was separated
  6. washthe aqueous layer was washed again with dichloromethane (100 mL)
  7. washThe combined organic layers were washed with brine (100 mL)
  8. dry with materialdried with MgSO4
  9. filtrationfiltered
  10. concentrationThe filtrate was concentrated in vacuo