HRID541896

反应详情

EQUATION

反应方程式

HRID 541896 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
60 °C

PROCEDURE

实验过程

Into the reaction flask was added tert-butyl [3-({2-[(tert-butoxycarbonyl)amino]-5-nitrophenyl}ethynyl)phenyl]carbamate (2.7 g, 6.0 mmol), methanol (70 mL), acetic acid (10 mL), and water (7 mL). Then iron powder (1.8 g, 30 mmol) was added. The reaction mixture was heated at 60° C. for 3 h. After filtration, the cake was rinsed with EtOAc. The filtrate was concentrated and the residue was diluted with NaHCO3 (aq) and EtOAc. After the layers were separated, the organic layer was dried, filtered and concentrated to give the desired product (2.3 g, 91%). LCMS for C24H30N3O4 (M+H)+: m/z=424.2.

WORKUP

后处理

  1. filtrationAfter filtration
  2. washthe cake was rinsed with EtOAc
  3. concentrationThe filtrate was concentrated
  4. additionthe residue was diluted with NaHCO3 (aq) and EtOAc
  5. customAfter the layers were separated
  6. customthe organic layer was dried
  7. filtrationfiltered
  8. concentrationconcentrated