HRID1370652

反应详情

EQUATION

反应方程式

HRID 1370652 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

5

PROCEDURE

实验过程

A suspension of sodium 4-(4-pyridyl)benzoate (425 mg, 1.92 mmol) in methylene chloride was treated with oxalyl chloride (0.840 mL, 9.60 mmol), followed by dimethylformamide (0.01 mL)). After 0.75 h, the mixture was concentrated in vacuo. The residue was then dissolved in methylene chloride and added dropwise to a solution of N4-(tert-butyloxycarbonyl)-3,4-pyridinediamine (400 mg, 1.92 mmol) and pyridine (0.31 mL) in methylene chloride (2 mL) and tetrahydrofuran (1 mL). After 16 h, the mixture was poured into ethyl acetate and 1 N aqueous sodium hydroxide. The organic layer was washed once with 1 N aqueous sodium hydroxide, once with saturated sodium chloride solution, dried (potassium carbonate), and filtered. The residue was purified by flash chromatography (silica gel, ethyl acetate/hexanes) to yield 75 mg (10%) of the title compound.

WORKUP

后处理

  1. concentrationthe mixture was concentrated in vacuo
  2. dissolutionThe residue was then dissolved in methylene chloride
  3. waitAfter 16 h
  4. washThe organic layer was washed once with 1 N aqueous sodium hydroxide, once with saturated sodium chloride solution
  5. dry with materialdried (potassium carbonate)
  6. filtrationfiltered
  7. customThe residue was purified by flash chromatography (silica gel, ethyl acetate/hexanes)