HRID1623266

反应详情

EQUATION

反应方程式

HRID 1623266 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
117.5 °C

PROCEDURE

实验过程

A mixture of 2,6-dibromopyridine (7.1 g, 30.0 mmol), NMP (16 ml), (3-fluorophenyl)methanamine (4.13 g, 33.0 mmol) and Hunig's Base (5.76 ml, 33.0 mmol) was flushed with argon. The crude reaction mixture was stirred at 115-120° C. for about 168 hours. LC/MS was used to monitor the reaction. The crude mixture was then cooled to room temperature, and then diluted with 250 ml of ethyl acetate, washed with saturated sodium bicarbonate (2×), water (2×), saturated. salt solution (1×), dried over sodium sulfate, filtered, and concentrated under reduced pressure to yield a residue. The residue was purified by silica gel chromatography using a 120 g column, eluting from 0%-20% ethyl acetate with hexane. The desired fractions were concentrated to yield, 7.11 grams of the titled compound as a free base, which was used in the next step without further purification. LCMS (m/z): 281.1/283.1 (MH+), retention time=1.03 min.

WORKUP

后处理

  1. customwas flushed with argon
  2. customThe crude reaction mixture
  3. customthe reaction
  4. washwashed with saturated sodium bicarbonate (2×), water (2×)
  5. dry with materialsalt solution (1×), dried over sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure
  8. customto yield a residue
  9. customThe residue was purified by silica gel chromatography
  10. washeluting from 0%-20% ethyl acetate with hexane
  11. concentrationThe desired fractions were concentrated
  12. customto yield
  13. custom7.11 grams of the titled compound as a free base, which was used in the next step without further purification