HRID1357920

反应详情

EQUATION

反应方程式

HRID 1357920 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

To a slurry of sodium hydride (47 mg, 60% in mineral oil, 1.2 mmol) in tetrahydrofuran at 0° C. was added 4-fluorothiophenol (0.1 mL, 0.94 mmol). The reaction mixture was warmed to rt. for 20 min, followed by addition of 4-(2-iodoeth-1-yl)-1-tert-butoxycarbonylpiperidine (265 mg, 0.78 mmol, from Step C). The reaction was then heated to reflux for 10 min, cooled and diluted with ether. The organic layer was washed with 1 N NaOH, dried over magnesium sulfate and concentrated to provide 252 mg (95%) of the title compound. ESI-MS: 340.0 (M+H); HPLC A: 4.07 min.

WORKUP

后处理

  1. temperatureThe reaction was then heated
  2. temperatureto reflux for 10 min
  3. temperaturecooled
  4. washThe organic layer was washed with 1 N NaOH
  5. dry with materialdried over magnesium sulfate
  6. concentrationconcentrated