HRID1864814

反应详情

EQUATION

反应方程式

HRID 1864814 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
115 °C

PROCEDURE

实验过程

To a solution of methyl 2-{[(2R)-2-[(tert-butylsulfinyl)amino]-2-(3,5-difluorophenyl)ethyl]thio}-2-methylpropanoate from Step C (428 mg, 1.09 mmol) in MeOH (20 mL), cooled to 0° C., was added anhydrous HCl gas for 1 minute. The reaction was sealed and allowed to sit at 0° C. for fifteen minutes, after which nitrogen was bubbled through the reaction for twenty minutes. The reaction was concentrated in vacuo. Additional MeOH (30 mL) was added and it was again concentrated in vacuo. This was repeated with another addition of MeOH and triethylamine (440. mg, 4.35 mmol). To the resulting residue was added toluene (10 mL) and triethylamine (440. mg, 4.35 mmol). A reflux condenser was attached and the mixture stirred at 115° C. After one week of stirring, the reaction was judged to be 90% complete by LCMS. The mixture was cooled to ambient temperature and concentrated in vacuo. The residue was diluted with diethyl ether (50 mL) and washed individually with 20 mL of each of the following aqueous solutions: 1 M HCl (twice), water, and saturated brine. The organic layer was then dried over sodium sulfate, filtered, and concentrated in vacuo to give a residue that was purified by silica gel chromatography, eluting with a gradient of MeOH:CH2Cl2-1:99 to 5:95, to give the title compound. MS: m/z=258 (M+1).

WORKUP

后处理

  1. customThe reaction was sealed
  2. waitto sit at 0° C. for fifteen minutes
  3. customafter which nitrogen was bubbled through the reaction for twenty minutes
  4. concentrationThe reaction was concentrated in vacuo
  5. additionAdditional MeOH (30 mL) was added
  6. concentrationit was again concentrated in vacuo
  7. customA reflux condenser was attached
  8. stirringAfter one week of stirring
  9. temperatureThe mixture was cooled to ambient temperature
  10. concentrationconcentrated in vacuo
  11. additionThe residue was diluted with diethyl ether (50 mL)
  12. washwashed individually with 20 mL of each of the following aqueous solutions
  13. dry with materialThe organic layer was then dried over sodium sulfate
  14. filtrationfiltered
  15. concentrationconcentrated in vacuo
  16. customto give a residue that
  17. customwas purified by silica gel chromatography
  18. washeluting with a gradient of MeOH