HRID401763

反应详情

EQUATION

反应方程式

HRID 401763 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
-78 °C

PROCEDURE

实验过程

N-(2,4-dimethoxybenzyl)-1,3-thiazol-2-amine (Preparation 6, 961 mg, 3.84 mmol, 1.0 eq) was suspended in THF (10 ml) and stirred at −78° C. for 10 minutes. 1,1,1,3,3,3-Hexanemethyldisilazane lithium salt (LiHMDS, 1M in THF, 4.2 ml, 4.2 mmol, 1.1 eq) was added dropwise maintaining the temperature below −70° C. and the reaction mixture stirred for a further 30 minutes. A solution of methyl 5-(chlorosulfonyl)pyridine-2-carboxylate (Preparation 16, 1 g, 3.8 mmol, 1 eq) in THF (5 ml) was added dropwise maintaining the reaction temperature below −72° C. and the reaction mixture allowed to warm to room temperature for 2 hours. The reaction mixture was diluted with water (10 ml), extracted into ethyl acetate (5 ml), dried over sodium sulphate, filtered and evaporated in vacuo. The crude material was dissolved in dioxane (5 ml), a solution of sodium hydroxide (311 mg, 7.77 mmol, 2 eq) in water (2 ml) was added and the reaction mixture stirred at room temperature for 30 minutes. The MeOH was evaporated and the remaining aqueous solution washed with ethyl acetate (10 ml). Brine (10 ml) was added to the aqueous phase and the solution extracted with ethyl acetate (10 ml). A precipitate formed in the organic phase which was collected by filtration to yield the title compound as a white solid (415 mg, 0.95 mmol, 25%).

WORKUP

后处理

  1. temperaturemaintaining the temperature below −70° C.
  2. stirringthe reaction mixture stirred for a further 30 minutes
  3. temperaturemaintaining the reaction temperature below −72° C.
  4. temperatureto warm to room temperature for 2 hours
  5. extractionextracted into ethyl acetate (5 ml)
  6. dry with materialdried over sodium sulphate
  7. filtrationfiltered
  8. customevaporated in vacuo
  9. dissolutionThe crude material was dissolved in dioxane (5 ml)
  10. stirringthe reaction mixture stirred at room temperature for 30 minutes
  11. customThe MeOH was evaporated
  12. washthe remaining aqueous solution washed with ethyl acetate (10 ml)
  13. additionBrine (10 ml) was added to the aqueous phase
  14. extractionthe solution extracted with ethyl acetate (10 ml)
  15. customA precipitate formed in the organic phase which
  16. filtrationwas collected by filtration