HRID2247636

反应详情

EQUATION

反应方程式

HRID 2247636 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

PROCEDURE

实验过程

To a solution of 5-({[t-butyl(dimethyl)silyl]oxy}methyl)-N′-hydroxyfuran-3-carboximidamide (0.14 g, 0.50 mmol) that was obtained in Example 1 (1d) and 4-phenyl-5-(trifluoromethyl)thiophene-2-carbonyl chloride (0.17 g, 0.60 mmol) in dichloromethane (10 ml) was added N,N-diisopropylethylamine (0.17 ml, 1.0 mmol) at 0° C. with stirring, and the resulting mixture was stirred for 1 hour. After stirring, a saturated aqueous solution of sodium hydrogencarbonate (1.0 ml) was added to the reaction mixture to quench the reaction, and the resulting mixture was poured into water (20 ml) and extracted with ether. The extract was washed with a saturated aqueous solution of sodium chloride and dried over magnesium sulfate. After filtration, the filtrate was evaporated in vacuo. Subsequently, to a solution of the residue obtained in tetrahydrofuran (1.0 ml) was added tetrabutylammonium fluoride (a 1.0 M solution in tetrahydrofuran, 0.75 ml, 0.75 mmol) with stirring, and the resulting mixture was stirred at 60° C. for 3 hours. After stirring, the reaction mixture was poured into water (20 ml) to quench the reaction and extracted with ether. The extract was washed with a saturated aqueous solution of sodium chloride and dried over magnesium sulfate. After filtration, the filtrate was evaporated in vacuo, and the crude product of the title compound thus obtained was purified by chromatography on a silica gel column using a mixed solvent of ethyl acetate and hexane (1:1) as the eluent to afford the title compound (0.20 g) in a yield of 10% as a white crystalline solid.

WORKUP

后处理

  1. stirringthe resulting mixture was stirred for 1 hour
  2. stirringAfter stirring
  3. customto quench
  4. customthe reaction
  5. extractionextracted with ether
  6. washThe extract was washed with a saturated aqueous solution of sodium chloride
  7. dry with materialdried over magnesium sulfate
  8. filtrationAfter filtration
  9. customthe filtrate was evaporated in vacuo
  10. customSubsequently, to a solution of the residue obtained in tetrahydrofuran (1.0 ml)
  11. stirringwith stirring
  12. stirringthe resulting mixture was stirred at 60° C. for 3 hours
  13. stirringAfter stirring
  14. customto quench
  15. customthe reaction
  16. extractionextracted with ether
  17. washThe extract was washed with a saturated aqueous solution of sodium chloride
  18. dry with materialdried over magnesium sulfate
  19. filtrationAfter filtration
  20. customthe filtrate was evaporated in vacuo