HRID46734

反应详情

EQUATION

反应方程式

HRID 46734 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

3.1 G. of 3,4-dihydro-2-methyl-3-oxo-2H-thieno[2,3-e]1,2-thiazine 1,1-dioxide are dissolved in 31 ml. of absolute dimethylsulfoxide under an atmosphere of nitrogen. 1.44 G. of freshly distilled triethylamine and 2.83 g. of 4-bromophenyl isocyanate are added to the solution and the mixture is then stirred for 24 hours at room temperature. This mixture is then poured into 225 ml. of 3-N hydrochloric acid and the prepcipitate which separates out is filtered on a sinter filter, washed three times with 20 ml. of distilled water each time and dried as much as possible. The precipitate is dissolved in 250 ml. of methylene chloride, dried over sodium sulfate, stirred with activated charcoal and filtered. The organic phase is shaken out four times with 250 ml. of saturated sodium bicarbonate solution each time and the aqueous phase is shaken again each time with a little methylene chloride. The combined aqueous phases are rendered strongly acid with concentrated hydrochloric acid. The product which separates out is extracted three times with 250 ml. of methylene chloride each time. The combined organic phases are dried over sodium sulfate, stirred with activated charcoal, filtered and the solvent is removed by distillation. The crystalline residue is dissolved in 50 ml. of chloroform. While boiling, activated charcoal is added and the mixture is filtered hot. The product is made to crystallize by scratching. The crystals are removed by filtration, digested with a little cold chloroform, and 4'-bromo-3-hydroxy-2-methyl-2H-thieno[2,3-e]1,2-thiazine-4-carboxanilide 1,1-dioxide, melting point 178° C. to 179° C. (decomposition), is obtained.

WORKUP

后处理

  1. additionThis mixture is then poured into 225 ml
  2. filtrationof 3-N hydrochloric acid and the prepcipitate which separates out is filtered on a sinter
  3. filtrationfilter
  4. washwashed three times with 20 ml
  5. dry with materialof distilled water each time and dried as much as possible
  6. dissolutionThe precipitate is dissolved in 250 ml
  7. dry with materialof methylene chloride, dried over sodium sulfate
  8. stirringstirred with activated charcoal
  9. filtrationfiltered
  10. stirringThe organic phase is shaken out four times with 250 ml
  11. stirringof saturated sodium bicarbonate solution each time and the aqueous phase is shaken again each time with a little methylene chloride
  12. extractionThe product which separates out is extracted three times with 250 ml
  13. dry with materialThe combined organic phases are dried over sodium sulfate
  14. stirringstirred with activated charcoal
  15. filtrationfiltered
  16. customthe solvent is removed by distillation
  17. dissolutionThe crystalline residue is dissolved in 50 ml
  18. additionactivated charcoal is added
  19. filtrationthe mixture is filtered hot
  20. customto crystallize
  21. customThe crystals are removed by filtration
  22. customis obtained