Reaktion #75012

Reaktionsgleichung

3,4-dihydro-2-methyl-3-oxo-2H-thieno[2,3-e]1,2-thiazine 1,1-dioxide

dimethylsulfoxide

4-bromophenyl isocyanate

→

4'-bromo-3-hydroxy-2-methyl-2H-thieno[2,3-e]1,2-thiazine-4-carboxanilide 1,1-dioxide

Lösungsmittel

triethylamine

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.ADDITIONThis mixture is then poured into 225 ml
2. 2
   Filtrationof 3-N hydrochloric acid and the prepcipitate which separates out is filtered on a sinter
3. 3
   Filtrationfilter
4. 4
   Waschenwashed three times with 20 ml
5. 5
   Trocknenof distilled water each time and dried as much as possible
6. 6
   workup.DISSOLUTIONThe precipitate is dissolved in 250 ml
7. 7
   Trocknenof methylene chloride, dried over sodium sulfate
8. 8
   workup.STIRRINGstirred with activated charcoal
9. 9
   Filtrationfiltered
10. 10
    workup.STIRRINGThe organic phase is shaken out four times with 250 ml
11. 11
    workup.STIRRINGof saturated sodium bicarbonate solution each time and the aqueous phase is shaken again each time with a little methylene chloride
12. 12
    ExtraktionThe product which separates out is extracted three times with 250 ml
13. 13
    TrocknenThe combined organic phases are dried over sodium sulfate
14. 14
    workup.STIRRINGstirred with activated charcoal
15. 15
    Filtrationfiltered
16. 16
    Sonstigethe solvent is removed by distillation
17. 17
    workup.DISSOLUTIONThe crystalline residue is dissolved in 50 ml
18. 18
    workup.ADDITIONactivated charcoal is added
19. 19
    Filtrationthe mixture is filtered hot
20. 20
    Sonstigeto crystallize
21. 21
    SonstigeThe crystals are removed by filtration
22. 22
    Sonstigeis obtained

Vorschrift

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.

Quelle