반응 #1099226
ord-4170cd07da2d42498a2c48950e0b8e3e
반응 방정식
반응물
시약
없음
용매
반응 조건
온도
0°CELSIUS
상세 조건
See reaction.notes.procedure_details.
후처리
- 1workup.ADDITIONAfter the addition
- 2온도the reaction mixture was heated
- 3온도under reflux for 4 hours
- 4온도to cool to room temperature
- 5workup.STIRRINGstirred overnight
- 6온도After further cooling in an ice bath the formed precipitate
- 7여과was filtered off
- 8세척washed with a little cold THF
- 9기타dried at 40° C. in vacuum
실험 절차
0.32 g (0.62 mmol) 2-{[2-((E)-{4-[ethyl(2-hydroxyethyl)amino]phenyl}-diazenyl)-4-(1-piperidinyl)-1,3-thiazol-5-yl]methylene}-1H-indene-1,3(2H)-dione were dissolved in 33 ml THF and cooled to 0° C. Then 0.11 g (0.93 mmol) chlorosulfonic acid were added slowly drop by drop with stirring. After the addition was completed, the reaction mixture was heated under reflux for 4 hours, allowed to cool to room temperature and stirred overnight. After further cooling in an ice bath the formed precipitate was filtered off, washed with a little cold THF and dried at 40° C. in vacuum.