반응 #1099226

ord-4170cd07da2d42498a2c48950e0b8e3e

용매

반응 조건

온도
0°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONAfter the addition
  2. 2
    온도the reaction mixture was heated
  3. 3
    온도under reflux for 4 hours
  4. 4
    온도to cool to room temperature
  5. 5
    workup.STIRRINGstirred overnight
  6. 6
    온도After further cooling in an ice bath the formed precipitate
  7. 7
    여과was filtered off
  8. 8
    세척washed with a little cold THF
  9. 9
    기타dried 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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07977482B2uspto-grants-2011_07