反应详情

The compound (202 mg) obtained in Example 129-1 was dissolved in carbon tetrachloride (7.1 ml) and added with N-bromosuccinimide (205 mg) and azobisisobutyronitrile (15.8 mg), followed by thermal reflux for 20 hours. The solution was further added with carbon tetrachloride (7.0 ml) and N-bromosuccinimide (51.3 mg), followed by thermal reflux for 4 hours. After having been stood to cool, the solution was added with water and then subjected to extraction with chloroform. The organic layer was washed with water and saturated saline solution and then dried with anhydrous sodium sulfate. The solvent was distilled off and the residue was then dissolved in DMF (5.8 ml). The solution was added with potassium phthalimide (359 mg) and stirred at room temperature for 16 hours. The residue obtained by distilling the solvent off was purified through silica gel column chromatography (hexane/ethyl acetate), thereby obtaining the subject compound (226 mg) as a white solid.

1. temperatureby thermal reflux for 20 hours
2. temperatureby thermal reflux for 4 hours
3. temperatureto cool
4. extractionsubjected to extraction with chloroform
5. washThe organic layer was washed with water and saturated saline solution
6. dry with materialdried with anhydrous sodium sulfate
7. distillationThe solvent was distilled off
8. dissolutionthe residue was then dissolved in DMF (5.8 ml)
9. additionThe solution was added with potassium phthalimide (359 mg)
10. customThe residue obtained
11. distillationby distilling the solvent
12. customoff was purified through silica gel column chromatography (hexane/ethyl acetate)