반응 #49410
ord-38c09a0431ed4c53b9a84c646106aade
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반응 조건
상세 조건
See reaction.notes.procedure_details.
후처리
- 1기타The solvent was evaporated under reduced pressure
- 2기타the residue was purified by thin-layer chromatography (chloroform/methanol=6/1)
실험 절차
4-Ethenesulfonyloxy-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone (0.0734 g, 0.133 mmol) was dissolved in methanol (1.5 mL), and the solution was added with 70% aqueous ethylamine solution (1.5 mL), followed by stirring at room temperature for 5 hours. The solvent was evaporated under reduced pressure and the residue was purified by thin-layer chromatography (chloroform/methanol=6/1) to obtain 4-[2-(ethylamino)ethanesulfonyloxy]-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone (0.0338 g, 43%).