反应详情

A solution of racemic (2′S,3S,4′R)-6-chloro-4′-[5-fluoro-2-(1-hydroxycarbonyl-1-methyl-ethoxy)-phenyl]-2′-(5-fluoro-2-methyl-phenyl)spiro[3H-indole-3,3′-piperidine]-2,6′(1H)-dione (100 mg, 0.18 mmol) and CDI (58 mg, 0.36 mmol) in DMF (5 mL) was heated at 60° C. for 0.5 h. Then to this solution was added a mixture of methanesulfonamide (475 mg, 5 mmol) and NaH (200 mg, 60%, 5 mmol) in DMF (5 mL), which had been stirred for 1 h at room temperature. After the resulting mixture was stirred at room temperature for 0.5 h, it was poured into water (5 mL) and the aqueous solution was acidified to “pH” 2-3 by concentrated aqueous hydrochloride. After the aqueous phase was extracted with EtOAc twice, the combined organic phases were dried over anhydrous Na2SO4, concentrated and the residue was purified by flash column to give the title compound as a white solid (80 mg).

1. additionThen to this solution was added
2. stirringAfter the resulting mixture was stirred at room temperature for 0.5 h
3. extractionAfter the aqueous phase was extracted with EtOAc twice
4. dry with materialthe combined organic phases were dried over anhydrous Na2SO4
5. concentrationconcentrated
6. customthe residue was purified by flash column