反应详情

A solution of methyl 3-cyclohexyl-2-(2-hydroxyphenyl)-1H-indole-6-carboxylate (prepared as described in International patent application publication WO2006/046030)(0.15 M) in DMF was treated with CsF (4 eq) in one portion; the resulting mixture was stirred for 20 min at RT then treated via dropping funnel over 30 min with a solution of tert-butyl (2R)-2-({[(4-nitrophenyl)sulfonyl]oxy}methyl)aziridine-1-carboxylate (1.3 eq) in DMF (0.5 M). The resulting solution was stirred at RT overnight. The reaction mixture was then placed into an ice bath and powdered KOtBu (1.4 eq) added slowly to the reaction mixture. After 1.5 h, the reaction was quenched with sat. aq. NH4C1 and extracted into EtOAc. The combined organic layers were washed with water and brine, before being dried over Na2SO4, filtered and concentrated in vacuo. The crude material was purified by FC (PE/EtOAc 80:20) affording the product as an off-white foam (85%). (ES+) m/z 505 (M+H)+

1. additionthen treated
2. customover 30 min
3. stirringThe resulting solution was stirred at RT overnight
4. customThe reaction mixture was then placed into an ice bath
5. waitAfter 1.5 h
6. customthe reaction was quenched with sat. aq. NH4C1
7. extractionextracted into EtOAc
8. washThe combined organic layers were washed with water and brine
9. dry with materialbefore being dried over Na2SO4
10. filtrationfiltered
11. concentrationconcentrated in vacuo
12. customThe crude material was purified by FC (PE/EtOAc 80:20)