反应详情

4-Morpholin-4-yl-4-oxo-2-benzylsulfonylmethyl-butyric acid (10.90 g, 40.15 mmol) was dissolved in 100 mL dry EtOH and set to stir at room temperature. NaOH pellets (4.81 g, 120.45 mmol) were added in one portion, and the reaction mixture was allowed to stir for 10 minutes. 1-Bromo-2-methyl propane (5.0 g, 36.49 mmol) was then added, and the reaction mixture was allowed to stir at ambient temperature for 20 hours. Upon completion (LCMS), the reaction mixture was diluted with water and the pH was lowered to ˜pH2. The reaction mixture was then washed 3× with EtOAc. The organic phase was concentrated in vacuo and then diluted with 200 mL aqueous MeOH. Oxone (10.02 g, 14.57 mmol) was added in one portion and the reaction was stirred at room temperature for 4 hours. Conversion of sulfide to sulfone was monitored via LCMS. Upon completion, reaction was quenched by the addition of sodium thiosulfate. Salts were filtered, and the reaction mixture was washed 3× with ethyl acetate and dried over sodium sulfate. The organics were evaporated by vacuum under reduced pressure. Product was purified via HPLC. Yield: 1.1 g, 23.1%. m/z (LCMS) M+ 322.01, Rf=2.03. δH 12.6 (1H, br s), 3.5 (4H, m), 3.5 (1H, m), 3.4 (4H, m), 3.25 (2H, d), 3.0 (2H, m), 2.9 (2H, d), 2.4 (1H, m), 1.3 (6H, d d).

1. additionwere added in one portion
2. stirringto stir for 10 minutes
3. stirringto stir at ambient temperature for 20 hours
4. washThe reaction mixture was then washed 3× with EtOAc
5. concentrationThe organic phase was concentrated in vacuo
6. additiondiluted with 200 mL aqueous MeOH
7. stirringthe reaction was stirred at room temperature for 4 hours
8. customUpon completion, reaction
9. customwas quenched by the addition of sodium thiosulfate
10. filtrationSalts were filtered
11. washthe reaction mixture was washed 3× with ethyl acetate
12. dry with materialdried over sodium sulfate
13. customThe organics were evaporated by vacuum under reduced pressure
14. customProduct was purified via HPLC