Sodium Hydroxide → (R)-3-(4-Methanesulfonyl-phenyl)-1-(2-methyl-pyridin-4-yl)-3-o-tolyl-propan-1-one
반응식
N1CCC[C@H]1C(O)=O.[OH-].[Na+].Br[C:12]1[CH:17]=[CH:16][C:15]([C@H:18]([C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][C:30]=2[CH3:35])[CH2:19][C:20]([C:22]2[CH:27]=[CH:26][N:25]=[C:24]([CH3:28])[CH:23]=2)=[O:21])=[CH:14][CH:13]=1.[CH3:36][S:37]([O-:39])=[O:38].[Na+]>CS(C)=O.[Cu]I.C(OCC)(=O)C.O>[CH3:36][S:37]([C:12]1[CH:17]=[CH:16][C:15]([C@H:18]([C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][C:30]=2[CH3:35])[CH2:19][C:20]([C:22]2[CH:27]=[CH:26][N:25]=[C:24]([CH3:28])[CH:23]=2)=[O:21])=[CH:14][CH:13]=1)(=[O:39])=[O:38]참가 물질
반응물 4
생성물 1
시약·촉매·용매 4
반응 조건
- 온도
- 110 °C
실험 절차
To a solution of L-proline (35 mg) in dimethyl sulfoxide (4 mL) was added at room temperature sodium hydroxide (12 mg). The reaction mixture was stirred at room temperature for 30 min. (R)-3-(4-Bromo-phenyl)-1-(2-methyl-pyridin-4-yl)-3-o-tolyl-propan-1-one (example 142, step 2, 150 mg), sodium methanesulfinate (311 mg) and copper(I) iodide (58 mg) were added. The reaction mixture was heated at 110° C. and stirred for 4 hours. Water and ethyl acetate were added, the phases were separated and the inorganic one was extracted with ethyl acetate (2×). The combined organic layers were washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo. The crude product was purified by flash chromatography on silica gel (50% to 100% ethyl acetate in n-heptane) to yield the title compound as an yellow oil (57%), MS (ESI+): m/z=394.0 ([M+H]+).
후처리
- additionwere added
- customthe phases were separated
- extractionthe inorganic one was extracted with ethyl acetate (2×)
- washThe combined organic layers were washed with brine
- dry with materialdried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated in vacuo
- customThe crude product was purified by flash chromatography on silica gel (50% to 100% ethyl acetate in n-heptane)
출처 및 근거
- ORD 기록
- ord-7bcda64f10c04681ac5fd7ea80edb62a
- 출처 데이터셋
- uspto-grants-2014_07
- 특허 번호
- US08765730B2
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