Hydrogen Peroxide → Odanacatib
반응식
[C:1]([C:3]1([NH:6][C:7](=[O:34])[C@H:8]([CH2:29][C:30]([F:33])([CH3:32])[CH3:31])[NH:9][C@@H:10]([C:15]2[CH:20]=[CH:19][C:18]([C:21]3[CH:26]=[CH:25][C:24](SC)=[CH:23][CH:22]=3)=[CH:17][CH:16]=2)[C:11]([F:14])([F:13])[F:12])[CH2:5][CH2:4]1)#[N:2].OO.[S:37]([O-:41])([O-])(=[O:39])=S.[Na+].[Na+].[C:44](OCC)(=O)C>C1(C)C=CC=CC=1.ClCCl>[C:1]([C:3]1([NH:6][C:7](=[O:34])[C@H:8]([CH2:29][C:30]([F:33])([CH3:31])[CH3:32])[NH:9][C@@H:10]([C:15]2[CH:16]=[CH:17][C:18]([C:21]3[CH:22]=[CH:23][C:24]([S:37]([CH3:44])(=[O:41])=[O:39])=[CH:25][CH:26]=3)=[CH:19][CH:20]=2)[C:11]([F:12])([F:13])[F:14])[CH2:4][CH2:5]1)#[N:2]참가 물질
실험 절차
To a 0° solution of the sulfide (0.265 g) from Step 10 in toluene (5 mL) and dichloromethane (5 mL) was added Na2WO4.2H2O (0.002 g) and n-Bu4 NHSO4 (0.01 g). 30% Hydrogen peroxide (0.137 mL) was then slowly added and the mixture was stirred at room temperature for 3 hours. The mixture was poured slowly onto a mixture of ice, dilute aqueous sodium thiosulfate and ethyl acetate. The organic layer was separated and the aqueous further extracted with ethyl acetate. The combined organic layers were washed with brine, dried with magnesium sulfate and the solvent was removed in vacuo to yield a residue which was purified on SiO2 using ethyl acetate, hexanes and dichloromethane (1:1:0.1) as eluant. The residue was triturated in diethyl ether to yield N1-(1-cyanocyclopropyl)-4-fluoro-N2-{(1S)-2,2,2-trifluoro-1-[4′-(methylsulfonyl)-1,1′-biphenyl-4-yl]ethyl}-L-leucinamide.
후처리
- customThe organic layer was separated
- extractionthe aqueous further extracted with ethyl acetate
- washThe combined organic layers were washed with brine
- dry with materialdried with magnesium sulfate
- customthe solvent was removed in vacuo
- customto yield a residue which
- customwas purified on SiO2
- customThe residue was triturated in diethyl ether
출처 및 근거
- ORD 기록
- ord-7fa021887d1e4f1c87c4f570a1c04708
- 출처 데이터셋
- uspto-grants-2014_07
- 특허 번호
- US08772336B2
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