1,4-Dioxane → Tert-butyl 4-{[6-formyl-2-(trifluoromethyl)pyrimidin-4-yl]amino}piperidine-1-carboxylate
반응식
C(O/C=C\[C:6]1[N:11]=[C:10]([C:12]([F:15])([F:14])[F:13])[N:9]=[C:8]([NH:16][CH:17]2[CH2:22][CH2:21][N:20]([C:23]([O:25][C:26]([CH3:29])([CH3:28])[CH3:27])=[O:24])[CH2:19][CH2:18]2)[CH:7]=1)C.I([O-])(=O)(=O)=O.[Na+].[O:36]1CCOC[CH2:37]1>O.[Os](=O)(=O)(=O)=O>[CH:37]([C:6]1[N:11]=[C:10]([C:12]([F:15])([F:14])[F:13])[N:9]=[C:8]([NH:16][CH:17]2[CH2:18][CH2:19][N:20]([C:23]([O:25][C:26]([CH3:29])([CH3:28])[CH3:27])=[O:24])[CH2:21][CH2:22]2)[CH:7]=1)=[O:36]참가 물질
6
반응물 3
생성물 1
시약·촉매·용매 2
실험 절차
tert-Butyl 4-{[6-[(Z)-2-ethoxyvinyl]-2-(trifluoromethyl)pyrimidin-4-yl]amino}piperidine-1-carboxylate (0.80 g, 1.9 mmol, from Step 2) was dissolved in 1,4-dioxane (56 mL) and water (14 mL), then sodium periodate (1.2 g, 5.8 mmol) was added followed by osmium tetraoxide (4 wt % in water, 0.424 mL, 0.0666 mmol). After stirring for 24 hours, the reaction mixture was partitioned between water and EtOAc, the phases were separated and the aqueous phase was extracted with additional EtOAc. The combined organic extracts were washed with water, then sat'd NaCl, dried over Na2SO4, filtered and solvent removed in vacuo. The crude product was used in the next reaction without purification. LCMS (M+H)+: 375.0; (M+H2O+H)+: 393.0.
후처리
- customthe reaction mixture was partitioned between water and EtOAc
- customthe phases were separated
- extractionthe aqueous phase was extracted with additional EtOAc
- washThe combined organic extracts were washed with water
- dry with materialdried over Na2SO4
- filtrationfiltered
- customsolvent removed in vacuo
- customThe crude product was used in the next reaction without purification
출처 및 근거
- ORD 기록
- ord-10d56eae0c6e44028d0e2ce66a2effa0
- 출처 데이터셋
- uspto-grants-2015_11
- 특허 번호
- US09193733B2
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