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[CH3:1][C:2]1[N:3]=[CH:4][NH:5][CH:6]=1.F[C:8]1[CH:13]=[CH:12][C:11]([N+:14]([O-])=O)=[CH:10][CH:9]=1.C([O-])([O-])=O.[K+].[K+]>CN(C=O)C>[CH3:1][C:2]1[N:3]=[CH:4][N:5]([C:8]2[CH:13]=[CH:12][C:11]([NH2:14])=[CH:10][CH:9]=2)[CH:6]=1참가 물질
실험 절차
To a solution of compound 6.0 4-methyl imidazole (1 mL, 10 mmol, 1 equiv.) in DMF at room temperature was added 1-fluoro-4-nitrobenzene 6.1 (820 mg, 10 mmol, 1 equiv.) and K2CO3 (1.38 g, 10 mmol, 1 equiv.). The resulting mixture was heated to 110° c for 4h before being cooled to room temperature, filtered through celite, and washed with EtOAc (20 mL×4). The collected filtrate was further washed with brine (50 mL×3) and dried over Na2SO4. After removal of solvent, the residue was diluted with MeOH (20 mL). Pd/C (50 mg, 5% mass equiv.) was added and the reaction flask was charged with a H2 balloon and stirred overnight at room temperature. The mixture was filtered through celite and washed with EtOAc (20 mL×3). The collected filtrate was concentrated and the residue was purified via flash chromatography (hexanes:EtOAc=1:1) to afford the desired product 6.3 4-(4-methyl-1H-imidazol-1-yl)benzenamine (1.0 g; 60%). LC-MS (M+H):174.15
후처리
- filtrationfiltered through celite
- washwashed with EtOAc (20 mL×4)
- washThe collected filtrate was further washed with brine (50 mL×3)
- dry with materialdried over Na2SO4
- customAfter removal of solvent
- additionthe residue was diluted with MeOH (20 mL)
- additionPd/C (50 mg, 5% mass equiv.) was added
- additionthe reaction flask was charged with a H2 balloon
- filtrationThe mixture was filtered through celite
- washwashed with EtOAc (20 mL×3)
- concentrationThe collected filtrate was concentrated
- customthe residue was purified via flash chromatography (hexanes:EtOAc=1:1)
출처 및 근거
- ORD 기록
- ord-00dfce051fc5487cb5574f6d0be9d388
- 출처 데이터셋
- uspto-grants-2014_11
- 특허 번호
- US08889706B2
연결된 노트
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