Methanol → {3-[(5-bromo-1H-pyrrolo[2,3-b]pyridin-3-yl)-hydroxy-methyl]-2,4-difluoro-phenyl}-carbamic acid methyl ester
반응식
[Br:1][C:2]1[CH:3]=[C:4]2[CH:10]=[CH:9][NH:8][C:5]2=[N:6][CH:7]=1.[CH3:11][O:12][C:13](=[O:25])[NH:14][C:15]1[CH:20]=[CH:19][C:18]([F:21])=[C:17]([CH:22]=[O:23])[C:16]=1[F:24].CO.[OH-].[K+]>O>[CH3:11][O:12][C:13](=[O:25])[NH:14][C:15]1[CH:20]=[CH:19][C:18]([F:21])=[C:17]([CH:22]([C:10]2[C:4]3[C:5](=[N:6][CH:7]=[C:2]([Br:1])[CH:3]=3)[NH:8][CH:9]=2)[OH:23])[C:16]=1[F:24]참가 물질
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
Into a reaction flask under nitrogen, 5-bromo-1H-pyrrolo[2,3-b]pyridine (4, 1.00 g, 5.08 mmol) is combined with (2,4-difluoro-3-formyl-phenyl)-carbamic acid methyl ester (3, 1.09 g, 5.08 mmol), 10 mL of methanol and potassium hydroxide (0.41 g, 7.31 mmol). The reaction is stirred at room temperature overnight, then diluted with 30 mL of water and extracted with 1×50 mL, then 2×30 mL of ethyl acetate. The organic layers are combined, dried over magnesium sulfate, filtered and the filtrate concentrated under vacuum. The resulting material is purified by silica gel column chromatography, eluting with a gradient of ethyl acetate:hexane. Appropriate fractions are combined and concentrated under vacuum to provide the desired compound (5, 1.91 g, 91%).
후처리
- extractionextracted with 1×50 mL
- dry with materialdried over magnesium sulfate
- filtrationfiltered
- concentrationthe filtrate concentrated under vacuum
- customThe resulting material is purified by silica gel column chromatography
- washeluting with a gradient of ethyl acetate
- concentrationconcentrated under vacuum
출처 및 근거
- ORD 기록
- ord-330b30895f254e13b1624ed59cbcd54f
- 출처 데이터셋
- uspto-grants-2016_09
- 특허 번호
- US09440969B2
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