3-(Difluoromethoxy)benzenesulfonyl chloride → 3-Difluoromethoxy-N-[2-(4-methyl-piperazin-1-yl)-pyridin-4-yl]-benzene sulfonamide
반응식
[CH3:1][N:2]1[CH2:7][CH2:6][N:5]([C:8]2[CH:13]=[C:12]([NH2:14])[CH:11]=[CH:10][N:9]=2)[CH2:4][CH2:3]1.[F:15][CH:16]([F:28])[O:17][C:18]1[CH:19]=[C:20]([S:24](Cl)(=[O:26])=[O:25])[CH:21]=[CH:22][CH:23]=1>N1C=CC=CC=1>[F:28][CH:16]([F:15])[O:17][C:18]1[CH:19]=[C:20]([S:24]([NH:14][C:12]2[CH:11]=[CH:10][N:9]=[C:8]([N:5]3[CH2:4][CH2:3][N:2]([CH3:1])[CH2:7][CH2:6]3)[CH:13]=2)(=[O:26])=[O:25])[CH:21]=[CH:22][CH:23]=1참가 물질
4
실험 절차
To a solution of 200 mg of 2-(4-methyl-piperazin-1-yl)-4-amino-pyridin (1.04 mmol) in 5 ml of pyridine 272 mg of (1.12 mmol) of 3-difluoromethoxybenzene sulfonylchloride (1.66 mmol) were added and the reaction mixture was stirred for 15 h at room temperature. The solvent was evaporated under reduced pressure and the residue was dissolved in dichloromethane. This mixture was washed with aqueous NaHCO3. The organic layer was dried over magnesium sulfate, filtered, and the solvent was evaporated under reduced pressure. The crude product was purified via silica gel chromatography with ethyl dichloromethane/methanol (0-15%) as eluent, yielding 231 mg of the purified product.
후처리
- customThe solvent was evaporated under reduced pressure
- dissolutionthe residue was dissolved in dichloromethane
- washThis mixture was washed with aqueous NaHCO3
- dry with materialThe organic layer was dried over magnesium sulfate
- filtrationfiltered
- customthe solvent was evaporated under reduced pressure
- customThe crude product was purified via silica gel chromatography with ethyl dichloromethane/methanol (0-15%) as eluent
출처 및 근거
- ORD 기록
- ord-426556b680484ac58f88921740542288
- 출처 데이터셋
- uspto-grants-2013_07
- 특허 번호
- US08497273B2
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