Methanesulfonyl chloride → 3-(4-(4-cyano-1-(tetrahydro-2H-pyran-2-yl)-1H-imidazo[4,5-c]pyridin-6-yl)-2-(trifluoromethyl)phenoxy)propyl methanesulfonate
반응식
[OH:1][CH2:2][CH2:3][CH2:4][O:5][C:6]1[CH:11]=[CH:10][C:9]([C:12]2[N:17]=[C:16]([C:18]#[N:19])[C:15]3[N:20]=[CH:21][N:22]([CH:23]4[CH2:28][CH2:27][CH2:26][CH2:25][O:24]4)[C:14]=3[CH:13]=2)=[CH:8][C:7]=1[C:29]([F:32])([F:31])[F:30].CCN(C(C)C)C(C)C.[CH3:42][S:43](Cl)(=[O:45])=[O:44]>CN1C(=O)CCC1.CCOC(C)=O>[CH3:42][S:43]([O:1][CH2:2][CH2:3][CH2:4][O:5][C:6]1[CH:11]=[CH:10][C:9]([C:12]2[N:17]=[C:16]([C:18]#[N:19])[C:15]3[N:20]=[CH:21][N:22]([CH:23]4[CH2:28][CH2:27][CH2:26][CH2:25][O:24]4)[C:14]=3[CH:13]=2)=[CH:8][C:7]=1[C:29]([F:31])([F:30])[F:32])(=[O:45])=[O:44]참가 물질
6
반응물 3
생성물 1
시약·촉매·용매 2
실험 절차
To a solution of 6-(4-(3-hydroxypropoxy)-3-(trifluoromethyl)phenyl)-1-(tetrahydro-2H-pyran-2-yl)-1H-imidazo[4,5-c]pyridine-4-carbonitrile (670 mg) and DIPEA (1.4 ml) in NMP (7.5 ml) at 0° C. was added methanesulphonyl chloride (0.2 ml). The mixture was allowed to stir for 45 minutes at room temperature, then diluted with EtOAc (75 ml) and washed with saturated sodium bicarbonate (70 ml), followed by water (2×40 ml). Organic layer was dried over sodium sulphate and solvent was evaporated under reduced pressure to yield 3-(4-(4-cyano-1-(tetrahydro-2H-pyran-2-yl)-1H-imidazo[4,5-c]pyridin-6-yl)-2-(trifluoromethyl)phenoxy)propyl methanesulfonate (720 mg).
후처리
- washwashed with saturated sodium bicarbonate (70 ml)
- dry with materialOrganic layer was dried over sodium sulphate and solvent
- customwas evaporated under reduced pressure
출처 및 근거
- ORD 기록
- ord-11f7150b347240caaf7a4f8dc29fedf4
- 출처 데이터셋
- uspto-grants-2011_04
- 특허 번호
- US07932251B2
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