Triethylamine → {4-[4-(Benzyloxycarbonylamino)phenoxy]pyridin-2-yl}-N-(phenoxycarbonyl)carbamic acid phenyl ester
반응식
[CH2:1]([O:8][C:9](=[O:25])[NH:10][C:11]1[CH:16]=[CH:15][C:14]([O:17][C:18]2[CH:23]=[CH:22][N:21]=[C:20]([NH2:24])[CH:19]=2)=[CH:13][CH:12]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(N([CH2:31][CH3:32])CC)C.Cl[C:34]([O:36][C:37]1[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=1)=[O:35]>O1CCCC1>[C:37]1([O:36][C:34](=[O:35])[N:24]([C:20]2[CH:19]=[C:18]([O:17][C:14]3[CH:15]=[CH:16][C:11]([NH:10][C:9]([O:8][CH2:1][C:2]4[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=4)=[O:25])=[CH:12][CH:13]=3)[CH:23]=[CH:22][N:21]=2)[C:9]([O:25][C:32]2[CH:31]=[CH:4][CH:3]=[CH:2][CH:1]=2)=[O:8])[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=1참가 물질
실험 절차
To a solution of [4-(2-aminopyridin-4-yloxy)phenyl]carbamic acid benzyl ester (500 mg) in tetrahydrofuran (15 ml) were added triethylamine (0.519 ml) and phenyl chloroformate (0.467 ml) while stirring in an ice water bath. The reaction mixture was stirred at room temperature for 30 min. The reaction mixture was partitioned between ethyl acetate (50 ml) and a saturated aqueous solution of sodium hydrogencarbonate (20 ml). The separated organic layer was washed with a saturated aqueous solution of sodium hydrogencarbonate (20 ml), water (20 ml) and brine (20 ml) in this order, and dried over anhydrous sodium sulfate. The solvent was concentrated under reduced pressure to provide a crude product of the titled compound as brown foam (935.6 mg).
후처리
- stirringThe reaction mixture was stirred at room temperature for 30 min
- customThe reaction mixture was partitioned between ethyl acetate (50 ml)
- washThe separated organic layer was washed with a saturated aqueous solution of sodium hydrogencarbonate (20 ml), water (20 ml) and brine (20 ml) in this order
- dry with materialdried over anhydrous sodium sulfate
- concentrationThe solvent was concentrated under reduced pressure
출처 및 근거
- ORD 기록
- ord-9815280601f54d11a07505a089c5c650
- 출처 데이터셋
- uspto-grants-2010_12
- 특허 번호
- US07855290B2
반응 노트
불러오는 중…