Lithium borohydride → 4-[1-(4-Benzyloxy-5-methoxy-2-nitro-phenyl)-2-hydroxy-ethylamino]-benzonitrile
반응식
C[O:2][C:3](=O)[CH:4]([C:14]1[CH:19]=[C:18]([O:20][CH3:21])[C:17]([O:22][CH2:23][C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=2)=[CH:16][C:15]=1[N+:30]([O-:32])=[O:31])[NH:5][C:6]1[CH:11]=[CH:10][C:9]([C:12]#[N:13])=[CH:8][CH:7]=1.[BH4-].[Li+]>C(COC)OC>[CH2:23]([O:22][C:17]1[C:18]([O:20][CH3:21])=[CH:19][C:14]([CH:4]([NH:5][C:6]2[CH:7]=[CH:8][C:9]([C:12]#[N:13])=[CH:10][CH:11]=2)[CH2:3][OH:2])=[C:15]([N+:30]([O-:32])=[O:31])[CH:16]=1)[C:24]1[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=1참가 물질
실험 절차
(4-Benzyloxy-5-methoxy-2-nitro-phenyl)-(4-cyano-phenylamino)-acetic acid methyl ester (4.5 g, 10 mmole) was dissolved in dimethoxyethane and lithium borohydride (0.210 g, 10 mmole) added. The reaction was heated to reflux for three hours and cooled to room temperature. The reaction was quenched with water containing acetic acid and diluted with ethyl acetate. After transferring to a separatory funnel, the organic layer was washed with water several times. The organic layer was dried over anhydrous sodium sulfate, filtered and the solvent removed. The crude material was then submitted to flash chromatography to yield 3.1 g of 4-[1-(4-Benzyloxy-5-methoxy-2-nitro-phenyl)-2-hydroxy-ethylamino]-benzonitrile (74%). 1HNMR(CDCl3):7.77 (s, 1H), 7.3-7.5 (m, 7H), 7.15 (s, 1H), 6.42 (d, 2H), 5.4 (bs, 1H), 5.18 (dd AB syst., 2H), 4.15 (dd, 1H), 3.83 (s, 3H), 3.79-3.86 (dd, 1H).
후처리
- temperatureThe reaction was heated
- temperatureto reflux for three hours
- customThe reaction was quenched with water
- additioncontaining acetic acid
- additiondiluted with ethyl acetate
- customAfter transferring to a separatory funnel
- washthe organic layer was washed with water several times
- dry with materialThe organic layer was dried over anhydrous sodium sulfate
- filtrationfiltered
- customthe solvent removed
출처 및 근거
- ORD 기록
- ord-58ede6e010ce49b7adfd0a152fc2179d
- 출처 데이터셋
- uspto-grants-2002_10
- 특허 번호
- US06472393B1
반응 노트
불러오는 중…