反応式
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]=1参加物
実験手順
(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).
後処理
- 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
出典と根拠
- ORDレコード
- ord-58ede6e010ce49b7adfd0a152fc2179d
- 出典データセット
- uspto-grants-2002_10
- 特許番号
- US06472393B1
関連ノート
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