反応式
[NH2:1][C@H:2]1[C@@H:7]([NH:8][C:9](=[O:17])[O:10][CH2:11][CH2:12][Si:13]([CH3:16])([CH3:15])[CH3:14])[CH2:6][C@H:5]2[C@@H:3]1[CH2:4]2.Cl[C:19]1[N:28]=[CH:27][C:26]2[C:21](=[CH:22][CH:23]=[C:24]([C:29]3[C:34]([Cl:35])=[C:33]([O:36][CH3:37])[CH:32]=[C:31]([O:38][CH3:39])[C:30]=3[Cl:40])[CH:25]=2)[N:20]=1.C(=O)(O)[O-].[Na+]>CN1CCCC1=O.C(OCC)(=O)C>[Cl:35][C:34]1[C:33]([O:36][CH3:37])=[CH:32][C:31]([O:38][CH3:39])=[C:30]([Cl:40])[C:29]=1[C:24]1[CH:25]=[C:26]2[C:21](=[CH:22][CH:23]=1)[N:20]=[C:19]([NH:1][C@H:2]1[C@@H:7]([NH:8][C:9](=[O:17])[O:10][CH2:11][CH2:12][Si:13]([CH3:14])([CH3:16])[CH3:15])[CH2:6][C@H:5]3[C@@H:3]1[CH2:4]3)[N:28]=[CH:27]2参加物
反応物 3
生成物 1
試薬・触媒・溶媒 2
実験手順
A solution of 2-(trimethylsilyl)ethyl (1S,2R,3S,5S)-2-aminobicyclo[3.1.0]hexan-3-ylcarbamate (250 mg, 0.977 mmol), 2-chloro-6-(2,6-dichloro-3,5-dimethoxyphenyl)quinazoline (300 mg, 0.814 mmol) and sodium bicarbonate (205 mg, 2.442 mmol) in N-methyl-2-pyrrolidone (10 mL) was stirred at 100° C. overnight. The reaction solution was cooled to room temperature, diluted with ethyl acetate (100 mL) and washed with water (eight times) and brine (50 mL). The organic layer was dried over sodium sulfate, filtered and concentrated to afford a crude product, which was purified by silica gel column chromatography (ethyl acetate:petroleum ether=4:2) to afford the title compound (300 mg, 52%) as a yellow solid. MS (ES+) C28H34Cl2N4O4Si requires: 588, 590, found: 589, 591 [M+H]+.
後処理
- washwashed with water (eight times) and brine (50 mL)
- dry with materialThe organic layer was dried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated
- customto afford a crude product, which
- customwas purified by silica gel column chromatography (ethyl acetate:petroleum ether=4:2)
出典と根拠
- ORDレコード
- ord-ea6964527a4d4262afbdc8f164fae667
- 出典データセット
- uspto-grants-2016_09
- 特許番号
- US09434700B2
関連ノート
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