反応式
Cl[C:2]1[N:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([C:12]3[C:17]([Cl:18])=[C:16]([O:19][CH3:20])[CH:15]=[C:14]([O:21][CH3:22])[C:13]=3[Cl:23])[CH:8]=2)[N:3]=1.[NH2:24][C@H:25]1[C@H:29]([OH:30])[CH2:28][CH:27]([C:31]([O:33][CH3:34])=[O:32])[CH2:26]1.C1CCN2C(=NCCC2)CC1>C(#N)C.CCOC(C)=O>[Cl:18][C:17]1[C:16]([O:19][CH3:20])=[CH:15][C:14]([O:21][CH3:22])=[C:13]([Cl:23])[C:12]=1[C:7]1[CH:8]=[C:9]2[C:4](=[CH:5][CH:6]=1)[N:3]=[C:2]([NH:24][C@H:25]1[C@H:29]([OH:30])[CH2:28][C@@H:27]([C:31]([O:33][CH3:34])=[O:32])[CH2:26]1)[N:11]=[CH:10]2参加物
6
反応物 3
生成物 1
試薬・触媒・溶媒 2
反応条件
- 温度
- 65 °C
実験手順
2-chloro-6-(2,6-dichloro-3,5-dimethoxyphenyl)quinazoline (0.576 g, 1.558 mmol), methyl (3R,4R)-3-amino-4-hydroxycyclopentane-1-carboxylate (0.372 g, 2.337 mmol) were taken up in acetonitrile (3 ml) and DBU (0.470 ml, 3.12 mmol) was added. The reaction was purged with N2 for 5 minutes then heated to 65° C. overnight. After cooling to room temperature, the solvent was removed under reduced pressure. The residue was purified via flash chromatography (0-100% Hex/EtOAc; 12 g column), and (1S,3R,4R)-methyl 3-((6-(2,6-dichloro-3,5-dimethoxyphenyl)quinazolin-2-yl)amino)-4-hydroxycyclopentanecarboxylate (0.520 g, 1.056 mmol, 67.8% yield) was recovered. MS (ES+) C23H23Cl2N3O5 requires: 492, found: 493 [M+H]+.
後処理
- customThe reaction was purged with N2 for 5 minutes
- temperatureAfter cooling to room temperature
- customthe solvent was removed under reduced pressure
出典と根拠
- ORDレコード
- ord-18577f484c0a489aa3234c21a76ea822
- 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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