反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[C:4]([F:9])[CH:3]=1.Cl.[CH2:11]([O:18][C:19]1[CH:28]=[C:27]2[C:22]([C:23](Cl)=[N:24][CH:25]=[N:26]2)=[CH:21][C:20]=1[O:30][CH3:31])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>N1C=CC=CC=1>[CH2:11]([O:18][C:19]1[CH:28]=[C:27]2[C:22]([C:23]([O:8][C:5]3[CH:6]=[CH:7][C:2]([Cl:1])=[CH:3][C:4]=3[F:9])=[N:24][CH:25]=[N:26]2)=[CH:21][C:20]=1[O:30][CH3:31])[C:12]1[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=1参加物
実験手順
4-Chloro-2-fluoro-phenol (264 mg, 1.8 mmol) was added to a solution of 7-benzyloxy-4-chloro-6-methoxyquinazoline hydrochloride (506 mg, 1.5 mmol), (prepared as described for the starting material in Example 1), in pyridine (8 ml) and the mixture heated at reflux for 45 minutes. The solvent was removed by evaporation and the residue partitioned between ethyl acetate and water. The organic layer was washed with 0.1M hydrochloric acid, water and brine, dried (MgSO4) and the solvent removed by evaporation. The solid residue was triturated with petroleum ether and the crude product collected by filtration and purified by flash chromatography eluting with methylene chloride/ether (9/1) to give 7-benzyloxy-4-(4-chloro-2-fluorophenoxy)-6-methoxyquinazoline (474 mg, 77%) as a cream solid.
後処理
- custom(prepared
- temperaturethe mixture heated
- temperatureat reflux for 45 minutes
- customThe solvent was removed by evaporation
- customthe residue partitioned between ethyl acetate and water
- washThe organic layer was washed with 0.1M hydrochloric acid, water and brine
- dry with materialdried (MgSO4)
- customthe solvent removed by evaporation
- customThe solid residue was triturated with petroleum ether
- filtrationthe crude product collected by filtration
- custompurified by flash chromatography
- washeluting with methylene chloride/ether (9/1)
出典と根拠
- ORDレコード
- ord-8df83238fa9745758f57a2fcb0296b6a
- 出典データセット
- uspto-grants-2002_03
- 特許番号
- US06362336B1
関連ノート
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