반응식
[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]=1참가 물질
실험 절차
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.
후처리
- 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)
출처 및 근거
- ORD 기록
- ord-8df83238fa9745758f57a2fcb0296b6a
- 출처 데이터셋
- uspto-grants-2002_03
- 특허 번호
- US06362336B1
연결된 노트
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