Sodium Methoxide → 6-Bromo-4-chloro-2-methoxy-8-methyl-3-(4-(trifluoromethoxy)phenyl)quinoline
反応式
[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[C:10]([CH3:12])[CH:11]=1)[N:8]=[C:7](Cl)[C:6]([C:14]1[CH:19]=[CH:18][C:17]([O:20][C:21]([F:24])([F:23])[F:22])=[CH:16][CH:15]=1)=[C:5]2[Cl:25].[CH3:26][O-:27].[Na+]>C1(C)C=CC=CC=1.C(Cl)Cl>[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[C:10]([CH3:12])[CH:11]=1)[N:8]=[C:7]([O:27][CH3:26])[C:6]([C:14]1[CH:19]=[CH:18][C:17]([O:20][C:21]([F:24])([F:23])[F:22])=[CH:16][CH:15]=1)=[C:5]2[Cl:25]参加物
5
反応条件
- 温度
- 110 °C
実験手順
A mixture of 6-bromo-2,4-dichloro-8-methyl-3-(4-(trifluoromethoxy)phenyl)quinoline (1.97 g, 4.367 mmol, Intermediate 58, step c) and sodium methoxide (1.18 g, 21.837 mmol) in toluene (20 mL) was heated in a sealed tube at 110° C. for 24 hours, cooled to RT, diluted with DCM, stirred at room temperature for 30 min, and filtered through Celite® rinsing several times with DCM. The solvents were removed under reduced pressure and the off-white solid product precipitated from MeOH, filtered and dried to provide the title compound.
後処理
- temperaturecooled to RT
- filtrationfiltered through Celite®
- washrinsing several times with DCM
- customThe solvents were removed under reduced pressure
- customthe off-white solid product precipitated from MeOH
- filtrationfiltered
- customdried
出典と根拠
- ORDレコード
- ord-d5ee121f8f854c18a885cfbf8d7a39ba
- 出典データセット
- uspto-grants-2016_04
- 特許番号
- US09309222B2
反応ノート
読み込み中…