3-Bromo-7-methoxyquinoline → 7-Methoxy-3-(3-methoxyphenyl)quinoline
反応式
Br[C:2]1[CH:3]=[N:4][C:5]2[C:10]([CH:11]=1)=[CH:9][CH:8]=[C:7]([O:12][CH3:13])[CH:6]=2.[CH3:14][O:15][C:16]1[CH:17]=[C:18](OB(O)O)[CH:19]=[CH:20][CH:21]=1>>[CH3:13][O:12][C:7]1[CH:6]=[C:5]2[C:10]([CH:11]=[C:2]([C:20]3[CH:19]=[CH:18][CH:17]=[C:16]([O:15][CH3:14])[CH:21]=3)[CH:3]=[N:4]2)=[CH:9][CH:8]=1参加物
3
実験手順
The compound is prepared by the reaction of 3-bromo-7-methoxyquinoline (255 mg, 1.07 mmol, 1.06 eq) and 3-methoxyphenylboric acid (154 mg, 1.01 mmol, 1 eq) according to method A in 4.5 h. Purification by column chromatography with a mixture of hexane/ethyl acetate 9/1 yields the desired product in a yield of 76% (215 mg).
後処理
- customPurification by column chromatography
- additionwith a mixture of hexane/ethyl acetate 9/1
出典と根拠
- ORDレコード
- ord-6410e7deb4224e908420774720bc98be
- 出典データセット
- uspto-grants-2013_10
- 特許番号
- US08546392B2
反応ノート
読み込み中…