2-Fluoro-5-nitrophenylboronic acid, pinacol ester → 4-(2-Fluoro-5-nitrophenyl)nicotinonitrile
反応式
Br[C:2]1[C:7]([C:8]#[N:9])=[CH:6][N:5]=[CH:4][CH:3]=1.[F:10][C:11]1[CH:16]=[CH:15][C:14]([N+:17]([O-:19])=[O:18])=[CH:13][C:12]=1B1OC(C)(C)C(C)(C)O1>>[F:10][C:11]1[CH:16]=[CH:15][C:14]([N+:17]([O-:19])=[O:18])=[CH:13][C:12]=1[C:2]1[C:7]([C:8]#[N:9])=[CH:6][N:5]=[CH:4][CH:3]=1参加物
3
実験手順
4-Bromonicotinonitrile (1.0 g, 5.5 mmol) was coupled to 2-(2-fluoro-5-nitrophenyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane (1.9 g, 7.1 mmol) using the method in Example 51. Purification by chromatography on silica gel eluting with dichloromethane gave 4-(2-fluoro-5-nitrophenyl)nicotinonitrile as a white solid: δH (400 MHz, CDCl3) 7.44-7.52 (2H, m), 8.38-8.47 (2H, m), 8.95 (1H, d, J 5), 9.06 (1H, s).
後処理
- customPurification by chromatography on silica gel eluting with dichloromethane
出典と根拠
- ORDレコード
- ord-20d17789d71d48749c6817666cd55990
- 出典データセット
- uspto-grants-2005_05
- 特許番号
- US06900215B2
反応ノート
読み込み中…