5-Bromo-2-thiopheneboronic Acid (contains varying amounts of Anhydride) → 2-(5-Bromo-thiophen-2-yl)-6-methyl-4-(4-trifluoromethyl-phenyl)-pyridine
反応式
I[C:2]1[CH:7]=[C:6]([C:8]2[CH:13]=[CH:12][C:11]([C:14]([F:17])([F:16])[F:15])=[CH:10][CH:9]=2)[CH:5]=[C:4]([CH3:18])[N:3]=1.[Br:19][C:20]1[S:24][C:23](B(O)O)=[CH:22][CH:21]=1>>[Br:19][C:20]1[S:24][C:23]([C:2]2[CH:7]=[C:6]([C:8]3[CH:13]=[CH:12][C:11]([C:14]([F:17])([F:16])[F:15])=[CH:10][CH:9]=3)[CH:5]=[C:4]([CH3:18])[N:3]=2)=[CH:22][CH:21]=1参加物
3
実験手順
The title compound was prepared from 2-iodo-6-methyl-4-(4-trifluoromethyl-phenyl)pyridine (example A.31) (1.00 g, 2.75 mmol) and commercially available 5-bromthiophene-2-boronic acid (0.570 g, 2.75 mmol) according to the general procedure IVb. Obtained as a light yellow solid (0.480 g, 43%). MS (ISP) 398.0 [(M+H)+] and 400.0 [(M+2+H)+].
出典と根拠
- ORDレコード
- ord-e8b87e17fb8143b785f5c6989e8f5141
- 出典データセット
- uspto-grants-2010_01