3-Bromo-2-fluoropyridine → 3-((1S)-1-(tert-Butyldimethylsilyloxy)-7-fluoro-2,3-dihydro-1H-inden-4-yl)-2-fluoropyridine
反応式
[C:1]([Si:5]([O:8][C@@H:9]1[C:17]2[C:12](=[C:13](B3OC(C)(C)C(C)(C)O3)[CH:14]=[CH:15][C:16]=2[F:18])[CH2:11][CH2:10]1)([CH3:7])[CH3:6])([CH3:4])([CH3:3])[CH3:2].Br[C:29]1[C:30]([F:35])=[N:31][CH:32]=[CH:33][CH:34]=1.BrC1C=CC(F)=C2C=1CC[C@H]2OC1C=CC2[C@H](CC(OC)=O)COC=2C=1>>[Si:5]([O:8][C@@H:9]1[C:17]2[C:12](=[C:13]([C:29]3[C:30]([F:35])=[N:31][CH:32]=[CH:33][CH:34]=3)[CH:14]=[CH:15][C:16]=2[F:18])[CH2:11][CH2:10]1)([C:1]([CH3:3])([CH3:4])[CH3:2])([CH3:6])[CH3:7]参加物
4
反応物 3
生成物 1
実験手順
The title compound is prepared from (S)-tert-butyl(7-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,3-dihydro-1H-inden-1-yloxy)dimethylsilane and 3-bromo-2-fluoropyridine following a procedure analogous to that described in Step 5 of Intermediate 1. LC (method 7): tR=1.31 min.; Mass spectrum (ESI+): m/z=362 [M+H]+.
出典と根拠
- ORDレコード
- ord-4b2e2ad181de49d2acc4f04aa52b4166
- 出典データセット
- uspto-grants-2014_02
- 特許番号
- US08642585B2
反応ノート
読み込み中…