4-Chloro-3-fluorophenylboronic Acid → (rac)-N-(4-(4-Chloro-3-fluorophenyl)-6,7-dihydro-5H-cyclopenta[c]pyridin-7-yl)propionamide
反応式
Br[C:2]1[C:3]2[CH2:10][CH2:9][CH:8]([NH:11][C:12](=[O:15])[CH2:13][CH3:14])[C:4]=2[CH:5]=[N:6][CH:7]=1.[Cl:16][C:17]1[CH:22]=[CH:21][C:20](B(O)O)=[CH:19][C:18]=1[F:26]>>[Cl:16][C:17]1[CH:22]=[CH:21][C:20]([C:2]2[C:3]3[CH2:10][CH2:9][CH:8]([NH:11][C:12](=[O:15])[CH2:13][CH3:14])[C:4]=3[CH:5]=[N:6][CH:7]=2)=[CH:19][C:18]=1[F:26]参加物
3
実験手順
In analogy to the procedure described for the preparation of example 1, (rac)-N-(4-bromo-6,7-dihydro-5H-cyclopenta[c]pyridin-7-yl)propionamide (intermediate A-4) was reacted with 4-chloro-3-fluorophenylboronic acid to give the title compound as grey solid in 87% yield. MS: 319.1 (M+H+, 1Cl).
出典と根拠
- ORDレコード
- ord-1cee0e26c8b6416ea5675a7c04c13870
- 出典データセット
- uspto-grants-2015_11
- 特許番号
- US09187429B2
反応ノート
読み込み中…