反応式
Cl[C:2]1[N:7]=[CH:6][C:5]([O:8][CH:9]2[CH2:14][CH2:13][N:12]([C:15]([O:17][C:18]([CH3:21])([CH3:20])[CH3:19])=[O:16])[CH2:11][CH2:10]2)=[CH:4][CH:3]=1.[F:22][C:23]1[CH:24]=[C:25]([S:32]([CH3:35])(=[O:34])=[O:33])[CH:26]=[C:27]2[C:31]=1[NH:30][CH:29]=[CH:28]2>>[C:18]([O:17][C:15]([N:12]1[CH2:13][CH2:14][CH:9]([O:8][C:5]2[CH:6]=[N:7][C:2]([N:30]3[C:31]4[C:27](=[CH:26][C:25]([S:32]([CH3:35])(=[O:33])=[O:34])=[CH:24][C:23]=4[F:22])[CH:28]=[CH:29]3)=[CH:3][CH:4]=2)[CH2:10][CH2:11]1)=[O:16])([CH3:21])([CH3:20])[CH3:19]参加物
3
実験手順
The title compound was prepared by following the similar procedure as described in Example-1 using tert-butyl 4-((6-chloropyridin-3-yl)oxy)piperidine-1-carboxylate (intermediate-06) and 7-Fluoro-5-(methylsulfonyl)-1H-indole (intermediate-22) (0.060 g, 23%).
出典と根拠
- ORDレコード
- ord-a37e85a0c3fc4747bb4be5fb838ebdaf
- 出典データセット
- uspto-grants-2015_04
- 特許番号
- US09000175B2
関連ノート
読み込み中…