4-(Trifluoromethyl)piperidine-1-carbonyl chloride → 6-Fluoro-1-(4-trifluoromethylpiperidine-1-carbonyl)-1H-indazol-3-yl 4-trifluoromethylpiperidine-1-carboxylate
反応式
[F:1][C:2]1[CH:10]=[C:9]2[C:5]([C:6]([OH:11])=[N:7][NH:8]2)=[CH:4][CH:3]=1.[F:12][C:13]([F:24])([F:23])[CH:14]1[CH2:19][CH2:18][N:17]([C:20](Cl)=[O:21])[CH2:16][CH2:15]1>>[F:12][C:13]([F:24])([F:23])[CH:14]1[CH2:19][CH2:18][N:17]([C:20]([O:11][C:6]2[C:5]3[C:9](=[CH:10][C:2]([F:1])=[CH:3][CH:4]=3)[N:8]([C:20]([N:17]3[CH2:16][CH2:15][CH:14]([C:13]([F:23])([F:12])[F:24])[CH2:19][CH2:18]3)=[O:21])[N:7]=2)=[O:21])[CH2:16][CH2:15]1参加物
3
実験手順
In analogy to example 1, 200 mg (1.315 mmol) of 6-fluoro-1H-indazol-3-ol were reacted with 340 mg (1.578 mmol) of 4-trifluoromethylpiperidine-1-carbonyl chloride.
出典と根拠
- ORDレコード
- ord-7478a93e1a65455db2ab8a7374a28b9e
- 出典データセット
- uspto-grants-2013_01
- 特許番号
- US08357698B2
反応ノート
読み込み中…