2-(4-Fluorophenyl)-2-oxoacetic Acid → (S)-2-(4-Fluoro-phenyl)-2-hydroxy-N-(3-methyl-1H-indazol-5-yl)-N-[2-(6-trifluoromethyl-pyridin-3-yl)-ethyl]-acetamide
反応式
[CH3:1][C:2]1[C:10]2[C:5](=[CH:6][CH:7]=[C:8]([NH2:11])[CH:9]=2)[NH:4][N:3]=1.[F:12][C:13]([F:24])([F:23])[C:14]1[N:19]=[CH:18][C:17]([CH2:20][C:21]#N)=[CH:16][CH:15]=1.[F:25][C:26]1[CH:31]=[CH:30][C:29]([C:32](=[O:36])[C:33](O)=[O:34])=[CH:28][CH:27]=1>>[F:25][C:26]1[CH:27]=[CH:28][C:29]([C@H:32]([OH:36])[C:33]([N:11]([C:8]2[CH:9]=[C:10]3[C:5](=[CH:6][CH:7]=2)[NH:4][N:3]=[C:2]3[CH3:1])[CH2:21][CH2:20][C:17]2[CH:18]=[N:19][C:14]([C:13]([F:24])([F:23])[F:12])=[CH:15][CH:16]=2)=[O:34])=[CH:30][CH:31]=1参加物
4
実験手順
In analogy to example 47, 3-Methyl-1H-indazol-5-ylamine, (6-Trifluoromethyl-pyridin-3-yl)-acetonitrile & (4-fluoro-phenyl)-oxo-acetic acid were successively coupled then reduced to give after silica gel and chiral chromatography the target compound. MS(m/e): 473.1 [M+H]+.
後処理
- customto give after silica gel and chiral chromatography the target compound
出典と根拠
- ORDレコード
- ord-5771199981f34e7a965c33497b8433a4
- 出典データセット
- uspto-grants-2012_03
- 特許番号
- US08133909B2
反応ノート
読み込み中…