HCID 86712345、化合物 → 1-(2-(2-(2-((1-Methyl-1H-pyrazol-4-yl)amino)-5-(trifluoromethyl)pyrimidin-4-yl)ethyl)phenyl)cyclopropanecarboxamide
反応式
[CH3:1][N:2]1[CH:6]=[C:5]([NH:7][C:8]2[N:13]=[C:12]([C:14]#[C:15][C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=3[C:22]3([C:25]([NH2:27])=[O:26])[CH2:24][CH2:23]3)[C:11]([C:28]([F:31])([F:30])[F:29])=[CH:10][N:9]=2)[CH:4]=[N:3]1>CN(C=O)C.CCOC(C)=O.CCN(CC)CC.[Pd]>[CH3:1][N:2]1[CH:6]=[C:5]([NH:7][C:8]2[N:13]=[C:12]([CH2:14][CH2:15][C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=3[C:22]3([C:25]([NH2:27])=[O:26])[CH2:24][CH2:23]3)[C:11]([C:28]([F:29])([F:31])[F:30])=[CH:10][N:9]=2)[CH:4]=[N:3]1参加物
6
実験手順
A mixture of 1-(2-((2-((1-methyl-1H-pyrazol-4-yl)amino)-5-(trifluoromethyl)pyrimidin-4-yl)ethynyl)phenyl)cyclopropanecarboxamide A75 (0.120 g, 0.281 mmol) and 10% Pd/C (0.135 g) in DMF (3 mL), EtOAc (5 mL) and Et3N (0.5 mL) was stirred under a hydrogen atmosphere for 16 hours. The mixture was filtered through Celite and concentrated under reduced pressure before purification by silica gel column chromatography (0-15% MeOH in EtOAc). The product was triturated with Et2O and the resulting precipitate was collected to give the title compound 65 (0.090 g, 74%). LCMS-D: rt 3.316 min; m/z 431.2 [M+H]+.
後処理
- filtrationThe mixture was filtered through Celite
- concentrationconcentrated under reduced pressure before purification by silica gel column chromatography (0-15% MeOH in EtOAc)
- customThe product was triturated with Et2O
- customthe resulting precipitate was collected
出典と根拠
- ORDレコード
- ord-f593faf02fe846d7b7e09c0f7a3cd65c
- 出典データセット
- uspto-grants-2016_01
- 特許番号
- US09238644B2
反応ノート
読み込み中…