4-(Trifluoromethyl)phenol → Rac-[5-methanesulfonyl-2-((s)-2,2,2-trifluoro-1-methyl-ethoxy)-phenyl]-[3-(4-trifluoromethyl-phenoxymethyl)-pyrrolidin-1-yl]-methanone
反応式
[OH:1][CH2:2][CH:3]1[CH2:7][CH2:6][N:5]([C:8]([C:10]2[CH:15]=[C:14]([S:16]([CH3:19])(=[O:18])=[O:17])[CH:13]=[CH:12][C:11]=2[O:20][C@@H:21]([CH3:26])[C:22]([F:25])([F:24])[F:23])=[O:9])[CH2:4]1.O[C:28]1[CH:33]=[CH:32][C:31]([C:34]([F:37])([F:36])[F:35])=[CH:30][CH:29]=1.C1(P(C2C=CC=CC=2)C2C=CC=CN=2)C=CC=CC=1.N(C(OC(C)(C)C)=O)=NC(OC(C)(C)C)=O>O1CCCC1.C(OCC)(=O)C>[CH3:19][S:16]([C:14]1[CH:13]=[CH:12][C:11]([O:20][C@@H:21]([CH3:26])[C:22]([F:24])([F:25])[F:23])=[C:10]([C:8]([N:5]2[CH2:6][CH2:7][CH:3]([CH2:2][O:1][C:28]3[CH:33]=[CH:32][C:31]([C:34]([F:37])([F:36])[F:35])=[CH:30][CH:29]=3)[CH2:4]2)=[O:9])[CH:15]=1)(=[O:17])=[O:18]参加物
7
反応物 4
生成物 1
試薬・触媒・溶媒 2
反応条件
- 温度
- 70 °C
実験手順
To a solution of 70 mg rac-(3-Hydroxymethyl-pyrrolidin-1-yl)-[5-methanesulfonyl-2-((S)-2,2,2-trifluoro-1-methyl-ethoxy)-phenyl]-methanone (Example C1) in 1.4 ml tetrahydrofuran were added 30 mg 4-hydroxybenzotrifluoride and 50 mg diphenyl-2-pyridylphosphine. 43 mg Di-tert-butyl azodicarboxylate was added. The mixture was stirred at 70° C. for 23 hours. The solvent was removed in vacuo. The oil was purified on silica gel (eluent: ethyl acetate) to yield a yellow gum. The gum was dissolved in ethyl acetate. The solution was washed 3 times with HCl 5N, once with water, dried over Na2SO4, filtered and concentrated in vacuo to provide the title compound as a light yellow foam. MS (m/e): 540.3 (M+H+, 100%).
後処理
- customThe solvent was removed in vacuo
- customThe oil was purified on silica gel (eluent: ethyl acetate)
- customto yield a yellow gum
- washThe solution was washed 3 times with HCl 5N
- dry with materialonce with water, dried over Na2SO4
- filtrationfiltered
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-65eb1d6bb9254bd2b1f1f32ac9968b90
- 出典データセット
- uspto-grants-2011_05
- 特許番号
- US07951836B2
反応ノート
読み込み中…