Water → 2-(4-{2-[4-(2-Bromo-5-fluorophenoxy)piperidin-1-yl]pyrimidin-5-yl}-1H-1,2,3-triazol-1-yl)propanoic acid
反応式
[Br:1][C:2]1[CH:32]=[CH:31][C:30]([F:33])=[CH:29][C:3]=1[O:4][CH:5]1[CH2:10][CH2:9][N:8]([C:11]2[N:16]=[CH:15][C:14]([C:17]3[N:18]=[N:19][N:20]([CH:22]([CH3:28])[C:23]([O:25]CC)=[O:24])[CH:21]=3)=[CH:13][N:12]=2)[CH2:7][CH2:6]1.[OH-].[Li+].O.OP([O-])(O)=O.[K+]>CO.C1COCC1>[Br:1][C:2]1[CH:32]=[CH:31][C:30]([F:33])=[CH:29][C:3]=1[O:4][CH:5]1[CH2:10][CH2:9][N:8]([C:11]2[N:16]=[CH:15][C:14]([C:17]3[N:18]=[N:19][N:20]([CH:22]([CH3:28])[C:23]([OH:25])=[O:24])[CH:21]=3)=[CH:13][N:12]=2)[CH2:7][CH2:6]1参加物
7
反応物 4
生成物 1
試薬・触媒・溶媒 2
実験手順
Into a 25 mL round-bottom flask equipped with a magnetic stirbar was added ethyl 2-(4-{2-[4-(2-bromo-5-fluorophenoxy)piperidin-1-yl]pyrimidin-5-yl}-1H-1,2,3-triazol-1-yl)propanate (55 mg, 0.11 mmol), 1 mL of THF and 0.5 mL of MeOH. A 1.0 M lithium hydroxide solution in water (0.53 mL, 0.53 mmol) was added and the reaction mixture was stirred at room temperature for 2 h. The mixture was poured into a 125 mL separatory funnel containing saturated aqueous KH2PO4 solution (75 mL) and the mixture was extracted with ethyl acetate (3×50 mL). The combined organic layers were washed with brine, dried over MgSO4, filtered and the solvent was evaporated under reduced pressure to yield a beige crystalline solid.
後処理
- customInto a 25 mL round-bottom flask equipped with a magnetic stirbar
- additionThe mixture was poured into a 125 mL separatory funnel
- extractionthe mixture was extracted with ethyl acetate (3×50 mL)
- washThe combined organic layers were washed with brine
- dry with materialdried over MgSO4
- filtrationfiltered
- customthe solvent was evaporated under reduced pressure
- customto yield a beige crystalline solid
出典と根拠
- ORDレコード
- ord-e84e0aa595b24d1c8e6ce1edb833dfdf
- 出典データセット
- uspto-grants-2009_09
- 特許番号
- US07582633B2
反応ノート
読み込み中…