Sodium Hydroxide → 1-{4-[(2-Phenyl-5-trifluoromethyl-oxazole-4-carbonyl)-amino]-phenyl}-piperidine-4-carboxylic acid
反応式
C[O:2][C:3]([CH:5]1[CH2:10][CH2:9][N:8]([C:11]2[CH:16]=[CH:15][C:14]([NH:17][C:18]([C:20]3[N:21]=[C:22]([C:29]4[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=4)[O:23][C:24]=3[C:25]([F:28])([F:27])[F:26])=[O:19])=[CH:13][CH:12]=2)[CH2:7][CH2:6]1)=[O:4].[OH-].[Na+]>CO.C1COCC1>[C:29]1([C:22]2[O:23][C:24]([C:25]([F:26])([F:27])[F:28])=[C:20]([C:18]([NH:17][C:14]3[CH:13]=[CH:12][C:11]([N:8]4[CH2:7][CH2:6][CH:5]([C:3]([OH:4])=[O:2])[CH2:10][CH2:9]4)=[CH:16][CH:15]=3)=[O:19])[N:21]=2)[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1参加物
反応物 2
生成物 1
試薬・触媒・溶媒 2
実験手順
The above 1-{4-[(2-phenyl-5-trifluoromethyl-oxazole-4-carbonyl)-amino]-phenyl}-piperidine-4-carboxylic acid methyl ester (470 mg, 1 mmol) was dissolved in a mixture of methanol (7 mL) and THF (2 mL). To this solution was added 1N sodium hydroxide solution (3 mL). The mixture was stirred at room temperature for 4 hrs until all starting material was consumed. Solvents were evaporated and the residue was diluted with water (8 mL). The solution was filtered and the filtrate was acidified with 1N hydrochloric acid (3.5 mL). The yellow precipitate was filtered and dried in the air to give 1-{4-[(2-phenyl-5-trifluoromethyl-oxazole-4-carbonyl)-amino]-phenyl}-piperidine-4-carboxylic acid (395 mg). 1H-NMR is consistent with the desired structure. LC-MS indicated a single peak (Rf=3.23 min). LRMS for C23H20F3N3O4 (m/e) calcd 459.14, obsd 460.2 (M+1).
後処理
- customwas consumed
- customSolvents were evaporated
- additionthe residue was diluted with water (8 mL)
- filtrationThe solution was filtered
- filtrationThe yellow precipitate was filtered
- customdried in the air
出典と根拠
- ORDレコード
- ord-5d4f95918fee4b3594c6f7e170adf721
- 出典データセット
- uspto-grants-2011_11
- 特許番号
- US08058299B2
反応ノート
読み込み中…