Hydrochloric Acid → 5-Chloro-2-hydroxy-N-({[3,5-bis(trifluoromethyl)phenyl]carbamoyl)-methyl)benzamide
反応式
[OH-].[Na+].C([O:6][C:7]1[CH:33]=[CH:32][C:31]([Cl:34])=[CH:30][C:8]=1[C:9]([NH:11][CH2:12][C:13](=[O:29])[NH:14][C:15]1[CH:20]=[C:19]([C:21]([F:24])([F:23])[F:22])[CH:18]=[C:17]([C:25]([F:28])([F:27])[F:26])[CH:16]=1)=[O:10])(=O)C.Cl>CO.O1CCCC1>[Cl:34][C:31]1[CH:32]=[CH:33][C:7]([OH:6])=[C:8]([CH:30]=1)[C:9]([NH:11][CH2:12][C:13](=[O:29])[NH:14][C:15]1[CH:16]=[C:17]([C:25]([F:27])([F:28])[F:26])[CH:18]=[C:19]([C:21]([F:22])([F:23])[F:24])[CH:20]=1)=[O:10]参加物
5
反応物 3
生成物 1
試薬・触媒・溶媒 1
実験手順
5N Aqueous sodium hydroxide (0.1 mL) was added to a solution of 2-acetoxy-5-chloro-N-({[3,5-bis(trifluoromethyl)phenyl]carbamoyl}methyl)benzamide (83.7 mg, 0.17 mmol) in methanol/tetrahydrofuran (2 mL+1 mL), and the mixture was stirred at room temperature for 20 minutes. The reaction mixture was poured into diluted hydrochloric acid and extracted with ethyl acetate. After the ethyl acetate layer was washed with water and brine, dried over anhydrous sodium sulfate, the residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=2:1) and washed with n-hexane under suspension to give the title compound (47.7 mg, 63.7%) as a white crystal.
後処理
- extractionextracted with ethyl acetate
- washAfter the ethyl acetate layer was washed with water and brine
- dry with materialdried over anhydrous sodium sulfate
- customthe residue obtained by evaporation of the solvent under reduced pressure
- customwas purified by column chromatography on silica gel (n-hexane:ethyl acetate=2:1)
- washwashed with n-hexane under suspension
出典と根拠
- ORDレコード
- ord-b6f8d379c38b4bfa8575aa4734836663
- 出典データセット
- uspto-grants-2010_04
- 特許番号
- US07700655B2
反応ノート
読み込み中…