Hydrochloric Acid → 2-(4-Carboxymethylamino-3-fluorophenyl)-6,8-difluoro-5-hexylamino-4H-1-benzopyran-4-one
反応式
C([N:4]([C:11]1[CH:16]=[CH:15][C:14]([C:17]2[O:18][C:19]3[C:27]([F:28])=[CH:26][C:25]([F:29])=[C:24]([NH:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH3:36])[C:20]=3[C:21](=[O:23])[CH:22]=2)=[CH:13][C:12]=1[F:37])[CH2:5][C:6]([O:8]CC)=[O:7])(=O)C.Cl.O>O1CCOCC1>[C:6]([CH2:5][NH:4][C:11]1[CH:16]=[CH:15][C:14]([C:17]2[O:18][C:19]3[C:27]([F:28])=[CH:26][C:25]([F:29])=[C:24]([NH:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH3:36])[C:20]=3[C:21](=[O:23])[CH:22]=2)=[CH:13][C:12]=1[F:37])([OH:8])=[O:7]参加物
5
反応物 3
生成物 1
試薬・触媒・溶媒 1
実験手順
143 mg (0.276 mmol) of Compound 74 obtained in Example 74 was dissolved in 12 ml of dioxane, 8 ml of concentrated hydrochloric acid was added and the mixture was heated ar reflux for 10 minutes. The reaction solution was cooled on ice, water was added and the mixture was extracted with ethyl acetate. The organic layer was washed twice with water and once with an aqueous saturated solution of sodium chloride and dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The residue was recrystallized from ethyl acetate/n-hexane to give 95 mg (77%) of Compound 75.
後処理
- temperaturethe mixture was heated ar
- temperaturereflux for 10 minutes
- additionwas added
- extractionthe mixture was extracted with ethyl acetate
- washThe organic layer was washed twice with water and once with an aqueous saturated solution of sodium chloride
- dry with materialdried over anhydrous sodium sulfate
- distillationthe solvent was distilled off under reduced pressure
- customThe residue was recrystallized from ethyl acetate/n-hexane
出典と根拠
- ORDレコード
- ord-7012fb3a54b6483a9cdf13bbea0d21c5
- 出典データセット
- uspto-grants-1996_07
- 特許番号
- US05539112
反応ノート
読み込み中…