Hydrochloric Acid → HCID 178488125、化合物
反応式
[CH3:1][O:2][C:3]1[CH:22]=[CH:21][C:6]2[NH:7][C:8]([S:10][CH2:11][C:12]3[C:17]([CH3:18])=[C:16](Cl)[C:15]([CH3:20])=[CH:14][N:13]=3)=[N:9][C:5]=2[CH:4]=1.[CH3:23][OH:24].C[O-].[Na+].Cl>C(OCC)(=O)C>[CH3:1][O:2][C:3]1[CH:22]=[CH:21][C:6]2[NH:7][C:8]([S:10][CH2:11][C:12]3[C:17]([CH3:18])=[C:16]([O:24][CH3:23])[C:15]([CH3:20])=[CH:14][N:13]=3)=[N:9][C:5]=2[CH:4]=1参加物
実験手順
First, 277 mg (0.92 mmol) of 5-methoxy-2-{[(4-chloro-3,5-dimethyl-2-pyridyl)methyl]thio}-1H-benzimidazole obtained in Example 21 and 1.00 g (5.20 mmol) of methanol 28% solution of sodium methoxide were introduced to a 3-necked flask (30 ml volume) equipped with a thermometer, a magnetic stirrer and a condenser tube, and the mixture was agitated for 10 hours while being slowly refluxed. Then the mixture was neutralized with dilute hydrochloric acid. Ethyl acetate (10 ml) was added thereto and an organic layer was separated, and an aqueous layer was extracted twice with 10 ml of ethyl acetate. The extracts and the above mentioned organic layer were combined and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure to give 232 mg of 5-methoxy-2-{[(4-methoxy-3,5-dimethyl-2-pyridyl)methyl]thio}-1H-benzimidazole (yield of 85%) with revealing the properties.
後処理
- customequipped with a thermometer, a magnetic stirrer and a condenser tube
- temperaturewhile being slowly refluxed
- customan organic layer was separated
- extractionan aqueous layer was extracted twice with 10 ml of ethyl acetate
- dry with materialdried over anhydrous magnesium sulfate
- customThe solvent was removed under reduced pressure
出典と根拠
- ORDレコード
- ord-4b5b552b356c4355b7ec698af979dc80
- 出典データセット
- uspto-grants-2002_02
- 特許番号
- US06350876B2
反応ノート
読み込み中…