反応式
[NH2:1][C:2]1[CH:3]=[C:4]([N:10]2[C:19]3[C:14](=[CH:15][C:16]([F:21])=[C:17]([Cl:20])[N:18]=3)[C:13](=[O:22])[C:12]([C:23]([O:25]CC)=[O:24])=[CH:11]2)[C:5]([F:9])=[CH:6][C:7]=1[F:8].Cl.C(O)(=O)C>O>[NH2:1][C:2]1[CH:3]=[C:4]([N:10]2[C:19]3[C:14](=[CH:15][C:16]([F:21])=[C:17]([Cl:20])[N:18]=3)[C:13](=[O:22])[C:12]([C:23]([OH:25])=[O:24])=[CH:11]2)[C:5]([F:9])=[CH:6][C:7]=1[F:8]参加物
4
反応物 2
生成物 1
試薬・触媒・溶媒 1
実験手順
To 0.6 g of ethyl 1-(3-amino-4,6-difluorophenyl)-7-chloro-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylate was added 4 ml of a 3N hydrochloric acid/acetic acid mixture. The solution was heated at reflux for 2 hours. Distilled water (3 ml) was added to the solution, which was refluxed for 5 minutes. The precipitate was collected by filtration and washed with ethanol to give 0.54 g of the title compound.
後処理
- temperatureThe solution was heated
- temperatureat reflux for 2 hours
- temperaturewas refluxed for 5 minutes
- filtrationThe precipitate was collected by filtration
- washwashed with ethanol
出典と根拠
- ORDレコード
- ord-615a00c25ab44f2f9c8282cad3cb2c6c
- 出典データセット
- uspto-grants-1999_06
- 特許番号
- US05910498
関連ノート
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