Hydrochloric Acid → 4-Chloro-6,7-dimethoxyquinoline-3-carboxylic acid
反応式
C([O:3][C:4]([C:6]1[CH:7]=[N:8][C:9]2[C:14]([C:15]=1[Cl:16])=[CH:13][C:12]([O:17][CH3:18])=[C:11]([O:19][CH3:20])[CH:10]=2)=[O:5])C.[OH-].[Na+].Cl>C(O)C.O>[Cl:16][C:15]1[C:14]2[C:9](=[CH:10][C:11]([O:19][CH3:20])=[C:12]([O:17][CH3:18])[CH:13]=2)[N:8]=[CH:7][C:6]=1[C:4]([OH:5])=[O:3]参加物
6
実験手順
4-chloro-6,7-dimethoxy-3-quinolinecarboxylic ethyl ester (ex RSL) (50 g) was suspended in ethanol (400 ml) and aqueous 2M sodium hydroxide (400 ml) was added with stirring, stirred for 24 hours. The reaction mixture was diluted with water (400 ml), cooled in an ice/water bath and brought to pH4 by carefully addition of concentrated hydrochloric acid. The resulting solid was filtered off, washed with water and dried in a vacuum oven at 50° C. To give 4-chloro-6,7-dimethoxy-3-quinolinecarboxylic acid (52.7 g, 98.7%).
後処理
- stirringstirred for 24 hours
- temperaturecooled in an ice/water bath
- filtrationThe resulting solid was filtered off
- washwashed with water
- customdried in a vacuum oven at 50° C
出典と根拠
- ORDレコード
- ord-88e97d518c1b403e8554a7da5a29042a
- 出典データセット
- uspto-grants-2003_10
- 特許番号
- US06638945B1
反応ノート
読み込み中…