反応式
[CH3:1][O:2][C:3]1[CH:11]=[CH:10][CH:9]=[CH:8][C:4]=1[C:5](Cl)=[O:6].[NH2:12][C:13]1[CH:14]=[CH:15][C:16]([Cl:25])=[C:17]([CH:24]=1)[C:18]([O:20][CH:21]([CH3:23])[CH3:22])=[O:19].C(N(CC)CC)C.O>CN(C1C=CN=CC=1)C.O1CCOCC1>[Cl:25][C:16]1[CH:15]=[CH:14][C:13]([NH:12][C:5](=[O:6])[C:4]2[CH:8]=[CH:9][CH:10]=[CH:11][C:3]=2[O:2][CH3:1])=[CH:24][C:17]=1[C:18]([O:20][CH:21]([CH3:23])[CH3:22])=[O:19]参加物
実験手順
2-Methoxybenzoyl chloride (8.8 g, 0.05 mole) was added at room temperature under a dry nitrogen atmosphere to a stirred mixture of 1-methylethyl 5-amino-2-chlorobenzoate (10.7 g, 0.05 mole), triethylamine (5.6 g, 0.055 mole) and 4-(N,N,-dimethylamino)pyridine (catalyst, 0.2 g) dissolved in dry p-dioxane (100 ml . A solid Precipitate formed. Following the initial exothermic reaction (temperature increased to about 45° C.), the reaction mixture was stirred under nitrogen at room temperature for 20 hours. Next, the reaction mixture was added to water (500 ml), resulting in the precipitation of a solid product, which was collected by vacuum filtration, washed with water (500 ml), and dried to yield 16.2 g of the title compound, m.p. 94°-96° C. NMR: (CDCl3) : 1.40 (6H,d) 4.05 (3H,s)5.28 (1H,m), 7.02 (1H,d), 7.11 (1H,m), 7.38 (1H,d), 7.49 (1H,m), 7.87 (1H,m), 7.95 (1H,d), 8.25 (1H,m), 9.86 (1H,s)
後処理
- customA solid Precipitate formed
- customexothermic reaction (temperature increased to about 45° C.)
- customresulting in the precipitation of a solid product, which
- filtrationwas collected by vacuum filtration
- washwashed with water (500 ml)
- customdried
出典と根拠
- ORDレコード
- ord-77d78e65566740bb92d633e4639e441e
- 出典データセット
- uspto-grants-1993_12
- 特許番号
- US05268389
関連ノート
読み込み中…