4-Amino-3,5-dimethylisoxazole → 7-Methoxy-2-methoxymethylbenzofuran-4-carboxylic acid (3,5-dimethylisoxazol-4-yl)-amide
反応式
[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([C:15]([OH:17])=O)=[C:7]2[C:11]=1[O:10][C:9]([CH2:12][O:13][CH3:14])=[CH:8]2.[CH3:18][C:19]1[C:23]([NH2:24])=[C:22]([CH3:25])[O:21][N:20]=1>>[CH3:18][C:19]1[C:23]([NH:24][C:15]([C:6]2[CH:5]=[CH:4][C:3]([O:2][CH3:1])=[C:11]3[O:10][C:9]([CH2:12][O:13][CH3:14])=[CH:8][C:7]=23)=[O:17])=[C:22]([CH3:25])[O:21][N:20]=1参加物
3
実験手順
Starting from 7-methoxy-2-methoxymethylbenzofuran-4-carboxylic acid (0.19 g) and 3,5-dimethylisoxazol-4-ylamine (88 mg). Purification by column chromatography on silica eluting with ethyl acetate afforded the title compound as a cream solid (0.18 g).
後処理
- customPurification by column chromatography on silica eluting with ethyl acetate
出典と根拠
- ORDレコード
- ord-e4399eb88f1e4dd5b69f17f5a1b2b566
- 出典データセット
- uspto-grants-2002_09
- 特許番号
- US06455561B1
反応ノート
読み込み中…