反応式
[N:1]1[CH:6]=[CH:5][C:4]([NH:7][C:8]2[CH:9]=[C:10]([CH:14]=[CH:15][CH:16]=2)[C:11](O)=[O:12])=[CH:3][CH:2]=1.[NH3:17]>>[N:1]1[CH:6]=[CH:5][C:4]([NH:7][C:8]2[CH:9]=[C:10]([CH:14]=[CH:15][CH:16]=2)[C:11]([NH2:17])=[O:12])=[CH:3][CH:2]=1参加物
3
実験手順
3-(4-Pyridinylamino)benzamide was prepared from 3-(4-pyridinylamino)benzoic acid and ammonia according to the procedure of Example 48, part (b), and was obtained in 50% yield as a colorless powder, m.p. 201°-203° C. when recrystallized from methanol.
後処理
- customwas obtained in 50% yield as a colorless powder, m.p. 201°-203° C. when
- customrecrystallized from methanol
出典と根拠
- ORDレコード
- ord-97b00eea7a994df3861f4e4a6b98738e
- 出典データセット
- uspto-grants-1986_09
- 特許番号
- US04610991
関連ノート
読み込み中…