2-Ethoxybenzoyl chloride → 3-Carbamoyl-2-(2-ethoxybenzamido)benzamide
反応式
[NH2:1][C:2]1[C:10]([C:11](=[O:13])[NH2:12])=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([NH2:6])=[O:5].[CH2:14]([O:16][C:17]1[CH:25]=[CH:24][CH:23]=[CH:22][C:18]=1[C:19](Cl)=[O:20])[CH3:15]>>[C:4]([C:3]1[C:2]([NH:1][C:19](=[O:20])[C:18]2[CH:22]=[CH:23][CH:24]=[CH:25][C:17]=2[O:16][CH2:14][CH3:15])=[C:10]([CH:9]=[CH:8][CH:7]=1)[C:11]([NH2:12])=[O:13])(=[O:5])[NH2:6]参加物
3
実験手順
The title compound was prepared from 2-amino-3-carbamoylbenzamide and 2-ethoxybenzoyl chloride following the procedure of Preparation 5 and was obtained as colorless crystals (33%), m.p. 224°-225° C. Found: C,62.57; H,5.18; N,12.81. C17H17N3O4 requires C,62.37; H,5.24; N,12.84%.
後処理
- customthe procedure of Preparation 5
出典と根拠
- ORDレコード
- ord-a1e7b3bc471340b6995f8e1c0cc9a602
- 出典データセット
- uspto-grants-1996_01
- 特許番号
- US05482941
反応ノート
読み込み中…