4-Fluorobenzoyl chloride → N-(4-fluorobenzoyl)isobutyrylmethylamine
反応式
Cl.[C:2]([CH2:7][NH2:8])(=[O:6])[CH:3]([CH3:5])[CH3:4].C(=O)(O)[O-].[Na+].[F:14][C:15]1[CH:23]=[CH:22][C:18]([C:19](Cl)=[O:20])=[CH:17][CH:16]=1>>[F:14][C:15]1[CH:23]=[CH:22][C:18]([C:19]([NH:8][CH2:7][C:2](=[O:6])[CH:3]([CH3:5])[CH3:4])=[O:20])=[CH:17][CH:16]=1参加物
4
実験手順
4.0 g of isobutyrylmethylamine hydrochloride, 6.1 g of sodium bicarbonate and 5.1 g of 4-fluorobenzoyl chloride are treated in the same manner as described in Preparation 1-(4). 5.8 g of N-(4-fluorobenzoyl)isobutyrylmethylamine are thereby obtained. Yield: 89.2%.
後処理
- customas described in Preparation 1-(4)
出典と根拠
- ORDレコード
- ord-2b415b9ba8c64dc1b48f47c9afb60913
- 出典データセット
- uspto-grants-1985_08
- 特許番号
- US04535089
反応ノート
読み込み中…