N-(2-Chloro-3-trifluoromethylbenzyl)-2-(2-methoxyphenyl)propionamide → N-(2-Chloro-3-trifluoromethylbenzyl)-2-(2-methoxyphenyl)propylamine
反応式
[Cl:1][C:2]1[C:21]([C:22]([F:25])([F:24])[F:23])=[CH:20][CH:19]=[CH:18][C:3]=1[CH2:4][NH:5][C:6](=O)[CH:7]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[O:15][CH3:16])[CH3:8].ClC1C(C(F)(F)F)=CC=CC=1CNCC(C1C=CC=CC=1Cl)C>>[Cl:1][C:2]1[C:21]([C:22]([F:23])([F:24])[F:25])=[CH:20][CH:19]=[CH:18][C:3]=1[CH2:4][NH:5][CH2:6][CH:7]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[O:15][CH3:16])[CH3:8]参加物
3
実験手順
The titled compound was prepared from N-(2-chloro-3-trifluoromethylbenzyl)-2-(2-methoxyphenyl)propionamide in 28% yield in the same manner as the preparation of N-(2-chloro-3-trifluoromethylbenzyl)-2-(2-chlorophenyl)propylamine in Example 184c. MS (ESI) 358 (MH+).
出典と根拠
- ORDレコード
- ord-a4d8ed50645d4413a7c2468ef2ec3066
- 出典データセット
- uspto-grants-2008_04
- 特許番号
- US07365085B2
反応ノート
読み込み中…