反応式
[C:1]1([CH:7]([CH2:11][CH:12]([CH3:14])[CH3:13])[C:8]([NH2:10])=O)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.COC1C=CC(C(C)CN)=CC=1>>[C:1]1([CH:7]([CH2:11][CH:12]([CH3:14])[CH3:13])[CH2:8][NH2:10])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1参加物
3
実験手順
The titled compound was prepared from 2-phenyl-4-methylpentanoic acid amide in 51% yield in the same manner as the preparation of 2-(4-methoxyphenyl)propylamine in Example 188c. MS (ESI) 178 (MH+)
出典と根拠
- ORDレコード
- ord-0139beff46494013a3dd85703b0d2ab8
- 出典データセット
- uspto-grants-2008_04
- 特許番号
- US07365085B2
関連ノート
読み込み中…