反応式
[CH3:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[CH3:11])[C:5]([OH:7])=O.N[NH:13][C@@H:14]([CH2:19][OH:20])[CH2:15][CH:16]([CH3:18])[CH3:17]>>[OH:20][CH2:19][C@H:14]([NH:13][C:5](=[O:7])[C:4]1[CH:8]=[CH:9][C:10]([CH3:11])=[C:2]([CH3:1])[CH:3]=1)[CH2:15][CH:16]([CH3:18])[CH3:17]参加物
3
実験手順
(R)—N-(1-hydroxy-4-methylpentan-2-yl)-3,4-dimethylbenzamide was prepared in a similar manner as described in example 4 using 3,4-dimethylbenzoic acid and with (R)-aminoleucinol. Yield: 75%. MS (M+H, 250.3).
出典と根拠
- ORDレコード
- ord-68997b4afbcf4dcaa1a97585d74276ea
- 出典データセット
- uspto-grants-2014_11
- 特許番号
- US08895050B2
関連ノート
読み込み中…