反応式
[OH:1][C:2]12[CH2:6][C:4]([NH:7][C:8](=[O:10])[CH3:9])([CH2:5]1)[CH2:3]2.[CH2:11]([C:15]1[CH:20]=[CH:19][C:18]([CH:21]([CH3:25])[C:22](Cl)=[O:23])=[CH:17][CH:16]=1)[CH:12]([CH3:14])[CH3:13]>>[CH2:11]([C:15]1[CH:16]=[CH:17][C:18]([CH:21]([CH3:25])[C:22]([O:1][C:2]23[CH2:6][C:4]([NH:7][C:8](=[O:10])[CH3:9])([CH2:5]2)[CH2:3]3)=[O:23])=[CH:19][CH:20]=1)[CH:12]([CH3:14])[CH3:13]参加物
3
実験手順
The general procedure of Example 1 Step 3 is repeated starting with N-(3-hydroxybicyclo[1.1.1]pentan-1-yl)acetamide (1) and using 2-(4-isobutylphenyl)propanoyl chloride in place of the acetyl chloride to produce 3-acetamidobicyclo[1.1.1]pentan-1-yl 2-(4-isobutylphenyl)propanoate (9).
出典と根拠
- ORDレコード
- ord-bd66d318b4f74252ae13b7b447a832ff
- 出典データセット
- uspto-grants-2016_09
- 特許番号
- US09447025B2
関連ノート
読み込み中…