反応式
I[C:2]1[CH:12]=[CH:11][C:5]([C:6]([O:8]CC)=[O:7])=[CH:4][CH:3]=1.[CH3:13][C@@H:14]1[CH2:18][O:17][C:16](=[O:19])[NH:15]1>>[CH3:13][C@@H:14]1[CH2:18][O:17][C:16](=[O:19])[N:15]1[C:2]1[CH:3]=[CH:4][C:5]([C:6]([OH:8])=[O:7])=[CH:11][CH:12]=1参加物
3
実験手順
By reaction and treatment in the same manner as in Preparation Example 18 and using ethyl 4-iodobenzoate (1.4 mL) and (R)-4-methyloxazolidin-2-one (860 mg) described in Preparation Example 25, the title compound (0.9 g) was obtained.
後処理
- customBy reaction and treatment in the same manner
- customas in Preparation Example 18
- customdescribed in Preparation Example 25
出典と根拠
- ORDレコード
- ord-e84e8c1253ee489a82819b91954e3aab
- 出典データセット
- uspto-grants-2013_01
- 特許番号
- US08354401B2
関連ノート
読み込み中…