6-(2,6-Dimethoxyphenyl)piperidin-2-one → 5-(2,6-Dimethoxyphenyl)-3-methylpyrrolidin-2-one
反応式
[NH2:1][CH:2]([C:11]1[C:16]([O:17][CH3:18])=[CH:15][CH:14]=[CH:13][C:12]=1[O:19][CH3:20])[CH2:3][CH:4]([CH3:10])[C:5](OCC)=[O:6].COC1C=CC=C(OC)C=1C1NC(=O)CCC1>>[CH3:20][O:19][C:12]1[CH:13]=[CH:14][CH:15]=[C:16]([O:17][CH3:18])[C:11]=1[CH:2]1[NH:1][C:5](=[O:6])[CH:4]([CH3:10])[CH2:3]1参加物
3
実験手順
5-(2,6-Dimethoxyphenyl)-3-methylpyrrolidin-2-one was prepared from ethyl 4-amino-4-(2,6-dimethoxyphenyl)-2-methylbutanoate according to the procedure described for 6-(2,6-dimethoxyphenyl)piperidin-2-one. Subsequent purification by FC (DCM/MeOH=20/1) afforded 5-(2,6-dimethoxyphenyl)-3-methylpyrrolidin-2-one as a light orange solid. LC-MS (conditions D): tR=0.84 min.; [M+H]+: 236.43 g/mol.
後処理
- customSubsequent purification by FC (DCM/MeOH=20/1)
出典と根拠
- ORDレコード
- ord-bd11ac94199e490a9bb7bc985002b7ec
- 出典データセット
- uspto-grants-2016_01
- 特許番号
- US09242970B2
反応ノート
読み込み中…