4-hydroxypiperidine-4-carboxylic Acid → Ethyl 4-hydroxypiperidine-4-carboxylate
反応式
[OH:1][C:2]1([C:8]([OH:10])=[O:9])[CH2:7][CH2:6][NH:5][CH2:4][CH2:3]1.Cl.[CH2:12](O)[CH3:13]>>[OH:1][C:2]1([C:8]([O:10][CH2:12][CH3:13])=[O:9])[CH2:7][CH2:6][NH:5][CH2:4][CH2:3]1参加物
3
実験手順
The 4-hydroxypiperidine-4-carboxylic acid (118 mg) obtained in the step (a) of Example 68 was dissolved in 1 N hydrochloric acid/ethanol (5 ml) solution, and the resulting solution was stirred at room temperature for 17 hours and then under reflux for 6 hours. The reaction mixture was concentrated to obtain crude ethyl 4-hydroxypiperidine-4-carboxylate. This crude ethyl 4-hydroxypiperidine-4-carboxylate was used in the following reaction without purification.
後処理
- temperatureunder reflux for 6 hours
- concentrationThe reaction mixture was concentrated
出典と根拠
- ORDレコード
- ord-9698b9aa8dcc4278a107e8bb6126e155
- 出典データセット
- uspto-grants-2003_06
- 特許番号
- US06576627B1
反応ノート
読み込み中…