Hydrochloric Acid → 1-(Pyridin-4-yl)piperidine-3-carboxylic acid hydrochloride
反応式
[N:1]1[CH:6]=[CH:5][C:4]([N:7]2[CH2:12][CH2:11][CH2:10][CH:9]([C:13]([O:15]CC)=[O:14])[CH2:8]2)=[CH:3][CH:2]=1.[ClH:18]>O1CCOCC1>[ClH:18].[N:1]1[CH:2]=[CH:3][C:4]([N:7]2[CH2:12][CH2:11][CH2:10][CH:9]([C:13]([OH:15])=[O:14])[CH2:8]2)=[CH:5][CH:6]=1参加物
4
実験手順
A mixture of 1.8 g of ethyl 1-(4-pyridyl)-piperidine-3-carboxylate, 50 ml of dioxane and 20 ml of 1 M hydrochloric acid was heated under reflux for 5 hours. The solvent was evaporated, and the residue was washed with ethyl acetate to obtain the title compound.
後処理
- temperaturewas heated
- temperatureunder reflux for 5 hours
- customThe solvent was evaporated
- washthe residue was washed with ethyl acetate
出典と根拠
- ORDレコード
- ord-8e3b448397e646fe82b0b737be53b5bf
- 出典データセット
- uspto-grants-2004_03
- 特許番号
- US06710056B2
反応ノート
読み込み中…