Potassium Carbonate → (3R,4S)-3-(1-phenyl-ethylamino)-piperidine-1,4-dicarboxylic acid 1-tert-butyl ester 4-ethyl ester
反応式
[CH2:1]([O:3][C:4]([C@@H:6]1[CH2:11][CH2:10][N:9]([C:12]([O:14][C:15]([CH3:18])([CH3:17])[CH3:16])=[O:13])[CH2:8][C@@H:7]1[NH:19][C@@H:20]([C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)[CH3:21])=[O:5])[CH3:2].C(=O)([O-])[O-].[K+].[K+]>C(O)C>[CH2:1]([O:3][C:4]([C@H:6]1[CH2:11][CH2:10][N:9]([C:12]([O:14][C:15]([CH3:16])([CH3:17])[CH3:18])=[O:13])[CH2:8][C@@H:7]1[NH:19][CH:20]([C:22]1[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=1)[CH3:21])=[O:5])[CH3:2]参加物
4
実験手順
In a dry flask (3R,4R)-3-[(R)-1-phenyl-ethylamino]-piperidine-1,4-dicarboxylic acid 1-tert-butyl ester 4-ethyl ester (31.32 g, 83.0 mmol) was dissolved in ethanol (400 mL). Potassium carbonate (68.72 g) was added and the mixture was refluxed for 6 hours. The reaction mixture was cooled, filtered through a bed of celite, and concentrated in vacuo to give a crude oil. Purification by flash column chromatography (20-50% ethyl acetate/hexanes) provided a colorless oil (4.59 g, 15%). Unepimerized ester was also isolated (23.49 g, 75%).
後処理
- temperaturethe mixture was refluxed for 6 hours
- temperatureThe reaction mixture was cooled
- filtrationfiltered through a bed of celite
- concentrationconcentrated in vacuo
- customto give a crude oil
- customPurification by flash column chromatography (20-50% ethyl acetate/hexanes)
出典と根拠
- ORDレコード
- ord-2b5b542d9bc64276b527f0839bd4b7b9
- 出典データセット
- uspto-grants-2005_09
- 特許番号
- US06949546B2
反応ノート
読み込み中…