Hydrochloric Acid → (3S,6R)-6-Methylpiperidine-3-carboxylic acid
反応式
[CH3:1][C@H:2]1[N:7](C(OCC2C=CC=CC=2)=O)[CH2:6][C@@H:5]([C:18]([O:20]C)=[O:19])[CH2:4][CH2:3]1.Cl>O1CCOCC1>[CH3:1][C@H:2]1[NH:7][CH2:6][C@@H:5]([C:18]([OH:20])=[O:19])[CH2:4][CH2:3]1参加物
反応条件
- 温度
- 100 °C
実験手順
Into a 75 mL sealable tube, were added 3-methyl 1-(phenylmethyl) (3S,6R)-6-methyl-1,3-piperidinedicarboxylate (10 g, 34.3 mmol), 1,4-dioxane (20 mL) and concentrated HCl (20 mL), and the mixture was stirred at 100° C. for 3 hours. The mixture was then cooled to room temperature. HPLC showed no starting material and NMR showed major was the desired product. The solution was transfered to a 500 mL round bottom flask, and concentrated to dryness. Trituration with Et2O and CH3CN afforded the HCl salt of the title compound (6.17 g) as a colorless oil that turned into a white solid after standing overnight. 1H NMR (400 MHz, CD3OD): δ 6.51 (s, 1H), 7.04 (m, 1H), 7.32 (m, 2H), 7.46 (dd, J=8.6, 1.3 Hz, 1H), 7.66 (m, 2H), 7.75 (dd, J=8.3, 0.8 Hz, 1H), 7.81 (s, 1H).
後処理
- temperatureThe mixture was then cooled to room temperature
出典と根拠
- ORDレコード
- ord-3eb76b93e6a7473c86d927b277a87055
- 出典データセット
- uspto-grants-2014_04
- 特許番号
- US08697685B2
反応ノート
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