Hydrochloric Acid → (3S,6R)-6-Methylpiperidine-3-carboxylic acid

HRID 2367441노트

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HRID 2367441 반응식
[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

참가 물질

4

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온도
100 °C

실험 절차

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).

후처리

  1. temperatureThe mixture was then cooled to room temperature

출처 및 근거

ORD 기록
ord-3eb76b93e6a7473c86d927b277a87055
출처 데이터셋
uspto-grants-2014_04
특허 번호
US08697685B2

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