Acetic Acid → 1-benzyl-N,4-dimethylpiperidin-3-amine

HRID 8701

반응식

HRID 8701 반응식
[CH2:1]([N:8]1[CH2:13][CH2:12][CH:11]([CH3:14])[C:10](=O)[CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CO.C(O)(=O)C.[CH3:22][NH2:23]>O1CCCC1>[CH2:1]([N:8]1[CH2:13][CH2:12][CH:11]([CH3:14])[CH:10]([NH:23][CH3:22])[CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

참가 물질

6

실험 절차

To a stirred solution of 1-benzyl-4-methyl-piperidin-3-one (2.3 grams, 11.5 mmol), prepared by the methods of Iorio, M. A. and Damia, G., Tetrahedron, 26, 5519 (1970) and Grieco et al., Journal of the American Chemical Society, 107, 1768 (1985), (modified using 5% methanol as a co-solvent), both references are incorporated by reference in their entirety, dissolved in 23 mL of 2 M methylamine in tetrahydrofuran was added 1.4 mL (23 mmol) of acetic acid and the resulting mixture stirred in a sealed tube for 16 hours at room temperature. Triacetoxy sodium borohydride (4.9 grams, 23 mmol) was added and the new mixture stirred at room temperature in a sealed tube for 24 h, at which time, the reaction was quenched upon addition of 1 N sodium hydroxide (50 mL). The reaction mixture was then extracted 3×80 mL with ether, the combined ether layers dried over sodium sulfate (Na2SO4) and concentrated to dryness in vacuo affording 1.7 grams (69%) of the title compound as a white solid. LRMS: 219.1 (M+1).

후처리

  1. stirringthe new mixture stirred at room temperature in a sealed tube for 24 h, at which time
  2. customthe reaction was quenched upon addition of 1 N sodium hydroxide (50 mL)
  3. extractionThe reaction mixture was then extracted 3×80 mL with ether
  4. dry with materialthe combined ether layers dried over sodium sulfate (Na2SO4)
  5. concentrationconcentrated to dryness in vacuo

출처 및 근거

ORD 기록
ord-8210397d84ee46a398b1d1f423bf0696
출처 데이터셋
uspto-grants-2006_08
특허 번호
US07091208B2

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