Nicotine → (S)-1-dec-3-ynyl-3-(1-methyl-pyrrolidin-2-yl)-pyridinium bromide

HRID 9817노트

반응식

HRID 9817 반응식
[N:1]1[CH:6]=[C:5]([C@@H:7]2[CH2:12][CH2:11][CH2:10][N:8]2[CH3:9])[CH:4]=[CH:3][CH:2]=1.[Br:13][CH2:14][CH2:15][C:16]#[C:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23]>CC(O)=O>[Br-:13].[CH2:14]([N+:1]1[CH:2]=[CH:3][CH:4]=[C:5]([C@@H:7]2[CH2:12][CH2:11][CH2:10][N:8]2[CH3:9])[CH:6]=1)[CH2:15][C:16]#[C:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23]

참가 물질

4

실험 절차

To a stirred solution of (S)-nicotine (0.46 g, 2.8 mmol) in AcOH (15 ml) was added 1-bromo-dec-3-yne (1.50 g, 6.91 mmol). The mixture was heated at reflux for 3 days. AcOH was evaporated and the residue was dissolved in CHCl3. The mixture was washed with saturated aqueous NaHCO3, water and brine successively and dried. Evaporation of the solvent followed by titration with ether afforded 0.55 g (51%) of (S)-1-dec-3-ynyl-3-(1-methyl-pyrrolidin-2-yl)-pyridinium bromide (NDNB-3y) as a brown oil. 1H NMR (300 MHz, CDCl3) δ 9.77 (1H, d, J=5.7 Hz), 9.14 (1H, s), 8.43 (1H, d, J=8.1 Hz), 8.04 (1H, dd, J=8.1, 5.7 Hz), 5.16 (2H, m), 3.52 (1H, t, J=8.1 Hz), 3.27 (1H, m), 3.03 (2H, m), 2.47 (2H, m), 2.26 (3H, s), 1.85–2.10 (4H, m), 1.70 (1H, m), 1.15–1.45 (8H, m), 0.86 (3H, t, J=7.2 Hz); 13C NMR (75 MHz, CDCl3) δ 145.91, 144.24, 144.12, 143.57, 128.02, 86.16, 73.98, 67.24, 60.66, 56.87, 40.70, 36.05, 31.44, 28.86, 28.75, 23.36, 22.71, 22.45, 18.82, 14.27; Anal. Calcd for C20H31BrN2.0.7H2O: C, 61.28; H, 8.33; N, 7.15. Found: C, 61.14; H, 8.21; N, 7.14.

후처리

  1. temperatureThe mixture was heated
  2. temperatureat reflux for 3 days
  3. customAcOH was evaporated
  4. dissolutionthe residue was dissolved in CHCl3
  5. washThe mixture was washed with saturated aqueous NaHCO3, water and brine successively
  6. customdried
  7. customEvaporation of the solvent

출처 및 근거

ORD 기록
ord-3fdcf2a8f87f46b7a88d01e0c4bc8690
출처 데이터셋
uspto-grants-2006_08
특허 번호
US07091357B2

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