Реакция #9905

Уравнение реакции

(S)-nicotine

(6-bromo-hexyl)-cyclopentane

→

(S)-1-(6-cyclopentyl-hexyl)-3-(1-methyl-pyrrolidin-2-yl)-pyridinium bromide hydrobromide salt

Выход 54.9%

Растворители

AcOH

Условия реакции

Обработка

1. 1
   ТемператураThe mixture was heated
2. 2
   Температураat reflux for 3 days
3. 3
   ДругоеAcOH was evaporated
4. 4
   Другоеthe residue was recrystallized in ethyl acetate-CHCl3

Методика

To a stirred solution of (S)-nicotine (0.43 g, 2.6 mmol) in AcOH (10 ml) was added (6-bromo-hexyl)-cyclopentane (1.50 g, 6.44 mmol). The mixture was heated at reflux for 3 days. AcOH was evaporated and the residue was recrystallized in ethyl acetate-CHCl3 to afford (S)-1-(6-cyclopentyl-hexyl)-3-(1-methyl-pyrrolidin-2-yl)-pyridinium bromide hydrobromide salt (NCyNB-5) (0.68 g, 54%) as hygroscopic white crystals: 1H NMR (300 MHz, CDCl3) δ 11.74 (1H, s), 10.52 (1H, s), 9.62 (1H, d, J=8.4 Hz), 8.99 (1H, d, J=6.0 Hz), 8.29 (1H, dd, J=7.8, 6.3 Hz), 5.80 (1H, m), 4.78 (2H, m), 4.01 (1H, m), 3.35 (1H, m), 2.98 (3H, d, J=5.1 Hz), 2.76 (1H, m), 2.45 (3H, m), 2.15 (2H, m), 1.70 (3H, m), 1.15–1.60 (12H, m), 1.02 (2H, m); 13C NMR (75 MHz, CDCl3) δ 147.78, 146.78, 144.41, 134.94, 128.90, 67.03, 63.14, 56.10, 40.26, 38.72, 36.23, 32.96, 32.11, 31.82, 29.48, 28.77, 26.55, 25.43, 21.89; Anal. Calcd for C21H36Br2N2.0.2H2O: C, 52.55; H, 7.64; N, 5.84. Found: C, 52.41; H, 7.56; N, 5.78.

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