Search results for Design and synthesis of potent N1-substituted indole melatonin receptor agonistsSelected data for 15: 1H NMR (200 MHz, CDCl3) δ 0.87–0.92 (t, 3H, CH3CH2, J = 7.3) 1.58–1.63 (quintet, 2H, CH2CH2CO, J = 7.3), 2.06–2.10 (t, 2H, CH2CO, J = 7.3) 2.86–2.89 (t, 2H, ArCH2, J = 6.8), 3.53–3.58 (q, 2H, CH2NH, J = 6.5), 3.83 (s, 3H, CH3O) 4.01 (s, 3H, CH3ON), 5.48 (br s, 1H, NHCO), 6.88–7.30 (m, 4H, Harom); 13C NMR (50 MHz, CDCl3) δ 13.7, 19.1, 25.3, 38.8, 39.4, 55.9, 65.7, 100.8, 108.6, 109.4, 112.9, 121.8, 122.7, 124.3, 154.5, 172.9. Anal. (C16H22N2O3) C, H, N.

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