Reaction Steps
2-(1-Piperidinyl)ethylamine (0.32 mL, 2.2 mmol) was added to a stirred solution of chloride 5 (165 mg, 0.7 mmol) in DME (30 mL) and the solution stirred at reflux temperature for 5 h. The solvent was evaporated and the residue was partitioned between DCM (100 mL) and dilute aqueous NH3 solution (50 mL). The organic fraction was dried and the solvent evaporated. The residue was purified by chromatography, eluting with a gradient (0-10%) of MeOH/DCM, to give 1-oxide 12 (205 mg, 88%) as a pale yellow solid: mp (MeOH) 152-155° C.; 1H NMR δ 7.53 (d, J=8.4 Hz, 1H, H-5), 7.38 (d, J=8.4 Hz, 1H, H-6), 5.90 (br s, 1H, NH), 3.60-3.66 (m, 2H, H-9), 3.48-3.54 (m, 2H, CH2N), 2.97 (br t, J=7.7 Hz, 2H, H-7), 2.57 (dd, J=6.1, 5.9 Hz, 2H, CH2N), 2.38-2.45 (m, 4H, 2×CH2N), 2.17 (br p, J=7.7 Hz, 2H, H-8), 1.55-1.61 (m, 4H, 2×CH2), 1.41-1.48 (m, 2H, CH2); 13C NMR δ 158.4, 149.0, 142.0, 137.3, 132.2, 129.1, 124.6, 56.9, 54.2 (2), 37.9, 35.3, 32.8, 25.9 (2), 24.8, 24.4. Anal. calcd for C17H23N5O: C, 65.2; H, 7.4; N, 22.4. Found: C, 65.1; H, 7.2; N, 22.5%.
