反应详情

This compound was synthesized from 1-(pyridin-3-yl)piperazine and 3-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzoic acid as described for example 37 step 3 (110 mg, yield 47%). 1H NMR (400 MHz, DMSO-d6) δ 8.32-8.31 (m, 1H), 8.18-8.15 (dt, J=6.7 Hz, 2.0 Hz, 1H), 8.08 (m, 1H), 8.03-8.02 (m, 1H), 7.76-7.71 (m, 2H), 7.36-7.33 (ddd, J=8.5 Hz, 3.0 Hz, 1.2 Hz, 1H), 7.25-7.22 (m, 1H), 3.81 (m, 2H), 3.50 (m, 2H), 3.21 (m, 4H). MS (ESI) m/z: Calculated for C19H16F3N6O2: 403.13. found: 404.2 (M+H)+