反应详情

Synthesized as described in Example 4 from 4-chloro-2-propyl-1H-indole-5-carbonitrile and 3-(chloromethyl)-5-[3-(trifluoromethyl)phenyl]-1,2,4-oxadiazole: 1H NMR (400 MHz, DMSO-d6) δ 8.30 (d, J=7.8 Hz, 1 H), 8.24 (s, 1 H), 8.07 (d, J=7.6 Hz, 1 H), 7.96 (d, J=1.0 Hz, 1 H), 7.89-7.80 (m, 1 H), 7.77 (d, J=8.7 Hz, 1 H), 7.58 (dd, J=8.5, 1.5 Hz, 1 H), 5.84 (s, 2 H), 2.91 (t, J=7.6 Hz, 2 H), 1.76-1.47 (m, 2 H), 0.92 (t, J=7.3 Hz, 3 H); MS (ES) m/z 445 (M+1).

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