“…1 H NMR (400 MHz, CDCl 3 ): δ 8.00 (s, 2H, indole-NH), 7.64 (d, J = 8.0 Hz, 2H, Ar−H), 7.36 (t, J = 8.4 Hz, 4H, Ar−H), 7 29. (d, J = 7.0 Hz, 1H, Ar−H), 7.18−7.24 (m, 3H, Ar−H), 6.99−7.08 (m, 5H, Ar−H), 6.63 (d, J = 7.8 Hz, 1H, CH 2 −NH), 6.17 (s, 1H, CH 2 NHCS−NH), 4.97 (t, J = 7.1 Hz, 1H, Ar 2 −CH), 4.43 (t, J = 5.4 Hz, 2H, CH 2 ); 13 C NMR (100 MHz, DMSO-d 6 ): δ 180.4, 139.6, 137.0, 130.4, 129.0, 127.2, 124.4, 123.2, 123.0, 121.4, 119.5, 118.7, 116.5, 111.9, 48.9, 33.5.…”