“…Addition of petroleum ether (20 mL) led to the precipitation of the target compounds which were isolated by centrifugation and recrystallized from methanol, yielding the β N-d 2 -alkanoyl-5-hydroxytryptamides in a purity of more than 99% (LC-MS, 1 m/z (%) 160.1 (100), 177 (12). 1 H NMR (400 MHz, d 6 -DMSO): δ/ppm 0.84 (t, 3H, J = 7.1 Hz, H-C(28)), 1.15-1.30 (m, 12 Â 2H, 2 Â 1H, H-C (14)(15)(16)(17)(18)(20)(21)(22)(23)(24)(25)(26)(27), H-C (19,20)), 1.47 (m, 2H, H-C(13)), 2.03 (t, 2H, J = 7.4 Hz, H-C(12)), 2.69 (t, 2H, J = 7.4 Hz, H-C(8)), 3.25 (q, 2H, J = 6.6 Hz, H-C(9)), 6.56 (dd, 1H, J = 8.56 Hz, J = 2.02 Hz, H-C(6)), 6.80 (d, 1H, J = 2.02 Hz, H-C(4)), 6.99 (d, 1H, J = 1.77 Hz, H-C(2)), 7.10 (d, 1H, J = 8.6 Hz, H-C(7)), 7.82 (t, 1H, J = 5.56 Hz, H-N(10)), 8.54 (s, 1H, HO-C(5)), 10.44 (d, 1H, J = 1.77 Hz, H-N(1)). 13 C NMR (100 MHz, d 6 -DMSO): δ/ppm 14.08 (CH 3 , C(28)), 25.35 (CH 2 , C(8,13)), 22.17-34.47 (CDH, CH 2 , C(14-27)), 35.53 (CH 2 , C(12)), 39.75 (CH 2 , C(9)), 102.66 (CH, C(4)), 111.80 (CH, C(6,7)), 112.66 (C, C(3)), 123.39 (CH, C(2)), 128.06 (C, C(3 0 )), 131.07 (C, C(7 0 )), 150.84 (C-OH, C(5)), 172.32 (CdO, C(11)).…”