1H NMR (293 K, d1-chloroform) d 1.14 (s, 6H, CH3), 1.28 (m, 4H, cyclohexyl-CH2), 1.31 (s, 6H, CH3), 1.70 (m, 2H, cyclohexyl-CH2), 1.99 (m, 2H, cyclohexyl-CH2), 3.39 (d, 3JHH = 12 Hz, 2H, CH2,), 3.69 (d, 2H, cyclohexyl-CH2), 4.16 (m, 2H, cyclohexyl-CH), 5.86 (s, 2H, NH), 9.34 (s, 2H, NH).
13C{1H} NMR (293 K d1-chloroform) d 21.1 (CH3), 24.7 (cyclohexyl-CH2), 27.3 (CH3), 32.7 (cyclohexyl-CH2), 57.9 (NCq(CH3)2), 59.8 (cyclohexyl-CH), 69.7 (CH2), 178.4 (NCqN).
IR (DCM layer, cm-1): 3240, 3072, 2930, 2857, 1594, 1527, 1462, 1411, 1369, 1259, 1230, 1051, 915, 731, 631.
Anal. Calcd. for C16H32N4S2O2: C, 51.03; H, 8.56; N, 14.88. Found: C, 50.87 ; H, 8.52; N, 14.78.
MS (EI) m/z 376 (M+).