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. 2003 Mar;69(3):1670–1679. doi: 10.1128/AEM.69.3.1670-1679.2003

TABLE 3.

1H NMR data of the substrate N-(2-hexylamino-4-phenylimidazol-1-yl)-acetamide and the products A, B, C, and E

Data for:
Proton assignmenta
Substrate
Product A
Product B
Product C
Product E
δ (ppm) 3J (Hz) δ (ppm) 3J (Hz) δ (ppm) 3J (Hz) δ (ppm) 3J (Hz) δ (ppm) 3J (Hz)
10.65 10.66 10.69 s, 1H, NH, NH—COCH3
7.65 7.8 7.65 8.2 7.62 8.2 7.64 7.8 7.70 7.8 d, 2H, H0, C6H5
7.30 7.8, 7.2 7.29 8.2, 7.3 7.3 8.2, 7.3 7.29 7.8, 7.3 7.46 7.8, 7.3 dd, 2H, Hm, C6H5
7.13 7.2 7.11 7.3 6.9 7.3 7.11 7.3 7.36 7.3 t, 1H, Hp, C6H5
7.08 7.07 7.1 7.09 7.49 s, 1H, CH, imidazol
5.5 6.01 s, 2H, NH2
5.83 5.7 5.84 5.8 7.88 5.98 5.8 7.85 6.1 t, 1H, NH, NH—CH2
3.21 3.21 3.31 3.24 3.38 m, 2H, CH2, CH2—NH
2.22 7.3 2.28 8.2 2.29 7.4 t, 2H, CH2, CH2—COOH
1.97 1.97 1.97 s, 3H, CH3
1.83 1.8 m, 2H, CH2, NH—CH2CH2—CH2COOH
1.54 1.59 m, 2H, CH2, CH2—CH3
1.29 1.5, 1.3 1.31 m, 6H, 3xCH2
0.87 6.6 0.88 6.7 t, 3H, CH3, CH3(CH2)5NH
a

Underlining reflects assignment of the single NMR signal.