JOURNAL OF THE CHINESE
CHEMICAL SOCIETY
Synthesis of Imidazole Derivatives
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characterization data for selected known products are
given below.
Data of selected products are represented as
follows:
4-(4,5-Diphenyl-1H-imidazol-2-yl)benzonitrile (Table
1
1, Entry 4). H NMR (400 MHz, DMSO): δ = 13.03 (s,
1H), 8.25 (d, 2H, J = 8.4 Hz), 7.94 (d, 2H, J = 8.4 Hz),
7.50–7.56 (m, 4H), 7.46 (t, 2H, J = 7.2Hz), 7.39–7.42 (m,
1H), 7.32 (t, 2H, J = 7.2Hz), 7.23–7.26 (m, 1H); 13C
NMR (100 MHz, DMSO): δ = 144.15, 138.51, 135.14,
134.72, 133.26, 131.06, 130.06, 129.20, 128.98, 128.73,
128.62, 127.56, 127.30, 125.98, 119.37, 110.56.
2-(4-Methoxyphenyl)-4,5-diphenylimidazole (Table
12. A. Mohammed, N. Lokare, J. Sangshetti, D. Shinde,
J. Korean Chem. Soc. 2007, 51, 418.
1
1, Entry 5). H NMR (400 MHz, DMSO): δ = 12.52
(s, 1H), 8.02 (d, 2H, J = 5.2 Hz), 7.34–7.55 (m, 7H),
7.30 (t, 2H, J = 6.8HZ), 7.19–7.23 (m, 1H), 7.05 (d,
2H, 4.8); 13C NMR (100 MHz, DMSO): δ = 159.86,
146.07, 137.19, 135.74, 131.65, 129.10, 128.80, 128.63,
128.09, 127.50, 127.15, 126.88, 123.54, 114,55, 55.66.
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ACKNOWLEDGMENTS
We are grateful to University of Mazandaran for
support of our research.
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