KARIMIAN AND DAVARPANAH
11 of 12
[8] Y. Li, Q. Xie, Q. Hu, C. Li, Z. Huang, X. Yang, H. Guo, Sci. Rep.
2016, 6, 30651.
(DMSO‐d6, 250 MHz, δ, ppm): 1.33 (t, J = 7.25 Hz, 3 H),
4.32 (q, J = 7.25 Hz, 2H), 7.52–7.89 (m, 3 H), 7.98–8.15
(m, 1 H), 8.29–8.36 (m, 2 H), 8.74–8.76 (m, 1 H), 13.46
(s, 1 H). Anal. Calcd for C16H14N2O2 (266.300) (%): C,
72.17; H, 5.30; N, 10.52. Found (%): C, 73.01; H, 5.41; N,
10.62.
[9] K. G. Laurier, F. Vermoortele, R. Ameloot, D. E. De Vos, J.
Hofkens, M. B. Roeffaers, J. Am. Chem. Soc. 2013, 135, 14488.
[10] Y.‐Z. Chen, R. Zhang, L. Jiao, H.‐L. Jiang, Coord. Chem. Rev.
2018, 362, 1.
[11] H.‐Y. Guan, R. J. LeBlanc, S.‐Y. Xie, Y. Yue, Coord. Chem. Rev.
2018, 369, 76.
4.3.6 | 2‐(Pyridin‐4‐yl)‐1H‐benzo [d]
imidazole
[12] C. Bolm, J. Legros, J. Le Paih, L. Zani, Chem. Rev. 2004, 104,
6217.
White solid; m.p. 215–217 °C. FT‐IR (KBr, cm−1): 686 (s),
[13] Q. Ding, B. Cao, X. Liu, Z. Zong, Y.‐Y. Peng, Green Chem. 2010,
12, 1607.
748 (s), 825 (s), 995 (s), 1319 (s), 1434 (s), 1604 (s), 3047
1
[14] a) A. Kamal, Y. V. V. Srikanth, M. N. A. Khan, T. B. Shaik, M.
Ashraf, Bioorg. Med. Chem. Lett. 2010, 20, 5229. b) N. Hazeri,
M. T. Maghsoodlou, S. M. Habibi‐Khorassani, J. Aboonajmi,
S. S. Sajadikhah, J. Chin. Chem. Soc. 2013, 60, 355.
(w). H NMR (DMSO‐d6, 250 MHz, δ, ppm): 7.22–7.29
(m, 2 H), 7.63–7.67 (m, 2 H), 8.08 (dd, J = 4.50,
J = 1.50 Hz, 2 H), 8.74 (dd, J = 4.50, J = 1.50 Hz, 2 H).
Anal. Calcd for C12 H9 N3 (195.230) (%): C, 73.83; H,
4.65; N, 21.52. Found (%): C, 73.92; H, 4.60; N, 21.79.
[15] M. Nasrollahzadeh, Y. Bayat, D. Habibi, S. Moshaee, Tetrahe-
dron Lett. 2009, 50, 4435.
[16] S. Majumdar, A. Chakraborty, S. Bhattacharjee, S. Debnath, D.
K. Maiti, Tetrahedron Lett. 2016, 57, 4595.
4.3.7 | 2‐(4‐Chlorophenyl)‐1H‐
benzimidazole
[17] B. Sreedhar, A. S. Kumar, D. Yada, Tetrahedron Lett. 2011, 52,
3565.
White solid; m.p. 294–295 °C. FT‐IR (KBr, cm−1): 1626
[18] D. Habibi, S. Vakili, Chin. J. Catal. 2015, 36, 620.
[19] P. Ghosh, R. Subba, Tetrahedron Lett. 2013, 54, 4885.
1
(C═ N), 3445 (NH). H NMR (DMSO‐d6, 250 MHz, δ,
ppm): 6.94–7.7.00 (m, 2 H), 7.19–7.26 (m, 3 H), 7.48 (m,
1 H), 7.91 (d, J = 8.50 Hz, 2 H). Anal. Calcd for C13 H9
Cl N2 (228.681) (%): C, 68.28; H, 3.97; N, 12.25. Found
(%): C, 68.35; H, 4.07; N, 12.38.
[20] P. Ghosh, B. Saha, G. C. Pariyar, A. Tamang, R. Subba, Tetra-
hedron Lett. 2016, 57, 3618.
[21] K. C. Prousis, N. Avlonitis, G. A. Heropoulos, T.
Calogeropoulou, Chin. J. Catal. 2014, 21, 937.
[22] H. Sharghi, J. Aboonajmi, M. Mozaffari, M. M. Doroodmand,
ACKNOWLEDGMENTS
M. Aberi, Appl. Organomet. Chem. 2018, 32, e4124.
[23] H. Sharghi, M. Jokar, M. M. Doroodmand, Adv. Synth. Catal.
2011, 353, 426.
Financial support of this work was provided by the
Baqiyatallah University of Medical Sciences.
[24] H. Sharghi, S. Ebrahimpourmoghaddam, M. M. Doroodmand,
Tetrahedron 2013, 69, 4708.
ORCID
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[27] P. Naik, P. Murumkar, R. Giridhar, M. R. Yadav, Bioorg. Med.
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