4-(1,2-Dihydro-2-phenylquinoxalin-3-yl)-N,N-dimethylbenzenamine (3g). (0.63 g, m.p. 190-192 °C, yields 96%), IR (KBr) (. max, cm-1): 3329, 3056, 2957, 1612, 1565, 1519, 1495. 1H NMR (500 MHz, CDCl3) d 3.01 (s, 6H, 2CH3), 4.41 (CH), 5.68 (s, 1H, NH), 6.50 (d, 1H, J = 7.7 Hz), 6.68 (d, 2H, J = 9.6 Hz), 6.81 (td, 1H, J = 7.6 Hz, 1.2 Hz), 6.98 (td, 1H, J = 7.6 Hz, 1.2 Hz), 7.21-7.30 (m, 5H), 7.44 (d, 1H, J = 7.7 Hz), 7.90 (d, 2H, J = 9.6 Hz) ppm. 13C NMR (125 MHz, CDCl3) d 40.08 (2CH3), 54.42 (CH), 111.44 (CH), 113.68 (CH), 118.93 (CH), 124.75 (C), 126.66 (CH), 127.37 (CH), 127.98 (CH), 128.65 (CH), 129.08 (CH), 133.86 (CH), 134.78 (C), 141.28 (C), 145.10 (C), 151.71 (C), 157.64 (C) ppm. Anal. Calcd. for C22H21N3 (327.43): C, 80.70; H, 6.46; N, 12.83%. Found: C, 80.58; H, 6.59; N, 12.58%. Acknowledgements We thank the Shahid Bahonar University for financial support as a Grant-in-Aid for Scientific Research. References 1. Katritzky, A. R.; Rees, C.W. Comprehensive Heterocyclic Chemistry, Pergamon: Oxford, Part 2B, 1984; Vol. 3, p 157. 2. Sherman, D.; Kawakami, J.; He, H. Y.; Dhun, F.; Rios, R.; Liu, H.; Pan, W.; Xu, Y. J.; Hong, S. P.; Arbour, M.; Labelle M.; Duncton, M. A. J. Tetrahedron Lett. 2007, 48, 8943. 3. (a) Loriga, M.; Piras, S.; Sanna, P.; Paglietti, G. Farmaco. 1997, 52, 157. (b) Seitz, L. E.; Suling, W. J.; Reynolds, R. C. J. Med. Chem. 2002, 45, 5604. (c) YB, K.; YH, K.; JY, P.; SK, K. Bioorg. Med. Chem. Lett. 2004, 14, 541. (d) Hui, X.; Desrivot, J.; Bories, C.; Loiseau, P. M.; Franck, X.; Hocquemiller, R.; Figadere, B. Bioorg. Med. Chem. Lett. 2006, 16, 815. (e) Lindsley, C. W.; Zhao, Z.; Leister, W. H.; Robinson, R. G.; Barnett, S. F.; Defeo-Jones, D.; Jones, R. E.; Hartman, G. D.; Huff, J. R.; Huber, H. E.; Duggan, M. E. Bioorg. Med. Chem. Lett. 2005, 15, 761. (f) Labarbera, D. V.; Skibo, E. B. Bioorg. Med. Chem. 2005, 13, 387. (g) Sarges, R.; Howard, H. R.; Browne, R. G.; Lebel, L. A.; Seymour, P. A.; Koe, B. K. J. Med. Chem. 1990, 33, 2240. (h) Srinivas, C.; Kumar, C. N. S. S. P.; Rao, V. J.; Palaniappan, S. J. Mol. Catal. A: Chem. 2007, 265, 227. (i) Ghomsi, N. T.; Ahabchane, N. E. H.; Es-Safi, N. E.; Garrigues, B.; Essassi, E. M. Spectroscopy Lett. 2007, 40, 741. 4. Sakata, G.; Makino, K.; Karasawa, Y. Heterocycles 1988, 27, 2481. 5. (a) Dell, A.; William, D. H.; Morris, H. R.; Smith, G. A.; Feeney, J.; Roberts, G. C. K. J. Am. Chem. Soc. 1975, 97, 2497. (b) Heravi, M. M.; Bakhtiari, K.; Tehrani, M. H.; Javadi, N. M.; Oskooie, H. A. ARKIVOC 2006, (xvi), 16. (c) Raw, S. A.; Wilfred, C. D.; Taylor, R. J. K. Chem. Commun. 2003, 18, 2286. 6. (a) Kumar, A.; Kumar, S.; Saxena, A.; De, A.; Mozumdar, S. Catal. Commun. 2008, 778. (b) Jaung, J. Y. Dyes and Pigments. 2006, 71, 45. 7. (a) Thomas, K. R. J.; Velusamy, M.; Lin, J. T.; Chuen, C. H.; Tao, Y. T. Chem. Mater. 2005, 17, 1860. (b) Dailey, S.; Feast, W. J.; Peace, R. J.; Sage, I. C.; Till, S.; Wood, E.
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