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Synthesis of methyl 2-[2-(alkylimino)-4-oxo-3-phenyl-1,3-thiazolan-5-yliden]acetate derivatives under solvent-free condition | ||
| Iranian chemical communication | ||
| مقاله 8، دوره 3، Issue 2, pp. 72-147, Serial No. 7، تیر 2015، صفحه 132-136 اصل مقاله (599.37 K) | ||
| نوع مقاله: Original Research Article | ||
| نویسندگان | ||
| Rahimeh Hajinasiri* 1؛ Sobhan Rezayati2 | ||
| 1Department of Chemistry, Islamic Azad University, Qaemshahr Branch, P.O. Box 163, Qaemshahr, Iran | ||
| 2Department of Chemistry, Payame Noor University, PO BOX 19395-4697 Tehran, Iran | ||
| چکیده | ||
| An efficient synthesis of Methyl 2-[2-(alkylimino)-4-oxo-3-phenyl-1,3-thiazolan-5-yliden]acetate derivatives via simple three-component reaction and one-pot reactions between isoquinoline, dimethyl acetylenedicarboxylate and N-phenylthiourea under solvent-free conditions without using any additional catalyst, is described. The mild reaction conditions and good yields and exhibit the synthetic advantage of this method. Also this method is environmentally friendly. The methods of green chemistry continue to grow in importance. Alternative processes help to conserve resources and can even reduce costs. The replacement of convention solvents with water or solvent-free conditions, which is harmless to health and is available in large quantities. The thiazolium rings are key units in agricultural compounds and drugs. | ||
| کلیدواژهها | ||
| Isoquinoline؛ solvent-free؛ N-phenylthiourea؛ thiazolan؛ green chemistry | ||
| مراجع | ||
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[1] A. Do¨mling, Comb. Chem. High. T. Scr., 1998, 1, 1-22.
[2] A. Do¨mling, I. Ugi, Angew. Chem. Int. Ed., 2000, 39, 3168.
[3] L. Weber, Drug Discovery Today, 2002, 7, 143-147.
[5] J. Zhu, H. Bienayme, Multicomponent Reactions, Eds. Wiley-VCH, Weinheim, Germany, 2005.
[6] P. Wipf, C. Kendall, Chem. Eur. J., 2002, 8, 1778-1784.
[7] G. Balme, E. Bossharth, N. Monteiro, Eur. J. Org. Chem., 2003, 4101-4111.
[8] A. Jacobi von Wangelin, H. Neumann, D. Gordes, S. Klaus, D. Strubing, M. Beller, Chem. Eur. J., 2003, 9, 4286-4294.
[9] S. Heck, A. Domling, Synlett., 2000, 424-426.
[10] L.Weber, Curr. Med. Chem., 2002, 9, 2085-2093.
[11] I. Yavari, A.S. Shahvelayati, A. Malekafzali, Journal of Sulfur Chemistry, 2010, 31, 499-508.
[12] P.M. Dewick, Medicinal natural products. A biosynthetic approach, 2nd eds; Wiley, Chichester, U.K. 2002.
[13] (a) R. Breslow, J. Am. Chem. Soc., 1958, 80, 3719-3726. (b) I. Yavari, S. A. Asgari, K. Porshamsian, M. Bagheri, J. Sulfur. Chem., 2007, 28, 477-482. (c) I. Yavari, M. Sabaghan, S. A. Asgari, K. Porshamsian, M. Bagheri, Z. Hossaini, Mol. Diversity, 2007, 11, 81-85.
[14] S. Miwatashi, Y. Arikawa, E. Kotani, M. Miyamoto, K.I. Naruo, H. Kimura, T. Tanaka, S. Asahi, S. Ohkawa, J. Med. Chem., 2005, 48, 5966-5979.
[15] Y. Kumar, R. Green, K.Z. Borysko, D.S. Wise, L.L. Wotring, L.B. Townsend, J. Med. Chem., 1993, 36, 3843-3848.
[16] R. Pereira, C. Gaudon, B. Iglesias, P. Germain, H. Gronemeyer, A.R. de Lera, Bioorg. Med. Chem. Lett., 2006, 16 , 49-54.
[17] Y. Tsurumi, H. Ueda, K. Hayashi, S. Takase, M. Nishikawa, S. Kiyoto, M. Okuhara, J. Antibiotic, 1995, 48, 1066-1072.
[18] F.W. Bell, A.S. Cantrell, M. Hoberg, S.R. Jaskunas, N.G. Johansson, C.L. Jordon, M.D. Kinnick, P. Lind, J.M. Morin, J. Med. Chem., 1995, 38, 4929-4936.
[19] D.S. Millan, R.H. Prager, C. Brand, P.H. Hart, Tetrahedron, 2000, 56, 811-816.
[20] W.L. Wang, D.Y. Yao, M. Gu, M.Z. Fan, J.Y. Li, Y.C. Xing, F.J. Nan, Bioorg. Med. Chem. Lett., 2005, 15, 5284-5287. | ||
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