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Novel Synthesis of 3-(Substituted phenyl)-2-[(substituted benzoyl)imino]-1,3-thiazolidine-4-one Derivatives from Substituted Thiourea
Corresponding Author(s) : Kh. Pourshamsian
Asian Journal of Chemistry,
Vol. 25 No. 1 (2013): Vol 25 Issue 1
Abstract
In this work, we proposed the synthesis of several new derivatives of 3-(substituted phenyl)-2-[(substituted benzoyl)imino]-1,3-thiazolidine-4-one by using substituted thiourea and chloroacetic acid. The structure of compounds were confirmed with IR, 1H NMR and 13C NMR spectroscopy.
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- M.K. Burghate and B.N. Berad, Asian J. Chem., 19, 3601 (2007).
- C. Boga, L. Forlani, C. Silvestroni, A.B. Corradi and P. Sagarabotto, J. Chem. Soc. Perkin Trans. I, 1363 (1999).
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- F. Aydogan, N. Ocal, Z. Turgut and C. Yolacan, Bull. Korean Chem. Soc., 22, 476 (2001).
- S.K. Sonwane, S.D. Srivastava and S.K. Srivastava, J. Sci., Islamic Republic of Iran, 20, 227 (2009).
- E.B. Akerblom, J. Med. Chem., 17, 609 (1974).
- A. Kausar, S. Zulfiqar, Z. Ahmad and M.I. Sarwar, Polym. Degrad. Stab., 10, 1016 (2010).
- D. Ugur, H. Arslan and N. Külcü, Russ. J. Coord. Chem., 32, 669 (2006).
- M.L. Xiao, F.H. Chen, Z.J. Chen, B.S. Guo, X.H. Lv and W.M. Tang, Chin. Chem. Lett., 18, 258 (2007).
- Kh. Pourshamsian, N. Montazeri, K. Rad-Moghadam and K.S. Aliasgari, J. Heterocycl. Chem., 47, 1439 (2010)
References
A.S. Galabov, B.S. Galabov and N.A. Neykova, J. Med. Chem., 23, 1048 (1980).
(a) L. Doub, L.M. Richardson, D.R. Herbst, M.L. Black, O.L. Stevenson, L.L. Bambas, G.P. Youmans and A.S. Youmans, J. Am. Chem. Soc., 80, 2205 (1958); (b) A.C. Glasser and R.M. Doughty, J. Pharm. Sci., 51, 1031 (1962).
G. Krause, R. Franke and G.N. Vasilev, Biochem. Physiol. Pflanz., 174, 128 (1979).
E.G. Ghalina and L. Chakarova, Eur. J. Med. Chem., 33, 875 (1998).
M.K. Burghate and B.N. Berad, Asian J. Chem., 19, 3601 (2007).
C. Boga, L. Forlani, C. Silvestroni, A.B. Corradi and P. Sagarabotto, J. Chem. Soc. Perkin Trans. I, 1363 (1999).
G. Capan, N. Ulusoy, N. Ergenc and M. Kiraz, Monatsh. Chem., 130, 1399 (1999).
M.G. Vigorita, R. Ottana, F. Monforte, R. Maccari, A. Trovato, M.T. Monforte and M.F. Taviano, Bioorg. Med. Chem. Lett., 11, 2791 (2001).
C.V. Kavitha, S. Basappa, S. Nanjunda, K. Mantelingu, S. Doreswamy, M.A. Sridhar, J.S. Prasad and K.S. Rangappa, Bioorg. Med. Chem., 14, 2290 (2006).
N. Ocal, C. Yolacan, S. Kaban, Y. Leonor, M. Vargas and V.J. Kouznetsov, Hetero. Chem., 38, 233 ( 2001).
F. Aydogan, N. Ocal, Z. Turgut and C. Yolacan, Bull. Korean Chem. Soc., 22, 476 (2001).
S.K. Sonwane, S.D. Srivastava and S.K. Srivastava, J. Sci., Islamic Republic of Iran, 20, 227 (2009).
E.B. Akerblom, J. Med. Chem., 17, 609 (1974).
A. Kausar, S. Zulfiqar, Z. Ahmad and M.I. Sarwar, Polym. Degrad. Stab., 10, 1016 (2010).
D. Ugur, H. Arslan and N. Külcü, Russ. J. Coord. Chem., 32, 669 (2006).
M.L. Xiao, F.H. Chen, Z.J. Chen, B.S. Guo, X.H. Lv and W.M. Tang, Chin. Chem. Lett., 18, 258 (2007).
Kh. Pourshamsian, N. Montazeri, K. Rad-Moghadam and K.S. Aliasgari, J. Heterocycl. Chem., 47, 1439 (2010)