Synthesis, crystal structure of some new 2-(4-methylbenzoylimino)-3-aryl-4- methyl-1,3-thiazolines

Journal of Heterocyclic Chemistry

Volumn 43, Issue 4, 2006, Pages 1027-1030

  Saeed, Aamer ^a   Parvez, Masood ^b  

^a QUAID I AZAM UNIVERSITY   (Pakistan)

^b UNIVERSITY OF CALGARY   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

1,3 THIAZOLINE DERIVATIVE; 2 (4 METHYLBENZOYLIMINO) 4 METHYL 1,3 THIAZOLINE DERIVATIVE; 3 (4 BROMOPHENYL) 2 (4 METHYLBENZOYLIMINO) 4 METHYL 1,3 THIAZOLINE; ACETONE; BROMINE; HETEROCYCLIC COMPOUND; THIAZOLE DERIVATIVE; THIOUREA DERIVATIVE; TRIETHYLAMINE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CRYSTAL STRUCTURE; CYCLIZATION; DRUG STRUCTURE; DRUG SYNTHESIS; INFRARED SPECTROSCOPY; MELTING POINT; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; X RAY DIFFRACTION;

EID: 33747398303     PISSN: 0022152X     EISSN: None     Source Type: Journal    
DOI: 10.1002/jhet.5570430431     Document Type: Article

References (29)

1. D. M. Vittoria, O. Mazzoni, E. Piscopo, A. Caligmano and A. Bolognese, J. Med. Chem., 35, 2910 (1992).
2. A. M. Omar, N. H. Eshba, J. Pharm. Sci. 73, 1166 (1984);
3. P. B. Patel, J. T. Trivedi, Indian Chem. Soc., 54, 765 (1987).
4. M. Chaudhary, S. S. Parmar, S. K. Chaudhari, and B. V. Ramasastry, J. Pharm. Sci., 65, 443 (1976).
5. F. A. Ragab, M. M. Hussain, M. M. Hanna and G. S. Hassan, J. Pharm. Sci., 82, 387 (1993).
6. H. Y. Hassan, N. A. El-Koussi and Z. S. Farghaly, Chem. Pharm. Bull., 46, 863 (1998).
7. G. Turan-Zitouni, D. M. Sivaci, Z. A. Kaplancikli and A. Ozdemir, Farmaco, 57, 569 (2002).
8. C. L. Lee and M. M. Sim, Tetrahedron Lett., 41, 5729 (2000).
9. I. Inamori, Y. Okamoto, Y. Takegawa, H. Tsujibo, Y. Sakagami, Y. Kumeda, M. Shibata and Numata, Biosci. Biotechnol. Biochem., 62, 1025 (1998).
10. N. S. Habib, S. M. Rida, E. A. M. Badawey, H. T. Y. Fahmy and H. Ghozlan, Eur. J. Med. Chem., 32, 759 (1997).
11. T. W. Sing, L. C. Lee, S. L. Yeo, S. P. Lim and M. M. Sim, Biorg. Med. Chem. Lett., 11, 91 (2001).
12. H. T. Y. Fahmy and A. A. Bekhit, Pharmazie, 57, 800 (2002).
13. F. Nagasaki, T. Yamada, E. Takahashi, Y. Kitagawa, R. Hatano, Japanese Patent JP 63250371 (1988); Chem. Abstr., 110, 192810 (1989).
14. H. Hoelzel, D. Creuzburg, P. Stohr, H. Dehne, J. Teller, L. Kranz, H. Luthardt, T. Roethling and A. Kaestner, German Patent DD 258168 (1988); Chem. Abstr., 111, 2681 (1989).
15. C. G. Bonde and N. J. Gaikwad, Bioorg. Med. Chem., 12, 2151 (2004);
16. A. Bodtke, W.-D Pfeiffer, N. Ahrens, P. Langer, Bioorg. Med. Chem. Lett., 14, 1509 (2004).
17. S. Bae, H-G. Hahn and K.D. Nam, J. Comb. Chem., 7, 7 (2005).
18. S. M. Sondhi, G. Bhattacharjee, R. K. Jameel, R. Shukla, R. Raghubir, O. Lozach, and L. Meijer, Cent. Eur. J. Chem., 2, 1 (2004).
19. M. Bouchekara, A. Djafri, N. Vanthuyne, and C. Roussel, ARKIVOC, 72 (2002).
20. S. E. Bramley, V. Dupplin, D. G. Goberdhan and G. D. Meakins, J. Chem. Soc., Perkin Trans, 1, 639 (1987);
21. N. De Kimpe, W. De Cock, M. Keppens, D. De Smaele and A. Meszaros, J. Heterocyclic Chem., 33, 1179 (1996).
22. H. Beyer, W. Lassig and E. Bulka, Chem. Ber., 87, 1385 (1987);
23. H. Beyer, and G. Wolter, Chem. Ber., 89, 1652 (1956).
24. E. Schmitz, and H. Striegler, J. Prakt. Chem., 312, 359 (1970);
25. A. K. Bhattacharya, J. Indian Chem. Soc., 44, 57 (1967).
26. T. H. Kim, N. Lee, G-J. Lee and J. N. Kim, Tetrahedron, 57, 7137 (2001).
27. M. D'hooghe, A. Waterinckx, and N. De Kimpe, J. Org. Chem., 70, 227 (2005).
28. B. Liu, H. Gao, and X. Zhou, Hauxe Yangbao, 5, 42 (1994);
29. A. Saeed, and M. Parvez, Cent. Eur. J. Chem. 3, 780 (2005).