Design, Synthesis, Spectral Charecterization of Some New Fully Unsaturated 2-Substituted-4, 6 Dichloro Symmetric Triazine- Based Chalcone Hybrids
Keywords:
fully unsaturated, 1, 3, 5-triazine-chalcone hybrids, spectral characterization
Abstract
Triazines and chalcones are interesting class of heterocyclic compounds with a prominent structural core system present in numerous pharmacologically active compounds. It is proved from the literature that the compounds containing 1,3,5-triazine moiety or chalcone bridge often shows significant biological activity profiles. Based on these observations, it was considered worthwhile to synthesize and characterize some new 1,3,5-triazine-chalcone hybrid molecules in the present investigation. As a part of our research program aimed at search for new hybrid pharmacophores as potential cytotoxic agents, we are interested to have α,β-unsaturated ketone linker to the 1,3,5-triazine basic nucleus to give a series of 1,3,5-triazinechalcone hybrid molecules. Therefore, in the present study an attempt has been made to synthesize and characterize various analogs of fully unsaturated 2-substituted-4,6 dichloro-1,3,5 triazine based chalcone hybrids.
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References
Ohsawa A., Arai H., Ohnishi H., Igeta H. (1981) Ohsawa A.; Arai H.; Ohnishi H.; Igeta H. J. Chem. Soc., Chem. 1981, 1174.
B. Grzegorz (2006) 62, 9507.
Kim H., Dietrich W., Hansch C., Dolnick J., Bertino R. (1980) Kim K. H.; Dietrich S. W.; Hansch C.; Dolnick B. J.; Bertino J. R. J. Med. 23, 1248.
Blaney M., Hansch C., Silipo C., Vittoria A.
Foster B.J., Harding B.J., Leyland-Jones B., Hoth D. (1986) Foster B.J.; Harding B.J. Leyland-Jones B.; Hoth D. Cancer Treat. 38, 197.
C. Labrid, G. Regnier, M. Laubie, Eur
Ono M., Kawahara N., Goto D., Wakabayashi Y., Ushiro S., Yoshida S., Izumi H., Kuwano M., Sato Y. (1996) Ono M.; Kawahara N.; Goto D.; Wakabayashi Y.; Ushiro S.; Yoshida S.; Izumi H.; Kuwano M.; Sato Y. 56(7), 1512.
Baker R., Ashton T. (1973) Baker B. R.; Ashton W. T. J. Med. 16, 209.
Sirawaraporn W., Sathitkul T., Sirawaraporn R., Y. Yuthavong, Santi V. Sirawaraporn W.; Sathitkul T.; Sirawaraporn R.; Yuthavong, Y.; Santi D.
R. Patel, P. Kumari, D. Rajani, K. Chikhalia (2011) Patel, R. V.; Kumari, P.; Rajani, D. P.; Chikhalia, K. H. Eur. J. of Med. 46, 4354.
Thurston T., Schaefer C., Dudley R, Holm- D., Illuminati G. (1951) Thurston J. T.; Schaefer F. C.; Dudley J. R; Holm- Hansen D. Illuminati G. J. Am. Chem. 73, 2992.
R. Patel (2011) V.; Kumari, P.; Rajani, D P.; Chikhalia, K H Eur J Med Chem. 46, 4354-4365.
N. Somayajulu, L. Divakara, V. Kasapu, A. Rao, B. Bugata, S. Yenupuri, J. Eur, Chem Somayajulu, N.; Divakara, L.; Kasapu, V.
Bugata, B.; Krishna, K.; Satya, V. V.; Avupati (2013) R.; Gavalapu, V.; Somayajulu, N.; Divakara, L.; Barla, S Eur J Chem. 4(4), 396-401.
J. Raval, Eur (2011) P Eur J Chem. 2(3), 388-393.
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2016-04-13
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