Year 2019,
Volume: 6 , 96 - 100, 25.07.2019
Onur Akyıldırım
Haydar Yuksek
Sevda Manap
References
-
Alam, M. M., Nazreen, S., Haider, S., Shafi, S., Yar, M. S., Hamid, H., & Alam., M. S. (2012). Synthesis of some new S-Alkylated 1,2,4-triazoles, their Mannich bases and their biological activities. Archiv der Pharmazie-Chemistry in Life Sciences, 345, 203–214. http://doi.org/10.1002/ardp.201100128
Bayrak, H., Demirbas, A., Karaoglu, S. A., Demirbas, N. (2009). Synthesis of some new 1,2,4-triazoles, their Mannich and Schiff bases and evaluation of their antimicrobial activities. European Journal of Medicinal Chemistry, 44, 1057-1066. http://doi.org/10.1016/j.ejmech.2008.06.019
Bekircan, O., Menteşe, E., Ülker, S., & Kucuk., C. (2014). Synthesis of some new 1,2,4-triazole derivatives starting from 3-(4-chlorophenyl)-5-(4-methoxybenzyl)-4H-1,2,4-triazol with anti-lipase and anti-urease activities. Archiv der Pharmazie-Chemistry in Life Sciences, 347, 387–397. http://doi.org/10.1002/ardp.201300344
Bektaş, H., Karaali, N., Şahin, D., Demirbaş, A., Karaoglu, Ş. A., Demirbaş, N. (2010). Synthesis and antimicrobial activities of some new 1,2,4-triazole derivatives. Molecules, 15, 2427-2438. http://doi.org/10.3390/molecules15042427
Demirbas, A., Sahin, D., Demirbas, N., Karaoglu, S. A. (2009). Synthesis of some new 1,3,4-thiadiazol-2-ylmethyl-1,2,4-triazole derivatives and investigation of their antimicrobial activities. European Journal of Medicinal Chemistry, 44, 2896–2903. http://doi.org/10.1016/j.ejmech.2008.12.005
Holla, B. S., Veerendra, B., Shivananda, M. K., Poojary, B. (2003). Synthesis characterization and anticancer activity studies on some Mannich bases derived from 1,2,4-triazoles. European Journal of Medicinal Chemistry, 38, 759–767. http://doi.org/10.1016/S0223-5234(03)00128-4
Nithinchandra, Kalluraya, B., Aamir, S., Shabaraya, A. R. (2012). Regioselective reaction: Synthesis, characterization and pharmacological activity of some new Mannich and Schiff bases containing sydnone. European Journal of Medicinal Chemistry, 54, 597-604. http://doi.org/10.1016/j.ejmech.2012.06.011
Ozdemir, Y., Gultekin, E., & Bekircan, O. (2017). Synthesis and biological significances of new heterocyclic compounds containing 5-(4-chlorobenzyl)-3-(4-chlorophenyl)-1H-1,2,4-triazol ring. Journal of The Chemical Society of Pakistan, 39, 1055–1067. http://doi.org/10.1002/ardp.201300344
Triloknadh, S., Rao, C. V., Nagaraju, K., Krishna, N. H., Ramaiah, C. V., Rajendra, W., Trinath, D., Suneetha, Y. (2018). Design, synthesis, neuroprotective, antibacterial activities and docking studies of novel thieno[2,3-d]pyrimidine-alkyne Mannich base and oxadiazole hybrids. Bioorganic & Medicinal Chemistry Letters, 28, 1663–1669. http://doi.org/10.1016/j.bmcl.2018.03.030
Synthesis and Characterization of Novel 1-(Morpholin-4-yl-methyl)-3-alkyl(aryl)-4-[3-ethoxy-4-(2-furylcarbonyloxy)-benzylidenamino]-4,5-dihydro-1H-1,2,4-triazol-5-ones
Year 2019,
Volume: 6 , 96 - 100, 25.07.2019
Onur Akyıldırım
Haydar Yuksek
Sevda Manap
Abstract
In
this study, six novel 1-(morpholin-4-yl-methyl)-3-alkyl(aryl)-4-[3-ethoxy-4-(2-furylcarbonyloxy)-benzylidenamino]-4,5-dihydro-1H-1,2,4-triazol-5-one (2) compunds were
synthesized from a reaction of type 1 compunds with formaldehyde and morpholine.
The finally part contains that synthesis of new compounds. The structures of
these novel compounds were characterized by using, IR, 1H NMR and 13C
NMR spectral data.
References
-
Alam, M. M., Nazreen, S., Haider, S., Shafi, S., Yar, M. S., Hamid, H., & Alam., M. S. (2012). Synthesis of some new S-Alkylated 1,2,4-triazoles, their Mannich bases and their biological activities. Archiv der Pharmazie-Chemistry in Life Sciences, 345, 203–214. http://doi.org/10.1002/ardp.201100128
Bayrak, H., Demirbas, A., Karaoglu, S. A., Demirbas, N. (2009). Synthesis of some new 1,2,4-triazoles, their Mannich and Schiff bases and evaluation of their antimicrobial activities. European Journal of Medicinal Chemistry, 44, 1057-1066. http://doi.org/10.1016/j.ejmech.2008.06.019
Bekircan, O., Menteşe, E., Ülker, S., & Kucuk., C. (2014). Synthesis of some new 1,2,4-triazole derivatives starting from 3-(4-chlorophenyl)-5-(4-methoxybenzyl)-4H-1,2,4-triazol with anti-lipase and anti-urease activities. Archiv der Pharmazie-Chemistry in Life Sciences, 347, 387–397. http://doi.org/10.1002/ardp.201300344
Bektaş, H., Karaali, N., Şahin, D., Demirbaş, A., Karaoglu, Ş. A., Demirbaş, N. (2010). Synthesis and antimicrobial activities of some new 1,2,4-triazole derivatives. Molecules, 15, 2427-2438. http://doi.org/10.3390/molecules15042427
Demirbas, A., Sahin, D., Demirbas, N., Karaoglu, S. A. (2009). Synthesis of some new 1,3,4-thiadiazol-2-ylmethyl-1,2,4-triazole derivatives and investigation of their antimicrobial activities. European Journal of Medicinal Chemistry, 44, 2896–2903. http://doi.org/10.1016/j.ejmech.2008.12.005
Holla, B. S., Veerendra, B., Shivananda, M. K., Poojary, B. (2003). Synthesis characterization and anticancer activity studies on some Mannich bases derived from 1,2,4-triazoles. European Journal of Medicinal Chemistry, 38, 759–767. http://doi.org/10.1016/S0223-5234(03)00128-4
Nithinchandra, Kalluraya, B., Aamir, S., Shabaraya, A. R. (2012). Regioselective reaction: Synthesis, characterization and pharmacological activity of some new Mannich and Schiff bases containing sydnone. European Journal of Medicinal Chemistry, 54, 597-604. http://doi.org/10.1016/j.ejmech.2012.06.011
Ozdemir, Y., Gultekin, E., & Bekircan, O. (2017). Synthesis and biological significances of new heterocyclic compounds containing 5-(4-chlorobenzyl)-3-(4-chlorophenyl)-1H-1,2,4-triazol ring. Journal of The Chemical Society of Pakistan, 39, 1055–1067. http://doi.org/10.1002/ardp.201300344
Triloknadh, S., Rao, C. V., Nagaraju, K., Krishna, N. H., Ramaiah, C. V., Rajendra, W., Trinath, D., Suneetha, Y. (2018). Design, synthesis, neuroprotective, antibacterial activities and docking studies of novel thieno[2,3-d]pyrimidine-alkyne Mannich base and oxadiazole hybrids. Bioorganic & Medicinal Chemistry Letters, 28, 1663–1669. http://doi.org/10.1016/j.bmcl.2018.03.030