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Bazı yeni 3-alkil(aril)-4-(3-metoksi-4-sinnamoiloksi)benzilidenamino-4,5- dihidro-1H-1,2,4-triazol-5-on bileşiklerinin sentezi, antioksidan ve asitlik özelliklerinin incelenmesi

Year 2018, Issue: 3, 1 - 6, 31.12.2018

Abstract

3-Alkil(aril)-4-amino-4,5-dihidro-1H-1,2,4-triazol-5-on (2) bileşiklerinin, 3-metoksi-4-sinnamoiloksibenzaldehid (3) ile reaksiyonları sonucunda dokuz yeni 3-alkil(aril)-4-(3-metoksi-4-sinnamoiloksi)-benzilidenamino-4,5-dihidro-1H-1,2,4-triazol5-on (4) bileşikleri sentezlendi. Yeni dokuz adet bileşiğin yapısı IR, 1H-NMR, 13C-NMR ve UV spektrum verileri ile aydınlatıldı. Sentezlenen bileşiklerin in vitro antioksidan aktiviteleri üç farklı yöntemle analiz edildi. Ayrıca, çözücülerin ve moleküler yapının asitlik üzerine etkisini incelemek için, 4 bileşikleri dört farklı çözücüde (izopropil alkol, tert-butil alkol, aseton ve N,Ndimetilformamid) tetrabutilamonyum hidroksid ile potansiyometrik metotla titre edildi. HNP ve pKa değerlerinin çözücüye ve
4,5-dihidro-1H-1,2,4-triazol-5-on yapısında C-3 pozisyonundaki substutiente bağlı değiştiği gözlendi.

References

  • 1. Sahu, J,K., Ganguly, S. and Kaushik, A., Triazoles: A valuable insight into recent developments and biological activities, Chin. J. Nat. Med. 2013, 11, 456-465.
  • 2. Ali, K.A., Ragab, E.A., Farghaly, T.A. and Abdalla, M.M., Synthesis of new functionalized 3-subsitituted [1,2,4]triazolo [4,3-a]pyrimidine derivatives: Potential antihypertensive agents, Acta Pol. Pharm. 2011, 68, 237-247.
  • 3. Li, Z.Y., Cao, Y., Zhan, P., Pannecouque, C., Balzarini, J., De Clercq, E. and Liu, X.Y., Synthesis and anti-HIV evaluation of novel 1,2,4-triazole derivatives as potential non-nucleoside HIV-1 reverse transcriptase inhibitors, Lett. Drug Des. Discov. 2013, 10, 27-34.
  • 4. Kaczor, A.A., Pitucha, M., Karczmarzyk, Z., Wysocki, W., Rzymowska, J. and Matosiuk, D., Structural and molecular docking studies of 4-benzyl-3-[(1-methylpyrrol- 2-yl)methyl]-4,5-dihydro-1H-1,2,4-triazol-5-one with anticancer activity, Med. Chem. 2013, 9, 313-328.
  • 5. Thakkar, S.S., Thakor, P., Doshi, H. and Ray, A., 1,2,4-Triazole and 1,3,4-oxadiazole analogues: Synthesis, MO studies, in silico molecular docking studies, antimalarial as DHFR inhibitor and antimicrobial activities, Bioorg. Med. Chem. 2017, 25, 4064-4075.
  • 6. Khalid, W., Badshah, A., Khan, A., Nadeem, H. and Ahmed, S., Synthesis, characterization, molecular docking evaluation, antiplatelet and anticoagulant actions of 1,2,4 triazole hydrazone and sulphonamide novel derivatives, Chem. Cent. J. 2018, 12:11, 1-16.
  • 7. Abuelhassan, A.H., Badran, M.M., Hassan, H.A., Abdelhamed, D., Elnabtity, S. and Aly, O.M., Design, synthesis, anticonvulsant activity, and pharmacophore study of new 1,5-diaryl-1H-1,2,4-triazole-3-carboxamide derivatives, Med. Chem. Res. 2018, 27, 928-938.
  • 8. Bahçeci, Ş., Yıldırım, N., Alkan, M., Gürsoy-Kol, Ö., Manap, S., Beytur, M. and Yüksek, H., Investigation of antioxidant, biological and acidic properties of new 3-alkyl(aryl)-4-(3-acetoxy-4-methoxybenzylidenamino)-4,5-dihydro-1H-1,2,4-triazol-5-ones, Pharm. Chem. J. 2017, 4, 91-101.
  • 9. Aktaş-Yokuş, Ö., Yüksek, H., Manap, S., Aytemiz, F., Alkan, M., Beytur, M. and Gürsoy-Kol, Ö., In-vitro biological activity of some new 1,2,4-triazole derivatives with their potentiometric titrations, Bulg. Chem. Commun. 2017, 49, 98-106.
  • 10. Yüksek, H. and Gürsoy-Kol, Ö., Preparation, characterization, and potentiometric titrations of some new di-[3-(3-alkyl/aryl-4,5-dihydro-1H-1,2,4-triazol-5-one-4-yl)-azomethinphenyl]-isophtalate/terephtalate derivatives, Turk. J. Chem. 2008, 32, 773-784.
  • 11. Hussain, H.H., Babic, G., Durst, T., Wright, J., Flueraru, M., Chichirau, A. and Chepelev, L.L., Development of novel antioxidants: Design, synthesis, and reactivity, J. Org. Chem. 2003, 68, 7023-7032.
  • 12. McClements, J. and Decker, E.A., Lipid oxidation in oil-in-water emulsions: Impact of molecular environment on chemical reactions in heterogeneous food systems, J. Food Sci. 2000, 65, 1270-1282.
  • 13. Dikusar, E.A. and Kozlov, N.G., Esters derived from vanillin and vanillal and aromatic and functionalized aliphatic carboxylic acids, Russ. J. Org. Chem. 2005, 41, 992-996.
  • 14. Oyaizu, M., Studies on products of browning reaction prepared from glucosamine, Japan. Nutri. 1986, 44, 307-316.
  • 15. Blois, M.S., Antioxidant determinations by the use of a stable free radical, Nature 1958, 181, 1199-1200.
  • 16. Dinis, T.C.P., Madeira, V.M.C. and Almeida, L.M., Action of phenolic derivatives (acetaminophen, salicylate, and 5-aminosalicylate) as inhibitors of membrane lipid-peroxidation and as peroxyl radical scavengers, Arch. Biochem. Biophys. 1994, 315, 161-169.
  • 17. Ikizler, A.A. and Un, R., Reactions of ester ethoxycarbonylhydrazones with some amine type compounds, Chim. Acta Turc. 1979, 7, 269-290; [Chem. Abstr. 1981, 94, 15645d].
  • 18. Ikizler, A.A. and Yuksek, H., Acetylation of 4-amino-4,5-dihydro-1H-1,2,4-triazol-5-ones, Org. Prep. Proced. Int. 1993, 25, 99-105.
  • 19. Meir, S., Kanner, J., Akiri, B. and Philosophhadas, S., Determination and involvement of aqueous reducing compounds in oxidative defense systems of various senescing leaves, J. Agr. Food Chem. 1995, 43, 1813-1819.
  • 20. Yildirim, A., Mavi, A. and Kara, A.A., Determination of antioxidant and antimicrobial activities of Rumex crispus L. extracts. J. Agr. Food Chem. 2001, 49, 4083-4089.
  • 21. Baumann, J., Wurn, G. and Bruchlausen, V., Prostaglandin synthetase inhibiting O2 - radical scavenging properties of some flavonoids and related phenolic compounds, Naunyn- Schmiedebergs Arch. Pharmacol. 1979, 308, R27.
  • 22. Soares, J.R., Dinis, T.C.P., Cunha, A.P. and Almeida, L.M., Antioxidant activities of some extracts of Thymus zygis, Free Radical Res. 1997, 26, 469-478.
  • 23. Duh, P.D., Tu, Y.Y. and Yen, G.C., Antioxidant activity of water extract of Harng Jyur (Chrysanthemum morifolium Ramat), Food Sci. Technol-Leb. 1999, 32, 269-277.
  • 24. Yamaguchi, F., Ariga, T., Yoshimura, Y. and Nakazawa, H., Antioxidative and anti-glycation activity of garcinol from Garcinia indica fruit rind, J. Agr. Food Chem. 2000, 48, 180-185.
  • 25. Strlic, M., Radovic, T., Kolar, J. and Pihlar, B., Anti- and prooxidative properties of gallic acid in fenton-type systems, J. Agr. Food Chem. 2002, 50, 6313-6317.
  • 26. Finefrock, A.E., Bush, A.I. and Doraiswamy, P.M., Current status of metals as therapeutic targets in Alzheimer’s disease, J. Am. Geriatr. Soc. 2003, 51, 1143-1148.
  • 27. Calis, I., Hosny, M., Khalifa, T. and Nishibe, S., Secoiridoids from Fraxinus angustifolia. Phytochemistry 1993, 33, 1453-1456.
  • 28. Gordon, M.H., Food Antioxidants, Elsevier, London, 1990.

Synthesis, antioxidant and acidic properties of some new 3-alkyl(aryl)-4-(3- methoxy-4-cinnamoyloxy)benzylideneamino-4,5-dihydro-1H-1,2,4-triazol5-ones

Year 2018, Issue: 3, 1 - 6, 31.12.2018

Abstract

Nine new 3-alkyl(aryl)-4-(3-methoxy-4-cinnamoyloxy)benzylideneamino-4,5-dihydro-1H-1,2,4-triazol-5-ones (4) were synthesized by the reactions of 3-alkyl(aryl)-4-amino-4,5-dihydro-1H-1,2,4-triazol-5-ones (2) with 3-methoxy-4-cinnamoyloxybenzaldehyde (3). The structures of new nine compounds were established from IR, 1H-NMR, 13C-NMR and UV spectral data. The synthesized compounds were analyzed for their in vitro potential antioxidant activities in three different methods. In addition, to investigate the effects of solvents and molecular structure upon acidity compounds 4 were titrated potentiometrically with tetrabutylammonium hydroxide in four non-aqueous solvents (isopropyl alcohol, tert-butyl alcohol, acetone and N,N-dimethylformamide).

References

  • 1. Sahu, J,K., Ganguly, S. and Kaushik, A., Triazoles: A valuable insight into recent developments and biological activities, Chin. J. Nat. Med. 2013, 11, 456-465.
  • 2. Ali, K.A., Ragab, E.A., Farghaly, T.A. and Abdalla, M.M., Synthesis of new functionalized 3-subsitituted [1,2,4]triazolo [4,3-a]pyrimidine derivatives: Potential antihypertensive agents, Acta Pol. Pharm. 2011, 68, 237-247.
  • 3. Li, Z.Y., Cao, Y., Zhan, P., Pannecouque, C., Balzarini, J., De Clercq, E. and Liu, X.Y., Synthesis and anti-HIV evaluation of novel 1,2,4-triazole derivatives as potential non-nucleoside HIV-1 reverse transcriptase inhibitors, Lett. Drug Des. Discov. 2013, 10, 27-34.
  • 4. Kaczor, A.A., Pitucha, M., Karczmarzyk, Z., Wysocki, W., Rzymowska, J. and Matosiuk, D., Structural and molecular docking studies of 4-benzyl-3-[(1-methylpyrrol- 2-yl)methyl]-4,5-dihydro-1H-1,2,4-triazol-5-one with anticancer activity, Med. Chem. 2013, 9, 313-328.
  • 5. Thakkar, S.S., Thakor, P., Doshi, H. and Ray, A., 1,2,4-Triazole and 1,3,4-oxadiazole analogues: Synthesis, MO studies, in silico molecular docking studies, antimalarial as DHFR inhibitor and antimicrobial activities, Bioorg. Med. Chem. 2017, 25, 4064-4075.
  • 6. Khalid, W., Badshah, A., Khan, A., Nadeem, H. and Ahmed, S., Synthesis, characterization, molecular docking evaluation, antiplatelet and anticoagulant actions of 1,2,4 triazole hydrazone and sulphonamide novel derivatives, Chem. Cent. J. 2018, 12:11, 1-16.
  • 7. Abuelhassan, A.H., Badran, M.M., Hassan, H.A., Abdelhamed, D., Elnabtity, S. and Aly, O.M., Design, synthesis, anticonvulsant activity, and pharmacophore study of new 1,5-diaryl-1H-1,2,4-triazole-3-carboxamide derivatives, Med. Chem. Res. 2018, 27, 928-938.
  • 8. Bahçeci, Ş., Yıldırım, N., Alkan, M., Gürsoy-Kol, Ö., Manap, S., Beytur, M. and Yüksek, H., Investigation of antioxidant, biological and acidic properties of new 3-alkyl(aryl)-4-(3-acetoxy-4-methoxybenzylidenamino)-4,5-dihydro-1H-1,2,4-triazol-5-ones, Pharm. Chem. J. 2017, 4, 91-101.
  • 9. Aktaş-Yokuş, Ö., Yüksek, H., Manap, S., Aytemiz, F., Alkan, M., Beytur, M. and Gürsoy-Kol, Ö., In-vitro biological activity of some new 1,2,4-triazole derivatives with their potentiometric titrations, Bulg. Chem. Commun. 2017, 49, 98-106.
  • 10. Yüksek, H. and Gürsoy-Kol, Ö., Preparation, characterization, and potentiometric titrations of some new di-[3-(3-alkyl/aryl-4,5-dihydro-1H-1,2,4-triazol-5-one-4-yl)-azomethinphenyl]-isophtalate/terephtalate derivatives, Turk. J. Chem. 2008, 32, 773-784.
  • 11. Hussain, H.H., Babic, G., Durst, T., Wright, J., Flueraru, M., Chichirau, A. and Chepelev, L.L., Development of novel antioxidants: Design, synthesis, and reactivity, J. Org. Chem. 2003, 68, 7023-7032.
  • 12. McClements, J. and Decker, E.A., Lipid oxidation in oil-in-water emulsions: Impact of molecular environment on chemical reactions in heterogeneous food systems, J. Food Sci. 2000, 65, 1270-1282.
  • 13. Dikusar, E.A. and Kozlov, N.G., Esters derived from vanillin and vanillal and aromatic and functionalized aliphatic carboxylic acids, Russ. J. Org. Chem. 2005, 41, 992-996.
  • 14. Oyaizu, M., Studies on products of browning reaction prepared from glucosamine, Japan. Nutri. 1986, 44, 307-316.
  • 15. Blois, M.S., Antioxidant determinations by the use of a stable free radical, Nature 1958, 181, 1199-1200.
  • 16. Dinis, T.C.P., Madeira, V.M.C. and Almeida, L.M., Action of phenolic derivatives (acetaminophen, salicylate, and 5-aminosalicylate) as inhibitors of membrane lipid-peroxidation and as peroxyl radical scavengers, Arch. Biochem. Biophys. 1994, 315, 161-169.
  • 17. Ikizler, A.A. and Un, R., Reactions of ester ethoxycarbonylhydrazones with some amine type compounds, Chim. Acta Turc. 1979, 7, 269-290; [Chem. Abstr. 1981, 94, 15645d].
  • 18. Ikizler, A.A. and Yuksek, H., Acetylation of 4-amino-4,5-dihydro-1H-1,2,4-triazol-5-ones, Org. Prep. Proced. Int. 1993, 25, 99-105.
  • 19. Meir, S., Kanner, J., Akiri, B. and Philosophhadas, S., Determination and involvement of aqueous reducing compounds in oxidative defense systems of various senescing leaves, J. Agr. Food Chem. 1995, 43, 1813-1819.
  • 20. Yildirim, A., Mavi, A. and Kara, A.A., Determination of antioxidant and antimicrobial activities of Rumex crispus L. extracts. J. Agr. Food Chem. 2001, 49, 4083-4089.
  • 21. Baumann, J., Wurn, G. and Bruchlausen, V., Prostaglandin synthetase inhibiting O2 - radical scavenging properties of some flavonoids and related phenolic compounds, Naunyn- Schmiedebergs Arch. Pharmacol. 1979, 308, R27.
  • 22. Soares, J.R., Dinis, T.C.P., Cunha, A.P. and Almeida, L.M., Antioxidant activities of some extracts of Thymus zygis, Free Radical Res. 1997, 26, 469-478.
  • 23. Duh, P.D., Tu, Y.Y. and Yen, G.C., Antioxidant activity of water extract of Harng Jyur (Chrysanthemum morifolium Ramat), Food Sci. Technol-Leb. 1999, 32, 269-277.
  • 24. Yamaguchi, F., Ariga, T., Yoshimura, Y. and Nakazawa, H., Antioxidative and anti-glycation activity of garcinol from Garcinia indica fruit rind, J. Agr. Food Chem. 2000, 48, 180-185.
  • 25. Strlic, M., Radovic, T., Kolar, J. and Pihlar, B., Anti- and prooxidative properties of gallic acid in fenton-type systems, J. Agr. Food Chem. 2002, 50, 6313-6317.
  • 26. Finefrock, A.E., Bush, A.I. and Doraiswamy, P.M., Current status of metals as therapeutic targets in Alzheimer’s disease, J. Am. Geriatr. Soc. 2003, 51, 1143-1148.
  • 27. Calis, I., Hosny, M., Khalifa, T. and Nishibe, S., Secoiridoids from Fraxinus angustifolia. Phytochemistry 1993, 33, 1453-1456.
  • 28. Gordon, M.H., Food Antioxidants, Elsevier, London, 1990.
There are 28 citations in total.

Details

Primary Language English
Subjects Chemical Engineering
Journal Section Research Article
Authors

Haydar Yüksek This is me 0000-0003-1289-1800

Buket Göksu This is me 0000-0001-8207-967X

Bahar Bankoğlu This is me 0000-0002-2931-077X

Songül Ulufer This is me 0000-0001-9533-0165

Sevda Manap 0000-0002-5025-9622

Murat Beytur 0000-0002-7098-5592

Özlem Gürsoy Kol 0000-0003-2637-9023

Publication Date December 31, 2018
Published in Issue Year 2018 Issue: 3

Cite

APA Yüksek, H., Göksu, B., Bankoğlu, B., Ulufer, S., et al. (2018). Synthesis, antioxidant and acidic properties of some new 3-alkyl(aryl)-4-(3- methoxy-4-cinnamoyloxy)benzylideneamino-4,5-dihydro-1H-1,2,4-triazol5-ones. Karadeniz Chemical Science and Technology(3), 1-6.
AMA Yüksek H, Göksu B, Bankoğlu B, Ulufer S, Manap S, Beytur M, Gürsoy Kol Ö. Synthesis, antioxidant and acidic properties of some new 3-alkyl(aryl)-4-(3- methoxy-4-cinnamoyloxy)benzylideneamino-4,5-dihydro-1H-1,2,4-triazol5-ones. Karadeniz Chem. Sci. Tech. December 2018;(3):1-6.
Chicago Yüksek, Haydar, Buket Göksu, Bahar Bankoğlu, Songül Ulufer, Sevda Manap, Murat Beytur, and Özlem Gürsoy Kol. “Synthesis, Antioxidant and Acidic Properties of Some New 3-alkyl(aryl)-4-(3- Methoxy-4-cinnamoyloxy)benzylideneamino-4,5-Dihydro-1H-1,2,4-Triazol5-Ones”. Karadeniz Chemical Science and Technology, no. 3 (December 2018): 1-6.
EndNote Yüksek H, Göksu B, Bankoğlu B, Ulufer S, Manap S, Beytur M, Gürsoy Kol Ö (December 1, 2018) Synthesis, antioxidant and acidic properties of some new 3-alkyl(aryl)-4-(3- methoxy-4-cinnamoyloxy)benzylideneamino-4,5-dihydro-1H-1,2,4-triazol5-ones. Karadeniz Chemical Science and Technology 3 1–6.
IEEE H. Yüksek, “Synthesis, antioxidant and acidic properties of some new 3-alkyl(aryl)-4-(3- methoxy-4-cinnamoyloxy)benzylideneamino-4,5-dihydro-1H-1,2,4-triazol5-ones”, Karadeniz Chem. Sci. Tech., no. 3, pp. 1–6, December 2018.
ISNAD Yüksek, Haydar et al. “Synthesis, Antioxidant and Acidic Properties of Some New 3-alkyl(aryl)-4-(3- Methoxy-4-cinnamoyloxy)benzylideneamino-4,5-Dihydro-1H-1,2,4-Triazol5-Ones”. Karadeniz Chemical Science and Technology 3 (December 2018), 1-6.
JAMA Yüksek H, Göksu B, Bankoğlu B, Ulufer S, Manap S, Beytur M, Gürsoy Kol Ö. Synthesis, antioxidant and acidic properties of some new 3-alkyl(aryl)-4-(3- methoxy-4-cinnamoyloxy)benzylideneamino-4,5-dihydro-1H-1,2,4-triazol5-ones. Karadeniz Chem. Sci. Tech. 2018;:1–6.
MLA Yüksek, Haydar et al. “Synthesis, Antioxidant and Acidic Properties of Some New 3-alkyl(aryl)-4-(3- Methoxy-4-cinnamoyloxy)benzylideneamino-4,5-Dihydro-1H-1,2,4-Triazol5-Ones”. Karadeniz Chemical Science and Technology, no. 3, 2018, pp. 1-6.
Vancouver Yüksek H, Göksu B, Bankoğlu B, Ulufer S, Manap S, Beytur M, Gürsoy Kol Ö. Synthesis, antioxidant and acidic properties of some new 3-alkyl(aryl)-4-(3- methoxy-4-cinnamoyloxy)benzylideneamino-4,5-dihydro-1H-1,2,4-triazol5-ones. Karadeniz Chem. Sci. Tech. 2018(3):1-6.