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Bis(Sülfonamid) İhtiva Eden Kalkon Türevlerinin Etkin Bir Şekilde Sentezi ve Karakterizasyonu

Year 2021, , 1341 - 1353, 01.06.2021
https://doi.org/10.21597/jist.852907

Abstract

Bu çalışmada, sülfonamid içeren yeni kalkon türevleri hızlı ve etkili bir şekilde sentezlendi. Kalkon iskelet yapısının sentezi, baz katalize Claisen-Schmidt kondenzasyon reaksiyon yöntemi kullanılarak yapıldı. 4-metoksi asetofenon, 4-nitrobenzaldehit ve NaOH’in reaksiyonu sonucu 3 nolu kalkon %80 verimle sentezlendi. Elde edilen 1-(4-metoksifenil)-3-(4-nitrofenil)prop-2-en-1-on (3) bileşiğindeki, nitro fonksiyonel grubunun SnCl2.2H2O ile indirgenmesiyle hedef bileşik 3-(4-aminofenil)-1-(4-metoksifenil)prop-2-en-1-on (4) %98 verimle elde edildi. Aminin (4), 3-(triflorometil)benzensülfonil klorür, 4-florobenzensülfonil klorür, 4-metoksibenzensülfonil klorür, naftalen-1-sülfonil klorür, pridin-3-sülfonil klorür ve metansülfonil klorür ile reaksiyonu sonucu Alzheimer hastalığı başta olmak üzere birçok farklı terapötik uygulamada kullanılabilme potansiyeline sahip olan moleküllerin sentezi başarılı bir şekilde gerçekleştirildi.

Supporting Institution

Kilis 7 Aralık Üniversitesi Bilimsel Araştırma Projeleri Koordinasyon Birimi

Project Number

12411

Thanks

Bu çalışma, Kilis 7 Aralık Üniversitesi Bilimsel Araştırma Projeleri Koordinasyon Birimi tarafından “12411” kodlu proje ile desteklenmiştir.

References

  • Akin Kazancioglu E, Guney M, Şentürk M, Supuran CT, 2010. Simple Methanesulfonates are Hydrolyzed by the Sulfatase Carbonic Anhydrase Activity. Journal of Enzyme Inhibition and Medicinal Chemistry, 27 (6): 880-885.
  • Akin Kazancioglu E, Senturk M, 2020. Synthesis of N-Phenylsulfonamide Derivatives and İnvestigation of Some Esterase Enzymes Inhibiting Properties. Bioorganic Chemistry, 104:104279.
  • Burmaoglu S, Akin Kazancioglu E, Kaya R, Kazancioglu M, Karaman M, Algul O, Gulcin I, 2020. Synthesis of Novel Organohalogen Chalcone Derivatives and Screening of Their Molecular Docking Study and Some Enzymes Inhibition Effects, Journal of Molecular Structure, 1208:127868.
  • Dong X, Du L, Pan Z, Liu T, Yang B, Hu Y, 2010. Synthesis And Biological Evaluation of Novel Hybrid Chalcone Derivatives as Vasorelaxant Agents. European Journal Of Medicinal Chemistry, 45 (9): 3986–3992.
  • Evranos AB, Ertan R, 2011. Chemical and Structural Properties of Chalcones I. Farad Journal of Pharmaceutical Sciences, 36, 223-242.
  • Fidan I, Salmas RE, Arslan M, Şentürk M, Durdagi S, Ekinci D, Şentürk E, Coşgun S, Supuran CT, 2015. Carbonic Anhydrase Inhibitors: Design, Synthesis, Kinetic, Docking and Molecular Dynamics Analysis of Novel Glycine and Phenylalanine Sulfonamide Derivatives. Bioorganic & Medicinal Chemistry, 23 (23): 7353-8.
  • Kim E, Namkoong K, Jeong J, Jang S, Kwon YJ, Jun KY, Jeon KH, Park M, Kim H, Na Y, 2020. Novel Compound and Pharmaceutical Composition Comprising Same as Active Ingredient. US Patent Aplication Publication, US20200190024.
  • Kocyigit UM, Budak Y, Eliguzel F, Taslimi P, Kılıc D, Gulcin I, Ceylan M, 2017. Synthesis and Carbonic Anhydrase Inhibition of Tetrabromo Chalcone Derivatives. Archiv der Pharmazie, 350 (12).
  • Kocyigit UM, Budak Y, Gurdere MB, Erturk F, Yencilek B, Taslimi P, Gulcin I, Ceylan M, 2018. Synthesis of Chalcone-Imide Derivatives and Investigation of Their Anticancer and Antimicrobial Activities, Carbonic Anhydrase and Acetylcholinesterase Enzymes Inhibition Profiles. Archives of Physiology and Biochemistry, 124 (1):61-68.
  • Kocyigit UM, Gezegen H, Taslimi P, 2020. Synthesis, Characterization, and Biological Studies of Chalcone Derivatives Containing Schiff Bases: Synthetic Derivatives for the Treatment of Epilepsy and Alzheimer's Disease. Archiv der Pharmazie, 353 (12):e2000202.
  • Mathew B, Mathew GE, Ucar G, Joy M, Nafna EK, Lohidakshan KK, Suresh J, 2017. Monoamine Oxidase İnhibitory Activity of Methoxy-Substituted Chalcones. International Journal of Biological Macromolecules, 104 (Pt A), 1321-1329.
  • Sonmez F, Sevmezler S, Atahan A, Ceylan M, Demir D, Gencer N, Arslan O, Kucukislamoglu M, 2011. Evaluation of New Chalcone Derivatives as Polyphenol Oxidase İnhibitors. Bioorganic & Medicinal Chemistry Letters. 15; 21(24): 7479-82.
  • Supuran CT, 2008. Carbonic Anhydrases: Novel Therapeutic Applications for Inhibitors and Activators. Nature Reviews Drug Discovery, 7 (2): 168-81.
  • Yazdan SK, Sagar DV, Shaik AB, 2015. Chemical and Biological Potentials of Chalcones: A Review. Organic & Medicinal Chemistry International Journal, 1 (1), 1-9. 10.
  • Zhuang C, Zhang W, Sheng C, Zhang W, Xing C, Miao Z, 2017. Chalcone: A Privileged Structure In Medicinal Chemistry, Chemical Reviews,117, 7762−7810.

Effective Synthesis and Characterization of Bis(Sulfonamide) Containing Chalcone

Year 2021, , 1341 - 1353, 01.06.2021
https://doi.org/10.21597/jist.852907

Abstract

In this study, new chalcone derivatives containing sulfonamide were synthesized rapidly and efficiently. The synthesis of the chalcone skeletal structure was performed using the base-catalyzed Claisen-Schmidt condensation reaction method. Chalcone 3 was synthesized with 80% yield as a result of the reaction of 4-methoxy acetophenone, 4-nitrobenzaldehyde and NaOH. Reduction of the nitro functional group in compound 1-(4-methoxyphenyl)-3-(4-nitrophenyl)prop-2-en-1-one (3) with SnCl2.2H2O obtained the target compound 3-(4-aminophenyl)-1-(4-methoxyphenyl)prop-2-en-1-one (4) in 98% yield. The synthesis of target molecules that has the potential to be used in many different therapeutic applications, including Alzheimer's disease, has been successfully achieved as a result of the reaction of amine (4) with 3-(trifluoromethyl)benzenesulfonyl chloride, 4-fluorobenzenesulfonyl chloride, 4-methoxybenzenesulfonyl chloride, naphthalene-1-sulfonyl chloride, pyridine-3-sulfonyl chloride and methanesulfonyl chloride.

Project Number

12411

References

  • Akin Kazancioglu E, Guney M, Şentürk M, Supuran CT, 2010. Simple Methanesulfonates are Hydrolyzed by the Sulfatase Carbonic Anhydrase Activity. Journal of Enzyme Inhibition and Medicinal Chemistry, 27 (6): 880-885.
  • Akin Kazancioglu E, Senturk M, 2020. Synthesis of N-Phenylsulfonamide Derivatives and İnvestigation of Some Esterase Enzymes Inhibiting Properties. Bioorganic Chemistry, 104:104279.
  • Burmaoglu S, Akin Kazancioglu E, Kaya R, Kazancioglu M, Karaman M, Algul O, Gulcin I, 2020. Synthesis of Novel Organohalogen Chalcone Derivatives and Screening of Their Molecular Docking Study and Some Enzymes Inhibition Effects, Journal of Molecular Structure, 1208:127868.
  • Dong X, Du L, Pan Z, Liu T, Yang B, Hu Y, 2010. Synthesis And Biological Evaluation of Novel Hybrid Chalcone Derivatives as Vasorelaxant Agents. European Journal Of Medicinal Chemistry, 45 (9): 3986–3992.
  • Evranos AB, Ertan R, 2011. Chemical and Structural Properties of Chalcones I. Farad Journal of Pharmaceutical Sciences, 36, 223-242.
  • Fidan I, Salmas RE, Arslan M, Şentürk M, Durdagi S, Ekinci D, Şentürk E, Coşgun S, Supuran CT, 2015. Carbonic Anhydrase Inhibitors: Design, Synthesis, Kinetic, Docking and Molecular Dynamics Analysis of Novel Glycine and Phenylalanine Sulfonamide Derivatives. Bioorganic & Medicinal Chemistry, 23 (23): 7353-8.
  • Kim E, Namkoong K, Jeong J, Jang S, Kwon YJ, Jun KY, Jeon KH, Park M, Kim H, Na Y, 2020. Novel Compound and Pharmaceutical Composition Comprising Same as Active Ingredient. US Patent Aplication Publication, US20200190024.
  • Kocyigit UM, Budak Y, Eliguzel F, Taslimi P, Kılıc D, Gulcin I, Ceylan M, 2017. Synthesis and Carbonic Anhydrase Inhibition of Tetrabromo Chalcone Derivatives. Archiv der Pharmazie, 350 (12).
  • Kocyigit UM, Budak Y, Gurdere MB, Erturk F, Yencilek B, Taslimi P, Gulcin I, Ceylan M, 2018. Synthesis of Chalcone-Imide Derivatives and Investigation of Their Anticancer and Antimicrobial Activities, Carbonic Anhydrase and Acetylcholinesterase Enzymes Inhibition Profiles. Archives of Physiology and Biochemistry, 124 (1):61-68.
  • Kocyigit UM, Gezegen H, Taslimi P, 2020. Synthesis, Characterization, and Biological Studies of Chalcone Derivatives Containing Schiff Bases: Synthetic Derivatives for the Treatment of Epilepsy and Alzheimer's Disease. Archiv der Pharmazie, 353 (12):e2000202.
  • Mathew B, Mathew GE, Ucar G, Joy M, Nafna EK, Lohidakshan KK, Suresh J, 2017. Monoamine Oxidase İnhibitory Activity of Methoxy-Substituted Chalcones. International Journal of Biological Macromolecules, 104 (Pt A), 1321-1329.
  • Sonmez F, Sevmezler S, Atahan A, Ceylan M, Demir D, Gencer N, Arslan O, Kucukislamoglu M, 2011. Evaluation of New Chalcone Derivatives as Polyphenol Oxidase İnhibitors. Bioorganic & Medicinal Chemistry Letters. 15; 21(24): 7479-82.
  • Supuran CT, 2008. Carbonic Anhydrases: Novel Therapeutic Applications for Inhibitors and Activators. Nature Reviews Drug Discovery, 7 (2): 168-81.
  • Yazdan SK, Sagar DV, Shaik AB, 2015. Chemical and Biological Potentials of Chalcones: A Review. Organic & Medicinal Chemistry International Journal, 1 (1), 1-9. 10.
  • Zhuang C, Zhang W, Sheng C, Zhang W, Xing C, Miao Z, 2017. Chalcone: A Privileged Structure In Medicinal Chemistry, Chemical Reviews,117, 7762−7810.
There are 15 citations in total.

Details

Primary Language Turkish
Journal Section Kimya / Chemistry
Authors

Elif Akın Kazancıoğlu 0000-0001-7486-685X

Project Number 12411
Publication Date June 1, 2021
Submission Date January 3, 2021
Acceptance Date January 27, 2021
Published in Issue Year 2021

Cite

APA Akın Kazancıoğlu, E. (2021). Bis(Sülfonamid) İhtiva Eden Kalkon Türevlerinin Etkin Bir Şekilde Sentezi ve Karakterizasyonu. Journal of the Institute of Science and Technology, 11(2), 1341-1353. https://doi.org/10.21597/jist.852907
AMA Akın Kazancıoğlu E. Bis(Sülfonamid) İhtiva Eden Kalkon Türevlerinin Etkin Bir Şekilde Sentezi ve Karakterizasyonu. Iğdır Üniv. Fen Bil Enst. Der. June 2021;11(2):1341-1353. doi:10.21597/jist.852907
Chicago Akın Kazancıoğlu, Elif. “Bis(Sülfonamid) İhtiva Eden Kalkon Türevlerinin Etkin Bir Şekilde Sentezi Ve Karakterizasyonu”. Journal of the Institute of Science and Technology 11, no. 2 (June 2021): 1341-53. https://doi.org/10.21597/jist.852907.
EndNote Akın Kazancıoğlu E (June 1, 2021) Bis(Sülfonamid) İhtiva Eden Kalkon Türevlerinin Etkin Bir Şekilde Sentezi ve Karakterizasyonu. Journal of the Institute of Science and Technology 11 2 1341–1353.
IEEE E. Akın Kazancıoğlu, “Bis(Sülfonamid) İhtiva Eden Kalkon Türevlerinin Etkin Bir Şekilde Sentezi ve Karakterizasyonu”, Iğdır Üniv. Fen Bil Enst. Der., vol. 11, no. 2, pp. 1341–1353, 2021, doi: 10.21597/jist.852907.
ISNAD Akın Kazancıoğlu, Elif. “Bis(Sülfonamid) İhtiva Eden Kalkon Türevlerinin Etkin Bir Şekilde Sentezi Ve Karakterizasyonu”. Journal of the Institute of Science and Technology 11/2 (June 2021), 1341-1353. https://doi.org/10.21597/jist.852907.
JAMA Akın Kazancıoğlu E. Bis(Sülfonamid) İhtiva Eden Kalkon Türevlerinin Etkin Bir Şekilde Sentezi ve Karakterizasyonu. Iğdır Üniv. Fen Bil Enst. Der. 2021;11:1341–1353.
MLA Akın Kazancıoğlu, Elif. “Bis(Sülfonamid) İhtiva Eden Kalkon Türevlerinin Etkin Bir Şekilde Sentezi Ve Karakterizasyonu”. Journal of the Institute of Science and Technology, vol. 11, no. 2, 2021, pp. 1341-53, doi:10.21597/jist.852907.
Vancouver Akın Kazancıoğlu E. Bis(Sülfonamid) İhtiva Eden Kalkon Türevlerinin Etkin Bir Şekilde Sentezi ve Karakterizasyonu. Iğdır Üniv. Fen Bil Enst. Der. 2021;11(2):1341-53.