skip to main content

Synthesis of Novel Ester-Based 5-Fluorouracil Derivatives

1Faculty of Pharmacy, University of Jember, Jember, East Java, Indonesia

2Department of Chemistry, Faculty of Mathematics and Natural Sciences, University of Jember, Jl. Kalimantan I/2 Jember 68121, East Java, Indonesia

Received: 6 Feb 2024; Revised: 2 Aug 2024; Accepted: 5 Aug 2024; Published: 31 Aug 2024.
Open Access Copyright 2024 Jurnal Kimia Sains dan Aplikasi under http://creativecommons.org/licenses/by-sa/4.0.

Citation Format:
Cover Image
Abstract
Fluorouracil (5-Fu, 1) is an antimetabolite cancer drug and the first-line drug of anticancer administration by WHO that has been widely used worldwide for more than 50 years. The development of 5-fluorouracil is an effort to obtain higher activity, decrease side effects, and create a specific target receptor compared to 5-fluorouracil. In this research, a series of novel 5-Fluorouracil (5-Fu) derivatives has been synthesized based on a benzoylation reaction (Schotten-Baumann reaction) of N1-hydroxylated 5-Fu called compound 2, 5-fluoro-1-(hydroxymethyl)-uracil. The benzoyl chloride substituents used in this research, including 3-chlorobenzoyl (4a), 2-chlorobenzoyl (4b), 3-nitrobenzoyl (4c), 4-methoxy benzoyl (4d), 4-trifluoromethylbenzoyl (4e), 3,4-dichlorobenzoyl (4f), and 4-nitrobenzoyl (4g) chloride become (4a-4f)-5Fu. This research meticulously examined the conditions (time and reaction temperature) at the second step of the synthesis reaction (esterification), ensuring the reliability of the results. The best synthesis conditions for 4a, 4b, 4c, 4d, and 4g compounds were found to be reflux at 40°C for 6 hours, whereas 4e and 4f compounds reactions were performed in an ice bath for 11 and 17 hours, respectively. All product syntheses, 4a-4g compound, were purified using column chromatography and eluted using eluent hexane: acetone (6:4), and the yields of 4a-4g compounds were around 61-79%. The pure compounds were characterized using FTIR and 1HNMR spectrometer, further validating the research. Based on these findings, it can be concluded that all 5-Fu derivatives can be synthesized using the Schotten-Baumann reaction method.
Fulltext View|Download
Keywords: 5-Fluorouracil; Derivatives; Synthesis; Benzoylation
Funding: Hibah Bersaing Research Grant

Article Metrics:

  1. Charles Heidelberger, N. K. Chaudhuri, Peter Danneberg, Dorothy Mooren, Lois Griesbach, Robert Duschinsky, R. J. Schnitzer, E. Pleven, J. Scheiner, Fluorinated Pyrimidines, A New Class of Tumour-Inhibitory Compounds, Nature, 179, 4561, (1957), 663-666 https://doi.org/10.1038/179663a0
  2. Jean L. Grem, 5-Fluorouracil: Forty-Plus and Still Ticking. A Review of its Preclinical and Clinical Development, Investigational New Drugs, 18, 4, (2000), 299-313 https://doi.org/10.1023/A:1006416410198
  3. Adrian Bogdan Țigu, Vlad-Alexandru Toma, Augustin Cătălin Moț, Ancuța Jurj, Cristian Silviu Moldovan, Eva Fischer-Fodor, Ioana Berindan-Neagoe, Marcel Pârvu, The Synergistic Antitumor Effect of 5-Fluorouracil Combined with Allicin against Lung and Colorectal Carcinoma Cells, Molecules, 25, 8, (2020), 1947 https://doi.org/10.3390/molecules25081947
  4. Chinmayee Sethy, Chanakya Nath Kundu, 5-Fluorouracil (5-FU) resistance and the new strategy to enhance the sensitivity against cancer: Implication of DNA repair inhibition, Biomedicine & Pharmacotherapy, 137, (2021), 111285 https://doi.org/10.1016/j.biopha.2021.111285
  5. Mounira Chalabi-Dchar, Tanguy Fenouil, Christelle Machon, Anne Vincent, Frédéric Catez, Virginie Marcel, Hichem C. Mertani, Jean-Christophe Saurin, Philippe Bouvet, Jérôme Guitton, Nicole Dalla Venezia, Jean-Jacques Diaz, A novel view on an old drug, 5-fluorouracil: an unexpected RNA modifier with intriguing impact on cancer cell fate, NAR Cancer, 3, 3, (2021), https://doi.org/10.1093/narcan/zcab032
  6. Seymour S. Cohen, Joel G. Flaks, Hazel D. Barner, Marilyn R. Loeb, Janet Lichtenstein, The Mode of Action of 5-Fluorouracil and Its Derivatives, Biochemistry, 44, 10, (1958), 1004-1012 https://doi.org/10.1073/pnas.44.10.1004
  7. Felix Steger, Matthias G. Hautmann, Oliver Kölbl, 5-FU-induced cardiac toxicity - an underestimated problem in radiooncology?, Radiation Oncology, 7, 1, (2012), 212 https://doi.org/10.1186/1748-717X-7-212
  8. M. Steiner, M. Seule, B. Steiner, I. Bauer, M. Freund, C. H. Köhne, P. Schuff-Werner, 5-Fluorouracil/irinotecan induced lethal toxicity as a result of a combined pharmacogenetic syndrome: report of a case, Journal of Clinical Pathology, 58, 5, (2005), 553 https://doi.org/10.1136/jcp.2004.022319
  9. Carmen J. Allegra, Dihydropyrimidine dehydrogenase activity: prognostic partner of 5-fluorouracil?, Clinical Cancer Research, 5, 8, (1999), 1947-1949
  10. André B. P. van Kuilenburg, Dihydropyrimidine dehydrogenase and the efficacy and toxicity of 5-fluorouracil, European Journal of Cancer, 40, 7, (2004), 939-950 https://doi.org/10.1016/j.ejca.2003.12.004
  11. M. B. Garg, L. F. Lincz, K. Adler, F. E. Scorgie, S. P. Ackland, J. A. Sakoff, Predicting 5-fluorouracil toxicity in colorectal cancer patients from peripheral blood cell telomere length: a multivariate analysis, British Journal of Cancer, 107, (2012), 1525-1533 https://doi.org/10.1038/bjc.2012.421
  12. Fu-Min Zhang, Xiao-Jun Yao, Xuan Tian, Yong-Qiang Tu, Synthesis and Biological Evaluation of New 4β-5-Fu-substituted 4'-Demethylepipodophyllotoxin Derivatives, Molecules, 11, 11, (2006), 849-857 https://doi.org/10.3390/11110849
  13. Sonani Mindt, Sihem Aida, Kirsten Merx, Annette Müller, Tobias Gutting, Maren Hedtke, Michael Neumaier, Ralf-Dieter Hofheinz, Therapeutic drug monitoring (TDM) of 5-fluorouracil (5-FU): new preanalytic aspects, Clinical Chemistry and Laboratory Medicine (CCLM), 57, 7, (2019), 1012-1016 https://doi.org/10.1515/cclm-2018-1177
  14. Dania A. Bukhari, Sarah K. Alessa, Safaa I. Beheiri, Corneal Epithelial Hyperplasia after 5-Fluorouracil Injection, Case Reports in Ophthalmology, 9, 1, (2018), 254-256 https://doi.org/10.1159/000487474
  15. Tae Hoon Lee, Dan Le, A Rare Case of Severe Lactic Acidosis from 5-Fluorouracil after mFOLFOX6 Treatment in a Patient with Advanced Gastric Cancer, Case Reports in Oncology, 14, 1, (2021), 545-549 https://doi.org/10.1159/000514296
  16. Jaskanwal D. Sara, Jasvinder Kaur, Ryan Khodadadi, Muneeb Rehman, Ronstan Lobo, Sakti Chakrabarti, Joerg Herrmann, Amir Lerman, Axel Grothey, 5-fluorouracil and cardiotoxicity: a review, Therapeutic Advances in Medical Oncology, 10, (2018), 1758835918780140 https://doi.org/10.1177/1758835918780140
  17. Chiara Focaccetti, Antonino Bruno, Elena Magnani, Desirée Bartolini, Elisa Principi, Katiuscia Dallaglio, Eraldo O. Bucci, Giovanna Finzi, Fausto Sessa, Douglas M. Noonan, Adriana Albini, Effects of 5-Fluorouracil on Morphology, Cell Cycle, Proliferation, Apoptosis, Autophagy and ROS Production in Endothelial Cells and Cardiomyocytes, PLOS ONE, 10, 2, (2015), e0115686 https://doi.org/10.1371/journal.pone.0115686
  18. Panagiotis Papanastasopoulos, Justin Stebbing, Molecular basis of 5-fluorouracil-related toxicity: lessons from clinical practice, Anticancer Research, 34, 4, (2014), 1531-1535
  19. Jason T. Weiss, Craig Fraser, Belén Rubio-Ruiz, Samuel H. Myers, Richard Crispin, John C. Dawson, Valerie G. Brunton, E. Elizabeth Patton, Neil O. Carragher, Asier Unciti-Broceta, N-alkynyl derivatives of 5-fluorouracil: susceptibility to palladium-mediated dealkylation and toxigenicity in cancer cell culture, Frontiers in Chemistry, 2, 56, (2014), https://doi.org/10.3389/fchem.2014.00056
  20. Xiaoyan Pan, Chen Wang, Fang Wang, Pengfei Li, Zhigang Hu, Yuanyuan Shan, Jie Zhang, Development of 5-Fluorouracil Derivatives as Anticancer Agents, Current Medicinal Chemistry, 18, 29, (2011), 4538-4556 http://dx.doi.org/10.2174/092986711797287584
  21. Jing Xiong, Hai-Feng Zhu, Ya-Juan Zhao, Yun-Jun Lan, Ji-Wang Jiang, Jing-Jing Yang, Shu-Feng Zhang, Synthesis and Antitumor Activity of Amino Acid Ester Derivatives Containing 5-Fluorouracil, Molecules, 14, 9, (2009), 3142-3152 https://doi.org/10.3390/molecules14093142
  22. Zhi-Yong Tian, Gang-Jun Du, Song-Qiang Xie, Jin Zhao, Wen-Yuan Gao, Chao-Jie Wang, Synthesis and Bioevaluation of 5-Fluorouracil Derivatives, Molecules, 12, 11, (2007), 2450-2457 https://doi.org/10.3390/12112450
  23. Andre Rosowsky, Sun-Hyuk Kim, Michael Wick, Synthesis and antitumor activity of an acyclonucleoside derivative of 5-fluorouracil, Journal of Medicinal Chemistry, 24, 10, (1981), 1177-1181 https://doi.org/10.1021/jm00142a011
  24. Tetsuji Kametani, Kazuo Kigasawa, Mineharu Hiiragi, Kikuo Wakisaka, Seiji Haga, Yasuo Nagamatsu, Hideo Sugi, Kazunaga Fukawa, Osamu Irino, Studies on the syntheses of heterocyclic compounds. 845. Studies on the synthesis of chemotherapeutics. 10. Synthesis and antitumor activity of N-acyl- and N-(alkoxycarbonyl)-5-fluorouracil derivatives, Journal of Medicinal Chemistry, 23, 12, (1980), 1324-1329 https://doi.org/10.1021/jm00186a008
  25. José F. Domı́nguez, Juan A. Marchal, Antonio Correa, Esmeralda Carrillo, Houria Boulaiz, Antonia Aránega, Miguel A. Gallo, Antonio Espinosa, Synthesis and evaluation of new 5-fluorouracil antitumor cell differentiating derivatives, Bioorganic & Medicinal Chemistry, 11, 3, (2003), 315-323 https://doi.org/10.1016/S0968-0896(02)00464-9
  26. Lolita Caram, Mech Doeleman, William J. Roberts, Richard J. Prankerd, John H. Perrin, William J. Underberg, Kenneth B. Sloan, Synthesis of 1- and 3-arylcarbonyl derivatives of 5-fluorouracil, Journal of Heterocyclic Chemistry, 36, 2, (1999), 397-401 https://doi.org/10.1002/jhet.5570360211
  27. A. F. Cook, M. J. Holman, M. J. Kramer, P. W. Trown, Fluorinated pyrimidine nucleosides. 3. Synthesis and antitumor activity of a series of 5'-deoxy-5-fluoropyrimidine nucleosides, Journal of Medicinal Chemistry, 22, 11, (1979), 1330-1335 https://doi.org/10.1021/jm00197a010
  28. Dikla Engel, Abraham Nudelman, Nataly Tarasenko, Inesa Levovich, Igor Makarovsky, Segev Sochotnikov, Igor Tarasenko, Ada Rephaeli, Novel Prodrugs of Tegafur that Display Improved Anticancer Activity and Antiangiogenic Properties, Journal of Medicinal Chemistry, 51, 2, (2008), 314-323 https://doi.org/10.1021/jm7009827
  29. Kazumasa Ikeda, Kunihiro Yoshisue, Eiji Matsushima, Sekio Nagayama, Kaoru Kobayashi, Charles A. Tyson, Kan Chiba, Yasuro Kawaguchi, Bioactivation of Tegafur to 5-Fluorouracil Is Catalyzed by Cytochrome P-450 2A6 in Human Liver Microsomes in Vitro, Clinical Cancer Research, 6, 11, (2000), 4409-4415
  30. Dai-shu Zuo, Tao Jiang, Hua-shi Guan, Kui-qi Wang, Xin Qi, Zhan Shi, Synthesis, Structure and Antitumor Activity of Dibutyltin Oxide Complexes with 5-Fluorouracil Derivatives. Crystal Structure of [(5-Fluorouracil)-1-CH2CH2COOSn(n-Bu)2]4O2, Molecules, 6, 8, (2001), 647-654 https://doi.org/10.3390/60800647
  31. Sheng Chen, Zhaohua Huang, Junlian Huang, Synthesis and characterization of novel kinds of polyethylene oxide drugs containing 5-fluorouracil and nitrogen mustard at one end and 4-amino-N-(2-pyrimidinyl) benzene sulfonamide at the other end, European Polymer Journal, 36, 8, (2000), 1703-1710 https://doi.org/10.1016/S0014-3057(99)00243-8
  32. Heping Li, Tao Yu, Shan Li, Long Qin, Jingheng Ning, Preparation and drug-releasing properties of chitosan-based thermosensitive composite hydrogel, Journal of the Korean Chemical Society, 56, 4, (2012), 473-477 https://doi.org/10.5012/jkcs.2012.56.4.473
  33. Cheng Wu Li, Gang Li, Ji Cheng Zuo, Synthesis and Characterization of 5-Fluorouracil and Polyethylene Glycol Esters as Prodrugs, Advanced Materials Research, 287-290, (2011), 1509-1512 https://doi.org/10.4028/www.scientific.net/AMR.287-290.1509
  34. Marri Venkateswarlu, Kamatala Chinna Rajanna, Mukka Satish Kumar, Utkoor Umesh Kumar, Soma Ramgopal, Pondichery Kuppuswamy Saiprakash, Rate enhancements in the acetylation and benzoylation of certain aromatic compounds with Vilsmeier-Haack reagents using acetamide, benzamide and oxychlorides under Non-conventional conditions, International Journal of Organic Chemistry, 1, 4, (2011), 233-241 http://dx.doi.org/10.4236/ijoc.2011.14034
  35. Giovanni Sartori, Roberto Ballini, Franca Bigi, Giovanna Bosica, Raimondo Maggi, Paolo Righi, Protection (and Deprotection) of Functional Groups in Organic Synthesis by Heterogeneous Catalysis, Chemical Reviews, 104, 1, (2004), 199-250 https://doi.org/10.1021/cr0200769
  36. Michael Schelhaas, Herbert Waldmann, Protecting Group Strategies in Organic Synthesis, Angewandte Chemie International Edition in English, 35, 18, (1996), 2056-2083 https://doi.org/10.1002/anie.199620561
  37. Ayik Rosita Puspaningtyas, Modifikasi Struktur 5-Fluorourasil dan Uji Sitotoksik Turunan 1-(Benzoiloksimetil)-5-Fluorourasil Hasil Modifikasi Terhadap Sel Kanker MCF-7 (Sebagai Upaya Pengembangan Senyawa Obat Antikanker Payudara), Farmasi, Universitas Airlangga, Surabaya, 2011
  38. Graham L. Patrick, An Introduction to Medicinal Chemistry, Oxford University Press, 2017,
  39. Frank Vella, Fundamentals of medicinal chemistry: Thomas, G., Biochemistry and Molecular Biology Education, 32, 3, (2004), 211-211 https://doi.org/10.1002/bmb.2004.494032039997

Last update:

No citation recorded.

Last update: 2024-09-26 05:33:43

No citation recorded.