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Synthesis of New 3-Morpholyl-Substituted 4-Aryl-2-Arylimino-2,3-Dihydrothiazole Derivatives and Their Anti-Inflammatory and Analgesic Activity

Iryna Drapak1, Borys Zimenkovsky1, Lina Perekhoda2, Hanna Yeromina2, Zinaida Ieromina2, Marianna Paykush1, Liliya Logoyda3, Vira Lubenets4, Tetiana Holubieva5, Roksolana Yaremkevych1, Oleksandr Shchur1, Nataliya Seredynska6
Affiliation: 
1 Danylo Halytsky Lviv National Medical University, 69, Pekarska St., Lviv, Ukraine 2 National University of Pharmacy, 53, Pushkinska St., Kharkiv, Ukraine 3 I. Horbachevsky Ternopil National Medical University, 1, Maidan Voli, Ternopil, Ukraine 4 Lviv Polytechnic National University, 12, S. Bandery St., Lviv, Ukraine 5 National University of Life and Environmental Sciences of Ukraine, Kyiv, Ukraine 6 Institute of Pharmacology and Toxicology, National Academy of Medical Sciences, 14, Anton Tsedik St., Kyiv, Ukraine iradrapak@ukr.net
DOI: 
https://doi.org/10.23939/chcht16.04.532
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Abstract: 
New 4-aryl-3-(morpholin-4-yl)-2-arylimino-2,3-dihydrothiazole derivatives 1.1-1.16 were obtained using the Hantzsch reaction by condensation of N-(morpholin-4-yl)-N'-arylthioureas with the corresponding α bromoacetophenones in alcohols. Synthesized hydrobromides 1.1-1.8 were formed as crystalline precipitates during the boiling of the reaction mixture. Bases 1.9-1.16 were obtained by neutralizing the corresponding hydrobromides with NH4OH solution. It has been proposed a possible mechanism of the reaction that is based on the study of the structure of the synthesized compounds. The structures of the synthesized compounds were confirmed by 1H NMR spectroscopy with its special techniques (NOESY and ROESY experiments). It has been shown the formation of the isomer 4-(4'-chlorophenyl)-3-(morpholin-4-yl)-2-(4'-chlorophenylamino)-2.3-dihydrothiazole on the basis of compound 1.14. Pharmacological screening of synthesized derivatives of 4-aryl-2-arylimino-2,3-dihydrothiazole compounds revealed the analgesic effect in the model of visceral pain caused by the introduction of acetic acid to white mice. The anti-inflammatory effect of the synthesized compounds was evaluated in vivo by reducing limb edema in rats with carrageenan-induced inflammation. Thus, the synthesized compounds have analgesic and anti-inflammatory activity.
References: 

[1] Haddani, F.Z.; Guich, A.; Youssoufi, T.; Boudhar, E.M.; Abouqal, R.; Achemlal, L.; Allali, F.; Bahiri, R.; Bouchti, E.I.; Maghraoui, E.I. et al. Comorbidities in Rheumatoid Arthritis: the RBSMR Study. Int. J. Clin. Rheumatol. 2020, 15(1), 10-14.

[2] Luque Ramos, A.; Redeker, I.; Hoffmann, F.; Callhoff, J.; Zink, A.; Albrecht, K. Comorbidities in Patients with Rheumatoid Arthritis and Their Association with Patient-reported Outcomes: Results of Claims Data Linked to Questionnaire Survey. J. Reumatol. 2019, 46(6), 547-571. https://doi.org/10.3899/jrheum.180668
https://doi.org/10.3899/jrheum.180668

[3] Roubille, C.; Fesler, P.; Combe, B. Shifting from a Rheumatologic Point of View toward Patient-centered Care in Rheumatoid Arthritis with an Integrated Management of Comorbidities. J. Reumatol. 2019, 46(6), 545-547. https://doi.org/10.3899/jrheum.181379
https://doi.org/10.3899/jrheum.181379

[4] Vogel, H. G.; Vogel W. H. Drug Discovery and Evaluation. Pharmacological Assays. Second Completely Revised, Updated, and Enlarged Edition; Springer, 2002. https://doi.org/10.1007/978-3-662-03333-3
https://doi.org/10.1007/978-3-662-03333-3

[5] Drapak, I.; Zimenkovsky, B.; Perekhoda, L.; Yeromina, H.; Lipakova, K.; Demchuk, I.; Rakhimovа, M. QSAR-Analysis of 1-[2-(R-Phenylimino)-4-methyl-3-(3-[morpholine-4-yl]propyl)-2,3-dihydro-1,3-thiazol-5-yl]ethane-1-ones Derivatives as Potential Antioxidants. Pharmacia 2019, 66(1), 33-40. https://doi.org/10.3897/pharmacia.66.e35083
https://doi.org/10.3897/pharmacia.66.e35083

[6] Drapak, I.; Suleiman, M.; Protopopov, M.; Yeromina, H.; Sych, I.; Ieromina, Z.; Sych, I.; Perekhoda, L. The Use of the Docking Studies with the Purpose of Searching Potential Antihypertensive Drugs. Res. J. Pharm. Technol. 2019, 12(10), 4889-4894. https://doi.org/10.5958/0974-360X.2019.00846.1
https://doi.org/10.5958/0974-360X.2019.00846.1

[7] Panasenko, N.; Bratenko, M.: Zvarych, V.; Stasevych, M.; Vovk, M. Synthesis and Evaluation of Hypoglycemic Activity of New Pyrazolothiazolidine Hybrid Structures. Chem. Chem. Technol. 2020, 14(3), 284-289. https://doi.org/10.23939/chcht14.03.284
https://doi.org/10.23939/chcht14.03.284

[8] Lelyukh, M.; Havrylyuk, D.; Lesyk, R. Synthesis and Anticancer Activity of Isatin, Oxadiazole and 4-Thiazolidinone Based Conjugates. Chem. Chem. Technol. 2015, 9(1), 29-36. https://doi.org/10.23939/chcht09.01.029
https://doi.org/10.23939/chcht09.01.029

[9] Yeromina, H.; Demchenko, N.; Kiz, O.; Ieromina, Z.; Demchenko, S. The Synthesis and Antimicrobial Properties of New 2-(R-Phenylimino)-1,3-thiazoline Derivatives Containing the N-Methylpiperazine Moiety. Chem. Chem. Technol. 2019, 13(2), 150-156. https://doi.org/10.23939/chcht13.02.150
https://doi.org/10.23939/chcht13.02.150

[10] Klenina, O.; Drapak, I.; Chaban, T.; Ogurtsov, V.; Chaban, I.; Golos, I. QSAR Studies of Some Thiazolo[4,5-b]pyridines as Novel Antioxidant Agents: Enhancement of Activity by Some Molecular Structure Parameters. Chem. Chem. Technol. 2013, 7(4), 397-404. https://doi.org/10.23939/chcht07.04.397
https://doi.org/10.23939/chcht07.04.397

[11] Perekhoda, L.; Georgiyants, V.; Yeromina, H.; Drapak, I.; Lubenets, V.; Ieromina, Z.; Sych, I.; Severina, H.; Demchenko, A. The Synthesis and in silico Antihypertensive Activity Prognosis of New Mannich Bases Containing the 1,2,4-Triazole Moiety. Chem. Chem. Technol. 2020, 14(2), 214-220. https://doi.org/10.23939/chcht14.02.214
https://doi.org/10.23939/chcht14.02.214

[12] Drapak, I.; Perekhoda, L.; Demchenko, N.; Suleiman, M.; Rakhimova, M.; Demchuk, I.; Taran, S.; Seredynska, N.; Gerashchenko, I. Cardioprotective Activity of Some 2-Arylimino-1,3-Thiazole Derivatives. Sci. Pharm. 2019, 87(1), 7. https://doi.org/10.3390/scipharm87010007
https://doi.org/10.3390/scipharm87010007

[13] Moldovan, C.M.; Oniga, O.; Pârvu, A.; Tiperciuc, B.; Verite, P.; Pîrnău, A.; Crişan, O.; Bojiţă, M.; Pop, R. Synthesis and Anti-Inflammatory Evaluation of Some New Acyl-Hydrazones Bearing 2-Aryl-Thiazole. Eur. J. Med. Chem. 2011, 46(2), 526-534. https://doi.org/10.1016/j.ejmech.2010.11.032
https://doi.org/10.1016/j.ejmech.2010.11.032

[14] Yeromina, H.O.; Drapak, I.V.; Perekhoda, L.O.; Yaremenko, V.D.; Demchenko, A.M. Synthesis of 2-(4-Aryl(adamantyl)-2-phenylіmіnothіazol-3-yl)-ethanol Derivatives and Prediction of Their Biological Activity. Der Pharma Chem. 2016, 8(3), 64-70.

[15] Karthikeyan, M.S. Synthesis, Analgesic, Anti-Inflammatory and Antimicrobial Studies of 2,4-Dichloro-5-fluorophenyl Containing Thiazolotriazoles. Eur. J. Med. Chem. 2009, 44(2), 827-833. https://doi.org/10.1016/j.ejmech.2008.04.022
https://doi.org/10.1016/j.ejmech.2008.04.022

[16] Nadtoka, O.; Syromyatnikov, V. The Influence of Chemical Structure of Chromophore on Polymerization of Methacrylic Azomonomers. Chem. Chem. Technol. 2014, 8(4), 389-394. https://doi.org/10.23939/chcht08.04.389
https://doi.org/10.23939/chcht08.04.389

[17] Rydchuk, P.; Labyk, O.; Oleksiv, L.; Tymoshuk, O.; Chaban, T. Voltammetric Determination of Pd(II) Using 5-Hydroxyimino-4-imino-1,3-thiazolidin-2-one after a Thermal Activation of the Interaction. Chem. Chem. Technol. 2021, 15(3), 324-329. https://doi.org/10.23939/chcht15.03.324
https://doi.org/10.23939/chcht15.03.324

[18] Stefanov, O.V. Doklinichni doslidzhennya likars'kykh zasobiv (metodychni rekomendatsiyi); Avitsena, 2001. (in Ukrainian)

[19] Winter, C.A.; Risley, E.A.; Nuss, G.W. Carrageenin-Induced Edema in Hind Paw of the Rat as an Assay for Antiinflammatory Drugs. Exp. Biol. Med. 1962, 111(3), 544-547. https://doi.org/10.3181/00379727-111-27849
https://doi.org/10.3181/00379727-111-27849