Next Article in Journal
Inhibitory Effects of AF-343, a Mixture of Cassia tora L., Ulmus pumila L., and Taraxacum officinale, on Compound 48/80-Mediated Allergic Responses in RBL-2H3 Cells
Previous Article in Journal
Chemical Composition and Determination of the Antibacterial Activity of Essential Oils in Liquid and Vapor Phases Extracted from Two Different Southeast Asian Herbs—Houttuynia cordata (Saururaceae) and Persicaria odorata (Polygonaceae)
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Molecules
Volume 25
Issue 10
10.3390/molecules25102433
molecules-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Synthesis, Characterization and Bioassay of Novel Substituted 1-(3-(1,3-Thiazol-2-yl)phenyl)-5-oxopyrrolidines

by
Birutė Sapijanskaitė-Banevič
1,
Božena Šovkovaja
1,
Rita Vaickelionienė
1,*,
Jūratė Šiugždaitė
2 and
Eglė Mickevičiūtė
3
1
Department of Organic Chemistry, Kaunas University of Technology, Radvilėnų Rd. 19, LT-50254 Kaunas, Lithuania
2
Department of Veterinary Pathobiology, Veterinary Academy, Lithuanian University of Health Sciences, Tilžės Str. 18, LT-47181 Kaunas, Lithuania
3
Department of Information Systems, Kaunas University of Technology, Studentų Str. 50, LT-51368 Kaunas, Lithuania
*
Author to whom correspondence should be addressed.
Molecules 2020, 25(10), 2433; https://doi.org/10.3390/molecules25102433
Submission received: 28 April 2020 / Revised: 19 May 2020 / Accepted: 20 May 2020 / Published: 22 May 2020
(This article belongs to the Section Organic Chemistry)
Browse Figures
Versions Notes

Abstract

:
Thiazole derivatives attract the attention of scientists both in the field of organic synthesis and bioactivity research due to their high biological activity. In the present study, thiazole ring was obtained by the interaction of 1-(4-(bromoacetyl)phenyl)-5-oxopyrrolidine-3-carboxylic acid with thiocarbamide or benzenecarbothioamide, as well as tioureido acid. A series of substituted 1-(3-(1,3-thiazol-2-yl)phenyl)-5-oxopyrrolidines with pyrrolidinone, thiazole, pyrrole, 1,2,4-triazole, oxadiazole and benzimidazole heterocyclic fragments were synthesized and their antibacterial properties were evaluated against Gram-positive strains of Staphylococcus aureus, Bacillus cereus, Listeria monocytogenes and Gram-negative Pseudomonas aeruginosa, Escherichia coli and Salmonella enterica enteritidis. The vast majority of compounds exhibited between twofold and 16-fold increased antibacterial effect against the test-cultures when compared with Oxytetracycline.

Graphical Abstract

1. Introduction

Heterocyclic compounds are one of the main groups of organic compounds possessing a wide range of applications in various areas of science and high technologies. Recently, greater attention has been paid to heterocyclic compounds such as azoles. The nitrogen-containing five-membered heterocycles–pyrrole, diazole, triazole, thiazole, thiadiazole, oxadiazole, benzimidazole demonstrate a wide diversity of biological properties. Thiazoles are commonly reported as active antimicrobial [1,2,3,4,5,6,7,8], anti-tuberculous [9,10,11,12], anti-HIV [13], antiviral [14,15], antihistamine [16,17], antipyretic [18], antitumor [3,19], antidepressant [20], fungicidal [21,22] property bearing compounds. 2-Aminothiazoles has found application in agriculture as herbicides and fungicides [23,24]. Pyrrole nucleus has been incorporated into a wide variety of therapeutically important medication candidates. For example, the pyrrole ring is present in the structure of the anti-cancerous drug Sunitinib [25,26], which is used for the treatment of several types of cancer. Compounds with a pyrrolidinone moiety in the structure show inhibition of human carbonic anhydrase [27,28]. Compounds containing a 1,2,4-triazole scaffold demonstrate different pharmacological actions such as analgesic [29,30], antiviral [31], anti-inflammatory [32], anticonvulsant [33,34], anticancer [35], antidepressant [36], antibacterial [37,38], antifungal [37,39], and are used as various pharmaceuticals. They have been approved as drugs such as Anastrazole, Letrozole, Rizatriptan, Ribavirin, Alprazolam, Fluconazole and Posaconazole (Figure 1). Therefore, many researchers looking for new medicines are still focused on the synthesis of 1,2,4-triazole derivatives. Benzimidazole is an important heterocyclic compound with the fused-ring system in the structure. Because of its similarity to the structure of purine bases, benzimidazole derivatives can compete with them in the course of bacterial membrane biosynthesis, thereby stimulating the death of bacteria [40,41].
This study focused on the synthesis of new, potentially biologically active 1,3-disubstituted 5-oxopyrrolidines with pyrrolidinone, thiazole, pyrrole, 1,2,4-triazole, oxadiazole, benzimidazole and quinoxaline heterocyclic fragments in the structure, and resulted in the discovery of compounds with significantly increased antibacterial activity.

2. Results and Discussion

2.1. Chemistry

In this work, the initial compound 1 was prepared from 4-aminoacetophenone and itaconic acid by a known method [42]. In order to obtain 2,5-disubstituted thiazole derivatives 3a–c, compound 1 was brominated with Br2 in acetic acid at room temperature (Scheme 1), and then used in the reactions with thiocarbonyl compounds. The bromination reaction resulted in the formation of α-bromocarbonyl compound 1-(4-(2-bromoacetyl)phenyl)-5-oxopyrrolidine-3-carboxylic acid (2). Cyclocondensation of α-bromoacyl derivative 2 with the corresponding thioamide, i.e., thiocarbamide, benzenecarbothioamide or thioureido acid, under different conditions was carried out to obtain the desired outcomes 3a–c. The a reaction was performed in acetic acid at 60 °C; in the cases of b and c, the reaction was carried out in refluxing acetone. A comparison of the 1H and 13C-NMR spectra of compounds 3a–c revealed the characteristic signals of the formed substituted thiazole moieties. In the spectra of compound 3a, the singlets at 6.96 (S–C=CH) and 7.07 (NH2, 1H-NMR) ppm, and the resonance lines at 100.9 (C–S), 138.1 (S–C=CH), 168.2 (C=N, 13C-NMR) ppm prove the presence of thiazole heterocycle in the molecule. The characteristic signals in the 1H (8.20 ppm, S–C=CH) and 13C (114.0, 154.7, 166.9 ppm, C–S, S–C=CH, C=N) NMR, as well as additional resonances in the aromatic field of the corresponding spectrum of 3b, provide the evidence of new 2-phenyl thiazole fragment. The formation of the 2-carboxyethyl-4-methylanilino moiety in compound 3c was confirmed by the presence of triplets at 2.40 (J = 7.9 Hz, NCH2CH2CO) and 4.10 (J = 7.9 Hz, NCH2CH2) ppm in the 1H-NMR spectrum. The signals of protons of the p-substituted benzene cycle resonated as two doublets at 7.26 and 7.32 ppm and the signal arising at 2.32 ppm indicated the presence of the methyl group. All NMR spectra of the synthesized compounds are given in Supplementary Materials.
Compounds 5a,b were prepared following the standard synthesis route, i.e., 5-oxopyrrolidine-3-carboxylic acids 3a,b were esterified with methanol in the presence of a catalytic amount of sulfuric acid to obtain esters 4a,b. The prepared esters were easily converted to the corresponding acid hydrazides 5a,b, when treated with hydrazine hydrate in refluxing propan-2-ol.
The condensation of acid hydrazides 5a,b with aromatic aldehydes in dimethylformamide or 1,4-dioxane afforded hydrazone-type compounds (6–8)a,b, and (9–12)b in good to excellent yield (62–99%, Scheme 2; the yields of all synthesized compounds are given in Table 1).
The synthesized hydrazones in DMSO-d6 solution, due to the restricted rotation around the CO-NH bond, exist as a mixtures of E/Z-amide conformers with the prevailing Z conformational structure [43,44,45]. However, geometric isomers are also possible due to the presence of the N=C double bond. The academic literature indicates that hydrazones obtained from acid hydrazides and aromatic aldehydes favour the sterically less-hindered and more stable geometric E-geometrical isomer [46,47,48].
The reaction of acid hydrazides 5a,b with hexane-2,5-dione (2,5-HD) resulted in the formation of 2,5-dimethylpyrrole derivatives 13a,b, as expected. Using the method of the formation of pyrrolidinone ring from aromatic amines and itaconic acid, hydrazide 5b as an amino group-containing compound was reacted with this dicarboxylic acid. The reaction was performed in toluene at reflux, and the synthesized compound 14b containing two pyrrolidinone rings connected by the amide bond was proved by double sets of the protons (1H-NMR) of the 2COCH2, 2CH and 2NCH2 groups, which gave rise in the ranges of 2.54–2.88, 3.25–3.42 and 3.55–4.16 ppm, respectively. In the 13C-NMR spectrum of 14b spectral lines at 31.3, 33.6, 34.2, 35.5, 49.7 and 50.3 ppm have been attributed to the COCH2, CH and NCH2 groups of two pyrrolidinone rings, and resonances at 170.9, 171.4, 171.8 and 174.6 ppm approve the presence of four carbonyl groups in this structure. NMR spectral data of compound 14b showed the presence of only one isomer in the DMSO-d6 solution. Unfortunately, attempts to grow single crystals suitable for stereochemical assignment by X-ray structural analysis were unsuccessful.
Thiosemicarbazide 15b was synthesized by treatment of acid hydrazide 5b with phenyl isothiocyanate in methanol. Singlets at 9.58, 9.68, 9.88, 10.12 and 10.22 ppm in the 1H-NMR spectrum of the compound are characteristic of the 3NH of the thiosemicarbazide moiety, and six additional resonance lines of the newly attached phenyl fragment in the 13C-NMR spectrum of 15b provide clear evidence of the compound structure. 2-(5-Oxo-1-(4-(2-phenylthiazol-5-yl)phenyl)pyrrolidine-3-carbonyl)-N-phenylhydrazine-1-carbothioamide (15b) was then converted to 1,2,4-triazole 16b by a base catalyzed intramolecular dehydrative cyclization reaction.
The reaction of hydrazide 5b with carbon disulfide in methanol under basic conditions (KOH/methanol) gave the intermediate, the potassium dithiocarbazate salt, which under the action of concentrated hydrochloric acid was cyclized to 5-thioxo-1,3,4-oxadiazole 17b. The treatment of potassium carbodithioate with hydrazine monohydrate afforded 4-aminotriazole 18b. The condensation of one equivalent of compound 18b containing free amino group with two equivalents of benzenecarbaldehyde in refluxing ethanol containing a catalytic amount of concentrated hydrochloric acid yielded the Schiff base 19b. The characteristic changes in the chemical shift of the resonances of the triazole moiety were observed because of the changed influence of the substituent at the nitrogen atom of the C–N–C=S fragment. In the case of 19b, the carbon atom of the C=S group resonated at 162.9 ppm, and the C=N–NH carbon atom peaked at 162.0 ppm in 13C-NMR spectrum. Additional spectral lines were observed in the aromatic region and were assigned to the carbon atoms of the newly incorporated benzene ring and formed azomethine group. The 1H-NMR spectrum of 1,2,4-triazole derivative 19b showed characteristic singlets at 10.14 ppm (N=CH) and 13.97 (NH), and the multiplet of the benzene rings integrated for 14 protons.
In the next stage of the work, the reactivity of acyl- 1 and α-bromo acyl 2 derivatives was investigated by reacting them with benzene-1,2-diamine (Scheme 3). The reactions were performed in different solvents. The reaction of the derivative 1 with diamine in ethanol yielded the condensation product 1-(4-(1-((2-aminophenyl)iminoethyl)phenyl)-5-oxopyrrolidine-3-carboxylic acid (20), while the bromoacyl derivative 2 under the same conditions afforded the compound 21 containing the quinoxaline moiety. The condensation in the compound 1 occurred in the acyl moiety. This resulted in a conjugated system with double bonds in the chain of the benzene ring-iminoethyl fragment-benzene ring, which gave the brightly brown-orange crystalline compound 20. The obtained compound 20 was easily identified by the data of the NMR spectra. In the 1H and 13C-NMR spectra of compound 21, the increased number of spectral lines in the aromatic regions of the respective spectra, the HRMS (High-resolution mass spectrometry) data, and the elemental analysis approved the formation of quinoxaline moiety. The second step of the investigation was to find out the products of the same reaction in refluxing 4 M hydrochloric acid. The reaction of compound 1, having an acyl group on the benzene ring with benzene-1,2-diamine in refluxing 4 M hydrochloric acid, afforded the benzimidazole derivative 22 [49]. Resynthesis was carried out according to a well-known Philips method (the heating of reagents in a 4 M HCl); however, extending it to 16 h and neutralizing the mixture with aqueous ammonium hydroxide to pH 7. This resulted in the increased yield of the desired product 22 (from 40 to 92%). The condensation of brominated compound 2 with diamine under the same conditions led to the formation of the complex mixture, and product separation was unsuccessful.
For more extensive analysis of biological properties of the compounds resynthesized benzimidazole 22 [49] was alkylated with iodoethane at solvent-free conditions and in the presence of potassium hydroxide and sodium carbonate.
The reaction provided N-alkylated compound 1-(4-acetylphenyl)-3-(1-ethyl-1H-benzimidazol-2-yl)-5-oxopyrrolidine (23).

2.2. Biological Activity

All synthesized compounds 2–19 and 21–23 were tested against Gram-positive bacteria strains of Staphylococcus aureus (ATCC 25923), Bacillus cereus (ATCC 10231), Listeria monocytogenes (ATCC 19111) as well as Gram-negative Pseudomonas aeruginosa (ATCC 10145), Escherichia coli (ATCC 8739) and Salmonella enterica enteritidis (ATCC 13076) bacteria for their in vitro antibacterial activity by broth dilution and spread-plate techniques [50,51,52]. Oxytetracycline was used as a control (C) for antibacterial activity screening. The determined values of the minimum inhibition (MIC, µg/mL) and the minimum bactericidal (MBC, µg/mL) concentrations are presented in Table 2. The investigations demonstrated that the synthesized compounds possessed higher antibacterial properties than those of the known antibiotic Oxytetracycline.
The in vitro evaluation of the above-mentioned compounds revealed the excellent antibacterial activity of compounds 3c, 5b, 15b and 16b. Their effect on Gram-positive bacteria strains (MIC 7.8 µg/mL and MBC 15.6 µg/mL) was 8 times higher, and against Gram-negative 16-fold higher, than those of the control Oxytetracycline.
It should also be noted that among the thiazoles 3a–c the amino thiazole 3c, containing the β-alanine moiety, displayed the best antibacterial results against all the tested bacteria strains.
Among all the tested compounds, methyl ester 4b, hydrazone 6b and oxadiazole derivative 17b should be distinguished. They demonstrated four times stronger inhibition effects against Gram-positive bacteria strains and showed 8-fold higher inhibition against Gram-negative bacteria in comparison with the control. Hydrazones 6a and (7–12)b in most cases displayed good to very good action against the tested bacteria species. However, the best activity showed hydrazone 9b with 4-fluorophenyl moiety in the molecule.
The comparison of the antibacterial activity of both benzimidazoles showed that the alkylated derivative 22 was more potent only against the strain of S. aureus. In all other cases, the effect of benzimidazole 20 and its derivative 22 on test-bacteria strains was completely the same. It is also noteworthy that S. aureus and E. coli were the most sensitive to the action of benzimidazoles 20 and 22. The minimum inhibition and minimum bactericidal concentrations of 31.25 µg/mL (MIC 15.6 µg/mL for S. aureus in case of 22) were sufficient in comparison with 62.5 and 125 µg/mL of Oxytetracycline for the inhibition of the growth and bactericidal action of the indicated test-cultures.
The quinoxaline fragment containing derivative 21 exhibited a more marked effect than the control Oxytetracycline only against B. cereus, L. monocytogenes and S. enterica enteritidis. In other cases, resistance of the test-bacteria was found to be the same as that of the used control antibiotic (except for MIC in the case of L. monocytogenes).
Comparing the data of the biological activity of the compounds containing different substituents (amino (a) or phenyl (b)) at the 2-position of thiazole ring, it can be asserted that derivatives with 2-phenylthiazol-5-yl moiety (3–6 and 13)b, show stronger inhibition and bactericidal effects than the derivatives with 2-aminothiazol-5-yl fragment (3–6 and 13)a. The MIC of compounds with phenyl group changes in range of 7.8–62.5 µg/mL, with prevailing MIC of 15.6 µg/mL, and the MBC vary from 15.6 to 125 µg/mL, with the prevailing value of 31.25 µg/mL. Accordingly, the data of compounds with amino group are as follows: the MIC vary from 15.6 to 62.5 µg/mL, with the prevailing value of 31.25 µg/mL; and the MBC changes in range of 31.25–125 µg/mL, with the prevailing concentration of 62.5 µg/mL. It should be noted that, among the compounds of group a, the 2-aminothiazole derivative 3a exhibited stronger activity only against S. aureus and E. coli in comparison with its analogue 3b.

3. Materials and Methods

3.1. Synthesis

Reagents and solvents were purchased from Sigma-Aldrich (St. Louis, MO, USA) and used without further purification. The reaction course and purity of the synthesized compounds were monitored by TLC (Thin layer chromatography) using aluminum plates pre-coated with Silica gel with F254 nm (Merck KGaA, Darmstadt, Germany). Melting points were determined with a Melt-Temp Melting Point Analyzer (Electrothermal, Bibby Scientific Company, Burlington, NJ, USA) and were uncorrected. NMR spectra were recorded on a Varian Unity Inova (300, 75 MHz) and Brucker BioSpin GmbH (400, 101 and 700, 175 MHz) spectrometers. Chemical shifts were reported in (δ) ppm relative to tetramethylsilane (TMS) with the residual solvent as internal reference ([D6]DMSO, δ = 2.50 ppm for 1H and δ = 39.5 ppm for 13C). The data are reported as follows: chemical shift, multiplicity, coupling constant [Hz], integration and assignment. IR spectra (ν, cm−1) were recorded on a Bruker TENSOR 27 spectrometer using KBr pellets. Mass spectra were measured on a Waters (Micromas) ZQ 2000 mass spectrometer (ESI 20 eV). Elemental analyses (C, H, N) were conducted using the Elemental Analyzer CE-440 (Exeter Analytical, Inc., North Chelmsford, MA, USA); their results were found to be in good agreement (± 0.3%) with the calculated values.
1-(4-Acetylphenyl)-5-oxopyrrolidine-3-carboxylic acid (1): White solid, yield 62.9 g, 86%, m. p. 170–171 °C (2-propanol) [42]. The 1H and 13C-NMR spectra agreed with that given in the study [42].
1-(4-(2-Bromoacetyl)phenyl)-5-oxopyrrolidine-3-carboxylic acid (2): To a stirred mixture of carboxylic acid 1 (2.47 g, 10 mmol) and acetic acid (5.5 mL) a solution of bromine (9.59 g, 60 mmol) and acetic acid (15 mL) was slowly added dropwise at room temperature, and then the resulting reaction mixture further was stirred for 4 h. Afterwards, the reaction mixture was poured into the ice/water mixture (350 mL). The residual bromine was removed by adding a few milliliters of 20% sodium thiosulfate solution. The obtained precipitate was filtered off, washed with plenty of water and recrystallized from water to give the title compound 2 (white solid, yield 2.34 g, 95%, m. p. 149–150 °C (water). 1H-NMR (400 MHz, DMSO-d6): δ = 2.67–2.92 (m, 2H, COCH2), 3.32–3.46 (m, 1H, CH), 3.94–4.20 (m, 2H, NCH2), 4.76, 4.89 (2s, 2H, CH2Br), 7.76–8.14 (m, 4H, HAr), 10.52 (br s, 1H, OH) ppm. 13C-NMR (101 MHz, DMSO-d6): δ = 33.9 (CH2Br), 35.0 (COCH2), 35.4 (CH), 49.8 (NCH2), 118.5, 128.6, 129.9, 143.7 (CAr), 172.8 (N–C=O), 174.1 (COOH), 190.6 (C=O) ppm. IR (KBr): νmax = 1738, 1691, 1660 (3C=O) cm–1. MS (ESI), m/z, % [M]+ = 326 (100), [M + 2]+ = 328 (98). Calcd. for C13H12BrNO4, %: C 47.87; H 3.71; N 4.29. Found, %: 47.78; H 3.68; N 4.29.
1-(4-(2-Aminothiazol-5-yl)phenyl)-5-oxopyrrolidine-3-carboxylic acid (3a): A mixture of carboxylic acid 2 (3.26 g, 10 mol), thiourea (1.52 g, 20 mol) and acetic acid (20 mL) was heated at 60 °C for 16 h, then the reaction mixture was diluted with water and the formed precipitate was filtered off, washed with water and hexane, and recrystallized from dimethylforamide/water (2:1) mixture to give the title compound 3 a (white solid, yield 2.0 g, 62%, m. p. 271–272 °C (DMF/water). 1H-NMR (400 MHz, DMSO-d6): δ = 2.69–2.82 (m, 2H, COCH2), 3.32–3.39 (m, 1H, CH), 3.93–4.13 (m, 2H, NCH2), 6.96 (s, 1H, CH=C), 7.07 (s, 2H, NH2), 7.66 (d, J = 8.8 Hz, 2H, HAr), 7.79 (d, J = 8.8 Hz, 2H, HAr), 12.81 (br s, 1H, OH) ppm. 13C-NMR (101 MHz, DMSO-d6): δ = 35.2 (COCH2), 35.3 (CH), 50.0 (NCH2), 100.9 (C–S), 119.3, 125.9, 130.8, 138.2, 149.4 (CH=C, CAr), 168.2 (C=N), 171.8 (C=O), 174.3 (COOH) ppm. IR (KBr): νmax = 3240 (NH2), 1684, 1664 (2C=O). Calcd. for C14H13N3O3S, %: C 55.43; H 4.32; N 13.85. Found, %: C 55.39; H 4.29; N 13.77.
5-Oxo-1-(4-(2-phenylthiazol-5-yl)phenyl)pyrrolidine-3-carboxylic acid (3b): A mixture of compound 2 (0.4 g, 0.123 mmol) and benzencarbothioamide (0.17 g, 0.123 mmol) was refluxed in acetone (5 mL) for 6 h, then cooled down, the formed crystalline precipitate was filtered off, washed with acetone, and recrystallized from methanol to give the title compound 3b (white solid, yield 0.19 g, 43%, m. p. 221–222 °C (methanol)). 1H-NMR (400 MHz, DMSO-d6): δ = 2.65–2.82 (m, 2H, COCH2), 3.28–3.41 (m, 1H, CH), 4.00–4.18 (m, 2H, NCH2), 7.51–7.61 (m, 3H, HAr), 7.75–7.86 (m, 2H, HAr), 8.01–8.18 (m, 4H, HAr), 8.20 (s, 1H, CH=C), 12.82 (s, 1H, OH) ppm. 13C-NMR (101 MHz, DMSO-d6): δ = 35.1 (COCH2), 35.3 (CH), 49.9 (NCH2), 114.0 (C–S), 119.4, 126.2, 126.5, 129.3, 129.7, 130.4, 133.0, 139.0 (CAr), 154.7 (CH=C), 166.9 (C=N), 172.0 (N–C=O), 174.2 (COOH) ppm. IR (KBr): νmax = 3446 (OH), 1727, 1651 (2C=O). MS (ESI), m/z, %: [M + H]+ = 365 (100). Calcd. for C20H16N2O3S, %: C 65.92; H 4.43; N 7.69. Found, %: C 65.82; H 4.35; N 7.62.
1-(4-(2-((2-Carboxyethyl)-4-methylanilino)-1,3-thiazol-5-yl)phenyl)-5-oxopyrrolidine-3-carboxylic acid (3c): To a solution of 3-(1-(p-tolyl)thioureido)propanoic acid (0.24 g, 1 mmol) in acetone (5 mL), compound 2 (0.42 g, 1.3 mmol) was added and the mixture was heated at reflux for 8 h. After the completion of the reaction, the mixture was cooled down, the formed crystalline solid was filtered off, washed with acetone, and dissolved in 10% aqueous sodium acetate solution (25 mL) by boiling, and then cooled down. The formed precipitate was filtered off, washed with water, and recrystallized from methanol to give the title compound 3 c (light yellow solid, yield 0.38 g, 82%, m. p. 196–197 °C (methanol)). 1H-NMR (400 MHz, DMSO-d6): δ = 2.32 (s, 3H, CH3), 2.40 (t, J = 7.9 Hz, 2H, CH2COO), 2.51–2.98 (m, 3H, COCH2 + CH), 3.88–4.05 (m, 2H, NCH2), 4.10 (t, J = 7.9 Hz, 2H, NCH2CH2), 6.99 (s, 1H, CH=C), 7.26 (d, J = 8.4 Hz, 2H, HAr2,, 6,), 7.32 (d, J = 8.3 Hz, 2H, HAr3,, 5,), 7.67 (d, J = 8.8 Hz, 2H, HAr2, 6), 7.82 (d, J = 8.7 Hz, 2H, HAr3, 5) ppm. 13C-NMR (101 MHz, DMSO-d6): δ = 20.7 (CH3), 35.0 (COCH2), 37.1 (CH), 37.5 (CH2), 50.2 (NCH2), 51.9 (CH2), 101.2 (C–S), 118.9, 125.9, 126.7, 130.1, 130.4, 136.5, 139.0, 142.2, 150.0 (CH=C, CAr), 169.1 (C=N), 173.7 (C=O), 174.5 (COOH), 176.0 (COOH) ppm. IR (KBr): νmax = 1683, 1605, 1575 (3C=O). MS (ESI), m/z, %: [M + H]+ = 466 (100). Calcd. for C24H23N3O5S, %: C 61.92; H 4.98; N 9.03. Found, %: C 61.68; H 4.62; N 8.91.

3.1.1. General Procedure for the Preparation of Esters 4a,b

To a solution of the corresponding carboxylic acid 3 (2.75 mmol) in methanol, concentrated sulfuric acid (1 mL) was added dropwise and the mixture was heated at reflux for 5 h. Then the solvent was evaporated under reduced pressure, and the residue neutralized with 7% (a) or 10% (b) sodium carbonate solution to pH 7. The obtained solid was filtered off, washed with plenty of water, and recrystallized from methanol to give the title compound 4a (light yellow solid, yield 0.54 g, 62%, m. p. 271–272 °C (methanol)) and 4b (light yellow solid, yield 0.71 g, 71%, m. p. 139–140 °C (methanol)).
Methyl 1-(4-(2-aminothiazol-5-yl)phenyl)-5-oxopyrrolidine-3-carboxylate (4a): 1H-NMR (400 MHz, DMSO-d6): δ = 2.64–2.89 (m, 2H, COCH2), 3.43–3.52 (m, 1H, CH), 3.68 (s, 3H, OCH3), 3.94–4.15 (m, 2H, NCH2), 6.95 (s, 1H, CH=C), 7.05 (s, 2H, NH2), 7.65 (d, J = 8.8 Hz, 2H, HAr), 7.79 (d, J = 8.8 Hz, 2H, HAr) ppm. 13C-NMR (101 MHz, DMSO-d6): δ = 34.9 (COCH2), 35.1 (CH), 49.7 (NCH2), 52.2 (OCH3), 100.9 (C–S), 119.2, 125.8, 130.8, 138.0, 149.3 (CH=C, CAr), 168.2 (C=N), 171.5 (C=O), 173.1 (COO) ppm. IR (KBr): νmax = 3430 (NH2), 1692, 1639 (2C=O). MS (ESI), m/z, %: [M + H]+ = 318 (100). Calcd. for C15H15N3O3S, %: C 56.77; H 4.76; N 13.24. Found, %: C 56.66; H 4.75; N 13.40.
Methyl 5-oxo-1-(4-(2-phenylthiazol-5-yl)phenyl)pyrrolidine-3-carboxylate (4b): 1H-NMR (400 MHz, DMSO-d6): δ = 2.71–2.80 (m, 2H, COCH2), 3.45–3.55 (m, 1H, CH), 3.70 (s, 3H, OCH3), 3.99–4.18 (m, 2H, NCH2), 7.44–7.62 (m, 3H, HAr), 7.77 (d, J = 8.8 Hz, 2H, HAr), 7.96–8.12 (m, 4H, AAr), 8.13 (s, 1H, CH=C) ppm. 13C-NMR (101 MHz, DMSO-d6): δ = 34.9 (COCH2), 35.1 (CH), 49.7 (NCH2), 52.2 (OCH3), 114.0 (C–S), 119.4, 126.2, 126.5, 129.3, 130.4, 133.0, 138.9, (CAr), 154.7 (CH=C), 166.9 (C=N), 171.7 (N–C=O), 173.1 (COO) ppm. IR (KBr): νmax = 1738, 1699 (2C=O). MS (ESI), m/z, %: [M + H]+ = 379 (100). Calcd. for C21H18N2O3S, %: C 66.65; H 4.79; N 7.40. Found, %: C 66.54; H 4.82; N 7.32.

3.1.2. General Procedure for the Preparation of Hydrazides 5a,b

A mixture of the corresponding methyl ester 4 (10 mmol), hydrazine monohydrate (2.5 g, 2.45 mL, 50 mmol) and propan-2-ol (30 mL) was heated at reflux for 10 h. After completion of the reaction (TLC), the mixture was cooled to room temperature, the formed precipitate filtered off, washed with water, and recrystallized from methanol to give the title compound 5a (white solid, yield 2.7 g, 81.4%, m. p. 248–248 °C) and 5b (white solid, yield 2.46 g, 65%, m. p. 231–232 °C).
1-(4-(2-Aminothiazol-5-yl)phenyl)-5-oxopyrrolidine-3-carbohydrazide (5a): 1H-NMR (400 MHz, DMSO-d6): δ = 2.53–2.81 (m, 2H, COCH2), 3.10–3.23 (m, 1H, CH), 3.88–4.08 (m, 2H, NCH2), 4.30 (s, 2H, NHNH2), 6.94 (s, 1H, CH=C), 7.04 (s, 2H, NH2), 7.65 (d, J = 8.4 Hz, 2H, HAr), 7.78 (d, J = 8.4 Hz, 2H, HAr), 9.28 (s, 1H, NH) ppm. 13C-NMR (101 MHz, DMSO-d6): δ = 34.1 (COCH2), 35.8 (CH), 50.7 (NCH2), 100.8 (C–S), 119.1, 125.8, 130.7, 138.2, 149.4 (CH=C, CAr), 168.2 (C=N), 171.6, 172.1 (2C=O) ppm. IR (KBr): νmax = 3391, 3316 (NH, NH2), 1674, 1643 (2C=O). MS (ESI), m/z, %: [M + H]+ = 317 (100).
5-Oxo-1-(4-(2-phenylthiazol-5-yl)phenyl)pyrrolidine-3-carbohydrazide (5b): 1H-NMR (400 MHz, DMSO-d6): δ = 2.62–2.80 (m, 2H, COCH2), 3.12–3.28 (m, 1H, CH), 3.86–4.08 (m, 2H, NCH2), 4.31 (s, 2H, NHNH2), 7.48–7.56 (m, 3H, HAr), 7.77 (d, J = 8.8 Hz, 2H, HAr), 7.98–8.09 (m, 4H, HAr), 8.12 (s, 1H, CH=C), 9.31 (s, 1H, NH) ppm. 13C-NMR (101 MHz, DMSO-d6): δ = 34.0 (COCH2), 35.8 (CH), 50.7 (NCH2), 113.9 (C–S), 119.3, 126.2, 126.5, 129.3, 129.6, 130.4, 133.0, 139.1 (CAr), 154.8 (CH=C), 166.9 (C=N), 171.5, 172.2 (2C=O) ppm. IR (KBr): νmax = 3318, 3281 (NH, NH2), 1682, 1638 (2C=O). MS (ESI), m/z, %: [M + H]+ = 379 (100). Calcd. for C20H18N4O2S, %: C 63.47; H 4.79; N 14.80. Found, %: C 63.37; H 4.72; N 14.71.

3.1.3. General Procedure for the Preparation of Hydrazones 6–12

A mixture of the corresponding hydrazide 5a,b (10 mmol), benzencarbaldehyde (11 mmol) or thiophene-2-carboxaldehyde (2.24 g, 20 mmol) and dimethylformamide (30 mL) was refluxed for 1–3 h. Afterwards, the reaction mixture was cooled down, diluted with water (50 mL), the obtained product was filtered off, washed with water and ether, and recrystallized from the indicated solvent.
1-(4-(2-Aminothiazol-5-yl)phenyl)-3-(benzylidenehydrazinocarbonyl)-5-oxopyrrolidine (6a): light yellow solid, yield 3.65 g, 90.2%, m. p. 239–240 °C (methanol). 1H-NMR (400 MHz, DMSO-d6): δ = Z/E 2.68–2.94 (m, 2H, COCH2), 3.36–3.41 (m, 0.35H, CH), 3.93–4.25 (m, 0.65H, CH + 2H, NCH2), 6.94, 6.95 (2s, 1H, CH=C), 7.05 (s, 2H, NH2), 7.24–7.90 (m, 9H, HAr), 8.05 (s, 0.65H, N=CH), 8.23 (s, 0.35H, N=CH), 11.58 (s, 0.65H, NH), 11.65 (s, 0.35H, NH) ppm. IR (KBr): νmax = 3398 (NH2), 1681, 1668 (2C=O). MS (ESI), m/z, %: [M + H]+ = 406 (100). Calcd. for C21H19N54O2S, %: C 62.21; H 4.72; N 17.27. Found, %: C 62.16; H 4.69; N 17.23.
3-(Benzylidenehydrazinocarbonyl)-1-(4-(2-phenylthiazol-5-yl)phenyl)-5-oxopyrrolidine (6b): light yellow solid, yield 4.05 g, 92%, m. p. 214–215 °C (methanol). 1H-NMR (400 MHz, DMSO-d6): δ = Z/E 2.73–2.95 (m, 2H, COCH2); 3.35–3.47 (m, 0.35H, CH); 3.95–4.31 (m, 0.65H, CH + 2H, NCH2); 7.38–7.61 (m, 6H, HAr), 7.66–7.78 (m, 2H, HAr), 7.81 (d, J = 8.6 Hz, 2H, HAr), 7.96–8.28 (m, 6H, HAr + CH=C + N=CH), 11.61 (s, 0.65H, NH), 11.68 (s, 0.35H, NH) ppm. IR (KBr): νmax = 3178 (NH), 1700, 1668 (2C=O). MS (ESI), m/z, %: [M + H]+ = 447 (100). Calcd. for C27H22N4O2S, %: C 69.51; H 4.75; N 12.01. Found, %: C 69.61; H 4.86; N 11.94.
1-(4-(2-Aminothiazol-5-yl)phenyl)-3-(4-chlorobenzylidenehydrazinocarbonyl)-5-oxopyrrolidine (7a): light yellow solid, yield 3.93 g, 89.5%, m. p. 254 °C (methanol). 1H-NMR (400 MHz, DMSO-d6): δ = Z/E 2.69–2.89 (m, 2H, COCH2), 3.34–3.38 (m, 0.4H, CH), 3.94–4.22 (m, 0.6H, CH + 2H, NCH2), 6.95 (s, 1H, CH=C), 7.04 (s, 2H, NH2), 7.48–7.82 (m, 8H, HAr), 8.03 (s, 0.65H, N=CH), 8.22 (s, 0.35H, N=CH), 11.64 (s, 0.65H, NH), 11.71 (s, 0.35H, NH) ppm. IR (KBr): νmax = 3252 (NH2), 1673, 1656 (2C=O). MS (ESI), m/z, %: [M + H]+ = 440 (100). Calcd. for C21H18ClN5O2S, %: C 57.33; H 4.12; N 15.92. Found, %: C 57.27; H 4.08; N 15.88.
3-(3-Chlorobenzylidenehydrazinocarbonyl)-1-(4-(2-phenylthiazol-5-yl)phenyl)-5-oxopyrrolidine (7b): yellow solid, yield 3.45 g, 69%, m. p. 141–142 °C (methanol). 1H-NMR (400 MHz, DMSO-d6): δ = Z/E 2.72–2.95 (m, 2H, COCH2), 3.34–3.45 (m, 0.4H, CH), 3.99–4.25 (m, 0.6H, CH + 2H, NCH2), 7.33–8.28 (m, 15H, HAr + CH=C + N=CH), 11.70 (s, 0.65H, NH), 11.80 (s, 0.35H, NH) ppm. IR (KBr): νmax = 3265 (NH), 1668, 1627 (2C=O). Calcd. for C27H21ClN4O2S, %: C 64.73; H 4.22; N 11.18. Found, %: C 64.67; H 4.19; N 11.29.
1-(4-(2-Aminothiazol-5-yl)phenyl)-3-(4-nitrobenzylidenehydrazinocarbonyl)-5-oxopyrrolidine (8a): light yellow solid, yield 2.79 g, 62%, m. p. 234–236 °C (ethanol). 1H-NMR (400 MHz, DMSO-d6): δ = Z/E 2.69–2.96 (m, 2H, COCH2), 3.35–3.44 (m, 0.35H, CH), 3.91–4.28 (m, 0.6H, CH + 2H, NCH2), 6.95 (s, 1H, CH=C), 7.04 (s, 2H, NH2), 7.50–8.41 (m, 9H, HAr + N=CH), 11.87 (s, 0.65H, NH), 11.94 (s, 0.35H, NH) ppm. IR (KBr): νmax = 3435 (NH2), 3245 (NH), 1681, 1656 (2C=O). MS (ESI), m/z, %: [M + H]+ = 451 (100). Calcd. for C21H18N6O4S, %: C 55.99; H 4.03; N 18.66. Found, %: C 55.96; H 4.01; N 18.55.
3-(4-Nitrobenzylidenehydrazinocarbonyl)-1-(4-(2-phenylthiazol-5-yl)phenyl)-5-oxopyrrolidine (8b): yellow solid, yield 4.55 g, 89%, m. p. 150–151 °C (methanol). 1H-NMR (400 MHz, DMSO-d6): δ = Z/E 2.77–2.96 (m, 2H, COCH2), 3.36–3.48 (m, 0.4H, CH), 4.01–4.27 (m, 0.6H, CH + 2H, NCH2), 7.45–8.38 (m, 15H, HAr + CH=C + N=CH), 11.90 (s, 0.65H, NH), 11.97 (s, 0.35H, NH) ppm. IR (KBr): νmax = 3221 (NH), 1674, 1612 (2C=O). Calcd. for C27H21N5O4S, %: C 63.39; H 4.14; N 13.69. Found, %: C 63.42; H 4.15; N 13.29.
3-(4-Fluorobenzylidenehydrazinocarbonyl)-1-(4-(2-phenylthiazol-5-yl)phenyl)-5-oxopyrrolidine (9b): light yellow solid, yield 3.97 g, 82%, m. p. 216–217 °C (methanol). 1H-NMR (400 MHz, DMSO-d6): δ = Z/E 2.77–2.91 (m, 2H, COCH2), 3.35–3.41 (m, 0.4H, CH), 4.01–4.24 (m, 0.6H, CH + 2H, NCH2), 7.22–8.26 (m, 15H, HAr + CH=C + N=CH), 11.61 (s, 0.65H, NH), 11.68 (s, 0.35H, NH) ppm. IR (KBr): νmax = 3265 (NH), 1668, 1604 (2C=O). Calcd. for C27H21FN4O2S, %: C 66.93; H 4.37; N 11.56. Found, %: C 66.72; H 4.25; N 11.49.
5-Oxo-1-(4-(2-phenylthiazol-5-yl)phenyl)-N’-(thiophen-2-ylmethylene)pyrrolidine-3-carbohydrazide (10b): light yellow solid, yield 3.54 g, 75%, m. p. 198–200 °C (methanol). 1H-NMR (400 MHz, DMSO-d6): δ = Z/E 2.72–2.90 (m, 2H, COCH2), 3.34–3.40 (m, 0.4H, CH), 3.82–4.30 (m, 0.6H, CH + 2H, NCH2), 7.10–8.18 (m, 13H, HAr + CH=C), 8.23 (s, 0.6H, N=CH), 8.45 (s, 0.4H, N=CH), 11.59 (s, 0.6H, NH), 11.62 (s, 0.4H, NH) ppm. IR (KBr): νmax = 3265 (NH), 1673, 1610 (2C=O). Calcd. for C25H20N4O2S2, %: C 66.54; H 4.27; N 11.86. Found, %: C 66.50; H 4.24; N 11.89.

3.1.4. General Procedure for the Preparation of Hydrazones 11b, 12b

A mixture of hydrazide 5b (1 g, 2.64 mmol) and dimethylformamide (11b) or 1,4-dioxane (12b) (10 mL) was heated to its boiling point and 3- or 4-pyridinecarbaldehyde (5.28 mmol) was added dropwise. The mixture was refluxed for 1 h, diluted with water (20 mL) (11b) or the solvent was evaporated under reduced pressure, the resin mass was poured with diethyl ether (10 mL), stirred and left in refrigerator (12b). The obtained precipitate was filtered off, washed with water and ether, and recrystallized 2-propanol to give the title compound 11b (yellow solid, yield 1.22 g, 99%, m. p. 203–204 °C (propan-2-ol) or 12b (yellow solid, yield 1.19 g, 96.5%, m. p. 236–237 °C (propan-2-ol).
5-Oxo-1-(4-(2-phenylthiazol-5-yl)phenyl)-N’-(pyridin-3-ylmethylene)pyrrolidine-3-carbohydrazide (11b): 1H-NMR (400 MHz, DMSO-d6): δ = Z/E 2.75–2.94 (m, 2H, COCH2), 3.34–3.46 (m, 0.35H, CH), 3.94–4.34 (m, 0.65H, CH + 2H, NCH2), 7.43–8.92 (m, 15H, HAr + CH=C + N=CH), 11.76 (s, 0.65H, NH), 11.85 (s, 0.35H, NH) ppm. IR (KBr): νmax = 3255 (NH), 1674, 1609 (2C=O). Calcd. for C26H21N5O2S, %: C 66.79; H 4.53; N 14.98. Found, %: C 66.76; H 4.48; N 14.89.
5-Oxo-1-(4-(2-phenylthiazol-5-yl)phenyl)-N’-(pyridin-4-ylmethylene)pyrrolidine-3-carbohydrazide (12b): 1H-NMR (400 MHz, DMSO-d6): δ = Z/E 2.71–3.02 (m, 2H, COCH2), 3.32–3.53 (m, 0.4H, CH), 4.00–4.27 (m, 0.6H, CH + 2H, NCH2), 7.47–8.27 (m, 13H, HAr + CH=C + N=CH), 8.57–8.79 (m, 2H, HPyr), 11.91 (s, 0.6H, NH), 11.97 (s, 0.4H, NH) ppm. IR (KBr): νmax = 3213 (NH), 1684, 1600 (2C=O). Calcd. for C26H21N5O2S, %: C 66.79; H 4.53; N 14.98. Found, %: C 62.68; H 4.48; N 14.76.

3.1.5. General Procedure for the Preparation of Pyrroles 13a,b

A mixture of the corresponding acid hydrazide 5a,b (10 mmol), hexane-2,5-dione (1.71 g, 1.8 mL, 15 mmol) glacial acetic acid (1.5 mL) and ethanol (30 mL) was heated at reflux for 10 h. Then the solvent was evaporated under reduced pressure, and the residue was poured with water (50 mL). The formed precipitate was filtered off, washed with water and ether, and recrystallized from the indicated solvent.
1-(4-(2-Aminothiazol-5-yl)phenyl)-N-(2,5-dimethyl-1H-pyrrol-1-yl)-5-oxopyrrolidine-3-carboxamide (13a): light yellow solid, yield 2.25 g, 57%, m. p. 257–258 °C (2-propanol). 1H-NMR (400 MHz, DMSO-d6): δ = 2.00 (s, 6H, 2CH3), 2.70–2.94 (m, 2H, COCH2), 3.43–3.52 (m, 1H, CH), 3.96–4.20 (m, 2H, NCH2), 5.65 (s, 2H, 2CH), 6.96 (s, 1H, CH=C), 7.05 (s, 2H, NH2), 7.68 (d, J = 8.8 Hz, 2H, HAr), 7.80 d, J = 8.8 Hz, 2H, HAr), 10.91 (s, 1H, NH) ppm. 13C-NMR (101 MHz, DMSO-d6): δ = 10.9, 11.0 (2CH3), 34.1 (COCH2), 35.7 (CH), 50.3 (NCH2), 100.9, 103.1, 119.3, 125.8, 126.7, 130.8, 138.1, 149.4 (CH=C, CAr, CPyr), 168.2 (C=N), 171.6, 171.9 (2C=O) ppm. IR (KBr): νmax = 3403 (NH2), 3325 (NH), 1693, 1678 (2C=O). MS (ESI), m/z, %: [M + H]+ = 396 (100). Calcd. for C20H21N5O2S, %: C 60.74; H 5.35; N 17.71. Found, %: C 60.67; H 5.31; N 17.69.
N-(2,5-Dimethyl-1H-pyrrol-1-yl)-5-oxo-1-(4-(2-phenylthiazol-5-yl)phenyl)pyrrolidine-3-carboxamide (13b): light brown solid, yield 4.2 g, 92%, m. p. 119–120 °C (methanol). 1H-NMR (400 MHz, DMSO-d6): δ = 2.01, 2.02 (2s, 6H, 2CH3), 2.73–2.99 (m, 2H, COCH2), 3.47–3.55 (m, 1H, CH), 4.02–4.24 (m, 2H, NCH2), 5.65 (s, 2H, 2CH), 7.50–7.57 (m, 3H, HAr), 7.81 (d, J = 8.8 Hz, 2H, HAr), 8.02–8.09 (m, 4H, HAr), 8.14 (s, 1H, CH=C), 10.93 (s, 1H, NH) ppm. 13C-NMR (101 MHz, DMSO-d6): δ = 11.0 (2CH3), 34.1 (COCH2), 35.8 (CH), 50.3 (NCH2), 103.1, 114.0, 119.5, 126.2, 126.5, 126.7, 129.3, 129.8, 130.4 133.0, 139.0 (CAr, CPyr), 154.7 (CH=C), 167.0 (C=N), 171.7, 171.8 (2C=O) ppm. IR (KBr): νmax = 3317 (NH), 1699, 1609 (2C=O). MS (ESI), m/z, %: [M + H]+ = 457 (100). Calcd. for C26H24N4O2S, %: C 68.40; H 5.30; N 12.17. Found, %: C 68.29; H 5.23; N 12.03.
5-Oxo-1-(5-oxo-1-(4-(2-phenylthiazol-5-yl)phenyl)pyrrolidine-3-carboxamido)pyrrolidine-3-carboxylic acid (14b): A mixture of acid hydrazide 5b (1 g, 2.64 mmol), itaconic acid (1.2 g, 9.23 mmol) and toluene (30 mL) was heated at reflux for 11 h, then cooled down, the obtained crystalline solid was filtered off, washed with water, and recrystallized from methanol to give the title compound 14b (light yellow solid, yield 0.70 g, 54%, m. p. 170–171 °C (methanol)). 1H-NMR (400 MHz, DMSO-d6): δ = 2.51–2.88 (m, 4H, 2COCH2), 3.25–3.42 (m, 2H, 2CH), 3.55–4.16 (m, 4H, 2NCH2), 7.50–7.56 (m, 3H, HAr), 7.75–7.80 (m, 2H, HAr), 8.03–8.11 (m, 4H, HAr), 8.13 (s, 1H, CH=C), 10.40 (s, 1H, NH), 12.84 (br s, 1H, OH) ppm. 13C-NMR (101 MHz, DMSO-d6): δ = 31.3, 33.6 (2COCH2), 34.2, 35.5 (2CH), 49.7, 50.3 (2NCH2), 114.0, 119.4, 126.2, 126.5, 129.3, 129.7, 130.4, 133.0, 139.0 (CAr), 154.7 (CH=C), 167.0 (C=N), 170.9, 171.4, 171.8, 174.1 (4C=O) ppm. IR (KBr): νmax = 3421 OH), 3274 (NH), 1726, 1717, 1699, 1682 (4C=O). Calcd. for C25H22N4O5S, %: C 61.21; H 4.52; N 11.42. Found, %: 61.28; H 4.62; N 11.50.
2-(5-Oxo-1-(4-(2-phenylthiazol-5-yl)phenyl)pyrrolidine-3-carbonyl)-N-phenylhydrazine-1-carbothioamide (15b): To a solution of hydrazide 5b (1 g, 2.64 mmol) in methanol (10 mL), phenyl isothiocyanate (0.714 g, 0.63 mL, 5.28 mmol) was added dropwise and the mixture was heated at reflux for 3 h. After completion of the reaction the mixture was cooled down, the obtained crystalline solid filtered off, washed with methanol and recrystallized from methanol to give the title compound 15b (white solid, yield 1.17 g, 86.5% m. p. 209–210 °C (methanol)). 1H-NMR (400 MHz, DMSO-d6): δ = 2.70–2.93 (m, 2H, COCH2), 3.31–3.42 (m, 1H, CH), 3.96–4.22 (m, 2H, NCH2), 7.08–7.22 (m, 1H, HAr), 7.31–7.59 (m, 8H, HAr), 7.69–7.83 (m, 2H, HAr), 7.92–8.10 (m, 3H, HAr), 8.13 (s, 1H, CH=C), 9.58 (s, 1H, NH), 9.68, 9.88 (2br s, 1H, NH), 10.12, 10.22 (2s, 1H, NH) ppm. 13C-NMR (101 MHz, DMSO-d6): δ = 34.0 (COCH2), 35.6 (CH), 50.3 (NCH2), 114.0 (C–S), 119.4, 126.2, 126.5, 128.1, 128.2, 129.3, 129.7, 130.4, 133.0, 139.1, 139.2 (CAr), 154.7 (CH=C), 166.9 (C=N), 167.8, 168.5, 172.1 (C=S, 2C=O) ppm. IR (KBr): νmax = 3163–3059 (NH), 1715, 1681 (2C=O). Calcd. for C27H23N5O2S2, %: C 63.14; H 4.51; N 13.63. Found, %: C 63.26; H 4.57; N 13.81.
3-(4-Phenyl-5-thioxo-4,5-dihydro-1H-1,2,4-triazol-3-yl)-1-(4-(2-phenylthiazol-5-yl)phenyl)-5-oxopyrrolidine (16b): A mixture of thiosemicarbazide 15b (1 g, 1.94 mmol) and 4% sodium hydroxide solution was refluxed for 6 h. Then, the reaction mixture was cooled down, acidified with diluted hydrochloric acid to pH 1, refluxed for 15 min, afterwards cooled down and neutralized with 10% sodium carbonate solution to pH 7. The formed solid was filtered off, washed with water, and recrystallized from methanol to give the title compound 16b (yellow solid, yield 0.86 g, 89.5%, m. p. 191–192 °C (methanol)). 1H-NMR (400 MHz, DMSO-d6): δ = 2.55–2.86 (m, 2H, COCH2), 3.42–3.76 (m, 1H, CH), 3.87–4.14 (m, 2H, NCH2), 7.25–8.11 (m, 14H, HAr), 8.13 (s, 1H, CH=C), 13.89 (s, 1H, NH) ppm. 13C-NMR (101 MHz, DMSO-d6): δ = 27.8 (COCH2), 36.2 (CH), 50.5 (NCH2), 114.0, 119.6, 126.2, 126.4, 128.6, 129.3, 129.6, 129.8, 130.4, 133.0, 133.5, 138.8, 152.9 (CAr), 154.7 (CH=C), 166.9, 168.4 (C=S, C=N), 171.3 C=O) ppm. IR (KBr): νmax = 3406 (NH), 1685 (C=O). Calcd. for C27H21N5OS2, %: C 65.43; H 4.27; N 14.13. Found, %: C 65.39; H 4.14; N 14.11.
3-(5-Thioxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-1-(4-(2-phenylthiazol-5-yl)phenyl)-5-oxopyrrolidine (17b): To a solution of potassium hydroxide (0.56 g, 10 mmol) in methanol (25 mL), carbon disulfide (0.76 g, 10 mmol) was added dropwise. The obtained mixture was stirred at room temperature for 15 min, and then methanolic solution of acid hydrazide 5b (1.89 g, 5 mmol/50 mL) poured over. The reaction mixture was refluxed for 15 h. After completion of the reaction (TLC), the solvent was evaporated under reduced pressure, the residue was poured with water (30 mL) and the mixture was acidified with diluted hydrochloric acid (1:1) to pH 1. The crystalline solid was filtered off, washed with plenty of water and recrystallized from methanol to give the title compound 17b (white solid, yield 3.21 g, 76.5%, m. p. 254–255 °C (methanol)). H-NMR (400 MHz, DMSO-d6): δ = 2.82–3.07 (m, 2H, COCH2), 3.94–4.04 (m, 1H, CH), 4.10–4.35 (m, 2H, NCH2), 7.49–7.58 (m, 3H, HAr), 7.78 (d, J = 8.8 Hz, 2H, HAr), 7.99–8.11 (m, 4H, HAr), 8.15 (s, 1H, CH=C), 14.42 (br s, 1H, NH) ppm. 13C-NMR (101 MHz, DMSO-d6): δ = 27.9 (COCH2), 35.2 (CH), 49.8 (NCH2), 114.1, 119.6, 126.2, 126.5, 129.3, 129.9, 130.4, 133.0, 138.8, 154.7, 163.9 (CH=C, CAr), 167.0 (C=N), 171.1, 178.0 (C=O, C=S) ppm. IR (KBr): νmax = 3110 (NH), 1658 (C=O). Calcd. for C21H16N4O2S2, %: C 59.98; H 3.84; N 13.32. Found, %: C 59.85; H 3.80; N 13.25.
3-(4-Amino-5-thioxo-4,5-dihydro-1H-1,2,4-triazol-3-yl)-1-(4-(2-phenylthiazol-5-yl)phenyl)-5-oxopyrrolidine (18b): A mixture of hydrazide 5b (0.7 g, 1.85 mmol), potassium hydroxide (0.01 g, 0.19 mmol), carbon disulfide (0.28 g, 3.7 mmol) and methanol (35 mL) was refluxed for 15 h. Then, the solvent was removed under reduced pressure, and the residue was poured with diethyl ether (15 mL). The formed crystalline solid was filtered off, washed with diethyl ether and dried. Afterwards, the solid was poured with water, hydrazine monohydrate (0.28 g, 5.6 mmol) was added and the mixture was refluxed for 10 h. After completion of the reaction, the mixture was cooled down, diluted with water (20 mL) and neutralized with 3 M hydrochloric acid to pH 7. The formed solid was filtered off, washed with water, and recrystallized from methanol to give the title compound 18b (light orange solid, yield 0.54 g, 67%, m. p. 245–246 °C (methanol)). 1H-NMR (400 MHz, DMSO-d6): δ = 2.62–3.08 (m, 2H, COCH2), 3.12–3.29 (m, 0.35H, CH), 3.85–4.34 (m, 0.65H, CH + 2H, NCH2), 5.59 (s, 2H, NH2), 7.40–8.10 (m, 9H, HAr), 8.14 (s, 1H, CH=C), 13.63 (s, 1H, NH) ppm. 13C-NMR (101 MHz, DMSO-d6): δ = 27.3 (COCH2), 35.4 (CH), 50.4 (NCH2), 114.1 (C–S), 119.6, 126.2, 126.5, 129.3, 129.8, 130.4, 133.0, 139.1, 152.6, 154.7, 158.4 (CAr), 166.9, 167.2, 172.2 (C=S, N–C=N, C=O) ppm. Calcd. for C21H18N6OS2, %: C 58.04; H 4.18; N 19.34. Found, %: C 57.95; H 4.05; N 19.27.
3-(4-(Benzylideneamino)-5-thioxo-4,5-dihydro-1H-1,2,4-triazol-3-yl)-1-(4-(2-phenylthiazol-5-yl)phenyl)-5-oxopyrrolidine (19b): To a mixture of compound 18b (1 g, 2.3 mmol), benzenecarbaldehyde (0.49 g; 0.47 mL, 4.6 mmol) and ethanol (50 mL) catalytic amount of concentrated hydrochloric acid was added (0.5 mL) and the mixture was refluxed for 5 h, then cooled down. The formed crystalline solid was filtered off, washed with water, and recrystallized from methanol to give the title compound 19b (light yellow solid, yield 1.06 g, 88%, m. p. 189–190 °C (methanol)). 1H-NMR (400 MHz, DMSO-d6): δ = 2.90–3.08 (m, 2H, COCH2), 4.03–4.13 (m, 1H, CH), 4.16–4.34 (m, 2H, NCH2), 7.40–7.70 (m, 6H, HAr), 7.78 (d, J = 8.7 Hz, 2H, HAr), 7.83–8.09 (m, 6H, HAr), 8.13 (s, 1H, CH=C), 10.14 (s, 1H, N=CH), 13.97 (s, 1H, NH) ppm. 13C-NMR (101 MHz, DMSO-d6): δ = 27.3 (COCH2), 35.5 (CH), 50.3 (NCH2), 114.0, 119.6, 126.2, 126.4, 128.6, 129.2, 129.3, 132.1, 133.0, 138.9, 151.5 (CH=N, CTh, CAr), 154.7 (CH=C), 162.0 (C=NNH), 162.9 (C=S), 166.9 (C=N), 171.7 (C=O) ppm. IR (KBr): νmax = 3278 (NH), 1681 (C=O), 1482 (C=N), 1134 (C=S). Calcd. for C28H22N6OS2, %: C 64.35; H 4.24; N 16.08. Found, %: C 64.24; H 4.22; N 15.96.
1-(4-(1-((2-aminophenyl)iminoethyl)phenyl)-5-oxopyrrolidine-3-carboxylic acid (20): A mixture of acid 1 (2.47 g, 0.01 mol) and benzene-1,2-diamine (2.16 g, 0.02 mol) in ethanol (25 ml) was refluxed for 20 h, then cooled down, the formed crystalline solid was filtered off, washed with ethanol, and recrystallized from water (twice) to give the title compound 20 (brown-orange solid, yield 2.76 g, 82%, m. p. 139–140 °C (water)). 1H-NMR (400 MHz, DMSO-d6): δ = 2.55 (s, 3H, CH3), 2.70–2.88 (m, 2H, COCH2), 3.29–3.45 (m, 1H, CH), 3.95–4.16 (m, 2H, NCH2), 5.98 (br s, 3H, OH + NH2), 6.31–6.44 (m, 2H, HAr), 6.44–6.63 (m, 2H, HAr), 7.81 (d, J = 8.6 Hz, 2H, HAr), 7.97 (d, J = 8.6 Hz, 2H, HAr) ppm. 13C-NMR (101 MHz, DMSO-d6): δ = 26.5 (CH3), 35.1 (COCH2), 35.4 (CH), 49.8 (NCH2), 114.6, 117.4, 118.4, 129.2, 132.1, 134.9, 143.1 (CAr), 172.6, 174.1 (2C=O), 196.7 (H3C–C=N) ppm. Calcd. for C19H19N3O3, %: C 67.64; H 5.68; N 12.46. Found, %: C 67.76; H 5.61; N 12.42.
5-Oxo-1-(4-(quinoxalin-2-yl)phenyl)pyrrolidine-3-carboxylic acid (21): A mixture of compound 2 (1 g, 3.08 mmol) and benzene-1,2-diamine (0.3 g, 2.77 mmol) in ethanol (12 mL) was refluxed for 5 h, then cooled down, the formed crystalline solid was filtered off, washed with methanol, and recrystallized from propan-2-ol to give the title compound 21 (brown solid, yield 0.72 g, 81%, m. p. 277–278 °C (propan-2-ol)). 1H-NMR (400 MHz, DMSO-d6): δ = 2.72–2.92 (m, 2H, COCH2), 3.36–3.45 (m, 1H, CH), 4.04–4.17 (m, 2H, NCH2), 7.78–7.92 (m, 4H, HAr), 8.04–8.15 (m, 2H, HAr), 8.36 (d, J =8.9 Hz, 2H, HAr), 9.56 (s, 1H, CH), 12.85 (s, 1H, OH) ppm. 13C-NMR (101 MHz, DMSO-d6): δ = 35.1 (COCH2), 36.4 (CH), 49.9 (NCH2), 119.3, 127.9, 128.8, 129.1, 129.6, 130.6, 131.2, 140.9, 141.1, 141.4, 143.5, 150.3 (CAr), 172.3 (C=O), 174.1 (COOH) ppm. IR (KBr): νmax = 3415 (OH), 3193 (NH), 1732, 1652 (2C=O). Anal Calcd for C19H15N3O3 m/z %: 334.1191 [M + H]+, found HRMS (ESI), m/z %: 334.1193 [M + H]+ (100%). Calcd. for C19H15N3O3, %: C 68.46; H 4.54; N 12.61. Found, %: 68.41; H 4.64; N 12.72.
1-(4-Acetylphenyl)-3-(1H-benzimidazol-2-yl)-5-oxopyrrolidine (22): A mixture of compound 1 (1 g, 4 mmol), 1,2-benzenediamine (0.86 g, 8 mmol) and 4N hydrochloric acid (15 mL) was heated at reflux for 16 h. After completion of the reaction (TLC), the reaction mixture was filtered off, the solvent was evaporated under reduced pressure, and the residue was neutralized with 25% aqueous ammonia to pH 7. Then, a liquid layer was decanted, the precipitate was poured over with 5% aqueous sodium carbonate solution (20 mL) and afterward boiled and filtered off until hot. The obtained crystalline solid was washed with plenty of water and recrystallized from methanol to give the title compound 22 (yellow solid, yield 1.17 g, 92%, m. p. 222–223 °C). 1H-NMR (400 MHz, DMSO-d6): δ = 2.55 (s, 3H, CH3), 2.99–3.14 (m, 2H, COCH2), 3.98–4.08 (m, 1H, CH), 4.25–4.38 (m, 2H, NCH2), 7.13–7.18 (m, 2H, HAr), 7.49–7.55 (m, 2H, HAr), 7.85 (d, J = 8.7 Hz, 2H, HAr), 7.99 (d, J = 8.7 Hz, 2H, HAr) ppm. 13C-NMR (101 MHz, DMSO-d6): δ = 26.5 (CH3), 30.6 (COCH2), 37.7 (CH), 52.0 (NCH2), 114.8 118.4, 121.5, 129.2, 132.1, 138.8, 143.2 (CAr), 155.0 (NHC=N), 172.8 (C=O), 196.6 (H3C–C=O) ppm. IR (KBr): νmax = 3056 (NH), 1699, 1683 (2C=O), 1601 (C=N). Calcd. for C19H17N3O2, %: C 71.46; H 5.37; N 13.16. Found, %: C 71.26; H 5.31; N 13.09.
1-(4-Acetylphenyl)-3-(1-ethyl-1H-benzimidazol-2-yl)-5-oxopyrrolidine (23): A mixture of benzimidazole 22 (1 g, 3 mmol), potassium hydroxide (0.36 g, 6.4 mmol), sodium carbonate (0.21 g, 2 mmol) and ethyl iodide (10 mL) was stirred at room temperature for 48 h. After completion of the reaction (TLC), a mixture was poured over with dry acetone and filtered off. The filtrate was evaporated under reduced pressure to dryness, and then the obtained oily mass was poured over with diethyl ether and left in refrigerator for several hours. The formed crystalline solid was filtered off, washed with diethyl ether, and recrystallized from methanol to give the title compound 23 (light yellow solid, yield 0.96 g, 88%, m. p. 175–176 °C). 1H-NMR (400 MHz, DMSO-d6): δ = 1.30 (t, J = 7.1 Hz, 3H, CH3), 2.96–3.18 (m, 2H, COCH2), 4.13–4.45 (m, 5H, CH + NCH2 + CH3CH2), 7.11–7.291 (m, 2H, HAr), 7.50–7.66 (m, 2H, HAr), 7.82 (d, J = 8.8 Hz, 2H, HAr), 7.94 (d, J = 8.8 Hz, 2H, HAr) ppm. 13C-NMR (101 MHz, DMSO-d6): δ = 15.2 (CH3), 26.5 (CH3), 28.4 (COCH2), 37.9 (CH + CH3CH2), 52.0 (NCH2), 110.2, 118.5, 118.8, 121.5, 122.0, 129.2, 132.1, 135.0, 142.0, 143.2 (CAr), 154.4 (N–C=N), 172.7 (N–C=O), 196.6 (H3C–C=O) ppm. IR (KBr): νmax = 1707, 1670 (2C=O). Calcd. for C21H21N3O2, %: C 72.60; H 6.09; N 12.10. Found, %: C 71.72; H 5.92; N 12.04.

3.2. Biological Activity

The determination of the antibacterial and antifungal activity by diffusion method in agar was carried out by diffusion in agar on a solid nutrient medium (beef-extract agar for bacteria, wort agar for fungi). Petri plates containing 20 mL of nutrient medium were used for all the tested microorganisms. The inoculum (the microbial loading 109 cells (spores)/1 mL) was spread on the surface of the solidified media and Whatman no. 1 filter paper discs (6 mm in diameter) impregnated with the test compound (0.1 and 0.5%) were placed on the plates. The duration of bacteria incubation was 24 h at 35 °C and that of fungi incubation was 48–72 h at 28–30 °C. The antimicrobial effect and degree of activity of the tested compounds were evaluated by measuring the inhibition zone diameters and the results were compared with the data for the well-known antibacterial/antifungal agent. Each experiment was repeated three times. The determination of minimal inhibitory (MIC) concentrations was achieved using the serial dilution method. The tested compounds were added to the nutrient medium (beef-extract broth for bacteria and wort for fungi) as solutions in dimethyl sulfoxide (DMSO) for ensuring the needed concentration (0.9–500.0 μg/mL). Bacteria and fungi inoculum were inoculated into nutrient medium (the microbial loading was 106 cells (spores)/1 mL). The duration of bacteria incubation was 24 h at 35 °C and that of fungi incubation was 48–72 h at 28–30 °C. The results were estimated by the microorganism growth measured by degree of microbial turbidity in nutrient medium. The MIC of any compound was defined as the lowest concentration, which completely inhibits visible growth (turbidity on liquid nutrient medium).

4. Conclusions

In this study, the condensation of 1-(4-(2-bromoacetyl)phenyl)-5-oxopyrrolidine-3-carboxylic acid with thiourea, benzenecarbothioamide and thioureido acid novel disubstituted thiazole derivatives were obtained. Some transformations of these compounds were carried out; compounds with pyrrolidine, pyrrole, triazole, oxadiazole fragments were synthesized; and their antibacterial properties were investigated. The antibacterial assay revealed that in most cases substituted phenylthiazole derivatives had stronger inhibition and bactericidal properties against the test-cultures Staphylococcus aureus (ATCC 25923), Bacillus cereus (ATCC 10231), Listeria monocytogenes (ATCC 19111), Pseudomonas aeruginosa (ATCC 10145), Escherichia coli (ATCC 8739) and Salmonella enterica enteritidis when compared with the corresponding aminothiazoles. Compounds 3c, 5b, 15b and 16 b were found to have an exceptional antibacterial potency against all tested bacteria strains. The MIC of these compounds was observed at 7.8 μg/mL, and MBC – at 15.6 μg/mL, while the minimum inhibitory and minimum bactericidal concentrations of Oxytetracycline for Gram-positive bacteria strains was determined to be 62.5 μg/mL, and 125 μg/mL for Gram-negative ones.

Supplementary Materials

The following are available online. Figure S1: 1H-NMR of compound 2, Figure S2: 13C-NMR of compound 2, Figure S3: 1H-NMR of compound 3 a, Figure S4: 13C-NMR of compound 3 a, Figure S5: 1H-NMR of compound 3 b, Figure S6: 13C-NMR of compound 3 b, Figure S7: 1H-NMR of compound 3 c, Figure S8: 13C-NMR of compound 3 c, Figure S9: 1H-NMR of compound 4 a, Figure S10: 13C-NMR of compound 4 a, Figure S11: 1H-NMR of compound 4 b, Figure S12: 13C-NMR of compound 4 b, Figure S13: 1H-NMR of compound 5 a, Figure S14: 13C-NMR of compound 5 a, Figure S15: 1H-NMR of compound 5 b, Figure S16: 13C-NMR of compound 5 b, Figure S17: 1H-NMR of compound 6 a, Figure S18: 1H-NMR of compound 6 b, Figure S19: 1H-NMR of compound 7 a, Figure S20: 1H-NMR of compound 7 b, Figure S21: 1H-NMR of compound 8 a, Figure S22: 1H-NMR of compound 8 b, Figure S23: 1H-NMR of compound 9 b, Figure S24: 1H-NMR of compound 10 b, Figure S25: 1H-NMR of compound 11 b, Figure S26: 1H-NMR of compound 12 b, Figure S27: 1H-NMR of compound 13 a, Figure S28: 13C-NMR of compound 13 a, Figure S29: 1H-NMR of compound 13 b, Figure S30: 13C-NMR of compound 13 b, Figure S31: 1H-NMR of compound 14 b, Figure S32: 13C-NMR of compound 14 b, Figure S33: 1H-NMR of compound 15 b, Figure S34: 13C-NMR of compound 15 b, Figure S35: 1H-NMR of compound 16 b, Figure S36: 13C-NMR of compound 16 b, Figure S37: 1H-NMR of compound 17 b, Figure S38: 13C-NMR of compound 17 b, Figure S39: 1H-NMR of compound 18 b, Figure S40: 13C-NMR of compound 18 b, Figure S41: 1H-NMR of compound 19 b, Figure S42: 13C-NMR of compound 19 b, Figure S43: 1H-NMR of compound 20, Figure S44: 13C-NMR of compound 20, Figure S45: 1H-NMR of compound 21, Figure S46: 13C-NMR of compound 21, Figure S47: 1H-NMR of compound 22, Figure S48: 13C-NMR of compound 22.

Author Contributions

Conceptualization, B.S.-B.; Methodology, B.S.-B. and R.V.; Software, E.M.; Validation, B.S.-B., B.Š., R.V. and J.Š.; Formal analysis, B.S.-B.; Investigation, B.S.-B., B.Š., R.V. and J.Š.; Resources, E.M.; Data curation, B.S.-B.; Writing—Original draft preparation, R.V. and J.Š.; Writing—Review and editing, B.S.-B.; Visualization, E.M.; Supervision and project administration, B.S.-B. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Salem, M.A. Synthesis of New Thiazole, Bithiazolidinone and Pyrano[2,3-d]thiazole Derivatives as Potential Antimicrobial Agents. Croat. Chem. Acta. 2017, 90, 7–15. [Google Scholar] [CrossRef]
  2. Bondock, S.; Fouda, A.M. Synthesis and evaluation of some new 5-(hetaryl)thiazoles as potential antimicrobial agents. Synth. Commun. 2018, 48, 561–573. [Google Scholar] [CrossRef]
  3. Abd Elhameed, A.A.; El-Gohary, N.S.; El-Bendary, E.R.; Shaaban, M.I.; Bayomi, S.M. Synthesis and biological screening of new thiazolo[4,5-d]pyrimidine and dithiazolo[3,2-a:5′,4′-e]pyrimidinone derivatives as antimicrobial, antiquorum-sensing and antitumor agents. Bioorg. Chem. 2018, 81, 299–310. [Google Scholar] [CrossRef] [PubMed]
  4. Nastasa, C.; Tiperciuc, B.; Duma, M.; Benedec, D.; Oniga, O. New Hydrazones Bearing Thiazole Scaffold: Synthesis, Characterization, Antimicrobial, and Antioxidant Investigation. Molecules 2015, 20, 17325–17338. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  5. Annadurai, S.; Martinez, R.; Canney, D.J.; Eidem, T.; Dunman, P.M.; Abou-Gharbia, M. Design and synthesis of 2-aminothiazole based antimicrobials targeting MRSA. Bioorg. Med. Chem. Lett. 2012, 22, 7719–7725. [Google Scholar] [CrossRef] [PubMed]
  6. El-Sayed, N.N.E.; AL-Balawi, N.A.; Alafeefy, A.M.; AL-Shaikh, M.A.; Khan, K.M. Synthesis, Characterization and Antimicrobial Evaluation of some Thiazole-Derived Carbamates, Semicarbazones, Amides and Carboxamide. J. Chem. Soc. Pak. 2016, 38, 358–368. [Google Scholar]
  7. Sharshira, E.M.; Hamada, N.M.M. Synthesis, Characterization and Antimicrobial Activities of Some Thiazole Derivatives. Am. J. Org. Chem. 2012, 2, 69–73. [Google Scholar] [CrossRef]
  8. Grybaitė, B.; Vaickelionienė, R.; Stasevych, M.; Komarovska-Porokhnyavets, O.; Kantminienė, K.; Novikov, V.; Mickevičius, V. Synthesis and antimicrobial activity of novel thiazoles with reactive functional groups. Chem. Select. 2019, 4, 6965–6970. [Google Scholar]
  9. Surineni, G.; Gao, Y.; Hussain, M.; Liu, Z.; Lu, Z.; Chhotaray, C.; Islam, M.M.; Adnan Hameed, H.M.; Zhang, T. Design, synthesis, and in vitro biological evaluation of novel benzimidazole tethered allylidenehydrazinylmethylthiazole derivatives as potent inhibitors of Mycobacterium tuberculosis. Med. Chem. Commun. 2019, 10, 49–60. [Google Scholar] [CrossRef]
  10. Pattan, S.R.; Krishna Reddy, V.V.; Manvi, F.V.; Desai, B.G.; Bhat, A.R. Synthesis of N-3-(4-(4-chlorophenyl thiazole-2-yl)(2-(amino)methyl)quinazoline-4(3H)-one and their derivatives for antitubercular activity. Indian J. Chem. 2006, 45, 1778–1781. [Google Scholar]
  11. Kesicki, E.A.; Bailey, M.A.; Ovechkina, Y.; Early, J.V.; Alling, T.; Bowman, J.; Zuniga, E.S.; Dalai, S.; Kumar, N.; Masquelin, T.; et al. Synthesis and Evaluation of the 2-Aminothiazoles as Anti-Tubercular Agents. PLoS ONE 2016, 11, 1–25. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  12. Pieroni, M.; Wan, B.; Cho, S.; Franzblau, S.G.; Costantino, G. Design, synthesis and investigation on the structure-activity relationships of N-substituted 2-aminothiazole derivatives as antitubercular agents. Eur. J. Med. Chem. 2014, 72, 26–34. [Google Scholar] [CrossRef] [PubMed]
  13. Fathalla, W. Syntheses and reactions of methyl [3-(4-phenyl-thiazol-2-yl)-thioureido]alkanoates and related compounds. Arkivoc 2008, 12, 245–255. [Google Scholar]
  14. Dawood, K.M.; Eldebss, T.M.; El-Zahabi, H.S.; Yousef, M.H. Synthesis and antiviral activity of some new bis-1,3-thiazole derivatives. Eur. J. Med. Chem. 2015, 102, 266–276. [Google Scholar] [CrossRef]
  15. Stankova, I.; Chuchkov, K.; Shishkov, S.; Kostova, K.; Mukova, L.; Galabov, A.S. Synthesis, antioxidative and antiviral activity of hydroxycinnamic acid amides of thiazole containing amino acid. Amino Acids 2009, 37, 383–388. [Google Scholar] [CrossRef]
  16. Hargrave, K.D.; Hess, F.K.; Oliver, J.T. N-(4-substituted-thiazolyl)oxamic acid derivatives, a new series of potent, orally active antiallergy agents. J. Med. Chem. 1983, 26, 1158–1163. [Google Scholar] [CrossRef]
  17. Brzezińska, E.; Stolarska, J.; Sobanska, A. A structure-activity relationship study of thiazole derivatives with H1-Antihistamine activity. 2011, 68, 677–686. Acta Pol. Pharm. 2011, 68, 677–686. [Google Scholar]
  18. Hammad Elgazwy, A.S.; Nassar, E.; Zaki, M.Y. Synthesis, Biological Evaluation of Some 2,3-dihydropyrazoles and Thiazoles as Anti-inflammatory and Antibacterial Agents. Org. Chem. Curr. Res. 2012, 1, 1000112. [Google Scholar] [CrossRef] [Green Version]
  19. Li, M.; Sim, Y.; Ham, S.W. Discovery of 2-Aminothiazole Derivatives as Antitumor Agents. Bull Korean Chem. Soc. 2010, 31, 1463–1465. [Google Scholar] [CrossRef] [Green Version]
  20. Harnett, J.J.; Roubert, V.; Dolo, C.; Charnet, C.; Spinnewyn, B.; Cornet, S.; Rolland, A.; Marin, J.-G.; Bigga, D.; Chabrierb, P.-E. Phenolic thiazoles as novel orally-active neuroprotective agents. Bioorg. Med. Chem. Lett. 2004, 14, 157–160. [Google Scholar] [CrossRef]
  21. Łączkowski, K.Z.; Konklewska, N.; Biernasiuk, A.; Malm, A.; Sałat, K.; Furgała, A.; Dzitko, K.; Bekier, A.; Baranowska-Łączkowska, A.; Paneth, A. Thiazoles with cyclopropyl fragment as antifungal, anticonvulsant, and anti-Toxoplasma gondii agents: synthesis, toxicity evaluation, and molecular docking study. Med. Chem. Res. 2018, 27, 2125–2140. [Google Scholar] [CrossRef] [Green Version]
  22. Shaquiquzzaman, N.S.; ur Rahman, M.; Arshad, M.F.; Ahsan, W.; Alam, M.S.; Ahmed, S. Synthesis, characterization and antimicrobial evaluation of some new 1,3-thiazole-2,4-diamine derivatives. Acta. Pol. Pharm. 2010, 67, 239–246. [Google Scholar]
  23. Yonova, P.A.; Stoilkova, G.M. Synthesis and biological activity of urea and thiourea derivatives from 2-aminoheterocyclic compounds. J. Plant Growth Regul. 2005, 23, 280–291. [Google Scholar] [CrossRef]
  24. Wilkes, M.C.; Lavrik, P.B.; Greenplate, J. Synthesis of N-benzoyl-N-alkyl-2-aminothiazole Heliothis virescens proinsecticides. J. Agric. Food Chem. 1991, 39, 1652–1657. [Google Scholar] [CrossRef]
  25. EMA/487080/2014. European Medicines Agency. 2014. Available online: https://www.ema.europa.eu/en/documents/overview/sutent-epar-summary-public_en.pdf (accessed on 15 December 2019).
  26. Le Tourneau, C.; Raymond, E.; Faivre, S. Sunitinib: a novel tyrosine kinase inhibitor. A brief review of its therapeutic potential in the treatment of renal carcinoma and gastrointestinal stromal tumors (GIST). Ther. Clin. Risk Manag. 2007, 3, 341–348. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  27. Balandis, B.; Ivanauskaitė, G.; Smirnovienė, J.; Kantminienė, K.; Matulis, D.; Mickevičius, V.; Zubrienė, A. Synthesis and structure-affinity relationship of chlorinated pyrrolidinone-bearing benzenesulfonamides as human carbonic anhydrase inhibitors. Bioorg. Chem. 2020, 97, 1–12. [Google Scholar] [CrossRef]
  28. Vaškevičienė, I.; Paketurytė, V.; Pajanok, N.; Žukauskas, Š.; Sapijanskaitė, B.; Kantminienė, K.; Mickevičius, V.; Zubrienė, A.; Matulis, D. Pyrrolidinone-bearing methylated and halogenated benzenesulfonamides as inhibitors of carbonic anhydrases. Bioorg. Med. Chem. 2019, 27, 322–337. [Google Scholar] [CrossRef]
  29. Khanage, S.G.; Raju, A.; Mohite, P.B.; Pandhare, R.B. Analgesic Activity of Some 1,2,4-Triazole Heterocycles Clubbed with Pyrazole, Tetrazole, Isoxazole and Pyrimidine. Adv. Pharm. Bull 2013, 3, 13–18. [Google Scholar]
  30. Goyal, P.K.; Bhandari, A.; Rana, A.C.; Jain, C.B. Synthesis, Characterization and Analgesic Activity of some 4H-1, 2, 4-Triazole Derivatives. Int. J. Chem. Tech. Res. 2010, 2, 1992–1997. [Google Scholar]
  31. El-Sayed, H.A.; Moustafa, A.H.; Haikal, A.-F.Z. Synthesis, Antiviral, and Antimicrobial Activity of 1,2,4-Triazole Thioglycoside Derivatives. Phosphorus, Sulfur Silicon Relat. Elem. 2013, 188, 649–662. [Google Scholar] [CrossRef]
  32. Paprocka, R.; Wiese, M.; Eljaszewicz, A.; Helmin-Basa, A.; Gzella, A.; Modzelewska-Banachiewicz, B.; Michalkiewicz, J. Synthesis and anti-inflammatory activity of new 1,2,4-triazole derivatives. Bioorg. Med. Chem. Lett. 2015, 25, 2664–2667. [Google Scholar] [CrossRef] [PubMed]
  33. Sari, S.; Kaynak, F.B.; Dalkara, S. Synthesis and anticonvulsant screening of 1,2,4-triazole derivatives. Pharmacol Rep. 2018, 70, 1116–1123. [Google Scholar] [CrossRef]
  34. Khanage, S.G.; Raju, S.A.; Mohite, P.B.; Pandhare, R.B. Synthesis and pharmacological evaluation of some new pyrimidine derivatives containing 1,2,4-triazole. Adv. Pharm. Bull. 2012, 2, 213–222. [Google Scholar] [PubMed]
  35. Kamel, M.M.; Megally Abdo, N.Y. Synthesis of novel 1,2,4-triazoles, triazolothiadiazines and triazolothiadiazoles as potential anticancer agents. Eur. J. Med. Chem. 2014, 86, 75–80. [Google Scholar] [CrossRef] [PubMed]
  36. Chelamalla, R.; Venkatesham, A.; Sarangapani, M. Novel water-soluble substituted pyrrolo[3,2-d]pyrimidines: design, synthesis, and biological evaluation as antitubulin antitumor agents. J. Pharm. Res. 2012, 5, 4739–4742. [Google Scholar]
  37. Gupta, D.; Jain, D.K. Synthesis, antifungal and antibacterial activity of novel 1,2,4-triazole derivatives. J. Adv. Pharm. Technol. Res. 2015, 6, 141–146. [Google Scholar] [CrossRef]
  38. Tumosienė, I.; Peleckis, A.; Jonuškienė, I.; Vaickelionienė, R.; Kantminienė, K.; Šiugždaitė, J.; Beresnevičius, Z.J.; Mickevičius, V. Synthesis of novel 1,2- and 2-substituted benzimidazoles with high antibacterial and antioxidant activity. Monatsh. Chem. 2018, 149, 577–594. [Google Scholar] [CrossRef]
  39. Jin, R.; Liu, J.; Zhang, G.; Li, J.; Zhang, S.; Guo, H. Design, Synthesis, and Antifungal Activities of Novel 1,2,4-Triazole Schiff Base Derivatives. Chem. Biodivers. 2018, 15, e1800263–e1800270. [Google Scholar] [CrossRef]
  40. Zhang, S.L.; Damu, G.L.V.; Zhang, L.; Geng, R.X.; Zhou, C.H. Synthesis and biological evaluation of novel benzimidazole derivatives and their binding behavior with bovine serum albumin. Eur. J. Med. Chem. 2012, 55, 164–175. [Google Scholar] [CrossRef]
  41. Zhang, H.Z.; Damu, G.L.V.; Cai, G.X.; Zhou, C.H. Design, synthesis and antimicrobial evaluation of novel benzimidazole type of Fluconazole analogues and their synergistic effects with Chloromycin, Norfloxacin and Fluconazole. Eur. J. Med. Chem. 2013, 64, 329–344. [Google Scholar] [CrossRef]
  42. Voskiene, A.; Mickevicius, V.; Mikulskiene, G. Synthesis and structural characterization of products condensation 4-carboxy-1-(4-styrylcarbonylphenyl)-2-pyrrolidinones with hydrazines. Arkivoc 2007, 15, 303–314. [Google Scholar]
  43. Quintanilla-Licea, R.; Colunga-Valladares, J.F.; Caballero-Quintero, A.; Rodríguez-Padilla, C.; Tamez-Guerra, R.; Gómez-Flores, R.; Waksman, N. NMR Detection of Isomers Arising from Restricted Rotation of the C-N Amide Bond of N-Formyl-o-toluidine and N,N’-bisFormyl-o-tolidine. Molecules 2002, 7, 662–673. [Google Scholar] [CrossRef]
  44. Palla, G.; Predieri, G.; Domiano, P.; Vignali, C.; Turner, W. Conformational behavior and E/Z isomerization of N-acyl and N-aroylhydrazones. Tetrahedron. 1986, 42, 3649–3654. [Google Scholar] [CrossRef]
  45. Syakaev, V.V.; Podyachev, S.N.; Buzykin, B.I.; Latypov, S.K.; Habicher, W.D.; Konovalov, A.I. NMR study of conformation and isomerization of aryl- and heteroarylaldehyde 4-tert-butylphenoxyacetylhydrazones. J. Mol. Struct. 2006, 788, 55–62. [Google Scholar] [CrossRef]
  46. Mazur, L.; Jarzembska, K.N.; Kami ´nski, R.; Wo´zniak, K.; Pindelska, E.; Zieli ´nska-Pisklak, M. Substituent and solvent effects on intermolecular interactions in crystals of N-acylhydrazone derivatives: Single-crystal X-ray, solid state NMR, and computational studies. Cryst. Growth Des. 2014, 14, 2263–2281. [Google Scholar] [CrossRef]
  47. Gu, W.; Wu, R.; Qi, S.; Gu, C.; Si, F.; Chen, Z. Synthesis and antibacterial evaluation of new N-acylhydrazone derivatives from dehydroabietic acid. Molecules 2012, 17, 4634–4650. [Google Scholar] [CrossRef] [Green Version]
  48. Cardoso, L.N.F.; Bispo, M.L.F.; Kaiser, C.R.; Wardell, J.L.; Wardell, S.M.S.V.; Lourenço, M.C.S.; Bezerra, F.A.F.; Soares, R.P.P.; Rocha, M.N.; de Souza, M.V.N. Anti-tuberculosis evaluation and conformational study of N-acylhydrazones containing the thiophene nucleus. Arch. Pharm. Chem. Life Sci. 2014, 347, 432–448. [Google Scholar] [CrossRef]
  49. Voskiene, A.; Mickevicius, V. Products from condensation of 1-(3(4)-acetylphenyl)-4-carboxy-2-pyrrolidinones with o-phenylenediamine and their properties. Chem. Heterocycl. Compd. 2007, 43, 1379–1384. [Google Scholar] [CrossRef]
  50. Lopez-Oviedo, E.; Aller, A.I.; Martín, C.; Castro, C.; Ramirez, M.; Pemán, J.M.; Cantón, E.; Almeida, C.; Martín-Mazuelos, E. Evaluation of Disk Diffusion Method for Determining Posaconazole Susceptibility of Filamentous Fungi: Comparison with CLSI Broth Microdilution Method. Antimicrob. Agents Chemother. 2006, 50, 1108–1111. [Google Scholar] [CrossRef] [Green Version]
  51. Goodson, B.; Ehrhardt, A.; Ng, S.; Nuss, J.; Johnson, K.; Giedlin, M.; Yamamoto, R.; Krebber, A.; Ladner, M.; Giacona, M.B.; et al. Characterization of Novel Antimicrobial Peptoids. Antimicrob. Agents Chemother. 1999, 43, 1429–1434. [Google Scholar] [CrossRef] [Green Version]
  52. Peleckis, A.; Anusevičius, K.; Šiugždaitiugė, J.; Mickevičius, V. Nucleophilic ring opening of 1,4-disubstituted 2-pyrrolidones with hydrazine. Synthesis of azoles with a high antibacterial activity. Chemija 2018, 29, 135–144. [Google Scholar] [CrossRef]
Sample Availability: Samples of the compounds are not available from the authors.
Molecules 25 02433 g001 550
Figure 1. Pharmaceuticals with 1,2,4-triazole scaffold in the molecule.
Figure 1. Pharmaceuticals with 1,2,4-triazole scaffold in the molecule.
Molecules 25 02433 g001
Molecules 25 02433 sch001 550
Scheme 1. Synthesis of disubstituted pyrrolidinone derivatives 2–5.
Scheme 1. Synthesis of disubstituted pyrrolidinone derivatives 2–5.
Molecules 25 02433 sch001
Molecules 25 02433 sch002 550
Scheme 2. Synthesis of compounds 6–19.
Scheme 2. Synthesis of compounds 6–19.
Molecules 25 02433 sch002
Molecules 25 02433 sch003 550
Scheme 3. Synthesis of compounds 20–23.
Scheme 3. Synthesis of compounds 20–23.
Molecules 25 02433 sch003
Table
Table 1. The yields of the synthesized compounds 2–23.
Table 1. The yields of the synthesized compounds 2–23.
CompoundYield, %CompoundYield, %CompoundYield, %
1867a9014b54
2957b6915b86
3a628a6216b90
3b438b8917b76
3c829b8218b67
4a6210b7519b88
4b7111b992082
5a8112b962181
5b6513a572292
6a9013b922388
6b92----
Table
Table 2. The determined MIC and MBC of the synthesized compounds (only the data for compounds that gave positive results in at least one case are included in the table).
Table 2. The determined MIC and MBC of the synthesized compounds (only the data for compounds that gave positive results in at least one case are included in the table).
CompoundGram-Positive Bacteria StrainsGram-Negative Bacteria Strains
S. aureusB. cereusL. monocytogenesP. aeruginosaE. coliS. enterica enteritidis
MICMBCMICMBCMICMBCMICMBCMICMBCMICMBC
µg/mL
3a15.631.2531.2562.531.2562.531.2562.531.2562.531.2562.5
3b31.2562.515.631.2515.631.2515.631.2562.512515.631.25
3c7.815.67.815.67.815.67.815.67.815.67.815.6
4a62.512531.2562.531.2562.531.2562.531.2562.531.2562.5
4b15.631.2515.631.2515.631.2515.631.2515.631.2515.631.25
5a31.2562.531.2562.531.2562.531.2562.531.2562.531.2562.5
5b7.815.67.815.67.815.67.815.67.815.67.815.6
6a31.2562.531.2562.531.2562.531.2562.531.2562.531.2562.5
6b15.631.2515.631.2515.631.2515.631.2515.631.2515.631.25
7b+-7.815.615.631.25+-15.631.2515.615.6
8b31.2562.531.2562.531.2562.531.2562.515.631.2531.2562.5
9b7.815.615.631.2515.631.2515.631.2515.631.2515.631.25
11b62.5125+-15.631.2515.631.2531.2562.515.631.25
12b31.2562.531.2562.531.2562.531.2562.531.2562.531.2562.5
13a31.2562.531.2562.531.2562.531.2562.531.2562.531.2562.5
13b31.2562.515.631.2515.631.2515.631.2531.2562.515.631.25
14b7.815.662.5125125250125250125250+-
15b7.815.67.815.67.815.67.815.67.815.67.815.6
16b7.815.67.815.67.815.67.815.67.815.67.815.6
17b15.631.2515.631.2515.631.2515.631.2515.631.2515.631.25
2162.512531.2531.2531.2562.5--12512531.2562.5
2231.2531.2531.2562.5--31.2562.531.2531.25--
2315.631.2531.2562.5--31.2562.531.2531.25--
C62.5125
+, the growth of microorganisms; -, the absence of growth inhibition and bactericidal action; C, control antibiotic Oxytetracycline.

Share and Cite

MDPI and ACS Style

Sapijanskaitė-Banevič, B.; Šovkovaja, B.; Vaickelionienė, R.; Šiugždaitė, J.; Mickevičiūtė, E. Synthesis, Characterization and Bioassay of Novel Substituted 1-(3-(1,3-Thiazol-2-yl)phenyl)-5-oxopyrrolidines. Molecules 2020, 25, 2433. https://doi.org/10.3390/molecules25102433

AMA Style

Sapijanskaitė-Banevič B, Šovkovaja B, Vaickelionienė R, Šiugždaitė J, Mickevičiūtė E. Synthesis, Characterization and Bioassay of Novel Substituted 1-(3-(1,3-Thiazol-2-yl)phenyl)-5-oxopyrrolidines. Molecules. 2020; 25(10):2433. https://doi.org/10.3390/molecules25102433

Chicago/Turabian Style

Sapijanskaitė-Banevič, Birutė, Božena Šovkovaja, Rita Vaickelionienė, Jūratė Šiugždaitė, and Eglė Mickevičiūtė. 2020. "Synthesis, Characterization and Bioassay of Novel Substituted 1-(3-(1,3-Thiazol-2-yl)phenyl)-5-oxopyrrolidines" Molecules 25, no. 10: 2433. https://doi.org/10.3390/molecules25102433

Article Metrics

Back to TopTop