Design, Synthesis and In Vitro Antimicrobial Activity of 6-(1H-Benzimidazol-2-yl)-3,5-dimethyl-4-oxo-2-thio-3,4-dihydrothieno[2,3-d]pyrimidines

Abstract

The rapid development in bacterial resistance to many groups of known antibiotics forces the researchers to discover antibacterial drug candidates with previously unknown mechanisms of action, one of the most relevant being the inhibition of tRNA (Guanine37-N1)-methyltransferase (TrmD). The discovery of selective TrmD inhibitors in the series of carboxamide derivatives of thienopyrimidines became a background for further modification of the similar structures aimed at the development of promising antibacterial agents. As part of this research, we carried out the construction of heterocyclic hybrids bearing the moieties of thieno[2,3-d]pyrimidine and benzimidazole starting from 3,5-dimethyl-4-oxo-2-thioxo-1H-thieno[2,3-d]pyrimidine-6-carboxylic acid, which was used as the pivotal intermediate. The hybrid molecule of 6-(1H-benzimidazol-2-yl)-3,5-dimethyl-2-thioxo-1H-thieno[2,3-d]pyrimidin-4-one prepared via condensation of the carboxylic acid with ortho-phenylenediamine was further alkylated with aryl/hetaryl chloroacetamides and benzyl chloride to produce the series of S-alkyl derivatives. The results of molecular docking studies for the obtained series of S-alkyl benzimidazole-thienopyrimidines showed their high affinity to the TrmD isolated from the P. aeruginosa. The results of antimicrobial activity screening revealed the antimicrobial properties for all of the studied molecules against both Gram-positive and Gram-negative bacteria and the Candida albicans fungal strain. The highest antimicrobial activity was determined for 2-{[6-(1H-benzimidazol-2-yl)-3,5-dimethyl-4-oxo-3,4-dihydrothieno[2,3-d]pyrimidin-2-yl]thio}-N-(4-isopropylphenyl)acetamide, which also had the highest affinity to the TrmD inhibitor’s binding site according to the docking studies results.

1. Introduction

Recently, the wide spread of the pathogenic strains of microorganisms and nosocomial infections caused by bacteria and fungi such as Staphylococcus aureus, Escherichia coli, Candida albicans has been observed. The resistance of many of these strains (Pseudomonas aeruginosa, for instance) to popular antibiotics almost reaches the scale of global threat [1]. All these factors motivate the research and development of the novel classes of small molecules suitable as antimicrobials. According to the results of the recent studies of thieno[2,3-d]pyrimidine derivatives, which showed the antimicrobial activity against both Gram-negative and Gram-positive bacteria [2,3,4,5], the molecules bearing this heterocyclic fragment are good candidates for the promising novel class of antibacterials.

In the last decade, we largely studied the antimicrobial activity of different synthetically prepared thieno[2,3-d]pyrimidines. The highest antimicrobial activity against Gram-negative bacteria (and P. aeruginosa in particular) was determined for 6-heterylthieno[2,3-d]pyrimidines with 1,3,4-oxadiazole I (Figure 1) [6], 2-aminothiazole II [7] and 1,3-benzoxazole moieties attached to thieno[2,3-d]pyrimidin-4-one or 4-thione moieties III [8].

The successful application of the hybrid pharmacophore concept achieved by the combination of thieno[2,3-d]pyrimidine with the other heterocycles has been reported by many other scientific groups. The modification of the position 6 of thieno[2,3-d]pyrimidine with a triazolothiadiazole cycle allowed the obtaining of highly effective antibacterial agents IV, which were also active against P. aeruginosa [9]. The antimicrobial and antifungal properties were found to be typical for the compounds V modified with 1,3,4-oxadiazole [10]; their analogs bore morpholine or piperidine cycles at position 4 of the core heterocycle (VI) also showed antimicrobial properties [11]. Other reports have shown some examples of successful modifications of other positions of the thieno[2,3-d]pyrimidine system as well as fusion of this ring system with different heterocycles (which led to the effective antimicrobials). The examples tetrahydrobenzo[4,5]thieno[2,3-d]pyrimidine derivatives [12,13], 5-furyl [14] and 2-thienyl theinopyrimidines fused with triazole [15] or pyrimidine cycles can also be mentioned [16].

The selective action on the specific enzymes of bacterial cells is of the great priority for discovery of the novel mechanisms of antibacterial action. An important advantage of some thieno[2,3-d]pyrimidine derivatives is their confirmed ability to selectively inhibit the enzymes of different microorganisms such as P. aeruginosa and M. tuberculosis. Some thienopyrimidines were found to be active against isoniazid resistant strains of M. tuberculosis due to their inhibitory activities of enoyl acyl-carrier protein reductase, which do not require activation of catalase-peroxidase [17,18]. It was also claimed that 4-amino-thieno[2,3-d]pyrimidine are the new scaffolds of the selective inhibitors of the QcrB subunit of the electron transport chain enzyme cytochrome bc1, which is a novel target for antitubercular agents [19]. The inhibition of QcrB results in the blockade of oxidative phosphorylation, which leads to the total death of M. tuberculosis cells [20].

One of the newly disclosed mechanisms of antimicrobial action is the inhibition of tRNA (Guanine37-N¹)-methyltransferase (TrmD) [21]. The derivatives of thieno[2,3-d]pyrimidine of general I (Figure 2) were the first series inhibitors for TrmD isolated from Haemophilus influenzae [22]. The most effective of these derivatives were the ligands that deeply immerse into the hydrophobic pocket, attaching to the site of methionine fragment of S-adenosylmethionine (SAM) cofactor. As a result of competing processes, the further methylation of tRNA is blocked; in this example of inhibitors, there is a compound II (Figure 2) with the terminal imidazole fragment. Another paper was about the modification of the structure and synthesis of the combinatorial library of the novel selective inhibitors of bacterial TrmD [23]. The complexes of different TrmD isolated from S. aureus, P. aeruginosa or M. tuberculosis with the different ligands were studied in detail, which allowed for the discovery of tyrosine-flipping mechanism of inhibitory action. The most active compounds reported were III and IV (Figure 2).

All the above-mentioned resulted undoubtedly show that modification of thieno[2,3-d]pyrimidine scaffolds is a promising method for the construction of novel antibacterial agents. Within the framework of the hybrid pharmacophore concept, we decided to modify thienopyrimidine moiety with benzimidazole (Figure 2). Benzimidazole was chosen as the substituent because many of its derivatives were reported as antibacterials [24,25], antituberculosis [26], antifungals [27] and antiparasitics [28] (Figure 2); a high affinity for bacterial enzymes was also reported for this heterocycle. It is also worth mentioning that benzimidazole is among the “privileged sub-structures” for drug discovery [29].

The outer membrane of Gram-negative bacteria is a reason for its high non-specific resistance to many antibiotics [30], it is also known that diffusion across the membrane is facilitated for lipophilic molecules. Therefore, the decision to introduce the sulphur atom at position 2 of thienopyrimidine together with the methyl groups at positions 3 and 5 was made in order to increase the lipophilicity.

The aim of this research was to search for effective antibacterials with 6-(1H-benzimidazol-2-yl)-3,5-dimethyl-4-oxo-2-thio-3,4-dihydrothieno[2,3-d]pyrimidine as a key structure.

2. Materials and Methods

2.1. General Information

All solvents and reagents were acquired from their commercial sources. The melting points were determined in a capillary using an electrothermal IA9100X1 (Bibby Scientific Limited, Staffordshire, UK) digital melting point apparatus. The elemental analyses was performed on a Euro Vector EA-3000 (Eurovector SPA, Redavalle, Italy) microanalyzer and were within 0.4% of the theoretical values. All the NMR spectra were recorded on Bruker Avance 500 ¹H NMR (500 MHz) and ¹³C NMR (125 MHz) in DMSO-d₆. TMS was used as an internal standard. LC-MS analysis of compounds was performed on an Agilent 1100 HPLC apparatus with diode array and mass-selective detectors (Agilent, Santa Clara, CA, USA, LC-MSD SL), Zorbax SB-C18 column (4.6 × 15 mm) with chemical ionization at atmospheric pressure (APCI).

2.2. Molecular Docking Study

The hardware used is the ASUS VivoBook X530UN S15 with an Intel Core i7 8550U 8thGen and Windows 10, 64-bit operating system. The molecular docking studies were performed with AutoDock Vina and AutoDockTools 1.5.6 programs [31]. The biomolecular target was acquired from Protein Data Bank [32]: TrmD Pseudomonas aeruginosa PDB ID—5ZHN [23]. The construction of the virtual base was done with BIOVIADraw 2017R2; the files were recorder in mol format. The structures were optimized with Chem3D using MM2 algorithm and saved as pdb. Their transformation to pdbqt format was performed with AutoDockTools-1.5.6 [33]. Discovery Studio Visualizer 2017/R2 was used for removal of the molecules of the solvent and the native ligand of the enzyme. The prepared macromolecule was saved in the pdb format. The program AutoDockTools-1.5.6 was used to add polar hydrogen atoms to the stricture of the enzyme and to save it as pdbqt. The size of the Grid box and its center was determined and validated using the native ligand of A subunit: TrmD (PDB ID 5ZHN): x = 40.04, y = 107.23, z = −3.40; size x = 18, y = 22, z = 20. To validate the docking method of the reference ligand, compound IV (Figure 2) [23], is extracted and then reused for the redocking process after given charged, set torque and saved as pdbqt. The calculation of the RMSD value was performed with ProFit Results available online. Discovery Studio V17.2.0.16349 was used for the visualization and analysis of the results.

2.3. Synthesis and Characterization of Compounds

Ethyl 3,5-dimethyl-4-oxo-2-thioxo-1,2,3,4-tetrahydrothieno[2,3-d]pyrimidine-6-carboxylate (which was used as the starting material) was prepared by the method reported in the paper [34].

2.3.1. Synthesis of 3,5-Dimethyl-4-oxo-2-thioxo-1,2,3,4-tetrahydrothieno[2,3-d]pyrimidine-6-carboxylic Acid (2)

To start, 4.20 g (0.105 mol) of sodium hydroxide and then 200 mL of water were added to 10.00 g (0.035 mol) of the ester 1. The reaction mixture was heated to 50–60 °C and allowed to stir at this temperature for 10 h. Then, the reaction mixture was cooled and acidified with orthophosphoric acid (85%). The precipitate formed was filtered and washed with plenty of water. The crystalline mass of the product was dried at 60 °C for 3 days.

Yield (7.98 g) 89%, m.p. >300 °C, grey solid. ¹H NMR (500 MHz, DMSO-d₆): δ 2.70 (s, 3H, CH₃), 3.56 (s, 3H, NCH₃), 13.56 (br. s, 1H, COOH). ¹³C NMR (125 MHz, DMSO-d₆): δ 14.6, 33.5, 117.0, 120.1, 143.6, 152.6, 157.5, 163.8, 175.3. LC-MS m/z (ES–) 255.0 (M–H)^–. Anal. calcd. for C₉H₈N₂O₃S₂ (256.30): C, 42.18; H, 3.15; N, 10.93. Found: C, 42.34; H, 3.27; N, 11.02.

2.3.2. Synthesis of 6-(1H-Benzimidazol-2-yl)-3,5-dimethyl-2-thioxo-1H-thieno[2,3-d]pyrimidin-4-one (3)

To start, 3.35 g (0.021 mol) of 1,1′-carbonyldiimidazole and 12 mL of dimethylformamide for peptide synthesis were added to 5.00 g (0.0195 mol) of 2. The reaction mixture was heated at 70–80 °C for 15 min. Then, 2.22 g (0.0205 mol) of o-phenylenediamine was added into the reaction mixture, the temperature was raised to 130 °C and the heating continued for 2.5 h. The reaction mixture was cooled and quenched with water. The precipitate formed was filtered off and washed with plenty of water.

Yield (3.71 g) 58%, m.p. >300 °C, yellow solid. ¹H NMR (500 MHz, DMSO-d₆): δ 2.82 (s, 3H, CH₃), 3.62 (s, 3H, NCH₃), 7,19 (m, 2H, Ar-H), 7,57 (m, 2H, Ar-H), 12.62 (br. s, 1H, NH). ¹³C NMR (125 MHz, DMSO-d₆): δ 14.4, 33.0, 116.5, 119.8, 122.2, 133.8, 145.6, 151.3, 157.0, 174.2. LC-MS m/z (ES+) 329.0 (MH⁺). Anal. calcd. for C₁₅H₁₂N₄OS₂ (328.42): C, 54.86; H, 3.68; N, 17.06. Found: C, 54.93; H, 3.77; N, 17.12.

2.3.3. General Method for Synthesis of 2-[6-(1H-Benzimidazol-2-yl)-3,5-dimethyl-4-oxo-thieno[2,3-d]pyrimidin-2-yl]sulfanyl-N-(aryl/heteryl)acetamides (4a-l) and 6-(1H-benzimidazol-2-yl)-2-(benzylsulfanyl)-3,5-dimethylthieno[2,3-d]pyrimidin-4(3H)-one (5)

To start, 0.6 mmol of the corresponding chloroacetamide or benzyl chloride and 0.66 mmol of triethylamine were added to the mixture of 0.2 g (0.6 mmol) of 6-(1H-benzimidazol-2-yl)-3,5-dimethyl-2-thioxo-2,3-dihydrothieno[2,3-d]pyrimidin-4(1H)-one (3) in 4 mL of dimethylformamide. The reaction mixture was stirred and heating (80 °C) until the clear solution is formed (1–2 h) and then additionally for 2 h. After the cooling reaction, the mixture was diluted with water and the precipitate formed was filtered off and dried. The product was additionally purified via crystallization from ethanol.

2-[6-(1H-Benzimidazol-2-yl)-3,5-dimethyl-4-oxo-thieno[2,3-d]pyrimidin-2-yl]sulfanyl-N-phenyl-acetamide (4a). Yield: 83%, m.p. >300 °C, yellowish powder. ¹H NMR (500 MHz, DMSO-d₆): 2.89 (s, 3H, CH₃), 3.45 (s, 3H, NCH₃), 4.26 (s, 2H, SCH₂), 7.07 (t, 1H, J = 7.4 Hz, Ar-H), 7.22 (m, 2H, Ar-H benzimidazole), 7.32 (t, 2H, J = 7.4 Hz, Ar-H), 7.59 (m, 4H, Ar-H benzimidazole), 10.22 (s, 1H, CONH), 12.41 (br. s, 1H, NH benzimidazole). ¹³C NMR (125 MHz, DMSO-d₆): δ 15.4, 30.5, 37.8, 119.7, 119.9, 122.5, 124.1, 129.3, 134.3, 139.4, 146.5, 158.3, 159.8, 163.1, 165.8. LC-MS m/z (ES+) 462.0 (MH⁺). Anal. calcd. for C₂₃H₁₉N₅O₂S₂ (461.57): C, 59.85; H, 4.15; N, 15.17. Found: C, 59.94; H, 4.29; N, 15.23.

2-[6-(1H-benzimidazol-2-yl)-3,5-dimethyl-4-oxo-thieno[2,3-d]pyrimidin-2-yl]sulfanyl-N-(p-methyl)acetamide (4b). Yield: 69%, m.p. 230–231 °C, yellowish powder. ¹H NMR (500 MHz, DMSO-d₆): δ: 2.24 (s, 3H, CH₃), 2.86 (s, 3H, CH₃), 3.5 (s, 3H, NCH₃), 4.23 (s, 2H, SCH₂), 7.12 (d, 2H, J = 7.9, Ar-H), 7.21 (m, 2H, Ar-H benzimidazole), 7.48 (d, 2H, J = 7.9, Ar-H), 7.59 (m, 2H, Ar-H benzimidazole), 10.33 (s, 1H, CONH), 12.54 (br. s, 1H, NH benzimidazole). ¹³C NMR (125 MHz, DMSO-d₆): δ 15.4, 21.0, 30.5, 37.8, 119.6, 119.8, 122.5, 129.7, 133.0, 134.3, 136.9, 146.5, 158.3, 159.8, 163.1, 165.5. LC-MS m/z (ES+) 476.0 (MH⁺). Anal. calcd. for C₂₄H₂₁N₅O₂S₂ (475.60): C, 60.61; H, 4.45; N, 14.73. Found: C, 60.73; H, 4.49; N, 14.86.

2-{[6-(1H-Benzimidazol-2-yl)-3,5-dimethyl-4-oxo-3,4-dihydrothieno[2,3-d]pyrimidin-2-yl]thio}-N-(2-ethylphenyl)acetamide (4c). Yield: 65%, m.p. 291–292 °C, white powder. ¹H NMR (500 MHz, DMSO-d₆): δ: 1.11 (t, 3H, J = 7.4, CH₃), 2.61 (q, 2H, J = 7.4, CH₂), 2.88 (s, 3H, CH₃), 3.52 (s, 3H, NCH₃), 4.27 (s, 2H, SCH₂), 7.15–7.23 (m, 2H, Ar-H benzimidazole), 7.32 (d, 1H, J = 7.1 Hz, Ar-H), 7.56–7.65 (m, 2H, Ar-H benzimidazole), 9.73 (s, 1H, CONH), 12.56 (br. s, 1H, NH benzimidazole). ¹³C NMR (125 MHz, DMSO-d₆): δ 14.9, 15.5, 24.3, 30.5, 36.9, 119.7, 122.5, 126.5, 126.6, 126.6, 129.1, 134.3, 135.9, 138.8, 146.5, 158.3, 159.8, 163.2, 166.2. LC-MS m/z (ES+) 490.2 (MH⁺). Anal. calcd. for C₂₅H₂₃N₅O₂S₂ (489.62): C, 61.33; H, 4.73; N, 14.30. Found: C, 61.35; H, 4.80; N, 14.33.

2-{[6-(1H-Benzimidazol-2-yl)-3,5-dimethyl-4-oxo-3,4-dihydrothieno[2,3-d]pyrimidin-2-yl]thio}-N-(4-isopropylphenyl)acetamide (4d). Yield: 79%, m.p. 189–190 °C, yellowish powder. ¹H NMR (500 MHz, DMSO-d₆): δ: 1.16 (d, 6H, J = 6.5, CH₃), 2.86 (m, 4H, CH, CH₃), 3.49 (s, 3H, CH₃), 4.24 (s, 2H, SCH₂), 7.10–7.33 (m, 4H, Ar-H), 7.41–7.70 (m, 4H, Ar-H), 10.34 (s, 1H, CONH), 12.55 (br. s, 1H, NH benzimidazole). ¹³C NMR (125 MHz, DMSO-d₆): δ 15.3, 24.4, 30.4, 33.3, 37.7, 119.5, 119.8, 122.4, 127.0, 134.2, 137.0, 144.1, 146.3, 158.2, 159.7, 163.0, 165.4, 204.3. LC-MS m/z (ES+) 504.2 (MH⁺). Anal. calcd. for C₂₆H₂₅N₅O₂S₂ (503.65): C, 62.01; H, 5.00; N, 13.91. Found: C, 62.14; H, 5.03; N, 14.06.

2-{[6-(1H-Benzimidazol-2-yl)-3,5-dimethyl-4-oxo-3,4-dihydrothieno[2,3-d]pyrimidin-2-yl]thio}-N-[3-(trifluoromethyl)phenyl]acetamide (4e). Yield: 89%, m.p. 278–279 °C, yellowish powder. ¹H NMR (500 MHz, DMSO-d₆): δ: 2.86 (s, 3H, CH₃), 3.51 (s, 3H, NCH₃), 4.28 (s, 2H, SCH₂), 7.20 (m, 2H, Ar-H benzimidazole), 7.42 (d, 1H, J = 7.4, Ar-H benzimidazole), 7.53 (d, 1H, J = 7.1, Ar-H), 7.58 (t, 1H, J = 7.9, Ar-H), 7.63 (d, 1H, J = 7.4, Ar-H benzimidazole), 7.77 (d, 1H, J = 8.2, Ar-H), 8.11 (s, 1H, Ar-H), 10.78 (s, 1H, CONH), 12.52 (br. s, 1H, NH benzimidazole). ¹³C NMR (125 MHz, DMSO-d₆): δ 15.4, 19.1, 30.5, 37.8, 56.6, 112.2, 115.7, 119.1, 119.6, 120.4, 122.5, 122.6, 123.2, 123.3, 130.7, 134.3, 135.4, 140.2, 143.7, 146.4, 158.2, 159.6, 163.0, 166.5. LC-MS m/z (ES+) 530.0 (MH⁺). Anal. calcd. for C₂₄H₁₈F₃N₅O₂S₂ (529.57): C, 54.43; H, 3.43; N, 13.22. Found: C, 54.58; H, 4.10; N, 13.56.

2-{[6-(1H-Benzimidazol-2-yl)-3,5-dimethyl-4-oxo-3,4-dihydrothieno[2,3-d]pyrimidin-2-yl]thio}-N-(2-ethoxyphenyl)acetamide (4f). Yield: 85%, m.p. 240–241 °C, grey powder. ¹H NMR (500 MHz, DMSO-d₆): δ: 1.31 (t, 3H, J = 6.8, CH₃), 2.89 (s, 3H, CH₃), 3.55 (s, 3H, NCH₃), 4.1 (q, 2H, J = 6.8, CH₂), 4.31 (s, 2H, SCH₂), 6.9 (t, 2H, J = 6.8, Ar-H), 7.01–7.06 (m, 2H, Ar-H), 7.22 (m, 2H, Ar-H benzimidazole), 7.55–7.64 (m, 2H, Ar-H benzimidazole), 7.94 (m, 1H, Ar-H), 9.3 (s, 1H, CONH), 12.44 (br. s, 1H, NH benzimidazole). ¹³C NMR (125 MHz, DMSO-d₆): δ 15.0, 15.4, 30.6, 37.4, 64.5, 112.2, 112.9, 119.2, 119.7, 120.8, 122.2, 122.6, 123.4, 125.2, 127.7, 134.3, 135.5, 143.8, 146.4, 149.2, 158.3, 159.6, 163.1, 165.9. LC-MS m/z (ES+) 506.0 (MH⁺). Anal. calcd. for C₂₅H₂₃N₅O₃S₂ (505.62): C, 59.39; H, 4.59; N, 13.85. Found: C, 59.47; H, 4.62; N, 13.90.

2-{[6-(1H-Benzimidazol-2-yl)-3,5-dimethyl-4-oxo-3,4-dihydrothieno[2,3-d]pyrimidin-2-yl]thio}-N-(4-ethoxyphenyl)acetamide (4g). Yield: 92%, m.p. 175–176 °C, white powder. ¹H NMR (500 MHz, DMSO-d₆): δ: 1.29 (t, 3H, J = 6.8, CH₃), 2.86 (s, 3H, CH₃), 3.5 (s, 3H, NCH₃), 3.97 (m, 2H, CH₂), 4.21 (s, 2H, SCH₂), 6.87 (d, 2H, J = 7.7, Ar-H), 7.21 (m, 2H, Ar-H benzimidazole), 7.48 (d, 2H, J = 7.7, Ar-H), 7.53–7.63 (m, 2H, Ar-H benzimidazole), 10.26 (s, 1H, CONH), 12.54 (br. s, 1H, NH benzimidazole). ¹³C NMR (125 MHz, DMSO-d₆): δ 15.1, 15.3, 30.4, 37.6, 63.5, 114.9, 119.5, 121.2, 122.4, 132.3, 134.2, 146.3, 155.1, 158.2, 159.7, 163.0, 165.1. LC-MS m/z (ES+) 506.0 (MH⁺). Anal. calcd. for C₂₅H₂₃N₅O₃S₂ (505.62): C, 59.39; H, 4.59; N, 13.85. Found: C, 59.41; H, 4.66; N, 13.94.

2-{[6-(1H-Benzimidazol-2-yl)-3,5-dimethyl-4-oxo-3,4-dihydrothieno[2,3-d]pyrimidin-2-yl]thio}-N-(3,4-dimethoxyphenyl)acetamide (4h). Yield: 67%, m.p. 185–186 °C, white powder. ¹H NMR (500 MHz, DMSO-d₆): δ: 2.86 (s, 3H, CH₃), 3.50 (s, 3H, NCH₃), 3.71 (m, 6H, OCH₃), 4.21 (s, 2H, SCH₂), 6.88–6.91 (d, 1H, J = 8.5, Ar-H), 7.06–7.09 (d, 1H, J = 8.5, Ar-H),7.21 (m, 2H, Ar-H benzimidazole), 7.31 (m, 1H, Ar-H), 7.54–7.63 (m, 2H, Ar-H benzimidazole), 10.28 (s, 1H, CONH), 12.53 (br. s, 1H, NH benzimidazole). ¹³C NMR (125 MHz, DMSO-d₆): δ 15.3, 30.4, 37.7, 55.8, 56.1, 104.8, 111.6, 112.0, 112.5, 119.0, 119.5, 122.4, 123.2, 132.9, 134.1, 145.5, 146.3, 149.0, 158.2, 159.7, 163.0, 165.2. LC-MS m/z (ES+) 522.0 (MH⁺). Anal. calcd. for C₂₅H₂₃N₅O₄S₂ (521.62): C, 57.57; H, 4.44; N, 13.43. Found: C, 57.63; H, 4.52; N, 13.48.

2-{[6-(1H-Benzimidazol-2-yl)-3,5-dimethyl-4-oxo-3,4-dihydrothieno[2,3-d]pyrimidin-2-yl]thio}-N-(5-chloro-2-methylphenyl)acetamide (4i). Yield: 86%, m.p. > 300 °C, yellowish powder. ¹H NMR (500 MHz, DMSO-d₆): δ: 2.25 (s, 3H, CH₃), 2.87 (s, 3H, CH₃), 3.50 (s, 3H, NCH₃), 4.29 (s, 2H, SCH₂), 7.12–7.14 (m, 1H, Ar-H), 7.18–7.26 (m, 3H, Ar-H benzimidazole), 7.50–7.49 (m, 3H, Ar-H benzimidazole), 9.83 (s, 1H, CONH), 12.54 (br. s, 1H, NH benzimidazole). ¹³C NMR (125 MHz, DMSO-d₆): δ 15.4, 17.9, 30.4, 37.0, 119.6, 122.4, 124.4, 125.4, 130.3, 130.7, 132.3, 134.2, 137.8, 146.3, 158.2, 159.7, 163.0, 166.2. LC-MS m/z (ES+) 510.0 (MH⁺). Anal. calcd. for C₂₄H₂₀ClN₅O₂S₂ (510.04): C, 56.52; H, 3.95; N, 13.73. Found: C, 56.51; H, 3.99; N, 13.83.

2-{[6-(1H-Benzimidazol-2-yl)-3,5-dimethyl-4-oxo-3,4-dihydrothieno[2,3-d]pyrimidin-2-yl]thio}-N-(3-chloro-4-fluorophenyl)acetamide (4j). Yield: 77%, m.p. 214–215 °C, white powder. ¹H NMR (500 MHz, DMSO-d₆): δ: 2.87 (s, 3H, CH₃), 3.52 (s, 3H, NCH₃), 4.24 (s, 2H, SCH₂), 7.20 (m, 2H, Ar-H benzimidazole), 7.37 (t, 1H, J = 9.0, Ar-H), 7.49 (m, 1H, Ar-H), 7.58 (m, 2H, Ar-H benzimidazole), 7.88 (d, 1H, Ar-H), 10.54 (s, 1H, CONH), 12.46 (br. s, 1H, NH benzimidazole). ¹³C NMR (125 MHz, DMSO-d₆): δ 15.3, 30.4, 37.6, 117.4, 117.6, 119.5, 119.9, 119.9, 121.0, 122.4, 134.2, 136.5, 146.3, 158.1, 159.5, 162.9, 166.1. LC-MS m/z (ES+) 514.0 (MH⁺). Anal. calcd. for C₂₃H₁₇ClFN₅O₂S₂ (514.00): C, 53.75; H, 3.33; N, 13.63. Found: C, 53.76; H, 3.48; N, 13.66.

Ethyl 4-[({[6-(1H-Benzimidazol-2-yl)-3,5-dimethyl-4-oxo-3,4-dihydrothieno[2,3-d]pyrimidin-2-yl]thio}acetyl)amino]benzoate (4k). Yield: 78%, m.p. 208–209 °C, yellowish powder. ¹H NMR (500 MHz, DMSO-d₆): δ: 1.31 (t, 3H, J = 6.3, CH₃), 2.88 (s, 3H, CH₃), 3.54 (s, 3H, NCH₃), 4.29 (s, 2H, SCH₂), 7.2 (m, 2H, Ar-H benzimidazole), 7.59 (m, 2H, Ar-H benzimidazole), 7.73 (d, 2H, J = 8.0, Ar-H), 7.93 (d, 2H, J = 8.0, Ar-H), 10.56 (s, 1H, CONH), 12.37 (br. s, 1H, NH benzimidazole). ¹³C NMR (125 MHz, DMSO-d₆): δ 14.7, 15.4, 30.5, 37.9, 61.0, 119.1, 119.6, 122.5, 125.1, 130.8, 134.3, 143.7, 146.4, 158.2, 159.6, 163.0, 165.8, 166.5. LC-MS m/z (ES+) 534.0 (MH⁺). Anal. calcd. for C₂₆H₂₃N₅O₄S₂ (533.63): C, 58.52; H, 4.34; N, 13.12. Found: C, 58.61; H, 4.36; N, 13.16.

2-{[6-(1H-Benzimidazol-2-yl)-3,5-dimethyl-4-oxo-3,4-dihydrothieno[2,3-d]pyrimidin-2-yl]thio}-N-1,3-thiazol-2-ylacetamide (4l). Yield: 83%, m.p. > 300 °C, yellowish powder. ¹H NMR (500 MHz, DMSO-d₆): δ: 2.85 (s, 3H, CH₃), 3.50 (s, 3H, NCH₃), 4.34 (s, 2H, SCH₂), 7.04–7.30 (m, 3H, Ar-H), 7.42–7.70 (m, 3H, Ar-H), 12.51 (s, 2H, CONH and NH benzimidazole). ¹³C NMR (125 MHz, DMSO-d₆): δ 15.4, 30.5, 36.3, 114.2, 119.6, 122.5, 134.3, 138.3, 146.4, 158.2, 158.5, 159.3, 162.9, 166.4. LC-MS m/z (ES+) 469.0 (MH⁺). Anal. calcd. for C₂₀H₁₆N₆O₂S₃ (468,58): C, 51.27; H, 3.44; N, 17.94. Found: C, 51.28; H, 3.47; N, 17.97.

6-(1H-benzimidazol-2-yl)-2-(benzylsulfanyl)-3,5-dimethylthieno[2,3-d]pyrimidin-4(3H)-one (5). Yield: 72%, m.p. 146–147 °C, pale yellow powder. ¹H NMR (500 MHz, DMSO-d₆): δ 2.88 (s, 3H, CH₃), 3.45 (s, 3H, NCH₃), 4.53 (s, 3H, SCH₂), 7.22 (m, 2H, Ar-H benzimidazole), 7.28 (t, 1H, J = 7.1 Hz, Ar-H), 7.34 (t, 2H, J = 7.4 Hz, Ar-H), 7.49 (d, 2H, J = 7.1 Hz, Ar-H), 7.52–7.68 (m, 2H, Ar-H benzimidazole), 12.50 (br. s, 1H, NH benzimidazole). ¹³C NMR (125 MHz, DMSO-d₆): δ 15.4, 30.4, 36.5, 112.2, 119.2; 119.7, 122.4, 122.63, 123.4, 128.1, 129.1, 129.9, 134.4, 135.5, 136.6, 143.8, 146.5, 158.4, 159.7, 163.2. LC-MS m/z (ES+) 419.0 (MH⁺). Anal. calcd. for C₂₂H₁₈N₄OS₂ (418.54): C, 63.13; H, 4.33; N, 13.39. Found: C, 63.25; H, 4.37; N, 13.39.

2.4. Antimicrobial Activity Study

According to the international recommendations and national standards [35,36,37], the following strains of micro-organisms were used as the test strains Staphylococcus aureus ATCC 25923, Escherichia coli ATCC 25922, Pseudomonas aeruginosa ATCC 27853, Proteus vulgaris ATCC 4636, Bacillus subtilis ATCC 6633 and Candida albicans ATCC653/885.

The microbial suspension of microorganisms was prepared using a Densi-La-Meter device (manufactured by PLIVA-Lachema, Czech Republic; wavelength 540 nm). The microbial load was 10⁷ microbial cells per 1 mL of medium and was established according to the MacFarland standard. An 18–24-h microorganism culture was used for the test. Muller–Hinton («HIMedia Laboratorles Pvt. Ltd. India») and Sabouraud agars («HIMedia Laboratorles Pvt. Ltd. India») were used in the studies. The studied compounds were administered in the form of DMSO solutions (concentration 100 μg/mL) in 0.3-mL aliquots, and Streptomycin was used in the form of a solution in DMSO (100 μg/mL). The measurement for each sample was repeated three times. The antibacterial activity was assessed by measuring the growth inhibition zones of the corresponding microorganism.

3. Results and Discussion

3.1. Docking Study

The discovery of the mechanism of selective inhibition of TrmD from different bacteria, which was confirmed for some carboxamide derivatives of thienopyrimidinones [23], allows for the estimation of the binding affinity of the thenopyrimidine structural analogs to TrmD with the help of molecular docking instruments. The molecular docking of the constructed hybrids was performed to the active site of selective inhibitors of TrmD; the model of the enzyme isolated from P. aeruginosa was used for the studies. Macromolecule of TrmD is a homodimer with two identical active sites for binding of its cofactor SAM. Among the TrmD inhibitors, N-(4-((octylamino)methyl)benzyl)-4-oxo-3,4-dihydrothieno[2,3-d]pyrimidine-5-carboxamide IV is the only known compound able to interact with both binding sites of SAM. It is a competitive inhibitor of TrmD with antibacterial activity against Gram-negative and Gram-positive bacteria and even Mycobacteria tuberculosis. The compound IV we used as the reference ligand for the assessment affinity of the novel derivatives of 6-(1H-benzimidazol-2-yl)-3,5-dimethyl-2-thio-2,3-dihydrothieno[2,3-d]pyrimidin-4(1H)-one. After redocking the binding energy of the reference ligand was −8.2 kcal/mol. The capacity of the docking algorithm for experimental modeling is presented in Figure 3a and in the

Table 1. The results of the target thieno[2,3-d]pyrimidines 3, 4a-l, 5 and the reference ligand docking studies to the active site of P. aeruginosa TrmD.

Ligand	Binding Energy Kcal/Mol	Hydrophobic Interaction	Hydrogen Interaction	Other Interaction
Reference ligand	−8.2	Tyr141, Ser93(2) #, Pro94 (4), Pro149(2), Ile138, Leu143, Gly 45, Gly146	Leu143, Gln95, Glu121, Gly139, Asp182	-
3	−7.9	Val142(3) *, Glu121, Gly122 *, Pro94(3)	Arg159, Leu143	-
4a	−9.3	Glu121(2), Gly122(2) *,Gly145, Gly146, Val142(3) *, Pro94(3), Leu143, Pro149	Tyt120, Thr177 *	Asp182 (Pi-Anion)
4b	−10.8	Val142(2) *, Gly145, Gly146, Ile138, Leu143(2), Tyr141, Pro94, Pro149	Arg159 *, Gly146, Tyr120, Ser144 *, Thr177(2) *	Asp159 * (Pi-Anion)
4c	−10.6	Glu121(2), Gly122(2) *, Gly145, Gly146, Pro94(3), Ile138, Leu143(2), Tyr141, Val142 *(2), Pro149	Gln95, Leu92 *, Tyr91 *	Asp159 * (Pi-Cation)
4d	−10.9	Gly145, Gly146, Leu92 * Ile138, Pro149(2), Leu143(3), Ile138, Leu228 *, Pro94(3), Val142 *, Pro149	Leu180*, Leu143	-
4e	−10.6	Val142(2) *, Gly179, Leu180 *, Ser144, Gly145(2), Gly146, Pro94(3), Pro149, Leu228	Leu180*, Leu143, Thr177 *	Leu92 *, Gly145 *, Ser93, (Halogen Fluorine)
4f	−10.0	Val142 *, Gly145(2), Gly146, Leu228 *, Pro94(3), Leu143, Pro149	Leu180*, Leu143, Leu92 *	Asp182
4g	−9.9	Val142(2) *, Gly145(2), Gly146, Leu228 *, Pro94(3), Leu143, Pro149	Leu180*, Leu143, Leu92 *	-
4h	−9.8	SER93, Pro94(4), Glu121, Gly122*, Val142(2) *,Leu143, Pro149	Gln95, Leu143, Gly139 *, Trp136	Arg159(2) *
4i	−10.4	Val142(2) *, Gly145(2), Gly146, Pro94(4), Leu143(2), Leu228 *, Pro149	Leu180 *, Leu143,	-
4j	−10.3	Val142(2) *, Gly145, Gly146, Pro94(4), Leu143(2), Leu228 *, Pro149	Leu180 *, Leu143,	Ser93 (Halogen Fluorine)
4k	−10.1	Val142(3) *, Gly179*, Leu180*, Gly145, Gly146, Leu228 *, Pro94(3), Pro149	Leu143, Glu121, Ser137*	Asp182 (Pi-Anion)
4l	−9.5	Val142(2) *, Gly145, Gly146, Pro94(2), Leu228 *	Leu143, Thr177 *	Asp182 (Pi-Anion)
5	−9.5	Glu121(2), Gly122(2) *, Gly145, Gly146, Val142(2) *, Pro94(3), Leu143, Pro149	Tyr120, Ser144 *, Thr177 *	Asp182 (Pi-Anion)

# The number of bonds is given in brackets. * The amino acids that do not interact with native ligand in the experiment.

. The validity of the docking study can be estimated by the value of RMSD, which characterizes the degree of reliable docking probability. For our research the RSMD value between the experimental and the reference conformation of the compound IV equals 1.952 Å; therefore, the study is reliable [38].

The reference interaction neatly reproduces the spatial arrangement of the ligand (yellow structure) comparatively to its natural position (blue structure) (Figure 3a). The ligand conformation is stabilized by the three loops of the active site, which are cover, bottom and wall loops [22,23]; all those crucial for ligand activity interactions (such as interaction with the tyrosine residues (Tyr141 ta 120)) were also well modelled.

The target thieno[2,3-d]pyrimidines showed much lesser values of the binding energies (−9.5 to −10.8 kcal/mol) comparatively to the native ligand (−8.2 kcal/mol). The only exception was the derivative 3, the scoring function value of which was −7.9 kcal/mol. The less favorable value of the scoring function in this case is explained by possible stabilization of the ligand conformation at the entrance to the hydrophobic pocket without the interaction with the amino acids of the SAM active site cavity. The visualization of the arrangements of the 4a-l molecules demonstrates their similarity to the native ligand (Figure 3); the character and the number of hydrophobic interactions allow for stabilization of the durable conformation in the active site of the enzyme (Table 1).

More detailed analysis of the arrangements of the ligands 4a-l shows the possibility of their longitudinal and deep immersion into the hydrophobic pocket with the ability to block the SAM methionine binding fragment, which includes interaction with the residues of glutamate (Gln95) and glycine (Gly 118, 145, 146) (Table 1, Figure 3b,c). The possibility of all the important hydrophobic interactions with the amino acids of the cover loop (proline (Pro94), the bottom loop (leucine (Leu143), tyrosine (Tyr143), isoleucine (Ile138)) and the wall loop (tyrosine (Tyr120) and glycine (Gly121)) was predicted. For all of the ligands, the ability of thieno[2,3-d]pyrimidine core structure to engage in hydrophobic interactions with the isopropyl substituent of valine (Val142), which according to the experimental results does not contribute into attachment of the ligand, although it was visualized in close proximity to the amino acids of the active site, proline (Pro94) in particular.

According to the docking studies results for all the thienopyrimidines 4 and 5 the high affinity level to the inhibitor binding site of TrmD isolated from P. aeruginosa was determined. The best affinity was found for the compound 4d with an iso-propyl substituent at the arylacetamide fragment (Figure 3b,c).

3.2. Chemical Synthesis

To achieve the objective of constructing of novel derivatives combining thieno[2,3-d]pyrimidine and benzimidazole fragments, the synthesis of the starting 3,5-dimethyl-4-oxo-2-thioxo-1H-thieno[2,3-d]pyrimidine-6-carboxylic acid 2 by hydrolysis of the previously reported and readily available ethyl ester 1 (Scheme 1) [34] was carried out. In particular, the high solubility of the starting ester 1 in alkaline water media allows for its hydrolysis at slight heating (50–60 °C) during a 10 hour period. These were found to be the optimal reaction conditions because the rise in the reaction temperature or the increase of alkali concentration produces more admixtures. The attempts to increase the solubility of the starting ester by addition of organic solvents such as ethanol or 1,4-dioxane decrease the yield of the acid 2 due to the problems with the product 3 precipitation.

The further synthesis of compound 3 combining thieno[2,3-d]pyrimidine and benzimidazole fragments was carried out via interaction of 5-methyl-4-oxo-2-thioxo-1,2,3,4-tetrahydrothieno[2,3-d]pyrimidine-6-carboxylic acid 2 imidazolide with o-phenylediamine in the way similarly to that reported previously [39]. In this case, the high solubility of the intermediate imidazolide of the acid 2 in such a highly-boiling solvent suitable for peptide synthesis as DMF allows for acylation and heterocyclization as a one pot procedure. It is a clear advantage that formation of benzimidazole ring takes place without any additional catalysts needed. The isolation of the product 3 is also an advantageous stage as it requires only dilution of the reaction mixture with water and further filtration of the crystalline product.

In the ¹H NMR spectrum of the compound 3 the signal of thiophene methyl group at 2.82 ppm and the signal of methyl group at position 3 of thieno[2,3-d]pyrimidine at 3.62 ppm are observed as singlets. The benzimidazole part of the molecule produces two multiplets at 7.19 and 7.57 ppm. The signal of NH proton of benzimidazole ring is observed at 12.62 ppm, while the signal of NHC=S is not observed because of the deuterium exchange.

Acetamide and benzyl fragments were introduced into the hybrid molecule 3 by alkylation of the sulfur atom at position 2 of thieno[2,3-d]pyrimidine system. The reaction was carried out in DMF using trimethylamine as a catalyst. The compound 3 is rather poorly soluble in DMF and therefore its alkylation requires relatively high temperature and prolonged time. The reaction is possible due to the good solubility of the products 4 and 5 in hot DMF.

The structure of the obtained compounds 4a-l and 5 was assigned using the data of ¹H and ¹³C NMR as well as LC-MS. If compared with the starting compound 3 the signals of methyl substituents of thienopyrimidine ring in ¹H NMR spectra of the derivatives 4a-l and 5 are observed in the region 2.85–2.89 ppm while the signal of NCH₃ is shifted and, for compounds 4, it is observed in the region 3.45–3.55 ppm. In the spectrum of the compound 5, the signal of methylene protons is observed at 4.53 ppm, although for the compounds 4a-l bearing acetamide substituents these signals are in the region 4.21–4.34 ppm. The acetamide NH signals are observed in the region 9.31–10.73 ppm; it should be mentioned that their position significantly depends on the type of amide substituent.

In the ¹³C NMR spectra of the compounds 4a-l and 5 the signals of CH₃ groups 14.7–15.4 (thiophene-CH₃) ta 30.4–30.6 ppm (NCH₃), which is almost similar to the positions of the signals for the same groups for the molecule of 3 14.4 ta 33.0 ppm respectively. For most of the compounds 4, the signal of the CH₂ Carbon atom is observed in the region 37.6–37.9 ppm; this signal slightly changes its position only for the derivatives 4c (2-ethtylphenyl amide) at 36.9 ppm, for 4l (2-aminothiazolyl amide) at 36.3 ppm and 4i (5-chloro-2-methylphenmyl amide) at 37.0 ppm (probably due to either ortho-substitution or heterocycle), while compound 5 shows this signal at 36.3 ppm. It should be also mentioned that the spectra of compounds 4 and 5 are lacking the signal in the 174–175 ppm region, which is typical for C=S Carbon and is present in the spectra of the compounds 2 and 3.

3.3. Antimicrobial Activity

According to the results of antimicrobial activity screening via agar diffusion test, all the studied compounds have shown antimicrobial and antifungal activity with the most pronounced influence on Gram-positive bacteria, i.e., S. aureus ATCC 25923 and B. subtilis ATCC 6633. It is worth mentioning that the studied tienopyrimidines have shown moderate activity in relation to the Gram-negative bacteria, but they were equal to the reference drug Streptomycine in relation to P. aeruginosa ATCC 27853 inhibition. The latter has been chosen as the reference drug for the experiment as a well-known and widely studied representative of aminoglycoside antibiotics with a broad spectrum of antibacterial activity, which is useful for experimental and clinical purposes [40,41,42]. Moreover, the aminoglycoside antibiotics were used as the reference drugs in the study of antibacterial activity spectrum for the selective inhibitors of TrmD [23], because among the TrmD inhibitors for now, there are not any approved and well-studied drugs with the confirmed mechanism of action on the market.

According to the results of antimicrobial activity screening (

Table 2. Screening data for antimicrobial activity of thieno[2,3-d]pyrimidine derivatives 3, 4a-l, 5.

Compounds *	Average Diameter (mm) of Growth Inhibition Zone, Number of Test Repetitions n = 3
	Gram-Positive Bacteria		Gram-Negative Bacteria			Fungus
	S. aureus ATCC 25923	B. subtilis ATCC 6633	E. coli ATCC 25922	P. vulgaris ATCC 4636	P. aeruginosa ATCC 27853	C. albicans ATCC 653/885
3	25, 25, 25	25, 26, 25	22, 21, 21	20, 21, 20	22, 21, 21	22, 21, 21
4a	23, 23, 23	27, 27, 26	21, 21, 21	21, 20, 20	21, 21, 21	22, 21, 21
4b	20, 21, 20	26, 26, 26	20, 21, 21	18, 18, 18	19, 20, 20	21, 21, 21
4c	22, 21, 21	27, 26, 26	20, 20, 20	19, 18, 18	21, 21, 21	22, 22, 22
4d	25, 26, 25	28, 28, 28	23, 24, 24	20, 21, 20	22, 21, 22	20, 21, 21
4e	25, 25, 25	26, 25, 25	23, 21, 22	19, 19, 19	22, 21, 21	22, 21, 21
4f	24, 24, 24	26, 25, 25	22, 22, 22	20, 19, 19	22, 21, 21	20, 21, 21
4g	22, 23, 23	26, 26, 26	23, 23, 23	20, 20, 20	20, 21, 21	22, 22, 22
4h	25, 26, 25	25, 26, 26	23, 24, 24	20, 20, 20	21, 21, 21	20, 20, 20
4i	23, 23, 23	25, 25, 25	22, 20, 21	21, 19, 20	21, 21, 21	22, 23, 22
4j	23, 23, 23	25, 26, 26	22, 21, 21	21, 19, 20	20, 20, 20	23, 23, 23
4k	22, 22, 22	27, 27, 27	20, 21, 20	20, 19, 20	21, 20, 20	21, 21, 21
4l	20, 21, 20	23, 24., 23	20, 19, 19	18, 18, 19	20, 21, 21	21, 21, 21
5	22, 23, 23	26, 26, 26	22, 22, 22	20, 20, 20	20, 21, 20	21, 21, 21
Streptomycin	26, 25, 25	27, 28, 27	25, 25, 25	22, 22, 22	22, 21, 21	– **

* The concentration of the compounds and the comparison drug streptomycin 100 µg/mL. ** Lack of antifungal activity.

), the most active compound 4d with iso-propyl substituent at the aromatic amide ring was more active than the reference drug against Gram-positive bacteria and showed similar to its activity for Gram-negative strains; it also inhibited the growth of the C. albicans strain.

In addition, the results of the antimicrobial activity study for the compound 3 (the activity of which was on a similar level with the other alkylated 4a-l derivatives) assumes the pivotal role of 6-(benzimidazol-2-yl)-3,5-dimethyl-2-thioxo-thieno[2,3-d]pyrimidin-4-one structure in the realization of the antimicrobial activity.

As the resistance of microorganisms to many antibiotics (Streptomycin among them) develops [43,44], the obtained results of antimicrobial activity screening and prediction of affinity to the binding site of selective inhibitors of TrmD for the novel benzimidazole-thienopyrimidines shows that further studies of them as antibacterial agents can be considered promising.

4. Conclusions

The successful application of the hybrid pharmacophore approach allowed us to obtain the novel antimicrobial agents among the hybrids of thieno[2,3-d]pyrimidin-4-ones with benzimidazole fragment at position 6. According to the docking studies results obtained for the benzimidazole-thienopyrimidines, they have a high affinity to the binding site of inhibitors of TrmD; this enzyme plays a crucial role in survival of most Gram-positive and Gram-negative bacteria, including P. aeruginosa (which is highly resistant to many known antibiotics). The optimal synthetic scheme for the preparation of 6-(1H-benzimidazol-2-yl)-3,5-dimethyl-2-thiothieno[2,3-d]pyrimidin-4-one with benzyl or the series of acetamide substituents attached to the Sulfur atom at position 2 of thienopyrimidine was developed. The antimicrobial activity screening results for the obtained compounds revealed their high level of growth inhibitory activity against Gram-positive bacteria (S. aureus and B. subtilis) and their moderate activity against Gram-negative bacterial strains with the activity to P. aeruginosa at the same level as that of the reference antibiotic. 2-{[6-(1H-Benzimidazol-2-yl)-3,5-dimethyl-4-oxo-3,4-dihydrothieno[2,3-d]pyrimidin-2-yl]thio}-N-(4-iso-propylphenyl)acetamide showed the highest in vitro antimicrobial activity among the tested compounds of the series; the same molecule has the highest affinity level to the active site of TrmD inhibitors isolated from P. Aeruginosa, according to the docking results. The obtained results can form the theoretical background for evaluation of the rationality of the further in vitro studies of the mechanism of antibacterial action of differently substituted derivatives of thieno[2,3-d]pyrimidine.