Synthesis and <i>In Vitro</i> Antimicrobial Evaluation of New 1,3,4-Oxadiazoles Bearing 5-Chloro-2-methoxyphenyl Moiety

Prasanna Kumar, Basavapatna N.; Mohana, Kikkeri N.; Mallesha, Lingappa; Harish, Kikkeri P.

doi:https://doi.org/10.1155/2013/725673

International Journal of Medicinal Chemistry

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Research Article | Open Access

Volume 2013 | Article ID 725673 | https://doi.org/10.1155/2013/725673

Synthesis and In Vitro Antimicrobial Evaluation of New 1,3,4-Oxadiazoles Bearing 5-Chloro-2-methoxyphenyl Moiety

Basavapatna N. Prasanna Kumar,¹Kikkeri N. Mohana,¹Lingappa Mallesha,²and Kikkeri P. Harish¹

Academic Editor: Jochen Lehmann

Received29 Dec 2012

Revised25 Feb 2013

Accepted13 Mar 2013

Published31 Mar 2013

Abstract

A series of new 1,3,4-oxadiazole derivatives, 4(a–h), containing 5-chloro-2-methoxy benzohydrazide moiety were synthesized by the reaction of 5-chloro-2-methoxybenzoate with different aromatic carboxylic acids. These newly synthesized compounds were characterized by FT-IR, ¹H NMR, mass spectra, and also by elemental analysis. All the newly synthesized compounds were screened for their antibacterial and antifungal activities. Antimicrobial studies revealed that compounds 4c, 4f, and 4g showed significant activity against tested strains.

1. Introduction

Resistance to number of antimicrobial agents among a variety of clinically significant bacteria is becoming increasingly important. There are various problems arising with the use of antimicrobials such as local tissue irritation, interference with wound healing process, hypersensitivity reactions, system toxicity, narrow antimicrobial spectrum, and emergency of resistance [1]. So, the increasing clinical importance of drug resistant microbial pathogens has additional urgency in microbiological and antifungal research. A wide variety of heterocyclic systems have been explored for developing pharmaceutically important molecules. Among them the derivatives of oxadiazoles have been playing an important role in the medicinal chemistry [2]. The 1,3,4-oxadiazole derivatives have been found to exhibit diverse biological activities such as antimicrobial [3, 4], anti HIV [5], antitubercular [6], antimalarial [7], anti-inflammatory [8, 9], anticonvulsant [10], and antitumor [11]. The 2,5-disubstituted-1,3,4-oxadiazole derivatives are known for various pharmacological activities such as antibacterial [12], antihypertensive [13], anticonvulsant [14], and antiproliferative [15]. The choice of 1,3,4-oxadiazole is due to its multiapplicability in the field of medicine. In the present study, some new 1,3,4-oxadiazoles 4(a–h) have been synthesized and characterized by different spectral studies. All the new compounds were screened for their antibacterial and antifungal studies.

2. Results and Discussion

2.1. Chemistry

The novel 1,3,4-oxadiazoles 4(a–h) were synthesized according to Scheme 1. Formation of 1,3,4-oxadiazole derivatives, 4(a–h), was confirmed by recording their elemental analyses, FT-IR, ¹H NMR, and mass spectra. The absorptions around 3050 cm⁻¹ in synthesized compounds confirm the aromatic C–H stretching vibrations and the appearance of a medium to strong absorption bands above 1600 cm⁻¹ due to a stretching vibration of the azomethine (C=N) bond formation in synthesized compound. The ¹H NMR spectra of 4c showed that singlet in the region of δ, 3.99–3.90, is due to the three protons of the methoxy groups. The mass spectra of 4c showed molecular ion peak at 317.0 which is in agreement with the molecular formula, C₁₆H₁₃ClN₂O₃. The elemental analyses data showed good agreement between the experimentally determined values and the theoretically calculated values within ±0.4%. The chemical structures and physical data of all the synthesized compounds are tabulated in Table 1.

2.2. In Vitro Antimicrobial Activity

The antibacterial activity of compounds 4(a–h) was evaluated and compared with bacteriomycin and gentamycin as standard drug (Table 2). All the tested compounds showed antibacterial activity against four pathogenic bacterial strains. Among the series, 4(a–h), compound 4c exhibited an elevated antibacterial activity against tested bacterial strains. Compounds 4f and 4g showed good antibacterial activity against all the tested organisms. Compounds 4h, 4b, 4a, 4d, and 4e showed moderate inhibitory activity.

The in vitro antifungal activity of the synthesized compounds 4(a–h) was studied against Fusarium oxysporum. The results were compared with the standard drug nystatin as in Table 2. Compounds 4c, 4f, and 4g showed good antifungal activity, when compared with other compounds in the series against F. oxysporum. Compounds 4h, 4b, 4a, 4d, and 4e were found to be moderately active against tested fungal strain.

In the present study, different electron withdrawing and electron donating groups attached to oxadaizole ring as substituents were linke to benzene ring. The close survey of antimicrobial efficacy indicated that the inhibition values of all the compounds exhibited a varied range of antibacterial and antifungal activities against all the tested microbial strains. The electron donating methoxy group in 4c showed good antimicrobial activity against tested microbial strains. The methoxy group and electron withdrawing fluorine atom in 4f and 4g produce enhanced antimicrobial activity. Compounds 4a, 4b, 4d, 4e and 4h exhibited moderate activity when compared 4c, 4f and 4g. The above studies reveal that the nature of the linkage (substituent on aromatic ring) influences the antimicrobial activity. Among the compounds, 4(a–h) showed antimicrobial activity in the order of 4c > 4f > 4g > 4h > 4b > 4a > 4d > 4e against tested bacterial and fungal strains.

3. Conclusion

In conclusion, series of new 1,3,4-oxadiazoles, 4(a–h), were synthesized in good yield and were characterized by different spectral studies and their antimicrobial activity has been evaluated. Compounds 4c, 4f, and 4g produced significant changes in activity against tested microbial strain. Therefore, this work presents a potent, wide-spectrum antimicrobial activity of the compounds. The nature of functional linkage and substituents (electron withdrawing and electron donating groups) on benzene ring is crucial for antimicrobial activities.

4. Experimental

4.1. Chemistry

Melting range was determined by Veego Melting Point VMP-III apparatus. Elemental analyses were recorded on VarioMICRO superuser V1.3.2 Elementar. The FT-IR spectra were recorded using KBr discs on FT-IR Jasco 4100 infrared spectrophotometer. ¹H NMR spectra were recorded on Bruker DRX-500 spectrometer at 400 MHz using CDCl₃ as solvent and TMS as an internal standard. Mass spectral data were obtained by LC/MSD Trap XCT. All solvents and reagents were purchased from Sigma-Aldrich Chemicals Pvt. Ltd.

4.1.1. Synthesis of Ethyl 5-Chloro-2-methoxybenzoate (2)

5-Chloro-2-methoxybenzoic acid (1) was converted into ethyl 5-chloro-2-methoxybenzoate (2) by the esterification reaction as per the reported procedure[16, 17]. The mixture of 5-chloro-2-methoxybenzoic acid (1, 0.01 mmol) was taken in ethanol (10 mL), and thionyl chloride (0.015 mmol) was added slowly and cooled to 5–10°C. Then the reaction mass was heated to reflux for 2 hr. The reaction mass was concentrated through rotavapor under reduced pressure. The residue was dissolved in dichloromethane and washed with water. The organic layer was concentrated under reduced pressure to get the product. Yield: 76%; mp 97–99°C.

4.1.2. Synthesis of 5-Chloro-2-methoxybenzohydrazide (3)

Compound 2 was converted into 5-chloro-2-methoxybenzohydrazide (3), by reacting with hydrazine hydrate in ethanol medium as per the reported procedure [18, 19]. To a mixture of ethyl 5-chloro-2-methoxybenzoate (2, 0.01 mmol) and ethanol (10 mL) at 0–5°C, hydrazine hydrate (0.02 mmol) was added. The reaction mass was heated to reflux for 6 hr. The reaction completion was monitored by TLC. The reaction mixture was concentrated to half volume. The solid obtained was filtered and washed with ethanol. The obtained solid was dried to get the pure product. Yield: 74%; mp 144–146°C.

4.1.3. General Procedure for the Synthesis of 1,3,4-Oxadiazole Derivatives 4(a–h)

An equimolar mixture of acid hydrazide (3, 0.2 mmol) with different aromatic carboxylic acids (0.0011 mmol) was refluxed with phosphorous oxychloride (5 volume with respect to the weight of compound 3). The mixture was refluxed at 100°C for 4 hr. The completion of the reaction was confirmed by the thin layer chromatography (TLC). After completion, the reaction mass was cooled to room temperature and quenched with ice cold water and stirred for 1 hr. The solid obtained was filtered and washed with water. Then recrystallised with ethanol and dried to get the pure product.

Synthesis of 2-(5-Chloro-2-methoxyphenyl)-5-(4-fluorophenyl)-1,3,4-oxadiazole (4a). White solid. FT-IR (KBr, cm⁻¹): 3070 (Ar C–H), 1615 (C=N), 1589 (C=C), 1076 (C–O stretch of oxadiazole ring). ¹H-NMR (400 MHz, CDCl₃): δ 8.09 (d, 2H), 7.98 (s, 1H), 7.47 (d, 2H), 7.01 (d, 2H), 4.01 (s, 3H). MS (ESI) : 304 (M⁺). Elemental analysis found (calculated) for C₁₅H₁₀ClFN₂O₂ (%): C, 59.22 (59.13); H, 3.40 (3.31); N, 9.02 (9.19).

Synthesis of 2-(5-Chloro-2-methoxyphenyl)-5-(4-nitrophenyl)-1,3,4-oxadiazole (4b). Yellow solid. FT-IR (KBr, cm⁻¹): 3060 (Ar C–H), 1655 (C=N), 1576 (C=C), 1054 (C–O stretch of oxadiazole ring). ¹H-NMR (400 MHz, CDCl₃): δ 8.43 (d, 2H), 8.36 (d, 2H), 8.04 (s, 1H), 7.54–7.05 (d, 2H), 4.02 (s, 3H). MS (ESI) : 331 (M⁺). Elemental analysis found (calculated) for C₁₅H₁₀ClN₃O₄ (%): C, 54.22 (54.31); H, 3.02 (3.04); N, 12.70 (12.67).

Synthesis of 2-(5-Chloro-2-methoxyphenyl)-5-(4-methoxyphenyl)-1,3,4-oxadiazole (4c). White solid. FT-IR (KBr, cm⁻¹): 3070 (Ar C–H), 1675 (C=N), 1576 (C=C), 1054 (C–O stretch of oxadiazole ring). ¹H-NMR (400 MHz, CDCl₃): δ 8.09 (d, 2H), 7.99 (s, 1H), 7.47 (d, 2H), 7.01–7.04 (d, 2H), 3.99 (s, 3H), 3.9 (s, 3H). MS (ESI) : 316 (M⁺). Elemental analysis found (calculated) for C₁₆H₁₃ClN₂O₃ (%): C, 60.50 (60.67); H, 4.20 (4.14); N, 8.66 (8.84).

Synthesis of 2-(5-Chloro-2-methoxyphenyl)-5-(4-chlorophenyl)-1,3,4-oxadiazole (4d). White solid. FT-IR (KBr, cm⁻¹): 3070 (Ar C–H), 1655 (C=N), 1580 (C=C), 1070 (C–O stretch of oxadiazole ring). ¹H-NMR (400 MHz, CDCl₃): δ 8.19 (d, 2H), 7.85 (s, 1H), 7.58 (d, 2H), 7.25–7.22 (d, 2H), 4.0 (s, 3H). MS (ESI) : 321 (M⁺). Elemental analysis found (calculated) for C₁₅H₁₀Cl₂N₂O₂ (%): C, 56.15 (56.10); H, 3.05 (3.14); N, 8.80 (8.72).

Synthesis of 2-(5-Chloro-2-methoxyphenyl)-5-(4-bromophenyl)-1,3,4-oxadiazole (4e). White solid. FT-IR (KBr, cm⁻¹): 3050 (Ar C–H), 1650 (C=N), 1570 (C=C), 1040 (C–O stretch of oxadiazole ring). ¹H-NMR (400 MHz, CDCl₃): δ 8.01 (d, 2H), 7.88 (s, 1H), 7.56 (d, 2H), 7.29–7.27 (d, 2H), 3.95 (s, 3H). MS (ESI) : 365 (M⁺). Elemental analysis found (calculated) for C₁₅H₁₀BrClN₂O₂ (%): C, 48.20 (49.28); H, 2.66 (2.76); N, 7.60 (7.66).

Synthesis of 2-(5-Chloro-2-methoxyphenyl)-5-(2-fluoro-3-methoxyphenyl)-1,3,4-oxadiazole (4f). Off-white solid. FT-IR (KBr, cm⁻¹): 3070 (Ar C–H), 1670 (C=N), 1570 (C=C), 1060 (C–O stretch of oxadiazole ring). ¹H-NMR (400 MHz, CDCl₃): δ 7.89 (s, 1H), 7.80 (s, 1H), 7.43 (d, 2H), 7.29 (d, 1H), 7.17 (m, 1H), 3.90 (s, 3H), 3.88 (s, 3H). MS (ESI) : 334 (M⁺). Elemental analysis found (calculated) for C₁₆H₁₂ClFN₂O₃ (%): C, 57.20 (57.41); H, 3.40 (3.61); N, 8.40 (8.37).

Synthesis of 2-(5-Chloro-2-methoxyphenyl)-5-(2-fluoro-5-methoxyphenyl)-1,3,4-oxadiazole (4g). Off white solid. FT-IR (KBr, cm⁻¹): 3060 (Ar C–H), 1665 (C=N), 1550 (C=C), 1050 (C–O stretch of oxadiazole ring). ¹H-NMR (400 MHz, CDCl₃): δ 7.94 (s, 1H), 7.80 (d, 2H), 7.43 (d, 2H), 7.07 (s, 1H), 4.0 (s, 3H), 3.95 (s, 3H). MS (ESI) : 334 (M⁺). Elemental analysis found (calculated) for C₁₆H₁₂ClFN₂O₃ (%): C, 57.30 (57.41); H, 3.52 (3.61); N, 8.40 (8.37).

Synthesis of 2-(5-Chloro-2-methoxyphenyl)-5-(2,6-difluorophenyl)-1,3,4-oxadiazole (4h). White solid. FT-IR (KBr, cm⁻¹): 3050 (Ar C–H), 1675 (C=N), 1585 (C=C), 1070 (C–O stretch of oxadiazole ring). ¹H-NMR (400 MHz, CDCl₃): δ 8.05 (s, 1H), 7.80 (d, 2H), 7.43 (d, 2H), 7.20 (m, 1H), 3.9 (s, 3H). MS (ESI) : 322 (M⁺). Elemental analysis found (calculated) for C₁₅H₉ClF₂N₂O₂ (%): C, 55.70 (55.83); H, 2.72 (2.81); N, 8.50 (8.68).

4.2. Antibacterial Activity

Antibacterial activity of the synthesized compounds was determined against Gram-positive bacteria (Bacillus subtilis MTCC 121 and Staphylococcus aureus MTCC 7443) and Gram-negative bacteria (Xanthomonas campestris MTCC 7908 and Escherichia coli MTCC 7410) in DMF by disc diffusion method on nutrient agar medium [20]. The sterile medium (nutrient agar medium, 15 mL) in each Petri plate was uniformly smeared with cultures of Gram-positive and Gram-negative bacteria. Sterile discs of 10 mm diameter (HiMedia) were placed in the Petri plates, to which 50 µL (1 mg/mL: i.e., 50 µg/disc) of the different synthesized compounds was added. The treatments also included 50 µL of DMF as negative, bacteriomycin and gentamycin as positive control for comparison. For each treatment, three replicates were maintained. The plates were incubated at 37 ± 2°C for 24 h and the zone of inhibition was determined.

4.3. Antifungal Activity

The synthesized compounds were screened for their antifungal activity against Fusarium oxysporum MTCC 2480 in DMF by poisoned food technique [21]. Potato dextrose agar (PDA) medium was prepared and about 15 mL of PDA was poured into each Petri plate and allowed to solidify. Five mm disc of seven-day old culture of the test fungi was placed at the center of the Petri plates and incubated at 26°C for 7 days. After incubation, the percentage inhibition was measured and three replicates were maintained for each treatment. Nystatin was used as standard. All the synthesized compounds were tested (at the dosage of 500 µL of the novel compounds/Petri plate, where concentration was 0.1 mg/mL) by poisoned food technique.

Acknowledgments

The authors would like to thank Dr. S. Satish, Department of Microbiology, University of Mysore, India, for carrying out antimicrobial studies. One of the authors (B. N. Prasanna Kumar) is grateful to Syngene International Private Limited, Bangalore, India, for giving an opportunity to continue the higher education.

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Copyright © 2013 Basavapatna N. Prasanna Kumar et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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