Table of Contents
Organic Chemistry International
Volume 2014 (2014), Article ID 748257, 5 pages
http://dx.doi.org/10.1155/2014/748257
Research Article

Synthesis and Antimicrobial Activities of N-(Heteroaryl-substituted)-p-toluenesulphonamides

Department of Pure and Industrial Chemistry, University of Nigeria, Nsukka, Enugu, Nigeria

Received 23 December 2013; Accepted 13 February 2014; Published 15 April 2014

Academic Editor: Ralph Nicholas Salvatore

Copyright © 2014 Ozoh Chinwe Francisca 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.

Abstract

A new class of N-(heteroaryl-substituted)-p-toluenesulphonamides has been synthesized exhibiting antibacterial and antifungal properties. The condensation reaction of p-toluenesulphonyl chloride 1 with appropriate substituted amino pyridines 2a–g in acetone furnished N-(heteroaryl-substituted)-p-toluenesulphonamides 3a–g. These derivatives were characterized by IR, 1H-, and 13C-NMR spectroscopy and were screened in vitro against gram-positive bacteria, gram-negative bacteria, and fungi organisms using agar-diffusion method. Results indicated improved biological activities over reference drugs such as Tetracycline (TCN) and Fluconazole (FLU).

1. Introduction

Sulphonamides are known to represent a class of medicinally important compounds which are extensively used as antimicrobial, antimalarial, and anticancer agents and inhibitors of carbonic anhydrase among others [1, 2]. Before the discovery of antibiotics in the 1940s, sulphonamides were the first efficient compounds used to treat microbial infections [3]. Sulphonamides are the amides of sulphonic acid which contain the basic group –SO2NH. They have been used against most gram-positive and many gram-negative organisms, fungi, and certain protozoa [4]. Sulphonamides are used in veterinary medicines to treat infections in livestock, also used in medicinal chemistry as potential therapeutic agents for depression, sleep disorder, pains, and hypertension among others [57]. Clinical sulphonamides have been used for the treatment of uncomplicated urinary tract infections [8]. Interest in the pharmacological activities of sulphonamide prompted the synthesis of scaffolds of sulphonamides and their derivatives. The discovery of sulphonamides started in the early 1930s, when Gerhard Domagk [9] discovered one of the dyes, Prontosil. Prontosil’s discovery ushered in the era of antibacterial and had a profound impact on pharmaceutical research, drug laws, and medical history. Prontosil is known as prodrug [10] which was reduced to sulphanilamide. The potency of these clinically useful drugs in treatment of microbial infections and other activities encouraged the development of some more potent and significant compounds.

In spite of recent advances in the development of sulphonamides as drugs, the synthesis and biological evaluation of N-heteroaryl derivatives of p-toluenesulphonamides remain largely unknown. Hence these led us to the synthesis of such new categories of p-toluenesulphonamides for evaluation of the antimicrobial activities.

2. Results and Discussion

2.1. Chemistry (Synthesis)

In this present investigation, a series of N-heteroaryl substituted sulphonamides 3a–g was prepared by condensation reaction of p-toluenesulphonyl chloride 1 and amino pyridine 2a–g in dry pyridine and acetone at room temperature for 24 hours. The structure of the derivatives was confirmed by IR, 1H-NMR, and 13C-NMR as described in the experimental section. The compound 3a was synthesized as white needle-like crystals with the melting point of 205°C-206°C. The IR spectrum revealed the presence of –NH group (3236 cm−1), aromatic C-H (3042 cm−1), and sulphonyl group (1133 cm−1) in the molecule. In 1H-NMR, the peaks at δ8.01 are assigned to NH-proton, δ7.76 is assigned to C7-proton, δ7.70 and δ6.86 (m, 8H) are due to aromatic protons, δ7.33 is assigned to C8-proton, δ7.14 is assigned to C9-proton, and δ2.32 is due to C10, aliphatic hydrogen. In 13C-NMR, peaks at δ153.57–δ114.10 are due to aromatic carbons () and δ21.49 is due to aliphatic carbon (CH3). The spectrum agrees with the assigned structure. On the basis of similar spectral characterization, the structures of the synthesized derivatives 3b–g were identified.

3. Antimicrobial Screening

The results of in vitro antibacterial and antifungal activities of the synthesized compounds against gram-positive bacteria, gram-negative bacteria, and fungi organisms using diffusion method are presented in Tables 2 and 3. The screening of the synthesized compounds showed inactive against gram-negative bacteria organisms. Some of the compounds, 3b, 3c, 3e, and 3g, showed good gram-positive antibacterial activity and compounds 3c–e showed moderate to little antifungal activity. Compound 3e is the most active against both antibacterial and antifungal activities (Table 1) (Scheme 1).

tab1
Table 1: Reactions of substituted amino pyridines with p-toluene sulphonyl chloride.
tab2
Table 2: Inhibition zone diameter (IZD in mm) at 2 mg/mL.
tab3
Table 3: Minimium inhibitory concentrations (MICs in mg/mL).
748257.sch.001
Scheme 1

4. Conclusion

The synthesis of N-(heteroaryl-substituted)-p-toluenesulphonamides has been achieved successfully. The assigned structures were supported by spectra analysis. The sulphonamides have good antimicrobial properties against some of the tested organisms.

4.1. Materials and Methods

The melting points were determined with Fischer John’s melting point apparatus and are uncorrected. IR spectra were recorded on 8400s Fourier transform infrared (FTIR) spectrophotometer and are reported in wave number (cm−1). IR analysis was done at National Research Institute for Chemical Technology (NARICT), Zaria, Kaduna State. 1H and 13C-NMR were determined using Jeol 400 MHz at Strathclyde University, Scotland. Chemical shifts are reported in δ scale. Tests for biological activities were carried in the Laboratories of the Faculty of Pharmacy Sciences, University of Nigeria, Nsukka. All reagents were of technical grade.

4.2. Synthesis

Compounds 3a–g were synthesized by the condensation reaction of compound 1 with different substituted amino pyridines 2a–g in the presence of acetone and dry pyridine.

4.3. Antimicrobial Screening

The antimicrobial properties of the sulphonamides were investigated in form of the general sensitivity testing and minimum inhibitory concentration (MIC) with respect to freshly cultured targeted organisms. The eight organisms used in this present study are gram-positive bacteria (Bacillus subtilis, Bacillus cereus, and Staphylococcus aureus), gram-negative bacteria (Klebsiella pneumonia, Pseudomonas aeruginosa, and Escherichia coli), and fungal organisms (Candida albicans and Aspergillus niger). The microorganisms were clinical isolates from Shanahan General Hospital Nsukka, and the S. aureus is of MRSA species. For each biological activity test, three experiments are performed and the average zone of inhibition is reported.

4.3.1. Sensitivity Test of Compounds

Agar-diffusion technique method as described by Okorie [11] was used to determine the antimicrobial (antibacterial and antifungal) activities of the synthesized compounds. Sensitivity test agar plates were seeded with 0.1 mL of 24-hour culture of each microorganism into its corresponding petri dish previously labeled using the molten agar already prepared. The plates were allowed to set after which cups were made in each sector previously drawn on the backside of the bottom-plate using marker. Using the pipette (sterile), each cup was filled with six drops of their corresponding antimicrobial agent (in appropriate solvent at a concentration of 2 mg/mL). The plates were finally incubated at 37°C for 24 hours for bacteria and 48 hours for fungi. It should be noted that the solubilizing solvent used was dimethyl formamide (DMF). Mueller Hinton agar was prepared in 20 mL portions kept molten at 45°C. The zone of inhibition (clearance) produced after 24 hours on incubation at 37°C was measured. The procedure was repeated for Tetracycline and Fluconazole drugs (standard).

4.3.2. Minimum Inhibitory Concentrations (MICs) Test of Compounds 3a–g

The MIC was determined by further dilution of the test sample found to be sensitive against a particular organism. Serial dilutions of the sulphonamides were prepared from 2 mg/mL solution of the sulphonamides to give 2.0–0.125 mg/mL. After dilution, the test solutions were added into their corresponding cups previously made in the molten agar starting from the lowest concentration (0.125–1.0 mg/mL). This was followed by incubation at the appropriate incubation temperature and time. The resultant inhibition zones of diameter (IZD) were measured and the value was subtracted from the diameter of the borer (8 mm) to give the inhibition zone diameter (IZD). The MIC was also determined using graph of IZD2 against logarithm of concentration for each plate containing a specific compound and a microorganism. The antilogarithm of the intercept on -axis gives the MIC.

5. Experimental Section

5.1. General Procedure for the Synthesis of the N-Heteroaryl-substituted-p-toluenesulphonamides (3a–g)

The preparation of 4-methyl-N-(pyridin-2-yl) benzenesulphonamide 3a described below is a typical procedure for the preparation of these new p-toluenesulphonamides. 2-Amino pyridine (0.94 g, 10.0 mmol) was dissolved in a mixture of anhydrous acetone (20 mL) and dry pyridine (2 mL). p-Toluenesulphonyl chloride (1.91 g, 10.0 mmol) was then added later. The reaction mixture was warmed to room temperature and allowed to stir. The reaction was left for 24 hours and 1.50 g of 4-methyl-N-(pyridin-2-yl) benzenesulphonamide 3a (product) was filtered off using suction filtration. On diluting the filtrate with distilled water, a further crop (1.25 g) was obtained. The total product was recrystallized from dimethylformamide (DMF). 4-Methyl-N-(5-nitropyridin-2-yl) benzenesulphonamide 3c and 4-methyl-N-(3-nitropyridin-2-yl) benzenesulphonamide 3d were recrystallized from methanol solvent and N-(3-hydroxypyridin-2-yl)-4-methyl benzenesulphonamide 3e was recrystallized from ethanol solvent. The products were dried in hot air oven under 50°C for 6 hours.

5.1.1. 4-Methyl-N-(pyridin-2-yl) Benzenesulphonamide (3a)

On condensation reaction of p-toluenesulphonyl chloride 1 and 2-amino pyridine 2a in dry pyridine and acetone at room temperature for 24 hours, 4-methyl-N-(pyridin-2-yl) benzenesulphonamide 3a was obtained as a white needle-like solid with a melting point of 205°C-206°C. IR (KBr) Ѵmax: 3236 cm−1 (N-H stret.), 3042 cm−1 (Ar C-H), 1133 cm−1 (SO2-functional group). 1H-NMR [DMSO-d6] δ: 8.01 (d;  Hz, 1H; NH), 7.76 (d; .14 Hz, 2H, Ar-H), 7.70 (m; 4H, phenyl-H), 7.33 (d;  Hz, 2H, Ar-H), 7.14 (d;  Hz, 1H, Ar-H), 6.86 (m; 4H, pyridyl-H), 2.32 (s; 3H, CH3-phenyl). 13C-NMR [DMSO-d6] δ: 153.57–144.10 (, Ar-C), 21.49 (, aliphatic carbon).

5.1.2. 4-Methyl-N-(4-methylpyridin-2-yl) Benzenesulphonamide (3b)

On condensation reaction of p-toluenesulphonyl chloride 1 and 2-amino-4-methyl pyridine 2b in acetone and dry pyridine at room temperature for 24 hours, 4-methyl-N-(4-methylpyridin-2-yl) benzenesulphonamide 3b was obtained as a white solid with a melting point of 217°C-218°C. IR (KBr) Ѵmax: 3229 cm−1 (N-H stret.), 3037 cm−1 (Ar C-H), 1141 cm−1 (SO2-functional group). 1H-NMR [DMSO-d6] δ: 7.81 (d; .87 Hz, 2H, Ar-H), 7.74 (d;  Hz, 2H, Ar-H), 7.31 (d;  Hz, 1H, Ar-H), 6.99 (s; 1H, Ar-H), 6.67 (d;  Hz, 1H, Ar-H), 3.39 (s; 1H, NH), 2.32 (s; 3H, CH3-pyridyl), 2.22 (s; 3H, CH3-phenyl).

5.1.3. 4-Methyl-N-(5–nitropyridin-2-yl) Benznesulphonamide (3c)

On condensation reaction of p-toluenesulphonyl chloride 1 and 2-amino-5-nitropyridine 2c in acetone and dry pyridine at room temperature for 24 hours, 4-methyl-N-(5-nitropyridin-2-yl) benzenesulphonamide 3c was obtained as a milky needle-like solid with a melting point of 183°C-184°C. IR (KBr) Ѵmax: 3259 cm−1 (N-H stret.), 3096 cm−1 (Ar C-H), 1518–1349 cm−1 (NO2 stret.), 1198 cm−1 (SO2-functional group). 1H-NMR [DMSO-d6] δ: 8.92 (d;  Hz, 1H, Ar-H), 8.26 (dd;  Hz,  Hz, 1H, Ar-H), 7.50 (d; J = 8.05 Hz, 2H, Ar-H), 7.13 (d;  Hz, 2H, Ar-H), 6.71 (d;  Hz, 1H, Ar-H), 5.30 (s, b; 1H; NH), 2.29 (s; 3H, CH3-phenyl).

5.1.4. 4-Methyl-N-(3-nitropyridin-2-yl) Benzenesulphonamide (3d)

On condensation reaction of p-toluenesulphonyl chloride 1 and 2-amino-3-nitropyridine 2d in acetone and dry pyridine at room temperature for 24 hours, 4-methyl-N-(3-nitropyridin-2-yl) benzenesulphonamide 3d was obtained as a yellowish needle-like solid with a melting point of 153°C-154°C. IR (KBr) Ѵmax: 3454 cm−1–3268 cm−1(N-H stret.), 3110 cm−1 (Ar C-H), 1333 cm−1 (NO2 stret.), 1162 cm−1 (SO2-functional group). 1H-NMR [DMSO-d6] δ: 8.41 (m, 7H, heteroaryl-H), 8.00 (s, b, 1H, NH), 7.51 (dt,  Hz,  Hz,  Hz, 2H, Ar-H), 7.13 (d,  Hz, 1H, Ar-H), 6.77 (dd,  Hz,  Hz, 1H, Ar-H), 2.29 (s, 3H, CH3-phenyl).

5.1.5. N-(3-Hydroxypyridin-2-yl)-4-methyl Benzenesulphonamide (3e)

On condensation reaction of p-toluenesulphonyl chloride 1 and 2-amino-3-hydroxyl pyridine 2e in acetone/DMF (in mol ratio of 2 : 1) and dry pyridine at room temperature for 24 hours, N-(3-hydroxypyridin-2-yl)-4-methyl benzenesulphonamide 3e was obtained as a pale white needle-like solid with a melting point of 105°C-106°C. IR (KBr)Ѵmax: 3474 cm−1 (OH stret.), 3287 cm−1(N-H stret.), 3138 cm−1 (Ar C-H), 1164 cm−1 (SO2-functional group). 1H-NMR [DMSO-d6]δ: 7.82 (m; 7H, heteroaryl-H), 7.43 (d;  Hz, 1H, NH), 7.29 (dd;  Hz,  Hz, 1H, Ar-H), 6.50 (dd,  Hz,  Hz, 1H, Ar-H), 5.97 (s; 1H, OH), 2.40 (s; 3H, CH3-phenyl). 13C-NMR [DMSO-d6]δ: 153.10–112.40 (C1–C9, Ar-C), 21.74 (C10, aliphatic carbon).

5.1.6. 4-Methyl-N-(6-methylpyridin-2-yl) Benzenesulphonamide (3f)

On condensation reaction of p-toluenesulphonyl chloride 1 and 2-amino-6-methyl pyridine 2f in acetone and dry pyridine at room temperature for 24 hours, 4-methyl-N-(6-methylpyridin-2-yl) benzenesulphonamide 3f was obtained as a yellowish liquid (oil). IR (KBr)Ѵmax: 3311 cm−1 (N-H stret.), 3161 cm−1 (Ar C-H), 1154 cm−1 (SO2-functional group). 1H-NMR [DMSO-d6]δ: 8.09 (m; 7H, heteroaryl-H), 8.0 (s,b; 1H, NH), 7.74 (t;  Hz, 1H, Ar-H), 7.52 (d; 8.02 Hz, 1H, Ar-H), 7.25 (d; .84 Hz, 1H, Ar-H), 7.12 (d;  Hz, 1H, Ar-H), 6.83 (d;  Hz, 1H, Ar-H), 6.62 (d; .03 Hz, 1H, Ar-H), 2.35 (s; 3H, CH3-pyridyl), 2.24 (s; 3H, CH3-phenyl).

5.2. 4-Methyl-N-(pyridin-4-yl) Benzenesulphonamide (3g)

On condensation reaction of p-toluenesulphonyl chloride 1 and 4-amino pyridine 2g in acetone and dry pyridine at room temperature for 24 hours, 4-methyl-N-(pyridin-4-yl) benzenesulphonamide 3g was obtained as a white solid with a melting point of 213°C-214°C. IR (KBr) Ѵmax: 3227 cm−1 (N-H stret.), 3061 cm−1 (Ar C-H), 1164 cm−1 (SO2-functional group). 1H-NMR [DMSO-d6]δ: 8.53 (d; .15 Hz, 2H, Ar-H), 7.87 (d;  Hz, Ar-H), 7.50 (d;  Hz, 2H, Ar-H), 7.44 (m; 4H, heteroaromatic-H), 7.12 (d;  Hz, NH), 2.28 (s; 3H, CH3-phenyl).

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

References

  1. A. Korolkovas, Essentials of Medicinal Chemistry, John Wiley & Sons, New York, NY, USA, 1988.
  2. M. Remko and C.-W. Von Der Lieth, “Theoretical study of gas-phase acidity, pKa, lipophilicity, and solubility of some biologically active sulfonamides,” Bioorganic and Medicinal Chemistry, vol. 12, no. 20, pp. 5395–5403, 2004. View at Publisher · View at Google Scholar · View at Scopus
  3. A. Ullman, “Pasteur-Koch: distinctive ways of thinking about infectious diseases,” American Society for Microbiology, vol. 2, no. 8, pp. 383–387, 2007. View at Google Scholar
  4. J. N. Delgado and W. H. Remers, in Textbook of Organic Medicinal and Pharmaceutical Chemistry, p. 223, Willian and Wilkins, Philadelphia, Pa, USA, 1998.
  5. N. S. El-Sayed, E. R. El-Bendary, S. M. El-Ashry, and M. M. El-Kerdawy, “Synthesis and antitumor activity of new sulfonamide derivatives of thiadiazolo[3,2-a]pyrimidines,” European Journal of Medicinal Chemistry, vol. 46, no. 9, pp. 3714–3720, 2011. View at Publisher · View at Google Scholar · View at Scopus
  6. M. J. Garcia-Galan, M. S. Diaz-Cruz, and D. Bercelo, “Identification and determination of metabolites and degradation products of sulfonamide antibiotics,” TrAC Trends in Analytical Chemistry, vol. 27, no. 11, pp. 1008–1022, 2008. View at Publisher · View at Google Scholar
  7. B. Pouw, M. Nour, and R. R. Matsumoto, “Effects of AMPA/kainate glutamate receptor antagonists on cocaine-induced convulsions and lethality in mice,” European Journal of Pharmacology, vol. 386, no. 2-3, pp. 181–186, 1999. View at Publisher · View at Google Scholar
  8. A. K. Gaded, C. S. Mahajanshetti, S. Nimbalkar, and A. Raichurkar, “Synthesis and antibacterial activity of some 5-guanylhydrazone/thiocyanato-6-arylimidazo[2,1-b]-1,3,4-thiadiazole-2-sulfonamide derivatives,” European Journal of Medicinal Chemistry, vol. 35, no. 9, pp. 853–857, 2000. View at Publisher · View at Google Scholar
  9. L. James, “Gerhard Domagk Discovery of Prontosil on Testing Variety of Azo Dyes,” Reed Business Information, vol. 107, no. 1465, pp. 53–54, 1985. View at Google Scholar
  10. J. Trefouel, J. M. Trefouel, F. Nitti, and D. Bovet, “Activities of p-aminophenylsulphonamides and Infection Streptococci experiment,” Comptes Rendus des Seances de la Societe de Biologie, no. 120, p. 756, 1935. View at Google Scholar
  11. V. C. Okorie, Pharmaceutical Microbiology: Principles of the Pharmaceutical Applications of Antimicrobial Agents, El 'Demak Publishers, Enugu, Nigeria, 2005.