Table of Contents
International Journal of Carbohydrate Chemistry
Volume 2013, Article ID 320892, 5 pages
Research Article

Synthesis and Antimicrobial Activity of Carbohydrate Based Schiff Bases: Importance of Sugar Moiety

1Campus São Gabriel, Universidade Federal do Pampa, Avenida Antônio Trilha 1847, 97300-000 São Gabriel, RS, Brazil
2Campus Cerro Largo, Universidade Federal da Fronteira Sul, R. Major Antônio Cardoso 590, 97900-000 Cerro Largo, RS, Brazil
3Ciências da Saúde, Centro Universitário Franciscano, Rua dos Andradas 1614-Centro, -97010-032 Santa Maria, RS, Brazil
4Departamento de Química, Universidade Federal de Santa Maria, 97105-900 Santa Maria, RS, Brazil

Received 25 September 2013; Revised 12 November 2013; Accepted 14 November 2013

Academic Editor: J. F. Vliegenthart

Copyright © 2013 Helmoz R. Appelt 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.


A series of D-glucosamine derivatives were synthesized (2–4) and evaluated for their antimicrobial activity. Some of the compounds investigated have shown significant antimicrobial activity against Gram-positive and Gram-negative bacterial strains as well as a few fungal strains. The results suggest that the presence of sugar moiety is necessary to biological activity.

1. Introduction

Carbohydrates are the most abundant class of biomolecules, making up 75% of the biomass on Earth [1]. Carbohydrates are used to store energy but also perform other important functions to life [2].

Recently, carbohydrates and their derivatives have emerged as an important tool for stereoselective synthesis and as a chiral pool for the design of chiral ligands. They are used as chiral building blocks, precursors for drug synthesis and chiral catalysts in asymmetric catalysis [38].

Despite the importance of carbohydrates in biological events, the pace of development of carbohydrate based therapeutics has been relatively slow. This is mainly due to practical synthetic and analytical difficulty. Recent advances in the field, however, have demonstrated that many of these problems can be circumvented and evidence the importance of carbohydrates as bioactive substances, with regard to antibacterial, antiviral, antineoplastic, antiprotozoal, and antifungal activity among others, related recently in literature [9, 10].

On the other hand, imines or Schiff bases are easily generated by condensation of carbonyl groups and primary amines. In carbohydrate chemistry, a large number of imines have been reported, both by reaction of sugar aldehydes with amines and by reaction of aminosugars with aldehydes [1116]. Schiff bases and their metal complexes have several applications as catalysts in oxygenations, hydrolysis, and other reactions, antimicrobial and antiviral activities, among other applications [1517]. Preparation of 4-anisaldehyde and cinnamaldehyde glucosamine imines and their acetylated derivatives is usually used as a convenient strategy for selective protecting of the amino group of the aminosugar [11, 18, 19].

Recent studies have shown that Schiff bases derived from glucosamine have antifungal [20] and antibacterial activity [21]. On the other hand, aldehydes present in essential oils may also have action against different microorganisms. Cinnamaldehyde, the main component of Cinnamomum zeylanicum essential oil, specie of Lauraceae family, has several activities such as antioxidant, antibacterial, and antifungal [22].

This field has been explored by our research group and in this context, we report herein the synthesis of Schiff bases 36 derived from D-glucosamine 1 or 2-aminoethanol 2 and aldehydes in order to evaluate the importance of the presence of carbohydrate moiety for antimicrobial activity.

2. Results and Discussion

The synthesis of compounds 36 is shown in Schemes 1 and 2. The Schiff bases are readily prepared from D-glucosamine and 2-aminoethanol in one or two straightforward steps.

Scheme 1: (i) 1N NaOH, anisaldehyde; (ii) 1N NaOH, cinnamaldehyde; (iii) acetic anhydride, pyridine.
Scheme 2: (i) Anisaldehyde; (ii) cinnamaldehyde; (iii) acetic anhydride, pyridine.

D-Glucosamine was first converted into the imines 3a or 3b by treatment with different aldehydes. The resultant imines were acetylated with acetic anhydride and pyridine to the tetra-acetylated glucosamine derivatives 4a and 4b (Scheme 1).

To evaluate the importance of the presence of D-glucosamine moiety for antimicrobial activity of the compounds obtained, we plan the synthesis of compounds with similar physical chemistry characteristics, but with simpler structures, without the aminosugar unit. The imines 5 and 6 were prepared, by 2-aminoethanol and the respective aldehyde condensation reaction, followed by acetylation of the hydroxyl group of aminoethanol (Scheme 2). The first step was carried out without the use of solvents, and the expected products were obtained quantitatively. Then we proceeded to the acetylation of 2-(arylidene-amino)ethanol 5 hydroxy group with acetic anhydride and pyridine. The yields of these reactions were very good (90 and 93%). All products were characterized by 1H and 13C NMR.

The compounds 36 were evaluated for their efficacy as antibacterial and antifungal agents by disk diffusion method [2325] against various microbial strains. The in vitro antibacterial activity of the synthesized compounds 36 was studied against the following bacterial strains of Gram-positive organisms: Staphylococcus aureus (ATCC 25923), Listeria monocytogenes (ATCC 7644), and Enterococcus faecalis (ATCC 29212), and Gram-negative organisms: Escherichia coli (ATCC 25922), Pseudomonas aeruginosa (ATCC 27853), Salmonella choleraesuis (ATCC 10708), and Klebsiella pneumoniae (ATCC 700603), by agar disk diffusion method. We also tested the antifungal activity of compounds 36 in Candida albicans (ATCC 90028). Imipenem and Sulfazotrin were used as standard drugs.

From the results shown in Table 1 it can be interpreted that the compounds 3-4 (entries 1–4)are active against Gram-positive, Gram-negative bacteria and fungi strains. It was observed that antibacterial activity of the compounds tested varied significantly depending on the bacteria studied, the highest sensitivity being against Gram-positive compared to Gram-negative strains. Another factor considered was the chemical structure of compounds. Comparing the compounds 3a and 3b in the deacetylated form with the acetylated compounds 4a and 4b it was verified that the compounds that showed greater antimicrobial activity were the deacetylated compounds. The compound with more activity was 3b, prepared by reaction of D-glucosamine with cinnamaldehyde. Apparently the presence of glucosamine moiety contributes significantly to antimicrobial activity. For compounds 5a, 5b, 6a, and 6b, derived from 2-aminoethanol, it was observed that these compounds showed no activity against the microorganisms evaluated (Table 1, entries 5–8). A possible explanation for the observed difference in activity between glucosamine derived Schiff bases and those derived from ethanol amine may stem from different rates of hydrolysis for the respective Schiff base.

Table 1: Antibacterial activity of compounds 3–6, by disk diffusion methoda.

When the results are compared with standard drugs Imipenem and Sulfazotrin (Table 1, entries 9-10), it was observed that only compound 3b presented the best activity against Listeria monocytogenes and Pseudomonas aeruginosa.

From the results of disk diffusion method, substances that presented inhibition zone (3a, 3b, 4a, and 4b) were studied to determine the minimal inhibitory concentration (MIC) by microdilution method. The results are shown in Table 2. These results confirm that the deacetylated compounds 3a and 3b are more active than acetylated derivatives. We also observed the greatest activity against Gram-positive bacteria compared to Gram-negative strains.

Table 2: Antibacterial activity of compounds 3-4, by microdilution methoda.

The last decade has witnessed a mass downsizing in pharmaceutical antibiotic drug discovery initiatives. Gram-positive infections are associated with high rates of morbidity and mortality. Indeed, reports estimate that in 2005 the Gram-positive cocci methicillin resistant S. aureus caused more US deaths than HIV/AIDS [26, 27].

The growing spread of multidrug-resistant bacteria, as exemplified by carbapenem-resistant Enterobacteriaceae carrying metallo-β-lactamase-1 (NDM-1, an enzyme that confers resistance to a broad range of β-lactam antibiotics), highlights the urgency to find new antimicrobial compounds [28].

When taken together, our results illustrate for the first time that antimicrobial effect of D-glucosamine derivatives is due to the presence of sugar moiety and these compounds can serve as a basis for the development of new antimicrobial agent, but more studies are necessary.

3. Material and Methods

All reagents and solvents used were of analytical grade. The 1H NMR (200 e 400 MHz) and 13C NMR (50 e 100 MHz) spectra were obtained from Bruker DPX200 and DPX400 spectrometers using tetramethylsilane as internal standard.

3.1. Synthesis of 2-Arylidene-2-deoxy-β-D-glucopyranose 3 (General Procedure)

In a 25 mL round-bottomed flask were added D-glucosamine hydrochloride 1 (1.00 g; 4.6 mmol), 1N NaOH (4.6 mL) and the correspondent aldehyde (4.6 mmol). The solution was stirred until a solid appeared (10–30 min) and then was maintained in the refrigerator for a few hours. The solid was filtered and washed with cold water and a solution of methanol/ether (1 : 1). The product was obtained pure enough.

3.2. 2-(4-Methoxybenzylidene)-2-deoxy-β-D-glucopyranose 3a

Yield: 80%. 1H NMR (DMSO-d6, 200 MHz): δ = 8.12 (s, 1H); 7.68 (d, = 8.5 Hz, 2H); 6.98 (d, 8.5 Hz, 2H); 5.01 (d, = 2.5 Hz, 1H); 3.78 (s, 3H); 3.6–3.1 (m, 10H). 13C NMR (DMSO-d6, 50 MHz): δ = 161.28, 161.03, 131.81, 129.61, 129.05, 114.50, 113.87, 95.61, 78.09, 76.80, 74.54, 70.34, 67.01, 61.22, 55.26.

3.3. 2-((E)-3-Phenylallylidene)-2-deoxy-β-D-glucopyranose 3b

Yield: 74%. 1H NMR (DMSO-d6, 200 MHz): δ = 7.94 (d, = 8.6 Hz, 1H); 7.63–7.56 (m, 2H); 7.45–7.30 (m, 3H); 7.12 (d, = 16 Hz, 1H); 6.90 (dd, = 16.0, 8.6 Hz, 1H); 5.02–4.97 (m, 1H); 3.78–3.10 (m, 9H); 2.72 (dd, = 8.6, 8.2 Hz, 1H). 13C NMR (DMSO-d6, 50 MHz): δ = 163.86, 141.26, 135.88, 129.20, 129.02, 128.47, 127.33, 95.72, 78.43, 77.03, 74.71, 70.42, 67.19, 61.39.

3.4. Synthesis of 1,3,4,6-Tetra-O-acetyl-2-arylidene-2-deoxy-β-D-glucopyranose 4 (General Procedure)

In a 25 mL round-bottomed flask, in an ice bath, was prepared a solution of pyridine (6 mL) and acetic anhydride. And to this solution was added the imine 3 (3 mmol). The mixture was allowed to stir for 5 min at 0°C and then the reaction was stirred at room temperature for 24 h. After completion of the reaction, the reaction mixture was poured on cold water (10 mL) and then was maintained in the refrigerator for a few hours. The solid was filtered and washed with cold water to remove pyridine excess.

3.5. 1,3,4,6-Tetra-O-acetyl-2-(4-methoxybenzylidene)-2-deoxy-β-D-glucopyranose 4a

Yield: 69%. 1H NMR (CDCl3; 400 MHz): δ = 8.16 (s, 1H); 7.64 (d, = 8.7 Hz, 2H); 6.91 (d, = 8.7 Hz, 2H); 5.94 (d, = 8.2 Hz, 2H); 5.42 (t, = 9.6 Hz, 1H); 5.12 (t, = 9.6 Hz, 1H); 4.35 (dd, = 12.3, 4.7 Hz 1H); 4.14 (dd, = 12.3, 1.9 Hz 1H); 3.99–3.94 (m, 1H); 3.83 (s, 3H); 3.47–3.41 (m, 1H); 2.08 (s, 3H); 2.02 (s, 3H); 2.00 (s, 3H); 1.87 (s, 3H). 13C NMR (CDCl3, 100 MHz): δ = 170.38; 169.66; 169.27; 168.48; 164.11; 162.37; 130.14; 128.47; 114.10; 93.25; 73.38; 72.98; 72.87; 68.37; 61.97; 55.30; 20.56; 20.52; 20.47; 20.31.

3.6. 1,3,4,6-Tetra-O-acetyl-2-((E)-3-phenylallylidene)-2-deoxy-β-D-glucopyranose 4b

Yield: 65%. 1H NMR (CDCl3, 200 MHz): δ = 8.00 (d, = 8.4 Hz, 1H); 7.61–7.27 (m, 5H); 7.04 (d, = 16.0 Hz, 1H); 6.86 (dd, = 16.0, 8.4 Hz, 1H); 5.90 (d, = 8.3, 1H); 5.39 (t, = 9.6, 1H); 5.13 (t, = 9.6, 1H); 4.38 (dd, = 12.5, 4.4 Hz, 1H); 4.12 (dd, = 12.5, 2.0 Hz, 1H); 3.97 (ddd, = 9.6, 4.4, 2.0 Hz, 1H); 3.39 (dd, = 9.6, 8.3 Hz, 1H); 2.10 (s, 3H); 2.07 (s, 3H); 2.04 (s, 3H); 1.96 (s, 3H). 13C NMR (CDCl3, 50 MHz): δ = 170.63; 169.85; 169.51; 168.63; 166.74; 143.92; 135.07; 129.76; 128.90; 127.47; 127.28; 93.04; 73.18; 72.96; 72.73; 67.99; 61.77; 20.78; 20.72; 20.64; 20.52.

3.7. Synthesis of 2-(Arylidene-amino)ethanol 5 (General Procedure)

In a 25 mL round-bottomed flask were added 2-aminoethanol 2 (3.05 g; 50 mmol) and the correspondent aldehyde (50 mmol) under strong stirring. After a few seconds there was a strong liberation of heat, with water formation. The mixture was stirred for 15 min and then evaporated in vacuum to eliminate water and unreacted reagents. The product was used without purification.

3.8. (E)-2-((4-Methoxybenzylidene)amino)ethanol 5a

Yield: quant. 1H NMR (CDCl3; 400 MHz): δ = 9.16 (s, 1H); 7.61 (d, = 8.8 Hz, 2H); 6.88 (d, = 8,8 Hz, 2H); 3.87 (t, = 4,6 Hz, 2H); 3.81 (s, 3H); 3.67 (t, = 4,6 Hz, 2H); 3.46 (s, 1H). 13C NMR (CDCl3; 100 MHz): δ = 162.3; 161.7; 129.7; 128.8; 113.9; 63.1; 62.2; 55.2.

3.9. 2-((E)-((E)-3-Phenylallylidene)amino)ethanol 5b

Yield: quant. 1H NMR (DMSO-d6; 400 MHz): δ = 8.06 (d, = 4.3 Hz, 1H); 7.6–7.3 (m, 5H); 7.08 (d, = 8 Hz, 1H); 6.89 (dd, = 8.0, 4.3 Hz, 1H); 3.63 (t, = 3 Hz, 2H); 3.54 (t, = 3 Hz, 2H); 3.41 (s, 1H). 13C NMR (DMSO-d6; 100 MHz): δ = 163.0; 140.7; 135.5; 128.8; 128.6; 128.0; 126.9; 63.2; 60.7.

3.10. Synthesis of 2-(Arylidene-amino)ethyl Acetate 6 (General Procedure)

In a 25 mL round-bottomed flask, in an ice bath, was prepared a solution of pyridine (6 mL) and acetic anhydride. And to this solution was added the imine 5 (10 mmol). The mixture was allowed to stir for 5 min at 0°C and then the reaction was stirred at room temperature for 24 h. After completion of the reaction, the reaction mixture was treated with saturated aqueous ammonium chloride solution and the whole mixture was extracted 3 times with CH2Cl2 and the combined organic fractions were collected, dried over MgSO4, and filtered and the solvent was then removed in vacuum. The crude mixture was purified by column chromatography on silica gel eluting with hexane ethyl acetate (9 : 1) and then with ethyl acetate.

3.11. (E)-2-((4-Methoxybenzylidene)amino)ethyl Acetate 6a

Yield: 90%. 1H NMR (CDCl3; 200 MHz): δ = 7.36–7.25 (m, 3H); 6.95–6.85 (m, 2H); 4.17–3.90 (m, 4H); 3.83 (s, 3H); 1.84 (s, 3H). 13C NMR (CDCl3; 50 MHz): δ = 168.080, 160.346, 159.696, 130.241, 127.959, 114.157, 65.508, 64.716, 55.245, 22.731.

3.12. 2-((E)-((E)-3-Phenylallylidene)amino)ethyl Acetate 6b

Yield: 93%. 1H NMR (CDCl3; 200 MHz): δ = 7.50–7.20 (m, 7H); 6.71 (dd, = 15.6, 10.0 Hz, 1H); 4.24–3.48 (m, 4H); 2.08 (s, 3H). 13C NMR (CDCl3; 50 MHz): δ = 170.976, 167.772, 134.484, 132.266, 128.666, 128.406, 127.937, 126.835, 65.717, 64.834, 22.615.

4. Conclusion

In summary, we presented in this report a simple and efficient approach for the preparation of sugar derived Schiff bases. The synthesized D-glucosamine derivatives were shown to possess biological activity when evaluated for antimicrobial activity against Gram-positive and Gram-negative bacterial and fungi strains.

Conflict of Interests

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


The authors wish to thank FAPERGS, CAPES, and UNIFRA for financial support of their research.


  1. V. F. Ferreira, D. R. da Rocha, and F. De Carvalho Da Silva, “Potentiality and opportunity in chemistry of sucrose and other sugars,” Quimica Nova, vol. 32, no. 3, pp. 623–638, 2009. View at Google Scholar · View at Scopus
  2. R. V. Stick, Carbohydrates: The Sweet Molecules of Life, Academic Press, 2001.
  3. M. Diéguez, O. Pàmies, A. Ruiz, Y. Díaz, S. Castillón, and C. Claver, “Carbohydrate derivative ligands in asymmetric catalysis,” Coordination Chemistry Reviews, vol. 248, pp. 2165–2192, 2004. View at Publisher · View at Google Scholar
  4. M. Diéguez, O. Pàmies, and C. Claver, “Ligands derived from carbohydrates for asymmetric catalysis,” Chemical Reviews, vol. 104, no. 6, pp. 3189–3216, 2004. View at Publisher · View at Google Scholar
  5. S. Woodward, M. Diéguez, and O. Pàmies, “Use of sugar-based ligands in selective catalysis: recent developments,” Coordination Chemistry Reviews, vol. 254, pp. 2007–2030, 2010. View at Publisher · View at Google Scholar
  6. M. Diéguez, C. Claver, and O. Pàmies, “Recent progress in asymmetric catalysis using chiral carbohydrate-based ligands,” European Journal of Organic Chemistry, vol. 2007, no. 28, pp. 4621–4634, 2007. View at Publisher · View at Google Scholar
  7. M. M. K. Boysen, “Carbohydrates as synthetic tools in organic chemistry,” Chemistry, vol. 13, no. 31, pp. 8648–8659, 2007. View at Publisher · View at Google Scholar
  8. H. R. Appelt, J. B. Limberger, M. Weber et al., “Carbohydrates in asymmetric synthesis: enantioselective allylation of aldehydes,” Tetrahedron Letters, vol. 49, no. 33, pp. 4956–4957, 2008. View at Publisher · View at Google Scholar · View at Scopus
  9. C. M. Nogueira, B. R. Parmanhan, P. P. Farias, and A. G. Corrêa, “A importância crescente dos carboidratos em química medicinal,” Revista Virtual de Química, vol. 1, no. 2, p. 149, 2009. View at Google Scholar
  10. C.-H. Wong, Ed., Carbohydrate-Based Drug Discovery, Wiley-VCH, Weinheim, Germany, 2003.
  11. M. Bergmann and L. Zervas, “Synthesen mit glucosamin,” Berichte der Deutschen Chemischen Gesellschaft, vol. 64, no. 5, pp. 975–980, 1931. View at Google Scholar
  12. Z. E. Jolles and W. T. Morgan, “The isolation of small quantities of glucosamine and chondrosamine,” Biochemical Journal, vol. 34, no. 8-9, pp. 1183–1190, 1940. View at Google Scholar
  13. A. N. Bedekar, A. N. Naik, and A. C. Pise, “Schiff base derivatives of 2-amino-2-deoxy-1,3,4,6-tetra-O-acetyl-β-D-glucopyranose,” Asian Journal of Chemistry, vol. 21, no. 9, pp. 6661–6666, 2009. View at Google Scholar · View at Scopus
  14. E. M. S. Pérez, M. Ávalos, R. Babiano et al., “Schiff bases from d-glucosamine and aliphatic ketones,” Carbohydrate Research, vol. 345, pp. 23–32, 2010. View at Publisher · View at Google Scholar
  15. J. Costamagna, L. E. Lillo, B. Matsuhiro, M. D. Noseda, and M. Villagrán, “Ni(II) complexes with Schiff bases derived from amino sugars,” Carbohydrate Research, vol. 338, no. 15, pp. 1535–1542, 2003. View at Publisher · View at Google Scholar · View at Scopus
  16. J. Costamagna, N. P. Barroso, B. Matsuhiro, and M. Villagrán, “Copper(II) complexes with aminosugar derived Schiff bases as ligands,” Inorganica Chimica Acta, vol. 273, no. 1-2, pp. 191–195, 1998. View at Google Scholar · View at Scopus
  17. S. Kumar, D. N. Dhar, and P. N. Saxena, “Applications of metal complexes of Schiff bases—a review,” Journal of Scientific and Industrial Research, vol. 68, pp. 181–187, 2009. View at Google Scholar
  18. G. Chauvière, B. Bouteille, B. Enanga et al., “Synthesis and biological activity of nitro heterocycles analogous to megazol, a trypanocidal lead,” Journal of Medicinal Chemistry, vol. 46, pp. 427–440, 2003. View at Publisher · View at Google Scholar
  19. M. Ávalos, R. Babiano, P. Cintas et al., “Synthesis of sugar isocyanates and their application to the formation of ureido-linked disaccharides,” European Journal of Organic Chemistry, vol. 3, pp. 657–671, 2006. View at Google Scholar
  20. Y. Xue-Qiong, H. Jian, Y. Chang-Jiang, L. Fang, and L. Qiang, “Synthesis and antifungal activity of D-glucosamine Schiff base,” Chemical Reagents, vol. 32, no. 11, pp. 961–964, 2010. View at Google Scholar
  21. L. Shurong, J. Shuxing, X. Yang, and L. Pu, “Detection of antibacterial activity of some new Schiffbase derivative,” Journal of Zhengzhou University Medical Sciences, no. 4, pp. 787–789, 2008. View at Google Scholar
  22. H. B. Singh, M. Srivastava, A. B. Singh, and A. K. Srivastava, “Cinnamon bark oil, a potent fungitoxicant against fungi causing respiratory tract mycoses,” Allergy, vol. 50, no. 12, pp. 995–999, 1995. View at Google Scholar · View at Scopus
  23. E. Margery Linday, Practical Introduction to Microbiology, E & FN Spon, London, UK, 1962.
  24. C. Perez, M. Paul, and P. Bazerque, “An antibiotic assay by the agar well-diffusion method,” Acta Biologiae et Medicine Experimentalis, vol. 15, pp. 113–115, 1990. View at Google Scholar
  25. D. Kalemba and A. Kunicka, “Antibacterial and antifungal properties of essential oils,” Current Medicinal Chemistry, vol. 10, no. 10, pp. 813–829, 2003. View at Publisher · View at Google Scholar · View at Scopus
  26. E. A. Bancroft, “Antimicrobial resistance: it's not just for hospitals,” The Journal of the American Medical Association, vol. 298, no. 15, pp. 1803–1804, 2007. View at Publisher · View at Google Scholar · View at Scopus
  27. R. M. Klevens, M. A. Morrison, J. Nadle et al., “Invasive methicillin-resistant Staphylococcus aureus infections in the United States,” The Journal of the American Medical Association, vol. 298, no. 15, pp. 1763–1771, 2007. View at Publisher · View at Google Scholar · View at Scopus
  28. K. Bush, “Alarming β-lactamase-mediated resistance in multidrug-resistant Enterobacteriaceae,” Current Opinion in Microbiology, vol. 13, no. 5, pp. 558–564, 2010. View at Publisher · View at Google Scholar