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Journal of Chemistry
Volume 2013 (2013), Article ID 472657, 9 pages
Research Article

Clean Procedure and DFT Study for the Synthesis of 2-Amino-3-ethoxycarbonyl-4-(aryl)-4H-pyrano-[3,2-c]-chromene-5-ones Derivatives: A Novel Class of Potential Antimicrobial and Antioxidant Agents

1Borj Cedria Higher Institute of Sciences and Technology of Environment, Touristic road of Soliman, B.P. 95, 2050 Hammam-Lif, Tunisia
2College of Science and Arts at Ar-Rass, Qassim University, P.O. Box 53, Ar-Rass, Saudi Arabia

Received 11 April 2012; Accepted 21 June 2012

Academic Editor: Benjamin Mwashote

Copyright © 2013 R. Medyouni 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.


2-Amino-3-ethoxycarbonyl-4-(aryl)-4H-pyrano-[3,2-c]-chromene-5-ones 5 is synthesized by the two-component reaction of 4-hydroxycouamrin with ethyl-2-cyano-3-(aryl) acrylate 3. The structures of the obtained compounds are confirmed by analytical IR, 1H, and 13C-NMR spectra to elucidate the different positions of protons and carbons and as well as theoretic studies (DFT/B3LYP). All the newly synthesized compounds are screened for their antibacterial. Furthermore, these compounds showed antioxidant activities of different extents with respect to individual compounds as well as to the antioxidant methods. The compounds 5a–e were found to be the most active antioxidant in the series then Trolox, which makes the investigated complexes a promising new class of antibacterial activity compounds.

1. Introduction

Coumarin and its derivatives represent one of the most active classes of compound possessing a wide spectrum of biological activity [13]. Novobiocin and chlorobiocin are established antimicrobials containing a coumarin skeleton [4]. Many of these compounds have proved to be active as antibacterial [57], antifungal [8], anti-inflammatory [9], anticoagulant [10], anti-HIV [11] and antitumor [12]; In addition, these compounds are used as additives to food and cosmetics [13]. Coumarin derivatives are commonly used as optical whiteners, luminescence dyes [14], active media for lasers [15] and solar collectors [16].

Several natural or synthetic coumarins with various hydroxyl and other substituents are found to inhibit lipid peroxydation and to scavenge hydroxyl radicals and superoxide anions [17]. 4H-chromenes with amino and cyano groups are also the synthons of some special natural products.

In continuation of the search for such potent molecules and as a part of our ongoing research, we plan to synthesize the hybrid structure having the lipohophilic functionality on the pyran ring. The current work highlights the synthesis as well as the theoritical studies of the important coumarin scaffold. The title compound is synthesized by the reaction of 4-hydroxycoumarin and (E) ethyl-2-cyano-3-(aryl) acrylate 3 in the presence of piperidine as a base catalyst and at reflux of DMC. Condensation of 1 with arylaldehydes in the presence of piperidine at room temperature gives the corresponding (E) ethyl-2-cyano-3-(aryl) acrylate 3, Scheme 1

Scheme 1: Synthesis of ethyl-2-cyano-3-(aryl) acrylate 3.

TLC is used to monitor the progress of the reaction; the structures of products are characterized by 1HNMR along with 13CNMR; and FT-IR spectral techniques, and they are in agreement with the structure of (E) ethyl-2-cyano-3-(aryl) acrylate 3. The IR spectrum of compound 3a shows a band in the region of 1664.62 cm−1 which is the characteristic for C=O. It shows strong bands at 2372 cm−1, 1952 cm−1, 3146 cm−1 due to (CΞN); (C=C); (C–H)arom functions, respectively. The 1H NMR spectrum of the synthesized compound 3a exhibits a multiplet signal in the region δ 7.37–7.93 due to the aromatic protons. A singlet in the region δ 8.0 ppm is also observed due to the CHAr proton. The quartet in the region δ 4.30 ppm and the triplet in the region δ 1.35 ppm in compounds 3a are observed due to methyl and methylene protons of the ethyl groups. Treatment of intermediate 3 with 4-hydroxycoumarin in the presence of piperidine at reflux of dimethylcarbonate gives 5 in high yield (Scheme 2).

Scheme 2: Synthesis of 2-amino-3-ethoxycarbonyl-4-(aryl)-4H-pyrano-[3,2-c]-chromene-5-ones 5.

The FT-IR spectra of compounds 5e shows absorption bands at 1582–1586 cm−1 corresponded with C=O and C–O linkage and 3705 cm−1 is observed due to the –NH group. The 1H NMR spectra of 5e displays a signal at δ 6.76 ppm that is ascribable to the NH2 protons. A characteristic singlet proton signal at δ 2.49 ppm is assigned to the CHAr proton. In addition, the aromatic protons (both coumarinic and aryl) are observed between δ 6.91 and δ 7.92 ppm (see Section 4), and the expected triplet for methylic protons is observed at δ 1.26 ppm. The singlet at δ 3.03 ppm is assigned to the three protons of the methoxy group.

Indeed the 13C{1H} NMR spectrum of 3e in DMSO-d6, shows the presence of 23 carbon atoms, such as: C1, Cf, C8,  Ch, and Ci and Cg are, respectively, 167.6, 164.6, 61.4, 35.2, and 39.5. The signals between (92.0 and 163.4 ppm) correspond to the ethylenic and aromatic carbons.

The formation of the 2-amino-3-ethoxycarbonyl-4-(aryl)-4H-pyrano-[3,2-c]-chromene-5-ones 5 occur via two steps: 4-hydroxycoumarin attacks the ethylenic double bond of the compound 3. The nonisolated intermediate (i2) rearranges to give (i3), who is cyclized to give 2-amino-3-ethoxycarbonyl-4-(aryl) 4H-pyrano-[3,2-c]-chromene-5-ones 5 as shown in Scheme 3.

Scheme 3: Proposed mechanism for the synthesis of 2-amino-3-ethoxycarbonyl-4-(aryl)-4H-pyrano-[3,2-c]-chromene-5-ones 5.

To further confirm the structure of the product 5 a systematic theoretical treatment of these compounds is performed by using the DFT/B3LYP approach implemented in the Gaussian 09 series of programs [18]. The B3LYP hybrid functional has been used in describing potential energy surfaces (PES).

The geometries of compounds 5 are fully optimized using analytic gradients. The harmonic vibrational frequencies of the stationary points of the PES have been calculated at the same level of theory in order to identify the local minima as well as to estimate the corresponding zero-point vibrational energy (ZPE) [19, 20].

For each atom no pseudopotential is used. A Def2-SVP EMSL basis set exchange is employed for each atom [21]. Optimized geometry for 5c is depicted in Figure 1. Values of selected geometrical parameters are listed in Table 1.

Table 1: DFT/B3LYP optimized geometrical parametersa.
Figure 1: DFT/B3LYP optimized geometries of 5c.

The value of the dihedral angle (3-3′-5′-6′= 96.8°) shows that the aryl group is orthogonal to the plan of the tricyclic structure 5. The bond length in compound 5c is more elongated than its counterparts in 5b–d, this is caused by the steric hindrance of the two methyl groups in positions 2 and 5. Another important information concerning the nature of the groups present in the structure 5 can be obtained by calculating the vibrational frequencies of these compounds. Values and intensities of the harmonic wave numbers calculated with the DFT/B3LYP method, and the corresponding experimental values of the compound 5c are presented in Table 2.

Table 2: Theoretical and experimental vibrational frequencies (cm−1) and theoretical infrared intensities (km mol−1) of 5c.

The values of the theoretical IR frequencies are in agreement with the experimental values with a shift to larger frequency values less than 10%. This shift is due to the approximations used in the DFT/B3LYP method.

The NBO analysis allows the determination of the atomic natural charges reports the natural charges of the acid protons in compound 5c calculated at DFT/B3LYP level of theory. We find that the protons Ha and Ha′ carried by the nitrogen atom are the most acidic Table 3.

Table 3: NBO charges of the acidic protons of compound 5c calculated at the DFT/B3LYP level of theory.

2. Antibacterial and Antioxidant Studies

2.1. Free Radical Scavenging Activity Assay

The free radical scavenging activity of the new 2-amino-3-ethoxycarbonyl-4-(aryl)-4H-pyrano-[3,2-c]-chromene-5-ones 5 is tested by utilizing DPPH scavenging.

DPPH is a free radical and accepts one electron or one hydrogen radical to become a stable diamagnetic molecule [22]. The reduction capability of the DPPH radical is determined by the decrease in absorbance induced by 2-amino-3-ethoxycarbonyl-4-(aryl)-4Hpyrano-[3,2-c]-chromene-5-ones 5. Briefly, 1.5 mL ethanolic solution of the synthesized compounds (0.2 mM) is added to 1.5 mL (0.2 mM) solution of DPPH radical in ethanol (final concentration of DPPH and synthesized compounds is 0.1 mM). The mixture is shaken vigorously and left standing for 30 min. After this, the absorbance at 534 nm is determined, and the percentage of scavenging activity is calculated using the following formula: where : absorbance of 0.1 mM ethanolic solution of DPPH at 534 nm, : absorbance of 0.1 mM ethanolic solution of test compound at 534 nm, and : absorbance of ethanolic mixture of the drug and DPPH at 534 nm.

Trolox was used as reference compound. All tests and analyses are done on triplicate and average on three samples. The results are illustrated in Scheme 4.

Scheme 4: Scavenging effect on 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical of compounds 5.

Among the compounds from the 2-amino-3-ethoxycarbonyl-4-(aryl)-4H-pyrano-[3,2-c]-chromene-5-ones 5 series, 5b showed moderate antioxidant activity. The activity exhibited by the compound 5e is the highest. In addition, the experimental data shows that compound 5a scavenges free radicals better than Trolox. Thus, we can conclude that substituents on the aryl group do not influence significantly the antioxidant activity.

One parameter that has been introduced recently for the interpretation of the results from the DPPH method is the effective concentration or EC50 value (otherwise called the IC50 value), which is defined as the concentration of substrate that causes 50% loss of the DPPH activity (color) and corresponds to the endpoint of the titration. In all cases, any residual (yellow) color from the reduced form or any nonspecific absorbance from the sample should be considered in defining the “endpoint” of the titration, that is, the 50% point. Additionally, this IC50 parameter has also the drawback of that the higher the antioxidant activity, the lower is the value of EC50. The EC50 values exhibited by 2-amino-3-ethoxycarbonyl-4-(aryl)-4H-pyrano-[3,2-c]-chromene-5-ones 5 are summarized in Table 4.

Table 4: The EC50 values exhibited by 2-amino-3-ethoxycarbonyl-4-(aryl)-4H-pyrano-[3,2-c]-chromene-5-ones 5.

From inspection of Table 4, it is evident that compounds 5e are more active than Trolox.

2.2. ABTS Radical Cation Decolorization Assay

The potential of 2-amino-3-ethoxycarbonyl-4-(aryl)-4Hpyrano-[3,2-c]-chromene-5-ones 5 to scavenge free radicals was also assessed by checking their ability to quench ABTS+• depicts the concentration-dependent decolourization of ABTS+•.

ABTS radical-scavenging activity of 2-amino-3-ethoxycarbonyl-4-(aryl)-4H-pyrano-[3,2-c]chromene-5-ones 5 is determined according to Re et al. [23]. The ABTS+•. The cation radical is produced by the reaction between 5 mL of 14 mM ABTS solution and 5 mL of 4.9 mM potassium persulfate (K2S2O8) solution, stored in the dark at room temperature for 16 h. Before use, this solution is diluted with ethanol to get an absorbance of 0.700 ± 0.020 at 734 nm. In a final volume of 1 mL, the reaction mixture comprised 950 μL of ABTS ± solution and 50 μL of the 2-amino-3-ethoxycarbonyl-4-(aryl)-4H-pyrano-[3,2-c]-xchromene-5-ones 5 at various concentrations. The reaction mixture is homogenized and its absorbance is recorded at 734 nm. Ethanol blanks were run in each assay, and all measurements were done after at least 6 min. Similarly, the reaction mixture of standard group was obtained by mixing 950 ll of ABTS+• solution and 50 μL of Trolox. As for the antiradical activity, ABTS scavenging ability is expressed as EC50 (mu g/mL). The inhibition percentage of ABTS radical was calculated using the following formula: where is the absorbance of the control at 30 min, and is the absorbance of the Sample at 30 min. All samples are analyzed in triplicate.

As shown for DPPH scavenging, these data indicate the higher capacity of 2-amino-3-ethoxycarbonyl-4-(aryl)-4H-pyrano-[3,2-c]-chromene-5-ones 5 to quench ABTS+Y as compared to the synthetic antioxidant Trolox, Scheme 5.

Scheme 5: Scavenging ability on ABTS radical of compounds 5.

The variation in the percentage of inhibition (PI) is almost constant starting from a value of the concentration equal to 1.34 mM. In addition, the synthesized products of the type 5 have antioxidant activities better than Trolox. Indeed, the antioxidant capacity seems to be attenuated when the concentration increases in the medium. This can be explained by the existence of the peroxide sites which are susceptible for oxidizing when the concentration increases. We have just shown that the synthesized 2-amino-3-ethoxycarbonyl-4-(aryl)-4H-pyrano-[3,2-c]-chromene-5-ones 5 has a good antioxidant activity under weak concentration, but it proves to be necessary to determine the reaction time necessary to highlight the antioxidant effect to be able to use these derivatives in pharmacy.

The EC50 values exhibited by 2-amino-3-ethoxycarbonyl-4-(aryl)-4H-pyrano-[3,2-c]-chromene-5-ones 5 are summarized in Table 5. The 2-amino-3-ethoxycarbonyl-4-(aryl)-4H-pyrano-[3,2-c]-chromene-5-ones 5 are shown to be efficient antioxidants, showing higher free radical scavenging activity than Trolox.

Table 5: The EC50 values exhibited by 2-amino-3-ethoxycarbonyl-4-(aryl)-4H-pyrano-[3,2-c]-chromene-5-ones 5.

These compounds have a remarkable oxidizing capacity which explains their susceptibility to fix free radicals DPPH and ABTS•+.

2.3. Antibacterial Activity

The cup-plate method [23, 24] using Mueller-Hinton agar medium was employed to study the preliminary antibacterial activity of 3a–e against Staphylococcus aureus, Bacillus subtilis, Escherichia coli, and Pseudomonas aeruginosa. Preparation of base-layer medium, agar medium, and peptone water is done as per the standard procedure. Each test compound (10 mg/mL) is prepared by dissolving 50 mg in 5 mL of dimethylformamide, and is used for testing same cup-plate method using PDA medium is employed to study the preliminary antifungal activity of 3a–e against Candida albicans and A. niger. The PDA medium was purchased from HImedia Laboratories Ltd, Mumbai, India. Preparation of nutrient broth, sub-culture, base-layer medium and PDA medium was done as per the standard procedure. For each test compound, a 50 μg/cup was used for testing.

The cups of 9 mm diameter were made by scooping out medium with a sterilized cork borer in a petri dish which was streaked with organisms. The solutions of each compound were added separately in the cups, and petri dishes were subsequently inoculated. Ampicillin and Griesofulvin (6 μg/cup and 25 μg/cup, resp.) were used as standard reference drugs and dimethylformamide (DMF) used as control which did not show any inhibition. Zone of inhibition produced by each compound was measured in mm, and the results are presented in Table 6.

Table 6: Zone of inhibition produced by each compounds.

All the tested compounds have shown antibacterial activity to some extent. Among the tested compounds 3b and 3d, show very good activity against the tested organisms.

Compounds 3a and 3e are moderate antibacterial activity. All the compounds synthesized possess electron-releasing groups, on both the aromatic rings. Therefore from the results, it is evident that compounds having electron-releasing groups like methyl, hydroxyl, and methoxy may be responsible for antibacterial activity.

3. Conclusion

In conclusion, an efficient green-chemistry method for the synthesis of 2-amino-3-ethoxycarbonyl-4-(aryl)-4H-pyrano-[3,2-c]-chromene-5-ones 5 derivatives by condensation of 4-hydroxycoumarin and (E) ethyl-2-cyano-3-(aryl)acrylate 3 is successfully established. In this method, the potential active compounds containingchromene heteroaromatic rings can be synthesizedeasily by two one-step reactions. Compared to other methods [25], this newsmethod has the advantage of good yields, mild reaction conditions, easy workup, inexpensive reagents, and environmentally friendly procedure. All the newly synthesized compounds are screened for their antibacterial effect against Staphylococcus aureus, Bacillus subtilis, Escherichia coli, and Pseudomonas aeruginosa.

4. Experimental Section

4.1. General Procedures

Flash chromatography was carried out on 0.04–0.063 mm (Merck) silica gel, thin-layer chromatography was carried out on aluminium-backed silica plates by Merck, and plates were revealed using a UV 254 light. 1H-NMR (300 MHz) and 13C-NMR (75 MHz) spectra were recorded on a Varian VXR 300 instrument at 293° K in CDCl3 or DMSO-d6. Spectra were internally referenced to TMS. Peaks are reported in ppm downfield of TMS. Multiplicities are reported as singlet (s), doublet (d), triplet (t), and quartet (q), some combinations of these were made by DEPT editing of the spectra. The IR-spectra were recorded on a Philips Analytical PU 9800 spectrometer. The melting points of compounds were determined in open-glass capillaries in a paraffin bath and are uncorrected.

4.2. Materials

1,1-diphenyl-2-picrylhydrazyl (DPPH) were obtained from Sigma. All other chemicals were of analytical grade purity. The 4-hydroxycoumarin, aromatic aldehydes, and ethylcyanoacetate were purchased from Fluka, DMF, were purified, dried, and distillated over CaH2 prior to use.

4.2.1. Synthesis of (E) Ethyl-2-cyano-3-(aryl)acrylate 3

Arylaldehyde (0.0199 mol), ethylcyanoacetate (0,0175 mol) and piperidine (0,0175 mol) are mixed in round bottomed flask. The latter is stirrer at r.t for 2 h. The reaction mixture was filtred, and the residue washed with acetone.

(E) Ethyl-2-cyano-3-(4-phenyl)acrylate 3a. Yield: 80%; mp = 80°C (MeOH); IR spectrum, cm−1: 2372 (CΞN); 1952 (C=C); 3146 (C–H)arom; 1105 (C–O)ester; 1685 (C=O)ester; 1H NMR spectrum (CDCl3, 300 MHz): 1,35 (t, 3H, CH3); 4,30 (q, 2H, CH2); 7,37–7,93 (m, 5H, Harom); 8,00 (s, 1H, CH); 13CNMR (CDCl3, 75 MHz): spectrum: 14,1 (Cc); 62,7 (Cb); 102,6 (C2); 115,4 (Ca); 127,9–133,4 (Carom); 155,3 (C3); 163,0 (C1).

(E) Ethyl-2-cyano-3-(4-methoxy-phenyl)acrylate 3b. Yield: 84%; mp = 83°C (MeOH); IR spectrum, cm−1: 2378 (CΞN); 1970 (C=C); 3100 (C–H)arom; 1112 (C–O)arom; 1685 (C=O)ester; 1H NMR spectrum (CDCl3, 300 MHz): 1,29 (t, 3H, CH3); 3,78 (s, 3H, OCH3); 4,26 (q, 2H, CH2); 6,88–7,90 (m, 4H, Harom); 8,03 (s, 1H, CH); 13CNMR (CDCl3, 75 MHz): spectrum: 14,1 (Cc); 55,6 (OCH3); 62,3 (Cb); 99,4 (C2); 116,1 (Ca); 114,7–163,0 (Carom); 154,2 (C3); 163,9 (C1).

(E) Ethyl-2-cyano-3-(2,5-dimethylaminophenyl)acrylate 3c. Yield: 78%; mp = 48°C (MeOH); IR spectrum, cm−1: 2373 (CΞN); 1934 (C=C); 3036  (C–H)arom; 1182 (C–O)ester; 1681 (C=O)ester; 1H NMR spectrum (CDCl3, 300 MHz): 1,38 (t, 3H, CH3); 2,34 (s, 3H, CH3); 2,37 (s, 3H, CH3); 4,36 (q, 2H, CH2); 7,12–7,21 (m, 3H, Harom); 8,50 (s, 1H, CH); 13CNMR (CDCl3, 75 MHz): 14,1 (Cc); 19,2 (CH3); 20,8 (CH3); 62,6 (Cb); 104,0 (C2); 115,4 (Ca); 128,8–136,7 (Carom); 153,3 (C3); 162,5 (C1).

(E) Ethyl-2-cyano-3-(4-nitro-phenyl)acrylate 3d. Yield: 72%; mp = 158°C (MeOH); IR spectrum, cm−1: 2382 (CΞN); 1950 (C=C); 3088 (C–H)arom; 1100 (C–O)ester; 1723 (C=O)ester; 1H NMR spectrum (CDCl3, 300 MHz): 1,44 (t, 3H, CH3); 4,36 (q, 2H, CH2); 8,08–8,32 (m, 4H, Harom); 8,24 (s, 1H, CH); 13CNMR (CDCl3, 75 MHz): 13,1 (Cc); 62,3 (Cb); 106,5 (C2); 113,5 (Ca); 123,3–148,8 (Carom); 150,7 (C3); 160,4 (C1).

(E) Ethyl-2-cyano-3-(4-dimethylamino phenyl)acrylate 3e. Yield: 47%; mp = 123°C (MeOH); IR spectrum, cm−1: 2208 (CΞN); 1927 (C=C); 1165 (C–O)ester; 1701 (C=O)ester; 1H NMR spectrum (CDCl3, 300 MHz): 1,26 (t, 3H, CH3); 3,05 (s, 6H, 2CH3); 4,22 (q, 2H, CH2); (m, 4H, Harom); 8,07 (s, 1H, CH). 13CNMR (CDCl3, 75 MHz): 14,1 (Cc); 39,5 (CH3); 39,8 (CH3); 61,4 (Cb) 104,0 (C2); 118,2 (Ca) 128,8–136,7 (Carom); 154,1 (C3); 163,4 (C1).

4.2.2. Synthesis of 2-Amino-3-ethoxycarbonyl-4-(aryl)-4H-pyrano-[3,2-c]-chromene-5-ones 5

The appropriate (E) ethyl-2-cyano-3-(4-arylphenyl)acrylate 3 (0.05 mol) and 4-hydroxycoumarin (0.005 mol) were dissolved in 10 mL of DMC in the presence of piperidine (0,00003 mol). The reaction mixture was refluxed for 7 h, then concentrated and cooled. The solid product was filtered off washed with the appropriate solvent.

2-Amino-3-ethoxycarbonyl-4-(phenyl)-4H-pyrano-[3,2-c]chromene-5-one 5a. Yiled: 65%; mp = 250°C (MeOH); IR spectrum, cm−1: 3439 (N–H); 1090 (C–O)ester; 1729 (C=O)ester; 1205 (C–O)ester; 1H NMR spectrum (CDCl3, 300 MHz): 1,56 (m, 3H, CH3); 2,53 (s, 1H, CH); 3,03 (t, 2H, CH2); 6,33 (s, 2H, NH2); 7,10–7,88 (d, 9H, Harom); 13CNMR (CDCl3, 75 MHz):19,5 (Cg); 36,1 (C8); 61,6 (Cf); 103,4 (C7); 115,4 (Cd); 152,5 (Cc); 103,4–130,8 (Carom); 142,4 (C6); 164,5 (C1); 167,6 (Ce).

2-Amino-3-ethoxycarbonyl-4-(4′-methoxyphenyl)-4H-pyrano-[3,2-c]-chromene-5-one 5b. Yiled: 70%; mp = 212°C (MeOH); IR spectrum, cm−1: 3414 (N–H); 1128 (C–O)ether; 1717 (C=Oester); 1186 (C–O)ester; 1H NMR spectrum (CDCl3, 300 MHz): 1,32 (t, 3H, CH3); 3,02 (t, 3H, OCH3); 3,70 (s, 1H, CH); 4,32 (q, 2H, CH2); 6,26 (s, 2H, NH2); 6,75–7,87 (d, 8H, Harom); 13CNMR (CDCl3, 75 MHz):22,1 (Cg); 35,3 (C8); 54,8 (OCH3); 62,0 (Cf); 79,1 (C7); 103,6–154,4 (Carom); 156,8 (C6); 162,3 (Cc); 164,6 (C1); 167,6 (Ce).

2-Amino-3-ethoxycarbonyl-4-(2,5-dimethylphenyl)-4H-pyrano-[3,2-c]-chromene-5-one 5c. Yiled: 75%; mp = 260°C (MeOH); IR spectrum, cm−1: 3436 (N–H); 1115 (C–O)ether; 1728 (C=O)ester; 1230 (C–O)ester; 1H NMR spectrum (CDCl3, 300 MHz):1,36 (m, 3H, CH3); 1,78 (s, 3H, CH3); 1,90 (s, 3H, CH3); 2,74 (t, 2H, CH2); 5,81 (s, 1H, CH); 6,52–7,59 (m, Harom et Hethyl); 7,97 (s, 2H, NH2); 13CNMR (CDCl3, 75 MHz):24,4 (Cg); 26,4 (CH3); 26,8 (CH3); 40,8 (C8); 49,0 (Cf); 84,4 (C7); 108,4–146,2 (Carom); 157,6 (Cc); 169,4 (C1); 173,2 (Ce).

2-Amino-3-ethoxycarbonyl-4-(4′-nitrophenyl)-4H-pyrano-[3,2-c]-chromene-5-one 5d. Yiled: 63%; mp = 142°C (MeOH); IRν (KBr, cm−1): 3000 (N–H); 1091 (C–O)ether; 1720 (C=O)ester; 1200 (C–O)ester; 1H NMR spectrum (CDCl3, 300 MHz): 1,30 (t, 3H, CH3); 3,68 (s, 1H, CH); 4,22 (q, 2H, CH2); 6,32 (s, 2H, NH2); 6,62–7,82 (d, 8H, Harom); 13CNMR (CDCl3, 75 MHz): 22,2 (Cg); 34,7 (C8); 62,2 (Cf); 78,2 (C7); 102,6–153,4 (Carom); 157,8 (C6); 163,3 (Cc); 164,2 (C1); 167,4 (Ce).

2-Amino-3-ethoxycarbonyl-4-(4′-dimethylaminophenyl)-4H-pyrano-[3,2-c]-chromene-5-one 5e. Yiled: 46%; mp = 122°C (MeOH); IRν (KBr, cm−1): 3705 (N–H); 1084 (C–O)ether; 1695 (C=O)ester; 1227 (C–O)ester; 1H NMR spectrum (CDCl3, 300 MHz): 1,26 (t, 3H, CH3); 3,00 (s, 6H, 2CH3); 4,00 (s, 1H, CH); 4,24 (q, 2H, CH2); 6,94 (d, 2H, NH2); 6,20–6,78 et 7,20–7,92 (m, Harom et Hethyl); 13CNMR (CDCl3, 75 MHz): 14,1 (Cg); 35,2 (C8); 39,5 (N(CH3)2); 61,4 (Cf); 92,0 (C7); 103,8 (Cb); 111,6 (C10 et C14); 115,3 (Cc); 118,3 (C5); 122,7 (C2); 127,2 (C3); 130,6 (C4); 133,7 (C11 et C13); 148,2 (C9); 152,5 (C12); 153,6 (Cd); 154,0 (C6); 163,4 (Ca); 164,6 (C1); 167,6 (Ce).


This work was carried out with financial aid of the Qassim University in KSA through project no. 1303.


  1. H. Zuo, G. Jose, Z. Boli, B. Hyunmoon, and D. S. Shin, “Microwave-assisted synthesis of fluorinated coumarino sulfonamides,” Arkivoc, vol. 2008, no. 2, pp. 183–189, 2008. View at Scopus
  2. S. Lee, K. Sivakumar, W. Seobshin, F. Xie, and Q. Wang, “Synthesis and anti-angiogenesis activity of coumarin derivatives,” Bioorganic and Medicinal Chemistry Letters, vol. 16, no. 17, pp. 4596–4599, 2006. View at Publisher · View at Google Scholar · View at Scopus
  3. K. Moghadam and M. Mohseni, “A route to the synthesis of novel coumarins,” Monatshefte fur Chemie, vol. 135, no. 7, pp. 817–821, 2004. View at Scopus
  4. S. V. Dekic, V. S. Dekic, B. R. Dekic, and M. S. Dekic, “Synthesis of new condensed and cyclized coumarin derivatives,” Chemical Papers, vol. 61, pp. 233–235, 2007.
  5. A. M. M. El-Saghier and A. Khodairy, “New synthetic approaches to condensed and spiro coumarins: coumarin-3-thiocarboxamide as building block for the synthesis of condensed and spiro coumarins,” Phosphorus, Sulfur and Silicon and Related Elements, vol. 160, pp. 105–119, 2000. View at Scopus
  6. B. Musicki, A. M. Periers, P. Laurin et al., “Improved antibacterial activities of coumarin antibiotics bearing 5',5'-dialkylnoviose: biological activity of RU79115,” Bioorganic and Medicinal Chemistry Letters, vol. 10, no. 15, pp. 1695–1699, 2000. View at Publisher · View at Google Scholar · View at Scopus
  7. J. Azizian, A. Mohammadi, I. Bidar, and P. Mirazaei, “KAl(SO4)2· 12H2O (alum) a reusable catalyst for the synthesis of some 4-substituted coumarins via Pechmann reaction under solvent-free conditions,” Monatshefte Für Chemie, vol. 139, no. 7, pp. 805–808, 2008. View at Publisher · View at Google Scholar
  8. V. S. V. Satyanarayana, P. Sreevani, A. Sivakumar, and V. Vijayakumar, “Synthesis and antimicrobial activity of new Schiff bases containing coumarin moiety and their spectral characterization,” Arkivoc, vol. 2008, no. 17, pp. 221–233, 2008. View at Scopus
  9. M. M. Garazd, O. V. Muzychka, A. I. Vovk, I. V. Nagorichna, and A. S. Ogorodniichuk, “Modified coumarins. 27. Ssynthesis and antioxidant activity of 3-substituted 5,7-dihydroxy-4-methylcoumarins,” Chemistry of Natural Compounds, vol. 43, no. 1, pp. 19–23, 2007. View at Publisher · View at Google Scholar · View at Scopus
  10. G. Smitha and R. Sanjeeva, “ZrCl4-catalyzed Pechmann reaction: synthesis of coumarins under solvent-free conditions,” Synthetic Communications, vol. 34, no. 21, pp. 3997–4003, 2004. View at Publisher · View at Google Scholar · View at Scopus
  11. A. Kotali, I. S. Lafazanis, and P. A. Harris, “Synthesis of 6,7-diacylcoumarins via the transformation of a hydroxy into a carbonyl group,” Synthetic Communications, vol. 38, no. 22, pp. 3996–4006, 2008. View at Publisher · View at Google Scholar · View at Scopus
  12. N. Hamdi, C. Lidrissi, M. Saoud, A. R. Nievas, and H. Zarrouk, “Synthesis of some new biologically active coumarin derivatives,” Chemistry of Heterocyclic Compounds, vol. 42, no. 3, pp. 320–325, 2006. View at Publisher · View at Google Scholar · View at Scopus
  13. M. Maheswara, V. Siddaiah, G. L. V. Damu, Y. K. Rao, and C. V. Rao, “A solvent-free synthesis of coumarins via Pechmann condensation using heterogeneous catalyst,” Journal of Molecular Catalysis A, vol. 255, no. 1-2, pp. 49–52, 2006. View at Publisher · View at Google Scholar · View at Scopus
  14. B. Rajitha, V. N. Kumar, P. Someshwar, J. V. Madhav, P. N. Reddy, and Y. T Reddy, “Dipyridine copper chloride catalyzed coumarin synthesis via Pechmann condensation under conventional heating and microwave irradiation,” Arkivoc, vol. 2006, no. 12, pp. 23–27, 2006. View at Scopus
  15. M. Zahradnik, The Production and Application of Fluorescent Brightening Agents, John Wiley & Sons, New York, NY, USA, 1992.
  16. Z. A. Sizova, A. A. Karasev, L. L. Lukatskaya, M. I. Rubtsov, and A. O. Doroshenko, “Acid-base properties of 3-benzazolylcoumarins and their imino analogs,” Theoretical and Experimental Chemistry, vol. 38, no. 3, pp. 168–172, 2002. View at Scopus
  17. M. Paya, B. Halliwell, and J. R. S. Hoult, “Interactions of a series of coumarins with reactive oxygen species. Scavening of superoxide, hypochlorous acid and hydroxyl radicals,” Biochemical Pharmacology, vol. 44, no. 2, pp. 205–214, 1992. View at Publisher · View at Google Scholar · View at Scopus
  18. M. J. Frisch, G. W. Trucks, H. B. Schlegel, et al., Gaussian 03, Revision C. 02, Gaussian, Wallingford, UK, 2004.
  19. A. D. Becke, “Density-functional thermochemistry. III. The role of exact exchange,” Journal of Chemical Physics, vol. 98, article 5648, 5 pages, 1993. View at Publisher · View at Google Scholar
  20. C. Lee, W. Yang, and R. G. Parr, “Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density,” Physical Review B, vol. 37, pp. 785–789, 1988. View at Publisher · View at Google Scholar
  21. F. Weigend and R. Ahlrichs, “Balanced basis sets of split valence, triple zeta valence and quadruple zeta valence quality for H to Rn: design and assessment of accuracy,” Physical Chemistry Chemical Physics, vol. 7, no. 18, pp. 3297–3305, 2005. View at Publisher · View at Google Scholar · View at Scopus
  22. S. Kirkiachiarian, R. Bakhchinian, H. Chidiak, M. Mazmanian, and C. Planche, Annales Pharmaceutiques Francaises, vol. 57, p. 251, 1999.
  23. A. L. Banty, The Antimicrobial Susceptibility Test, Principle and Practice, Edited by I. Lea and Febiger, 1976.
  24. H. W. Seely and P. J. Van Demark, Microbes in Action: A Laboratory Manual of Microbiology, DB Taraporevala Sons & Co, Bombay, India, 1975.
  25. H. Mehrabi and H. Abusaidi, “Synthesis of biscoumarin and 3,4-dihydropyrano[c]chromene derivatives catalysed by sodium dodecyl sulfate (SDS) in neat water,” Journal of the Iranian Chemical Society, vol. 7, pp. 890–894, 2010.