Design, Synthesis and Characterization of Novel Sulfonamides Derivatives as Anticancer Agent Targeting EGFR TK, and Development of New Methods of Synthesis by Microwave Irradiation ()
1. Introduction
Cancer is a worldwide health problem and the most deadly disease in humans [1] [2], and it is considered the second leading cause of mortality after cardiovascular diseases [2]. There are several methods for the treatment of cancer such as Surgery, Chemotherapy, Hormonal therapy, Immunotherapy [3] [4], and Phototherapy [5]. Today, anticancer chemotherapy is still the main method applied in the treatment of cancer [6]. Chemotherapy drugs include antitumor antibiotics, anti-metabolites, mitotic inhibitors, hormonal therapies. Cancer chemotherapy offers a unique advantage: it can treat the entire body, even the cells that may have escaped from the primary tumor [4] [7].
Among the wide range of compounds tested as potential anticancer agents, derivatives of sulfonamide have attracted reasonable attention [8].
The compounds which contain SO2NH2 functional group are called sulfonamides. The general formula of sulfonamides is RSO2NH2 [9] (Figure 1).
Sulfa drugs are amphoteric, they have pKa 4.79 to 8.56 and act as weak organic acids. They are weakly soluble in water, their solubility is increased at alkaline pH. The lipophilicity of the N1 group has the largest effect on protein binding [10]. Sulfonamide derivatives comprise an important class of drugs with diverse biological applications [11]. Over 30 drugs containing this functional group are in clinical use, including antihypertensive, antibacterial, antiprotozoal, antifungal, anti-inflammatory, non-peptidic vasopressin receptor antagonists, translation initiation inhibitors, rheumatoid arthritis, antimalarial, anti-leishmanial, anti-thyroid, Antidepressant [10] [11] [12], hypoglycemics, anticonvulsants [13], diuretic, receptor tyrosine kinase inhibitors, and antipsychotics [1]. They are also used to treat ulcerative colitis, urinary, intestinal, and ophthalmic infections [14]. Recently, sulfonamides have been used as anti-cancer, anti-viral, and anti-HIV [15] [16], and in Alzheimer’s disease [13].
Epidermal growth factor receptor (EGFR) is a member of the tyrosine kinase family and is usually overexpressed in several types of cancer, such as non-small-cell lung cancer, breast, esophageal, head, cervical, and neck cancer [17] [18]. The TMLR (T790M/L858R) mutation, the L858R mutation is located in the tyrosine kinase domain of EGFR in exon 2 and deletions within exon 19, and T790M is located in exon 20 of EGFR within the kinase domain where the threonine gatekeeper residue Thr790 is exchanged for methionine T790M [19] [20] [21].
Recently, some sulfonamide derivatives carrying pyrrole and pyrrolopyrimdine cycles have been synthesized by Ghorab et al. in 2014 and have antitumor activity. Most of the synthesized compounds showed good activity as cytotoxic
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Figure 1. The structure of sulfanilamide.
agents with better IC50 than doxorubicin as a reference drug. The molecular docking study was performed on the human c-Src for all synthesized compounds [22].
Ihmaid et al. in 2018 designed and synthesized some novel anthranilate sulfonamide derivatives having anticancer activity. The molecular docking study was performed against EGFR [6].
In the past few years, the use of microwave as an energy resource to induce organic reactions has been a useful technique in organic synthesis. Microwave irradiation has been shown to dramatically reduce reaction times, increase product yields and enhance product purities by reducing unwanted side reactions compared to conventional heating methods [23] [24] [25].
Due to our interest in the development of novel anticancer agents, in this study, we report the design and synthesis of some novel sulfonamide derivatives and we expect that these new compounds might show significant anticancer activity.
2. Materials and Methods
Protein Data Bank (PDB), PubMed and software like ChemSketch version 14.01, Marvin sketch version 21.2, and Molegro Virtual Docker (MVD) version 2011.4.3 were implemented within the current study.
A Monowave 300 microwave oven was used for microwave synthesis (Anton Paar, Austria) and we used reaction vial G30 equipped with snap caps and silicon septa. Melting points were determined in open capillary on a BÜCHI Melting Point B-540 apparatus (BÜCHI Labortechnik, Switzerland). Analytical thin-layer chromatography (TLC) was performed with silica gel 60 F254 aluminum sheets (Macherey-Nagel, Germany). IR spectra (KBr disc) were recorded using an ATR-FTIR Bruker spectrophotometer (Bruker, Billerica, Massachusetts). 1H-NMR spectra were scanned on JEOL-ECA NMR spectrophotometer (Joel, Tokyo, Japan), operating at 400 MHz for 1H and 13C. Chemical shifts are expressed in δ-values (ppm), using DMSO-d6 as a solvent. Mass spectra (MS) were scanned by the triple quadrupole mass spectrometer with positive ionization (Sciex, Framingham, USA). The m/z values of the more intense peaks are mentioned.
EGFR structure
The 3D crystal structure of EGFR Kinase T790M/L858R (TMLR) (PDB ID: 5EDQ) domain was retrieved from PDB and has a resolution of 2.8 Å. The kinase domain consists of 327 residues between 695 - 1022 residues. The resolved EGFR structure was co-crystallized as holo-form with a known kinase inhibitor (N-(7-Chloro-1H-indazol-3-yl)-7,7-dimethyl-2-(1H-pyrazol-4-yl)-5H-furo[3,4-d]pyrimidin-4-amine) (5N3) (Figure 2).
Define the binding pocket:
The binding pocket was defined using the co-crystallized ligand as a center of the pocket, which had a volume of 312.32 Å, and fitted to the polar surface area for designed compounds (Figure 3).
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Figure 2. Co-crystal structure of the EGFR TMLR (PDB ID: 5EDQ) kinase domain in complex with 5N3.
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Figure 3. EGFR (TMLR) binding pocket (PDB ID: 5EDQ) used to dock the designed compounds.
Compounds preparation:
Structures of designed compounds were drawn and optimized by using Marvin Sketch and saved as mol2. The preparation of compounds was performed using the default setting to assign bonds, create explicit hydrogens, assign bond orders and hybridization, assign charges (calculated by MVD), assign tripos atom types, and detect flexible torsions in ligands.
Molecular Docking:
The Molecular Docking was performed in MVD. The following parameters were used for docking in the EGFR kinase (Table 1).
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Table 1. Parameters of Molegro Virtual Docker.
The results of docking compounds with the receptors were compared with Osimertinib and Rociletinib which are in use to treat non-small cell lung cancer (NSCLC). Osimertinib docked with EGFR with mutation T790M, L858R, and exon 19 deletions, and Rociletinib docked with EGFR including T790M mutation.
General procedures for the synthesis of compounds:
• Synthesis of compound 1b
Pyridine (10 ml) was placed in a 100 ml round flask fitted with a magnetic stirrer and heated to 70˚C. Sulfamethoxazole (5 mmol) was added to the warmed liquid in several portions, creating a homogeneous yellow solution. The warm solution was stirred while benzoyl chloride (5 mmol) was added dropwise. The mixture was stirred for 30 minutes with maintaining the temperature at 70˚C. The mixture was cooled in a cold water bath, then poured into chipped ice to produce a white precipitate, then, filtration, drying at 100˚C and recrystallizing from ethanol.
• Synthesis of compound 1c
(11.6 mmol) of sulfanilamide dissolved in 20 ml of 4% NaOH and placed in a 100 ml conical flask. Then, (23.2 mmol) of benzoyl chloride was added slowly with vigorous shaking. The flask was closed and shaken for further 30 min or till the odor of benzoyl chloride can no longer be detected. When the reaction finished, a white precipitate was formed, then, filtration, drying and recrystallizing from hot methanol.
• Synthesis of compound 3b
A mixture of sulfamethoxazole (8 mmol) and triethylamine (2 ml) in dry DMF (10 mL) were stirred under reflux for 1 h. A solution of phthalic acid (8 mmol) was then added dropwise. The reaction mixture was heated under reflux at 200˚C in oil bath for 3 h. After cooling, the reaction mixture was poured into ice water and the formed solid was collected by filtration and recrystallized from acetonitrile.
• Synthesis of compound 3d
Sulfanilamide (11.6 mmol) and triethylamine (2 ml) in dry DMF (10 mL) were stirred under reflux for 1 h. Phthalic acid (11.6 mmol) was then added dropwise. The reaction mixture was heated under reflux at 200˚C in oil bath for 2.5 h. After cooling, the reaction mixture was poured into ice water and the product was collected by filtration and recrystallized from DMF.
Synthesis of compounds by microwave irradiation:
• Synthesis of compound 1b
A mixture of sulfamethoxazole (5 mmol) and benzoyl chloride (5 mmol) was dissolved in 5 ml pyridine and placed in a 30-mL sealed vial. Then, it is put in the microwave and heated to 120˚C, and maintained at this temperature for 10 min. Finally, the reaction was cooled to 55˚C. After completion of the reaction, the mixture of reaction was poured into cold water to produce a white precipitate which was filtered, washed with water and methanol, and dried.
• Synthesis of compound 1c
(5.8 mmol) of sulfanilamide dissolved in 5 ml pyridine and placed in a 30-mL sealed vial, then, (11.6 mmol) of benzoyl chloride was added and put in the microwave, then, was heated to 100˚C and was maintained at this temperature for 5 min. Then, the reaction was cooled to 55˚C. When the reaction finished, a white precipitate was formed, which was filtered, washed with water and methanol, and dried.
• Synthesis of compound 3b
Sulfamethoxazole (4 mmol) and phthalic acid (4 mmol) were dissolved in 5 ml pyridine and placed in a 30-mL sealed vial. The reaction mixture was heated to 200˚C and was kept at this temperature for 20 min. Then, the reaction was cooled to 55˚C. After cooling, the reaction mixture was poured into ice water and the formed solid was collected by filtration, washing with water and methanol, and drying.
• Synthesis of compound 3d
A mixture of Sulfanilamide (5.8 mmol) and phthalic acid (5.8 mmol) was dissolved in 10 ml pyridine and placed in a 30-mL sealed vial. The reaction mixture was heated to 200˚C and was kept at this temperature for 20 min. Then, the reaction was cooled to 55˚C. After cooling, a white precipitate was formed which was filtered, washed with water and methanol, and dried.
3. Results and Discussion
Sulfonamide derivatives
The core scaffold of the sulfonamide shown in (Figure 4) was used to design several derivatives in the current study. The structure of designed sulfonamide derivatives is shown in (Table 2).
Molecular Docking results
The list of compounds was docked into the EGFR (TMLR) receptor binding pocket using the validated docking methods. Docking results tabulated between
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Table 2. Structure of sulfonamide derivatives considered in the study.
the EGFR (TMLR) binding pocket and the derivatives of sulfonamide are shown (Table 3).
Validation docking method
Validation of docking was used to ensure the orientation and position of ligand binding obtained from docking studies by MVD program. Therefore, the parameters must be validated by re-dock the native ligand into the crystal structure (PDB ID: 5EDQ). After that, it was extracted and re-docked into the binding pocket to generate the X-ray binding mode. The ability of the docking algorithm to generate the active biding mode of the ligands was evaluated by
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Table 3. The energy docking of ligands with receptors.
calculating the RMSD (Root Mean Square Deviation) between the docking solutions and the X-ray binding mode. RMSD < 2 Å considered as a threshold in the computer-aided drug design.
The RMSD value for the top-ranked docking solution of ligand was 0.565382. Thus, the applied docking methods were able to generate the X-ray binding mode of the ligand.
The interactions between the binding pocket residues of the EGFR (TMLR) receptor and the sulfonamide derivatives together with energy docking are shown in Table 4.
Synthesis of compounds
• Mechanism of synthesis
Compound 1b
The reaction of sulfamethoxazole (1) with benzoyl chloride (2) in pyridine with refluxing, results in the desired N-{4-[(5-methyl-1,2-oxazol-3-yl)sulfamoyl] phenyl}benzamide (1b) in 84% yield, and in 89% yield by microwave synthesis (Figure 5).
Compound 1c
The reaction of sulfanilamide (3) with benzoyl chloride (2) in NaOH with shaking, results in the desired N-{[4 (benzoylamino)phenyl]sulfonyl}benzamide (1c) in 50% yield, and in 82% yield by microwave synthesis (Figure 6).
Compound 3b
The reaction of sulfamethoxazole (1) with phthalic acid (4) in DMF with refluxing, results in the desired 4-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-N-(5- methyl-1,2-oxazol-3-yl) benzenesulfonamide (3b) in 50% yield, and in 88% yield by microwave synthesis (Figure 7).
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Figure 5. The mechanism of synthesis of N-{4-[(5-methyl-1,2-oxazol-3-yl) sulfamoyl]phenyl}benzamide (1b).
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Figure 6. The mechanism of synthesis of N-{[4 (benzoylamino)phenyl]sulfonyl} benzamide (1c).
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Table 4. Interaction of the amino acids in 5EDQ with ligands.
Compound 3d
The reaction of sulfanilamide (3) with phthalic acid (4) in DMF with refluxing, results in the desired 4-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl) benzenesulfonamide (3d) in 91% yield, and in 97% yield by microwave synthesis (Figure 8).
• Analytical data
N-{4-[(5-methyl-1,2-oxazol-3-yl)sulfamoyl]phenyl}benzamide (1b)
White powder, mp 278˚C - 280˚C. TLC; the mobile phase was used acetate
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Figure 7. The mechanism of synthesis of 4-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-N- (5-methyl-1,2-oxazol-3-yl)benzenesulfonamide (3b).
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Figure 8. The mechanism of synthesis of 4-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl) benzenesulfonamide (3d).
ethyl: petrolatum ether 9:1, which the Rf for sulfamethoxazole 0.8 and the Rf for compound (1b) 0.88. IR spectrum (νmax, cm−1): 3362 (N–H), 3061 (C–H arom), 2987, 2882 (C–H), 1660 (C=O), 1604, 1589, 1578 (C=C), 1529 (N–O), 1372, 1332 (S=O), 1318 (C–N) (Figure 9) [26]. 1H-NMR spectrum (DMSO-d6, δ, ppm): 2.3 (s, 3H, CH3), 6.1 (s, 1H, =CH–), 7.5 (t, 1H, Ar–H), 7.58 (t, 1H, Ar–H), 7.8 (d, 1H, Ar–H), 7.9 (d, 1H, Ar–H), 7.97 (d, 1H, Ar–H), 10.6 (s, 1H, NH), 11.3 (s, 1H, SO2–NH) (Figure 10). 13C-NMR (DMSO-d6, δ, ppm): 12.5, 96, 120.5, 128.3, 128.4, 129, 132.5, 135, 144, 158, 166.6, 170.8 (Figure 11) [27]. Mass spectrum
(m/z, ESI): showed molecular ion [M + H]+ peak at 358.12 corresponding to the molecular formula of C17H15N3O4S, and [M + Na]+ peak at 380.07.
N-{[4 (benzoylamino)phenyl]sulfonyl}benzamide (1c)
White powder, mp 296˚C - 300˚C. TLC; the mobile phase was used acetate ethyl: petrolatum ether 9:1, which the Rf for sulfanilamide 0.69 and the Rf for compound (1c) 0.79. IR spectrum (νmax, cm−1): 3359, 3264 (N–H), 1650 (C=O), 1590, 1513, 1484 (C=C), 1396, 1294 (S=O), 1266 (C–N) (Figure 12) [26]. 1H-NMR spectrum (DMSO-d6, δ, ppm): 7.2 (t, 1H, Ar–H), 7.5 (t, 1H, Ar–H), 7.55 (t, 1H, Ar–H), 7.75 (d, 1H, Ar–H), 7.8 (d, 1H, Ar–H), 7.95 (d, 1H, Ar–H), 10.5 (s, 1H, NH) (Figure 13). 13C-NMR (DMSO-d6, δ, ppm): 120.3, 127.05, 127.1, 128.3, 128.29, 128.31, 129, 132.4, 135.02, 135.04, 139.25, 139.3, 142.7, 166.5 (Figure 14) [27]. MS (m/z, ESI): The major peak for compound showed molecular ion [M + H]+ peak at 381.15 corresponding to the molecular formula of C22H20N2O2S, and [M + Na]+ peak at 403.21.
4-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-N-(5-methyl-1,2-oxazol-3-yl)benzenesulfonamide (3b)
Pale white powder, mp 255˚C - 258˚C. TLC; the mobile phase was used acetate ethyl: petrolatum ether 7:3, which the Rf for sulfamethoxazole 0.67 and the Rf for compound (3b) 0.8. IR spectrum (νmax, cm−1): 3476 (N–H), 3107 (C–H arom), 3026, 3001 (C–H), 1739, 1713 (C=O), 1610, 1594, 1500 (C=C), 1413, 1380 (S=O), 1333 (C–N) (Figure 15) [26]. 1H-NMR spectrum (DMSO-d6, δ, ppm):2.3 (s, 3H, CH3), 6.1 (s, 1H, =CH–), 7.7 (d, 1H, Ar–H), 7.9 (d, 1H, Ar–H), 7.95 (d, 1H, Ar–H), 8 (d, 1H, Ar–H), 11.5 (s, 1H, SO2–NH) (Figure 16). 13C-NMR
(DMSO-d6, δ, ppm): 12.5, 96, 124.1, 128, 128.2, 132, 135.5, 136.7, 138.9, 158, 167, 171 (Figure 17) [27]. MS (m/z, ESI): showed [M + H]+ peak at 384.05 corresponding to the molecular formula of C18H13N3O5S, and [M + Na]+ peak at 406.03.
4-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)benzenesulfonamide (3d)
White powder, mp 364˚C - 368˚C. TLC; the mobile phase was used acetate ethyl: petrolatum ether 6:4, which the Rf for sulfanilamide 0.44 and the Rf for compound (3d) 0.62. IR spectrum (νmax, cm−1): 3362, 3258 (N–H), 1703 (C=O), 1615, 1594, 1498 (C=C), 1393, 1340 (S=O), 1299, 1286 (C–N), 1224 (C–O) (Figure 18) [26]. 1H-NMR spectrum (DMSO-d6, δ, ppm): 7.4 (s, 1H, SO2–NH), 7.66 (d, 1H, Ar–H), 7.88 (d, 1H, Ar–H), 7.93 (t, 1H, Ar–H), 7.95 (d, 1H, Ar–H) (Figure 19). 13C-NMR (DMSO-d6, δ, ppm): 124, 127, 128, 132, 135.3, 135.5, 143.8, 167.18 (Figure 20) [27]. MS (m/z, ESI): showed [M + 2H]+ peak at 304.26 corresponding to the molecular formula of C14H10N2O4S, and [M + Na]+ peak at 325.03.
All the designed compounds were bound to receptors and given energy docking. Only one compound showed higher docking scores toward the receptor than the reference ligand, Table 3. The compounds 4b, 6c, and 5b were shown higher energy binding with EGFR (TMLR) binding pocket than other compounds.
Most of the compounds were given hydrogen bonds and van der Waals bonds to receptors with different bond lengths and binding energies. The ligand displayed hydrogen bonds with 9 amino acid residues of 5EDQ: Thr854, Lys745, Asn842, Asp855, Met793, Arg858, Arg841. To stabilize the compounds in the binding pocket; most compounds displayed van der Waals interactions between the amino acid residues and the ligands.
The predicted binding modes of 4b and 6c and their interactions with the residues in the EGFR (TMLR) binding pocket are shown in (Figure 21).
A series of four sulfonamides were synthesized in basic media by simple reactions of amino-group-containing drug; sulfamethoxazole and sulfanilamide with carbonyl group in benzoyl chloride and phthalic acid. The compounds were obtained in good to excellent yield (50% - 91%), and the yield by microwave synthesis was excellent (82% - 97%). The synthesized compounds were characterized by FT-IR; the characteristics band at 3258 - 3476 cm−1 for (N–H) and 1650 - 1739 cm−1 for (C=O) and 1413 - 1294 cm−1 of S=O stretching and 1266 - 1333 cm−1 for (C-N) for all compounds reveals the formation of sulfonamides. Mass spectral data of all synthesized compounds was obtained by ESI-MS. The major peak for compounds was showed good agreement with the calculated molecular masses of the concerned compound. The structures of all the compounds were also confirmed by 1H NMR by dissolving in DMSO. 1H NMR spectra of compounds,
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Table 5. Comparison of conventional heating method and microwave synthesis.
*C: conventional heating, *M: microwave heating.
there were two signals for solvent at 2.5 and 3.3 ppm. The protons for the benzene ring appeared at 7.2 - 8 ppm. In 1b and 3b compounds, there were signals in 2.3 and 6.1 for methyl and CH in oxazole, respectively. In the 13C NMR spectra for compounds, there was a signal for solvent at 40 ppm. Aromatic carbons of benzene ring appeared at chemical shift 120.3 - 144 ppm. The chemical shift value of C=O was observed at 166.5 - 167.18 ppm. In 1b and 3b compounds, three carbons were visible at 96,158 and 171 ppm, and the carbon for methyl group was noted at chemical shift 12.5 ppm.
From the results, all the newly synthesized compounds are in agreement with the spectroscopic analysis. And we noted that the microwave synthesis gave a higher yield than the conventional heating method with less time and higher temperature (Table 5).
4. Conclusion
Several sulfonamide derivatives were docked into the EGFR (TMLR) binding pocket using the Molegro Virtual Docker software. The binding free energy was calculated to predict their affinity toward EGFR kinase TMLR to select novel candidates as EGFR inhibitors for treating cancer. The results showed that 4b, and 6c gave the highest energy docking −147.213, −132.14 Kcal/mol toward the EGFR (TMLR) receptor. Their corresponding binding modes were predicted. The obtained results suggested that these compounds may be novel candidates in lung cancer treatment by targeting EGFR tyrosine kinase T790M/L858R. Then, some of new sulfonamide derivatives were synthesized with a simple procedure in one step starting from sulfanilamide and sulfamethoxazole with benzoyl chloride and phthalic acid in basic media. The reactions conditions were easy and excellent yields of compounds were obtained and progress of reaction was monitored by TLC and their structures were confirmed by spectral and elemental analysis. These novel sulfonamide derivatives were also synthesized in rationally good yields by the microwave-assisted method. This is environmentally compassionate technique which gives higher yields and lesser reaction time and easy work-up method. Finally, more studies are still needed to identify the mechanism of action of these derivatives and we are hoping that it will show significant anticancer activity.
Acknowledgements
The authors are thankful to University of Marburg, Institute of Pharmacy, Department of Pharmaceutical Chemistry, Germany, for analyze our synthesized compounds by IR spectrum, mass spectrum, and H-NMR and 13C NMR spectrum.