Green Chemical Synthesis and Analgesic Activity of Fluorinated Thiazolidinone, Pyrazolidinone, and Dioxanedione Derivatives

Sachdeva, Harshita; Dwivedi, Diksha; Goyal, Pradeep

doi:https://doi.org/10.1155/2013/976032

Organic Chemistry International

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Abstract Introduction Results and Discussion Experimental Conclusion Acknowledgments References Copyright Related Articles

Research Article | Open Access

Volume 2013 | Article ID 976032 | https://doi.org/10.1155/2013/976032

Green Chemical Synthesis and Analgesic Activity of Fluorinated Thiazolidinone, Pyrazolidinone, and Dioxanedione Derivatives

Harshita Sachdeva,¹Diksha Dwivedi,¹and Pradeep Goyal²

Academic Editor: William Setzer

Received07 Apr 2013

Revised28 Jun 2013

Accepted28 Jun 2013

Published21 Jul 2013

Abstract

Facile lemon juice catalyzed green and efficient synthesis of a series of new classes of 5-(fluorinatedbenzylidene)-2-thioxo-1,3-thiazolidin-4-ones (3a–e), 5-methyl-4-(fluorinatedbenzylidene)-2-phenylpyrazolidin-3-ones (5a–e), and 2,2-dimethyl-5-(fluorinatedbenzylidene)-1,3-dioxane-4,6-diones (7a–e) by the reaction of fluorinated aromatic aldehydes with active methylene compounds is reported. Lemon juice is natural acid catalyst which is readily available, cheap, nontoxic, and ecofriendly. This method is experimentally simple, clean, high yielding, green, and with reduced reaction times. The product is purified by simple filtration followed by washing with water and drying process. Some of the synthesized compounds have been evaluated “in vivo” for their analgesic activity and all the synthesized compounds are characterized by IR, ¹H NMR, ¹³C NMR, ¹⁹F NMR, and mass spectral studies.

1. Introduction

The steady growth of interest in the synthesis of heterocyclic compounds is connected with their raised biological activity and also with the fact that these compounds make possible the development of novel materials of unique properties. Pyrazolone is a biologically important scaffold associated with multiple pharmacological activities such as antimicrobial [1], anti-inflammatory [2], analgesic [3], antidepressant [4], anticonvulsant [5], antidiabetic [6], antihyperlipidemic [7], antiviral [8], antitubercular [9], antioxidant [10], and anticancer activites [11, 12]. The synthesis of pyrazolone and its derivatives has engrossed substantial attention from organic and medicinal chemists for many years as they belong to a class of compounds with proven utility in medicinal chemistry.

One very interesting and promising class of heterocycles is the 4-thiazolidinone ring system. It represents a class of chemical products with interesting pharmacological and biological activities [13–18] including antidiabetic, antitubercular, anti-HIV, antiparasitic, hypnotic, and anathematic agents. Furthermore, the reactivity of the Meldrum’s acid (2,2-dimethyl-1,3-dioxan-4,6-dione) as a methylene active compound was explored about 40 years after its preparation, when the structure was correctly attributed by Davidson and Bernhard [19] assigning the acidic proton to the central carbon, and its high acidity is still object of study [20]. It is known that the Meldrum’s acid undergoes standard Knoevenagel condensation with aromatic and heteroaromatic aldehydes furnishing the corresponding arylidene derivatives, which are versatile substrates for different kinds of reactions [21, 22]. They are useful intermediates for cycloaddition reaction and for the synthesis of heterocyclic compounds with potential pharmacological activity [23].

Several methods have been developed for the preparation of thiazolidinone, pyrazolone, and dioxanedione derivatives. The most common is Knoevenagel condensation between aromatic aldehydes and various active methylene compounds carried out in glacial acetic acid containing anhydrous sodium acetate [24]. Instead of sodium acetate, acetic anhydride [25], ethanolamine [26], and ammonium chloride in ammonia [27–29] have also been used as catalysts. Other derivatives were also prepared using glycine and sodium carbonate as catalysts, ionic liquid, and acidic alumina as solid support, borate zirconia [30–34].

More recent methods for the preparation of 5-benzylidene-2-thioxothiazolidin-4-ones, 4-arylidene-3-methyl-1-phenyl-5-pyrazolone derivatives, and 5-benzylidene-2,2-dimethyl-1,3-dioxane-4,6-dione have been reported which involve Knoevenagel condensation of aromatic aldehydes with 2-thioxothiazolidin-4-one/3-methyl-1-phenyl-1H-pyrazol-5(4H)-one/Meldrum acid catalyzed by a basic functionalized ionic liquid [35], nanoparticles [36, 37], triphenylphosphine [38], and 1-butyl-3-methylimidazolium hydroxide ([bmim][OH]) [39, 40]. Knoevenagel condensation is also reported under microwave irradiation for the synthesis of 5-arylidene-4-thiazolidinones [41]. These derivatives are also synthesized using tetrabutylammonium bromide (TBAB) as a phase transfer catalyst in water under microwave irradiation [42]. However, in spite of their utility, some methods suffer from disadvantages like long reaction times, low yields, chemical hazards, and environmental pollution.

In recent years, organic research is mainly focused on the development of green methods to synthesize various organic compounds through the use of alternative green catalyst to replace hazardous strong acidic or basic catalyst commonly used in organic synthesis. Nowadays, many organic transformations have been carried out using biocatalysts or intact plant systems. Recently, use of lemon juice as natural catalyst is reported [43] in few chemical reactions because it is inexpensive, most abundant in nature, nonhazardous, and ecofriendly. It exhibits unique reactivity and selectivity. As lemon juice is acidic in nature (pH ≈ 2-3) and percentage of citric acid (5%–7%) is more than other acids, it works as acid catalyst.

In addition, incorporation of fluorine further enhances the biological activity by increasing solubility in lipoid material and fat deposits in the body. Compounds of medicinal interest containing trifluoromethyl substituents, including anaesthetics, antipsychotics, antibiotics and a few antimalarials were reviewed in 1958 [44]. Antibiotic multi drug resistance is a major and continuing public health concern and some clinicians are switching to replacements such as the fluoroquinolones [45]. A recent review [46] has highlighted pesticides containing the CF₃O group, and its authors have argued that a CF₃O substituent can advantageously replace a fluorine atom in most molecules with the benefit of increased lipid solubility. Many drugs with enhanced effectiveness and selectivity contain the CF₃O moiety (e.g., celikalim, roflumilast and riluzole) (Figure 1).

In Scheme 1, we have synthesized for the first time a series of new class of fluorine containing olefinic compounds from Knoevenagel condensation of fluoro-substituted aromatic aldehydes (1) with active methylene compounds, 2-thioxo-4-thiazolidinone (2)/3-methyl-1-phenyl-2-pyrazolin-5-one (4)/Meldrum’s acid (6) in the presence of lemon juice as natural acid catalyst at room temperature. The compounds synthesized by various methods have been characterized by their melting points, elemental analyses, IR, ¹HNMR, ¹³CNMR, ¹⁹FNMR, and mass spectral studies.

2. Results and Discussion

In continuation to our interest on environmentally benign synthesis of heterocyclic compounds [47–50], we now report the green synthesis of fluorinated thiazolidinone (3a–e), pyrazolidinone (5a–e) and dioxanedione derivatives (7a–e) via Knoevenagel condensation at room temperature in the presence of catalytic amount of lemon juice as natural acid catalyst (Scheme 1). We have extensively studied the title reaction taking two parameters, namely, type of catalysts and type of solvent. In order to optimize the reaction conditions, the synthesis of compound 3a was used as a model reaction and a mixture of 3-fluoro benzaldehyde and 2-thioxo-4-thiazolidinone was magnetically stirred in presence of various catalysts as shown in Table 1. When reaction was carried out in aqueous medium in the presence of oxalic acid, boric acid, alum, and lemon juice (Table 1, entry 1–4), lemon juice provided the best yield as compared to other catalysts.

Furthermore, we studied the role of solvent on the synthesis of title compounds and found that the solvent played a crucial role in this reaction (Table 2, entry 1, 2, 3). Ethanol, methanol, dichloromethane were all able to facilitate but it took longer time (4-5 hrs) to complete the reaction with low yield (66–75%) of the product. We extended our studies and carried out the reaction in the absence of any solvent and presence of lemon juice at room temperature, 92% yield of the product was obtained in 1.5 hrs. (Table 2, entry 4). With these optimal conditions in hand, we examined the scope of this Knoevenagel condensation reaction. Results indicate that lemon juice is the best catalyst at room temperature for the synthesis of olefinic compounds (Table 3). As lemon juice is acidic in nature (pH ≈ 2-3) and percentage of citric acid (5%–7%) is more than other acids, it works as acid catalyst for the synthesis of fluorinated thiazolidinone (3a–e), pyrazolidinone (5a–e), and dioxanedione derivatives (7a–e). Using this methodology, these reactions were completed in shorter reaction times (1-2 hrs) at room temperature (25°C) with yields of the product ranging from 90% to 95%. For the Knoevenagel condensation reaction, we have used extract of Citrus limonum species of lemon as natural catalyst for synthesis of arylidenes. To our satisfaction, we found that the use of 2 mL of lemon juice resulted in quantitative yield (90%–95%) of the corresponding olefinic compounds within 1 to 2 hrs. The purity of the compounds was checked by TLC using silica gel-G as adsorbent. We have also carried out this reaction using citric acid separately; reaction took place successfully as observed on TLC.

The product is isolated in pure form and does not require further purification and crystallization. Hence, other compounds were also synthesized at room temperature following the similar procedure. The chemical structures all the synthesized compounds have been confirmed by IR, ¹HNMR, ¹⁹FNMR, ¹³CNMR, and mass spectral studies.

The IR spectra of 3a–e showed absorption bands at 3320–3350 cm⁻¹ due to NH stretching of amide, 1680–1692 cm⁻¹ due to C=O, 1578–1596 cm⁻¹ due to C=C, and 1131–1211 cm⁻¹ due to C=S Stretching, which confirms with the formation of compounds 3a–e. The ¹HNMR spectrum of 3b showed peaks at δ 8.65 (s, 1H, NH), 8.02 (s, 1H, CH), and 6.79–7.98 (m, 4H, Ar-H) ppm. Formation of compound 3b was further confirmed on the basis of ¹³CNMR spectrum. In the ¹³CNMR spectrum, sharp signals were observed at δ 200 (C=S), 168.37 (C=O), 161.23 (C-O), 143 (CH), 120.48 (C=C, aliphatic carbon), 122 (OCF₃), and 138.25–119.36 (aromatic carbons) ppm. Mass spectrum of compound 3b showed molecular ion peak [M⁺ + 1] at 306 m/z (54%) corresponding to its molecular weight along with base peak observed at m/z 122 (100%) and other relevant peaks were observed at m/z 246 (39%), 236 (84%), 220 (70%), 95 (15%), and 79 (58%).

The IR spectra of 5a–e showed absorption bands at 2915–3129 cm⁻¹ due to CH str of methine, 1670–1688 cm⁻¹ due to C=O str, and 1586–1591 cm⁻¹ due to C=C, which confirms with the formation of compounds 5a–e. The ¹HNMR spectrum of 5d showed peaks at δ 7.73 (s, 1H, CH), 7.19–7.71 (comp, 8H, Ar-H), 3.51 (s, 1H, CH), 2.52 (s, 1H, NH), and 1.24 (s, 3H, CH₃) ppm. Formation of compound 5d was further confirmed on the basis of ¹³CNMR spectrum. In the ¹³CNMR spectrum, sharp signals were observed at δ 162.50 (C=O), 134.82 (CH), 130.82 (C=C, aliphatic carbon), 123.13 (CF₃), 139.82–112.12 (aromatic carbons), and 21.73 (CH₃) ppm.

The IR spectra of 7a–e showed absorption bands at 2915–3083 cm⁻¹ due to CH str of methine, 1630–1685 cm⁻¹ due to C=O str, 1554–1590 cm⁻¹ due to C=C, and 1055–1145 cm⁻¹ (C-O) which confirms with the formation of compounds. The ¹HNMR spectrum of 7a showed peaks at δ 8.97 (s, 1H, CH), 7.70–7.84 (m, 4H, Ar-H), and 2.12 (s, 6H, CH₃) ppm. Formation of compound 7a was further confirmed on the basis of ¹³CNMR spectrum. In the ¹³CNMR spectrum, sharp signals were observed at δ 164.91 (C=O), 160.42 (C-F), 154.08 (CH), 123.74 (C=C, aliphatic carbon), 134.02–118.12 (aromatic carbons), 105.18 (O-C-O), and 26.16 (CH₃) ppm. The mass spectrum of compound 7a showed molecular ion peak [M⁺] at 250 m/z (30%) corresponding to its molecular weight along with base peak observed at m/z 176 (100%) and other relevant peaks were observed at m/z 123 (13%), 100 (34%), and 63 (9%). Spectral analyses of all the synthesized compounds are given in Tables 4, 5, and 6.

3. Experimental

General. Reagents and solvents were obtained from commercial sources and used without further purification. Melting points were determined on a Toshniwal apparatus. The ¹H NMR and ¹³C NMR of synthesized compounds have been carried out at SAIF, Punjab University, Chandigarh, India. IR spectra of compounds have been carried out at FET, MITS, Laxmangarh, Sikar, Rajasthan, India. The purity of compounds was checked on thin layers of silica gel in various nonaqueous solvent systems, for example, ethyl acetate : n-hexane (1 : 9). IR spectra were recorded in KBr on a PerkinElmer Infrared L1600300 Spectrum Two Li Ta spectrophotometer and ¹H NMR spectra were recorded on Bruker Avance II 400 NMR spectrometer using DMSO-d₆ and CDCl₃ as solvent and tetramethylsilane (TMS) as internal reference standard. The analgesic activity of synthesized compounds was carried out in Goenka College of Pharmacy, Department of Pharmacology, Lakshmangarh, Sikar, Rajasthan, India.

General Procedure for Extraction of Lemon Juice. Fresh lemon was cut by using knife and then pieces were pressed manually using domestic presser to extract juice. Then juice was then filtered through cotton/muslin cloth and then through filter paper to remove solid material and to get clear juice which was used as a catalyst.

General Procedure for the Preparation of 3a–e, 5a–e, and 7a–e. A mixture of fluorinated aromatic aldehyde (1 mmol) and 2-thioxo-4-thiazolidinone/3-methyl-1-phenyl-2-pyrazolin-5-one/Meldrum’s acid (1 mmol) was taken in single neck round bottom flask and to this lemon juice (2 mL) was added as catalyst. The reaction mixture was stirred at room temperature for the appropriate time required for the completion of reaction given in Table 2. The progress of reaction was monitored by TLC using ethyl acetate : n-hexane (1 : 9) as eluent. After the completion of the reaction, mixture was poured onto crushed ice, and the solid product obtained was filtered and isolated in pure form with no need of further purification. For comparative studies, 3a was synthesized using various solvents and catalysts. Results of synthesis of 3a under different reaction conditions are given in Tables 1 and 2. The structures of the newly synthesized compounds are determined on the basis of their FTIR, ¹H NMR, ¹⁹F NMR, ¹³C NMR, and mass spectral data.

4. Analgesic Activity

Few compounds have been screened for analgesic activity. The analgesic properties of the target compounds were tested using a model of central analgesia where the painful stimulus is represented by a hot plate heated to 56°C. Seven groups of 6 mice, each having an average weight of 25–35 g, were taken for study. The animals were kept for a week before the experiment under standard laboratory environment, with access to water ad libitum. The experiment consisted in measuring the reaction to pain as the time (in seconds) between the moment when the animal was placed on the plate and the moment when it begins to lick its back paws in response to painful stimulus.

The animals were treated as follows. Group 1: control group received 0.5% sodium CMC (1 mg/kg) I.P. Group 2: nimesulide 5 mg/kg was administered I.P. Group 3: the 3a in dose level of 50 mg/kg was administered I.P. Group 4: the 3b in dose level of 50 mg/kg was administered I.P. Group 5: the 3d in dose level of 50 mg/kg was administered I.P. Group 6: the 5b in dose level of 50 mg/kg was administered I.P. Group 7: the 5d in dose level of 50 mg/kg was administered I.P.The time response of the animal to painful stimulus was evaluated at 0, 30, 60, and 90 minutes interval after the administration of the tested substances. The recorded results were used to calculate for each group of animals the average response time to painful stimulus and the standard error. Statistical analysis (ANOVA followed by using Dunnett’s test) was performed for analgesic activity to ascertain the significance of the exhibited activity. Compounds 3b, 5d, and 5d have shown excellent analgesic activity as compared to other compounds which indicate that OCF₃ group is more potent than CF₃ and NO₂ groups (Table 7, Figure 2).

5. Conclusion

The use lemon juice as green catalyst offers a convenient, nontoxic, inexpensive reaction medium for the synthesis of olefinic compounds. This procedure is simpler, economical, milder, and faster, including cleaner reactions, high yields of products and a simple experimental and work-up procedure, which makes it a useful and attractive process and is also consistent with the green chemistry theme which affords excellent yields. Compounds bearing OCF₃ group possess excellent analgesic activity. With further molecular modification and manipulation of these compounds, several other promising bioactive molecules can be developed in future.

Acknowledgments

The authors are thankful to the Dean and HOD (Science and Humanities), FET, MITS, for providing necessary research facilities in the department. Financial assistance from FET, MITS is gratefully acknowledged. They are also thankful to SAIF, Punjab University, Chandigarh, India for the spectral analyses and Goenka College of Pharmacy, Department of Pharmacology, Lakshmangarh, Rajasthan, India for helping in performing analgesic activity.

References

Ş. G. Küçükgüzel, S. Rollas, H. Erdeniz, M. Kiraz, A. Cevdet Ekinci, and A. Vidin, “Synthesis, characterization and pharmacological properties of some 4-arylhydrazono-2-pyrazoline-5-one derivatives obtained from heterocyclic amines,” European Journal of Medicinal Chemistry, vol. 35, no. 7-8, pp. 761–771, 2000.
View at: Publisher Site | Google Scholar
S. A. F. Rostom, I. M. El-Ashmawy, H. A. Abd El Razik, M. H. Badr, and H. M. A. Ashour, “Design and synthesis of some thiazolyl and thiadiazolyl derivatives of antipyrine as potential non-acidic anti-inflammatory, analgesic and antimicrobial agents,” Bioorganic and Medicinal Chemistry, vol. 17, no. 2, pp. 882–895, 2009.
View at: Publisher Site | Google Scholar
S. Khode, V. Maddi, P. Aragade et al., “Synthesis and pharmacological evaluation of a novel series of 5-(substituted)aryl-3-(3-coumarinyl)-1-phenyl-2-pyrazolines as novel anti-inflammatory and analgesic agents,” European Journal of Medicinal Chemistry, vol. 44, no. 4, pp. 1682–1688, 2009.
View at: Publisher Site | Google Scholar
M. Abdel-Aziz, G. E. A. Abuo-Rahma, and A. A. Hassan, “Synthesis of novel pyrazole derivatives and evaluation of their antidepressant and anticonvulsant activities,” European Journal of Medicinal Chemistry, vol. 44, no. 9, pp. 3480–3487, 2009.
View at: Publisher Site | Google Scholar
Z. S. Quan, R. L. Li, and Y. Z. Ling, “Study of the relationship between structure and anticonvulsant activities of 5-substituted-1-butry-3-pyrazolidinones and their synthesis,” Acta Pharmaceutica Sinica, vol. 27, no. 9, pp. 711–716, 1992.
View at: Google Scholar
N. Das, A. Verma, P. K. Shrivastava, and S. K. Shrivastava, “Synthesis and biological evaluation of some new aryl pyrazol-3-one derivatives as potential hypoglycemic agents,” Indian Journal of Chemistry B, vol. 47, no. 10, pp. 1555–1558, 2008.
View at: Google Scholar
G. A. Idrees, O. M. Aly, G. E. A. A. Abuo-Rahma, and M. F. Radwan, “Design, synthesis and hypolipidemic activity of novel 2-(naphthalen-2-yloxy)propionic acid derivatives as desmethyl fibrate analogs,” European Journal of Medicinal Chemistry, vol. 44, no. 10, pp. 3973–3980, 2009.
View at: Publisher Site | Google Scholar
G. Ouyang, Z. Chen, X. Cai et al., “Synthesis and antiviral activity of novel pyrazole derivatives containing oxime esters group,” Bioorganic and Medicinal Chemistry, vol. 16, no. 22, pp. 9699–9707, 2008.
View at: Publisher Site | Google Scholar
D. Castagnolo, F. Manetti, M. Radi et al., “Synthesis, biological evaluation, and SAR study of novel pyrazole analogues as inhibitors of Mycobacterium tuberculosis: part 2. Synthesis of rigid pyrazolones,” Bioorganic and Medicinal Chemistry, vol. 17, no. 15, pp. 5716–5721, 2009.
View at: Publisher Site | Google Scholar
K. B. Umesha, K. M. L. Rai, and M. A. Harish Nayaka, “Antioxidant and antimicrobial activity of 5-methyl-2-(5-methyl-1,3-diphenyl-1H-pyrazole-4-carbonyl)-2,4-dihydro-pyrazol-3-one,” International Journal of Biomedical Science, vol. 5, no. 4, pp. 359–368, 2009.
View at: Google Scholar
R. Tripathy, A. Ghose, J. Singh et al., “1,2,3-Thiadiazole substituted pyrazolones as potent KDR/VEGFR-2 kinase inhibitors,” Bioorganic and Medicinal Chemistry Letters, vol. 17, no. 6, pp. 1793–1798, 2007.
View at: Publisher Site | Google Scholar
H. Park, K. Lee, S. Park et al., “Identification of antitumor activity of pyrazole oxime ethers,” Bioorganic and Medicinal Chemistry Letters, vol. 15, no. 13, pp. 3307–3312, 2005.
View at: Publisher Site | Google Scholar
R. Murugan, S. Anbazhagan, and S. S. Narayanan, “Synthesis and in vivo antidiabetic activity of novel dispiropyrrolidines through [3 + 2] cycloaddition reactions with thiazolidinedione and rhodanine derivatives,” European Journal of Medicinal Chemistry, vol. 44, no. 8, pp. 3272–3279, 2009.
View at: Publisher Site | Google Scholar
S. Chandrappa, C. V. Kavitha, M. S. Shahabuddin et al., “Synthesis of 2-(5-((5-(4-chlorophenyl)furan-2-yl)methylene)-4-oxo-2-thioxothiazolidin-3-yl)acetic acid derivatives and evaluation of their cytotoxicity and induction of apoptosis in human leukemia cells,” Bioorganic and Medicinal Chemistry, vol. 17, no. 6, pp. 2576–2584, 2009.
View at: Publisher Site | Google Scholar
E. W. Brooke, S. G. Davies, A. W. Mulvaney et al., “Synthesis and in vitro evaluation of novel small molecule inhibitors of bacterial arylamine N-acetyltransferases (NATs),” Bioorganic and Medicinal Chemistry Letters, vol. 13, no. 15, pp. 2527–2530, 2003.
View at: Publisher Site | Google Scholar
S. Ozkirimli, F. Kazan, and Y. Tunali, “Synthesis, antibacterial and antifungal activities of 3-(1,2,4-triazol-3-yl)-4-thiazolidinones,” Journal of Enzyme Inhibition and Medicinal Chemistry, vol. 24, no. 2, pp. 447–452, 2009.
View at: Publisher Site | Google Scholar
S. Chandrappa, S. B. Benaka Prasad, K. Vinaya, C. S. Ananda Kumar, N. R. Thimmegowda, and K. S. Rangappa, “Synthesis and in vitro antiproliferative activity against human cancer cell lines of novel 5-(4-methyl-benzylidene)-thiazolidine-2,4-diones,” Investigational New Drugs, vol. 26, no. 5, pp. 437–444, 2008.
View at: Publisher Site | Google Scholar
A. Verma and S. K. Saraf, “4-Thiazolidinone—a biologically active scaffold,” European Journal of Medicinal Chemistry, vol. 43, no. 5, pp. 897–905, 2008.
View at: Publisher Site | Google Scholar
D. Davidson and S. A. Bernhard, “The structure of Meldrum's supposed β-lactonic acid,” Journal of the American Chemical Society, vol. 70, no. 10, pp. 3426–3428, 1948.
View at: Google Scholar
K. Byun, Y. Mo, and J. Gao, “New insight on the origin of the unusual acidity of Meldrum's acid from αβ-initio and combined QM/MM simulation study,” Journal of the American Chemical Society, vol. 123, no. 17, pp. 3974–3979, 2001.
View at: Publisher Site | Google Scholar
B. Chen, “Meldrum's acid in organic synthesis,” Heterocycles, vol. 32, no. 3, pp. 529–597, 1991.
View at: Google Scholar
L. F. Tietze and U. Beifuss, “The knoevenagel reaction,” in Comprehensive Organic Synthesis, vol. 2, pp. 341–394, 1991.
View at: Google Scholar
B. Pita, E. Sotelo, M. Suárez et al., “Pyridazine derivatives. Part 21: synthesis and structural study of novel 4-aryl-2,5-dioxo-8-phenylpyrido[2,3-d]pyridazines,” Tetrahedron, vol. 56, no. 16, pp. 2473–2479, 2000.
View at: Publisher Site | Google Scholar
F. C. Brown, C. K. Bradsher, and S. M. Bond, “Some 5-substituted rhodanines,” Industrial & Engineering Chemistry, vol. 45, pp. 1030–1032, 1953.
View at: Google Scholar
K. Ramkumar, V. N. Yarovenko, A. S. Nikitina et al., “Design, synthesis and structure-activity studies of rhodanine derivatives as HIV-1 integrase inhibitors,” Molecules, vol. 15, no. 6, pp. 3958–3992, 2010.
View at: Publisher Site | Google Scholar
J. Iwao and K. J. Tomino, “Synthesis of pyrazolo [3, 4-b] pyridine by knovengel condensation,” Pharmaceutical Society of Japan, vol. 76, pp. 748–755, 1956.
View at: Google Scholar
B. A. Alekseenko, T. E. Gorizdra, and S. N. Baranov, “Synthesis and structure of noncondensed bicyclic thiazolidino-4-one derivatives,” Khimiya Geterotsiklicheskikh Soedinenii, vol. 5, pp. 230–231, 1969.
View at: Google Scholar
G. G. Allan, D. Maclean, and G. T. Newbold, “Condensation products of rhodanine, and keto-acids,” Journal of the Chemical Society, pp. 5132–5153, 1952.
View at: Google Scholar
F. C. Brown, C. K. Bradsher, S. G. McCallum, and M. Potter, “Rhodanine derivatives of ketones,” Journal of Organic Chemistry, vol. 15, no. 1, pp. 174–176, 1950.
View at: Google Scholar
M. M. Chowdhry, D. M. P. Mingos, A. J. P. White, and D. J. Williams, “Syntheses and characterization of 5-substituted hydantoins and thiazolines - Implications for crystal engineering of hydrogen bonded assemblies. Crystal structures t of 5-(2-pyridylmethylene)-hydantoin, 5-(2-pyridylmethylene)-2-thiohydantoin, 5-(2-pyridylmethylene)thiazolidine-2,4-dione, 5-(2-pyridylmethylene)rhodanine and 5-(2-pyridylmethylene)pseudothiohydantoin,” Journal of the Chemical Society, Perkin Transactions 1, vol. 1, no. 20, pp. 3495–3504, 2000.
View at: Publisher Site | Google Scholar
R. V. Hangarge, D. V. Jarikote, and M. S. Shingare, “Knoevenagel condensation reactions in an ionic liquid,” Green Chemistry, vol. 4, no. 3, pp. 266–268, 2002.
View at: Publisher Site | Google Scholar
S. S. Shindalkar, B. R. Madje, and M. S. Shingare, “Microwave induced, solvent-free Knoevenagel condensation of 4-oxo-(4H)-1-benzopyran-3-carbaldehyde with Meldrum's acid using alumina support,” Indian Journal of Chemistry B, vol. 45, no. 11, pp. 2571–2573, 2006.
View at: Google Scholar
S. Santosh, B. R. Shindalkar, R. V. Madje, P. T. Hangarge, M. K. D. Patil, and M. S. Shingare, “Borate zirconia mediated Knoevenagel condensation reaction in water,” Journal of the Korean Chemical Society, vol. 49, pp. 377–380, 2005.
View at: Google Scholar
S. S. Shindalkar, B. R. Madje, and M. S. Shingare, “Ultrasonically accelerated Knoevenagel condensation reaction at room temperature in distilled water,” Indian Journal of Chemistry B, vol. 44, no. 7, pp. 1519–1521, 2005.
View at: Google Scholar
N. B. Darvatkar, A. R. Deorukhkar, S. V. Bhilare, and M. M. Salunkhe, “Ionic liquid-mediated knoevenagel condensation of Meldrum's acid and aldehydes,” Synthetic Communications, vol. 36, no. 20, pp. 3043–3051, 2006.
View at: Publisher Site | Google Scholar
J. M. Khurana and K. Vij, “Nickel nanoparticles catalyzed chemoselective Knoevenagel condensation of Meldrum's acid and tandem enol lactonizations via cascade cyclization sequence,” Tetrahedron Letters, vol. 52, no. 28, pp. 3666–3669, 2011.
View at: Publisher Site | Google Scholar
S. Ghosh, J. Das, and S. Chattopadhyay, “A novel light induced Knoevenagel condensation of Meldrum's acid with aromatic aldehydes in aqueous ethanol,” Tetrahedron Letters, vol. 52, no. 22, pp. 2869–2872, 2011.
View at: Publisher Site | Google Scholar
A. M. Dumas, A. Seed, A. K. Zorzitto, and E. Fillion, “Triphenylphosphine mediated Knoevenagel condensation of Meldrum's acid with aromatic aldehydes,” Tetrahedron Letters, vol. 48, pp. 7072–7276, 2007.
View at: Google Scholar
K. Gong, Z. He, Y. Xu, D. Fang, and Z. Liu, “Green synthesis of 5-benzylidene rhodanine derivatives catalyzed by 1-butyl-3-methyl imidazolium hydroxide in water,” Monatshefte fur Chemie, vol. 139, no. 8, pp. 913–915, 2008.
View at: Publisher Site | Google Scholar
K. F. Shelke, S. B. Sapkal, B. R. Madja, B. B. Shingate, and M. S. Shingare, “Ionic liquid promoted an efficient synthesis of 5-arylidene-2, 4-thiazolidinedione,” Bulletin of the Catalysis Society of India, vol. 8, pp. 30–34, 2009.
View at: Google Scholar
J. Zhou, Y. Song, F. Zhu, and Y. Zhu, “Facile synthesis of 5-benzylidene rhodamine derivatives under microwave irradiation,” Synthetic Communications, vol. 36, no. 22, pp. 3297–3303, 2006.
View at: Publisher Site | Google Scholar
K. Bourahla, A. Derdour, M. Rahmouni, F. Carreaux, and J. P. Bazureau, “A practical access to novel 2-amino-5-arylidene-1,3-thiazol-4(5H)-ones via sulfur/nitrogen displacement under solvent-free microwave irradiation,” Tetrahedron Letters, vol. 48, no. 33, pp. 5785–5789, 2007.
View at: Publisher Site | Google Scholar
S. Patil, S. D. Jadhav, and U. P. Patil, “Natural acid catalyzed synthesis of schiff base under solvent-free condition: as a green approach,” Journal of Applied Sciences Research, vol. 4, no. 2, pp. 1074–1078, 2012.
View at: Google Scholar
H. L. Yale, “The trifluoromethyl group in medicinal chemistry,” Journal of Medicinal and Pharmaceutical Chemistry, vol. 1, no. 2, pp. 121–133, 1959.
View at: Google Scholar
P. C. Appelbaum and P. A. Hunter, “The fluoroquinolone antibacterials: past, present and future perspectives,” International Journal of Antimicrobial Agents, vol. 16, no. 1, pp. 5–15, 2000.
View at: Publisher Site | Google Scholar
F. M. D. Ismail, G. B. D. Michael, and J. Michael, “Modulation of drug pharmacokinetics and pharmacodynamics by fluorine substitution,” Chemistry today, vol. 27, no. 3, pp. 18–21, 2009.
View at: Google Scholar
H. Sachdeva, D. Dwivedi, K. Arya, S. Khaturia, and R. Saroj, “Anti-inflammatory activity, and QSAR study of some Schiff bases derived from 5-mercapto-3-( $4^{'}$ -pyridyl)-4H-1,2,4-triazol-4-yl-thiosemicarbazide,” Medicinal Chemistry Research, 2013.
View at: Publisher Site | Google Scholar
A. Dandia, H. Sachdeva, and R. Singh, “Improved synthesis of 3-spiro indolines in dry media under microwave irradiation,” Synthetic Communications, vol. 31, no. 12, pp. 1879–1892, 2001.
View at: Publisher Site | Google Scholar
H. Sachdeva, D. Dwivedi, and S. Khaturia, “Aqua mediated facile synthesis of 2-(5/7-fluorinated-2-oxoindolin-3-ylidene)-N- (4-substituted phenyl) hydrazine carbothioamides,” Research Journal of Pharmaceutical, Biological and Chemical Sciences, vol. 2, no. 2, pp. 213–219, 2011.
View at: Google Scholar
H. Sachdeva and D. Dwivedi, “Lithium-acetate-mediated biginelli one-pot multicomponent synthesis under solvent-free conditions and cytotoxic activity against the human lung Cancer Cell line A549 and Breast Cancer cell line MCF7,” The Scientific World Journal, vol. 2012, Article ID 109432, 9 pages, 2012.
View at: Publisher Site | Google Scholar

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Copyright © 2013 Harshita Sachdeva 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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