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Current Organic Synthesis

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ISSN (Print): 1570-1794
ISSN (Online): 1875-6271

Research Article

Facile Synthesis of Naphtha-quinoxaline Derivatives from β-lapachone Using Graphene Oxide as Catalyst

Author(s): Pooja Vyas, Barkha Darra Wadhwani, Ravindra Singh Rao and Poonam Khandelwal*

Volume 17, Issue 2, 2020

Page: [91 - 97] Pages: 7

DOI: 10.2174/1570179416666191210102358

Price: $65

Abstract

Objective: To develop efficient method for the synthesis of naphtha-quinoxaline derivatives via the reaction of β-lapachone with various 1,2-diamines.

Methods: A mixture of β-lapachone (1mmol), 1,2-diamine (1mmol) and graphene oxide (20mg) in methanol (3mL) was heated at 60°C, under constant stirring for appropriate time. After completion of the reaction, the catalyst was filtered off, washed with ethyl acetate (3x3mL) and the combined filtrate was washed with H2O, dried (anhy. Na2SO4) and concentrated under vacuum. The residue was chromatographed over a column of silica gel eluting with a mixture of hexane and ethyl acetate in different ratios, to afford the desired product. All synthesized compounds were assigned with the help of analytical and 1H, 13C NMR, IR, and mass spectral studies.

Results: To establish the catalytic role of GO in the synthesis of naphtha-quinoxaline derivatives, the reaction of β-lapachone with 3,4-diaminotoluene was selected as a model reaction. The catalytic activity of graphene oxide in comparison with other catalysts like acidic resin amberlyst-15 and solid acid catalyst like montmorillonite K-10 were studied. The reaction was also observed in various solvents such as water, acetonitrile, toluene, dichloromethane, ethanol and 1,4-dioxane using GO as a catalyst. Excellent yields were obtained at 60°C in methanol. The efficacy of the present protocol was investigated by the reaction of β- lapachone with other 1,2-diamines.

Conclusion: An attractive green metal free carbocatalyst Graphene Oxide (GO) has been successfully utilized for the expedient synthesis of naphtha-quinoxaline derivatives. GO showed high catalytic activity which is attested by the desired products being produced in shorter time. The main advantage of this method is the reusability of the catalyst which makes the procedure sustainable.

Keywords: Graphene oxide, β-lapachone, 1, 2-naphthoquinone, 1, 2-diamines, acid catalyst, naphtha-quinoxaline.

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[1]
Li, C.J.; Wang, C.; Pardee, A.B. Induction of apoptosis by β-lapachone in human prostate cancer cells. Cancer Res., 1995, 55(17), 3712-3715.
[PMID: 7641181]
[2]
Dolan, M.E.; Frydman, B.; Thompson, C.B.; Diamond, A.M.; Garbiras, B.J.; Safa, A.R.; Beck, W.T.; Marton, L.J. Effects of 1,2-naphthoquinones on human tumor cell growth and lack of cross-resistance with other anticancer agents. Anticancer Drugs, 1998, 9(5), 437-448. Available at
[http://dx.doi.org/10.1097/00001813-199806000-00011] [PMID: 9660542]
[3]
Pink, J.J.; Wuerzberger-Davis, S.; Tagliarino, C.; Planchon, S.M.; Yang, X.; Froelich, C.J.; Boothman, D.A. Activation of a cysteine protease in MCF-7 and T47D breast cancer cells during beta-lapachone-mediated apoptosis. Exp. Cell Res., 2000, 255(2), 144-155. Available at
[http://dx.doi.org/10.1006/excr.1999.4790] [PMID: 10694431]
[4]
Woo, H.J.; Choi, Y.H. Growth inhibition of A549 human lung carcinoma cells by beta-lapachone through induction of apoptosis and inhibition of telomerase activity. Int. J. Oncol., 2005, 26(4), 1017-1023.
[PMID: 15753997]
[5]
Vyas, P.; Yadav, D.K. Khandelwal. P. Tectona grandis (teak) - A review on its phytochemical and therapeutic potential. Nat. Prod. Res, 2018. [Formerly Natural Product Letters]. Available at
[http://dx.doi.org/10.1080/14786419.2018.1440217] [PMID: 29506390]
[6]
a) Singh, P.; Khandelwal, P.; Hara, N.; Asai, T.; Fujimoto, Y. Radermachol and naphthoquinone derivatives from Tecomella undulata: Complete 1H and 13C NMR assignments of radermachol with the aid of computational 13C shift prediction. Indian J. Chem., 2008, 47B, 1865-1870.
b) Singh, P.; Krishna, V.; Khandelwal, P.; Sharma, K.K.; Sharma, M.C. Chemistry of lapachol - Syntheses of some new biogenetically related naphthoquinones, naphthoquinone dimers, naphthaquinoxaline and naphthazaquinoxaline derivatives from lapachol. J. Indian Chem. Soc., 2010, 87, 85-95.
c) Khandelwal, P.; Singh, P. Tabebuin and tecomaquinone-III- dimeric quinones from Tabebuia rosea. J. Indian Chem. Soc., 2008, 85, 310-312.
d) Khandelwal, P.; Singh, P.; Taniguchi, T.; Monde, K.; Uekusa, H.; Masubuti, H.; Fujimoto, Y. Revision of the relative and absolute stereochemistries of 3-hydroxy-dehydroiso-α-lapachone and its 8-hydroxy derivative. Phytochem. Lett., 2014, 10, 224-229. Available at
[http://dx.doi.org/10.1016/j.phytol.2014.10.004]
[7]
Martinez, M.J.A.; Benito, P.B. Biological activity of quinones. Studies in Natural Products Chemistry, 2005, 30, 303-366. Available at
[http://dx.doi.org/10.1016/S1572-5995(05)80036-5]
[8]
Sacau, E.P.; Estévez-Braun, A.; Ravelo, A.G.; Ferro, E.A.; Tokuda, H.; Mukainaka, T.; Nishino, H. Inhibitory effects of lapachol derivatives on epstein-barr virus activation. Bioorg. Med. Chem., 2003, 11(4), 483-488. Available at
[http://dx.doi.org/10.1016/S0968-0896(02)00542-4] [PMID: 12538012]
[9]
O’Brien, P.J. Molecular mechanisms of quinone cytotoxicity. Chem. Biol. Interact., 1991, 80(1), 1-41. Available at
[http://dx.doi.org/10.1016/0009-2797(91)90029-7] [PMID: 1913977]
[10]
de Almeida, E.R.; da Silva Filho, A.A.; dos Santos, E.R.; Lopes, C.A. Antiinflammatory action of lapachol. J. Ethnopharmacol., 1990, 29(2), 239-241. Available at
[http://dx.doi.org/10.1016/0378-8741(90)90061-W] [PMID: 2374436]
[11]
Guiraud, P.; Steiman, R.; Campos-Takaki, G.M.; Seigle-Murandi, F.; Simeon de Buochberg, M. Comparison of antibacterial and antifungal activities of lapachol and β-lapachone. Planta Med., 1994, 60(4), 373-374. Available at
[http://dx.doi.org/10.1055/s-2006-959504] [PMID: 7938274]
[12]
Ioset, J.R.; Marston, A.; Gupta, M.P.; Hostettmann, K. Antifungal and larvicidal meroterpenoid naphthoquinones and a naphthoxirene from the roots of Cordia linnaei. Phytochemistry, 1998, 47(5), 729-734. Available at
[http://dx.doi.org/10.1016/S0031-9422(97)00695-X] [PMID: 9542168]
[13]
a) Rao, C.N.; Sood, A.K.; Subrahmanyam, K.S.; Govindaraj, A. Graphene: the new two-dimensional nanomaterial. Angew. Chem. Int. Ed. Engl., 2009, 48(42), 7752-7777. Available at
[http://dx.doi.org/10.1002/anie.200901678] [PMID: 19784976]
b) Hummers, W.S.; Offemann, R.E. Preparation of Graphitic Oxide. J. Am. Chem. Soc., 1958, 80, 1339. Available at
[http://dx.doi.org/10.1021/ja01539a017]
c) Brodie, C.B. Sur le poids atomique du graphite. Ann. Chim. Phys., 1860, 59, 466-472.
d) Wu, J.; Pisula, W.; Müllen, K. Graphenes as potential material for electronics. Chem. Rev., 2007, 107(3), 718-747. Available at
[http://dx.doi.org/10.1021/cr068010r] [PMID: 17291049]
e) Boehm, P.H.; Eckel, M.; Scholz, W. Anorg. Z. Untersuchungen am Graphitoxid V. Über den Bildungsmechanismus des Graphitoxids. Allg. Chem., 1967, 353, 236-242. Available at
[http://dx.doi.org/10.1002/zaac.19673530503]
f) Eda, G.; Fanchini, G.; Chhowalla, M. Large-area ultrathin films of reduced graphene oxide as a transparent and flexible electronic material. Nat. Nanotechnol., 2008, 3, 270-274.
g) Geim, A.K. Graphene: Status and prospects. Science, 2009, 324, 1530-1534. 9h) Allen M.J.; Tung V. C.; Kaner R.B. Honeycomb Carbon: A review of graphene. Chem. Rev.,2010, 110, 132-145.(i) Nakajima T.; Matsuo Y. Formation process and structure of graphite oxide. Carbon, 1994, 32, 469-475.
[14]
Szabo, T.; Tombacz, E.; Illes, E.; Dekany, I. Enhanced acidity and pH‐dependent surface charge characterization of successfully oxidized graphite oxide. Carbon, 2006, 44, 537-545. Available at
[http://dx.doi.org/10.1016/j.carbon.2005.08.005]
[15]
a) Li, D.; Kaner, R.B. Materials science. Graphene-based materials. Science, 2008, 320(5880), 1170-1171. Available at
[http://dx.doi.org/10.1126/science.1158180] [PMID: 18511678]
b) Eigler, S.; Hirsch, A. Chemistry with graphene and graphene oxide-challenges for synthetic chemists. Angew. Chem. Int. Ed. Engl., 2014, 53(30), 7720-7738. Available at
[http://dx.doi.org/10.1002/anie.201402780] [PMID: 24962439]
c) Navalon, S.; Dhakshinamoorthy, A.; Alvaro, M.; Garcia, H. Carbocatalysis by graphene-based materials. Chem. Rev., 2014, 114(12), 6179-6212. Available at
[http://dx.doi.org/10.1021/cr4007347] [PMID: 24867457]
d) Rajesh, U.C.; Wang, J.; Prescott, S.; Tsuzuki, T.; Rawat, D.S. RGO/ZnO Nanocompositae: An efficient sustainable, heterogenous, amphiphilic catalyst for synthesis of 3-substituted indoles in water. ACS Sustain. Chem.& Eng., 2015, 3, 9-18. Available at
[http://dx.doi.org/10.1021/sc500594w]
e) Dreyer, D.R.; Todd, A.D.; Bielawski, C.W. Harnessing the chemistry of graphene oxide. Chem. Soc. Rev., 2014, 43(15), 5288-5301. Available at
[http://dx.doi.org/10.1039/C4CS00060A] [PMID: 24789533]
[16]
Jia, H.P.; Dreyer, D.R.; Bielawski, C.W. Graphite oxide as an auto-tandem oxidation–hydration–aldol coupling catalyst. Adv. Synth. Catal., 2011, 353, 528-532. Available at
[http://dx.doi.org/10.1002/adsc.201000748]
[17]
Hamdouchi, C.; Ezquerra, J.; Vega, J.A.; Vaquero, J.J.; Alvarez-Builla, J.; Heinz, B.A. Short synthesis and anti-rhinoviral activity of imidazo[1,2-a]pyridines: the effect of acyl groups at 3-position. Bioorg. Med. Chem. Lett., 1999, 9(10), 1391-1394. Available at
[http://dx.doi.org/10.1016/S0960-894X(99)00193-6] [PMID: 10360742]
[18]
a) Dreyer, D.R.; Park, S.; Bielawski, C.W.; Ruoff, R.S. The chemistry of graphene oxide. Chem. Soc. Rev., 2010, 39(1), 228-240. Available at
[http://dx.doi.org/10.1039/B917103G] [PMID: 20023850]
b) Boehm, H.P.; Clauss, A.; Fischer, G.; Hofmann, U. The adsorption behavior of very thin carbon films. Z. Anorg. Allg. Chem., 1962, 316, 119-127. Available at
[http://dx.doi.org/10.1002/zaac.19623160303]
c) Dreyer, D.R.; Jia, H-P.; Todd, A.D.; Geng, J.; Bielawski, C.W. Graphite oxide: a selective and highly efficient oxidant of thiols and sulfides. Org. Biomol. Chem., 2011, 9(21), 7292-7295. Available at
[http://dx.doi.org/10.1039/c1ob06102j] [PMID: 21909587]
d) Jia, H-P.; Dreyer, D.R.; Bielawski, C.W. C–H oxidation using graphite oxide. Tetrahedron, 2011, 67, 4431-4434. Available at
[http://dx.doi.org/10.1016/j.tet.2011.02.065]
e) Huang, H.; Huang, J. Liu Y-M., He, H.Y.; Cao Y. and Fan, K.N. Graphite oxide as an efficient and durable metal-free catalyst for aerobic oxidative coupling of amines to imines. Green Chem., 2012, 14, 930-934. Available at
[http://dx.doi.org/10.1039/c2gc16681j]
f) Kumar, A.V.; Rao, K.R. Recyclabe graphite oxide catalysed Friedel-crafts addition of indoles to alpha, beta-unsaturated ketone. Tetrahedron Lett., 2011, 52, 5188-5191. Available at
[http://dx.doi.org/10.1016/j.tetlet.2011.08.002]
[19]
Dreyer, D.R.; Jia, H.P.; Bielawski, C.W. Graphene oxide: a convenient carbocatalyst for facilitating oxidation and hydration reactions. Angew. Chem. Int. Ed. Engl., 2010, 49(38), 6813-6816. Available at
[http://dx.doi.org/10.1002/anie.201003238] [PMID: 20602388]
[20]
a) Basu, B.; Kundu, S.; Sengupta, D. Graphene oxide as a carbocatalyst: The first example of a one-pot sequential dehydration–hydrothiolation of secondary aryl alcohols. RSC Advances, 2013, 3, 22130-22134. Available at
[http://dx.doi.org/10.1039/c3ra44712j]
b) Roy, B.; Sengupta, D.; Basu, B. Graphene oxide (GO)-catalyzed chemoselective thioacetalization of aldehyde under solvent free conditions. Tetrahedron Lett., 2014, 55, 6596-6600. Available at
[http://dx.doi.org/10.1016/j.tetlet.2014.10.043]
[21]
a) Hummers, W.S., Jr; Offeman, R.E. Preparation of Graphitic Oxide. J. Am. Chem. Soc., 1958, 80, 1339. Available at
[http://dx.doi.org/10.1021/ja01539a017]
b) Liao, K.H.; Mittal, A.; Bose, S.; Leighton, C.; Mkhoyan, K.A.; Macosko, C.W. Aqueous only route toward graphene from graphite oxide. ACS Nano, 2011, 5(2), 1253-1258. Available at
[http://dx.doi.org/10.1021/nn1028967] [PMID: 21271739]
[22]
Marcano, D.C.; Kosynkin, D.V.; Berlin, J.M.; Sinitskii, A.; Sun, Z.; Slesarev, A.; Alemany, L.B.; Lu, W.; Tour, J.M. Improved synthesis of graphene oxide. ACS Nano, 2010, 4(8), 4806-4814. Available at
[http://dx.doi.org/10.1021/nn1006368] [PMID: 20731455]
[23]
Santra, S.; Hota, P.K.; Bhattacharyya, R.; Bera, P.; Ghosh, P.; Mandal, S.K. Palladium nanoparticles on graphite oxide: A recyclable catalyst for synthesis of biaryl cores. ACS Catal., 2013, 3, 2776-2789. Available at
[http://dx.doi.org/10.1021/cs400468h]
[24]
Dhopte, K.B.; Zambare, R.S.; Patwardhan, A.V.; Nemade, P.R. Role of graphene oxide as heterogeneous acid catalyst and benign oxidant for synthesis of benzimidazoles and benzothiazoles. RSC Advances, 2016, 6, 8164-8172. Available at
[http://dx.doi.org/10.1039/C5RA19066E]
[25]
Khandelwal, P.; Vyas, P.; Yadav, D.K.; Koolwal, N.; Singh, P. Synthesis of new heterocycles through the reaction of β-lapachone with 1,2-diamines using Triton X-100 surfactant as catalyst in aqueous medium. Synth. Commun., 2017, 47, 688-694. Available at
[http://dx.doi.org/10.1080/00397911.2017.1281420]
[26]
Singh, P.; Dandia, A.; Khandelwal, P. Studies on novel polycyclic heterocycles: Synthesis of new naphthaquinoxaline and naphthazaquinoxaline derivatives from naturally occurring quinones. Indian J. Chem., 2008, 47B, 427-433.

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