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Current Organic Synthesis

Editor-in-Chief

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

Research Article

One-pot Multicomponent Synthesis of pyrrolo[1,2-d][1,4]benzoxazines and pyrrolo[1, 2-a]pyrazines in Water Catalyzed by Fe3O4@SiO2@L-Arginine-SA Magnetic Nanoparticles

Author(s): Hedieh Rostami and Lotfi Shiri*

Volume 17, Issue 6, 2020

Page: [473 - 482] Pages: 10

DOI: 10.2174/1573409916666200128163047

Price: $65

Abstract

Aims: Synthesis of pyrrolo[1,2-d][1,4]benzoxazines and pyrrolo[1,2-a]pyrazines using magnetic nanoparticles.

Background: One-pot, three component reaction for the synthesis of pyrrolo[1,2-d][1,4]benzoxazines and pyrrolo[1,2-a]pyrazines is reported. For the synthesis of pyrrolo[1,2-d][1,4]benzoxazines use of 2- aminophenols, dialkylacetylenedicarboxylates and β -nitrostyrene derivatives and Pyrrolo[1,2-a]pyrazines synthesized from reaction of ethylenediamine, dialkylacetylenedicarboxylates and β-nitrostyrene derivatives is discussed.

Materials and Methods: 2-aminophenol (0.5 mmol) and dimethylacetylenedicarboxylate (0.5 mmol) in water (3 ml) were stirred at room temperature for 10 min. Then, β-nitrostyrene (0.5 mmol) and Fe3O4@SiO2@LArginine- SA MNPs (0.07 g) were added and the mixture was refluxed for 5 h. After completion of the reaction, the mixture was cooled to room temperature and the catalyst was separated with external magnet and product extracted with dichloromethane. More purification of products was performed by column chromatography (nhexane/ ethyl acetate 4:1). Ethylenediamine (0.6 mmol) was added to dialkylacetylenedicarboxylate (0.6 mmol) in 3 ml water and was stirred for 10 min at room temperature. Later, β -nitrostyrene (0.5 mmol) and Fe3O4@SiO2@L-Arginine-SA MNPs (0.06 g) were added to mixture reaction and refluxed for 3 h. After completion, the mixture reaction was cooled to room temperature and the catalyst was separated by an external magnet. Then, the product was extracted with dichloromethane. For more purification column chromatography was used (n-hexane/ethylacetate 1:1).

Results and Discussions: In this research, we have synthesized new derivatives of pyrrolo[1,2- d][1.4]benzoxazines and pyrrolo[1,2-a]pyrazines in green conditions consisting of use of water as a green solvent and magnetic nanoparticles.

Conclusion: In this research, we have synthesized new derivatives of pyrrolo[1,2-d][1.4]benzoxazines and pyrrolo[1,2-a]pyrazines in green conditions consisting of use of water as a green solvent and magnetic nanoparticles which were easily separated from mixture with an external magnet and had the capability to be recovered and reused. Also, in this work, the yield was good and the time of reactions was low compared with prior research.

Keywords: Three component reaction, pyrrolo[1, 2-d][1, 4]benzoxazines, pyrrolo[1, 2-a]pyrazines, β-nitrostyrene derivatives, nanoparticles, scanning electron microscopy.

Graphical Abstract

[1]
Yavari, I.; Moradi, L. A synthesis of isoxazoles through the reaction of activated acetylenes and alkyl 2-nitroethanoates in the presence of triphenylphosphine. Tetrahedron Lett., 2006, 47, 1627-1629.
[http://dx.doi.org/10.1016/j.tetlet.2005.12.112]
[2]
Bloxam, J.; Dell, C.P.; Smith, C.W. Preparation of some new benzylidenemalononitriles by an SNAr reaction: application to naphtho[1, 2‐b]pyran synthesis. Heterocycles, 1994, 38, 399-408.
[http://dx.doi.org/10.3987/COM-93-6594]
[3]
Yavari, I.; Hossaini, Z.; Sabbaghan, M. A synthesis of pyrrolo [2, 1-a] isoquinolines through the reaction of activated acetylenes and isoquinoline in the presence of ethyl bromopyruvate. Tetrahedron Lett., 2006, 47, 6037-6040.
[http://dx.doi.org/10.1016/j.tetlet.2006.06.113]
[4]
Denny, W.A.; Rewcastle, G.W.; Baguley, B.C. Potential antitumor agents. 59. Structure-activity relationships for 2-phenylbenzimidazole-4-carboxamides, a new class of “minimal” DNA-intercalating agents which may not act via topoisomerase II. J. Med. Chem., 1990, 33, 814-819.
[http://dx.doi.org/10.1021/jm00164a054] [PMID: 2153829]
[5]
Del Poeta, M.A.; Schell, W.C.; Dykstra, C.K.; Jones, S.R.; Tidwell, R.; Czamy, A.; Bajic, M.; Kumar, A.; Boykin, D.R.; Perfect, J. Structure-In vitro activity relationships of pentamidine analogues and dication-substituted bis-benzimidazoles as new antifungal agents antimicrob. Agents Chemother, 1998, 4, 2495-2502.
[http://dx.doi.org/10.1128/AAC.42.10.2495]
[6]
Lehuédé, J.; Fauconneau, B.; Barrier, L.; Ourakow, M.; Piriou, A.; Vierfond, J. Synthesis and antioxidant activity of new tetraarylpyrroles. Eur. J. Med. Chem., 1999, 34, 991-996.
[http://dx.doi.org/10.1016/S0223-5234(99)00111-7] [PMID: 10889322]
[7]
Commandeur, M.; Commandeur, C.; De Paolis, M.; Edmunds, A.J.F.; Maienfisch, P.; Ghosez, L. Studies related to the total synthesis of the sesquiterpene core of the pyrrolobenzoxazine natural products CJ-12662 and CJ-12663. Tetrahedron Lett., 2009, 50, 3359-3362.
[http://dx.doi.org/10.1016/j.tetlet.2009.02.105]
[8]
Park, S.; Jung, Y.; Kim, I. Diversity-oriented decoration of pyrrolo[1, 2-a]pyrazines. Tetrahedron, 2014, 70, 7534-7550.
[http://dx.doi.org/10.1016/j.tet.2014.08.003]
[9]
Ouberai, M.; Asche, C.; Carrez, D.; Croisy, A.; Dumy, P.; Demeunynck, M. 3,4-Dihydro-1H-[1,3]oxazino[4,5-c]acridines as a new family of cytotoxic drugs. Bioorg. Med. Chem. Lett., 2006, 16, 4641-4643.
[http://dx.doi.org/10.1016/j.bmcl.2006.05.101] [PMID: 16777412]
[10]
Li, X.; Manjunatha, U.H.; Goodwin, M.B.; Knox, J.E.; Lipinski, C.A.; Keller, T.H.; Barry, C.E., III; Dowd, C.S. Synthesis and antitubercular activity of 7-(R)- and 7-(S)-methyl-2-nitro-6-(S)-(4-(trifluoromethoxy) benzyloxy)-6,7-dihydro-5H-imidazo[2,1-b][1,3]oxazines, analogues of PA-824. Bioorg. Med. Chem. Lett., 2008, 18, 2256-2262.
[http://dx.doi.org/10.1016/j.bmcl.2008.03.011] [PMID: 18358721]
[11]
Mathew, B.P.; Kumar, A.; Sharma, S.; Shukla, P.K.; Nath, M. An eco-friendly synthesis and antimicrobial activities of dihydro-2H-benzo- and naphtho-1,3-oxazine derivatives. Eur. J. Med. Chem., 2010, 45, 1502-1507.
[http://dx.doi.org/10.1016/j.ejmech.2009.12.058] [PMID: 20116901]
[12]
Sawant, R.; Bhangale, L.; Wadekar, J.; Gaikwad, P. Substituent Selection for Design and Synthesis of Antimicrobial 1, 3 Oxazines, a Topliss Modified Approach. Farmacia, 2012, 60, 32-39.
[13]
Henry, B.L.; Desai, U.R. Recent research developments in the direct inhibition of coagulation proteinases--inhibitors of the initiation phase. Cardiovasc. Hematol. Agents Med. Chem., 2008, 6, 323-336.
[http://dx.doi.org/10.2174/187152508785909519] [PMID: 18855645]
[14]
Sawant, R.L.; Mhaske, M.S.; Wadekar, J.B. A series of Schiff bases of 1, 3-oxazines were synthesized via reaction of 1, 3-oxazine-2-amine with substituted benzaldehyde and they exhibited. Int. J. Pharma Sci., 2012, 4, 320-323.
[15]
Chang-Fong, J.; Addo, J.; Dukat, M.; Smith, C.; Mitchell, N.A.; Herrick-Davis, K.; Teitler, M.; Glennon, R.A. Evaluation of isotryptamine derivatives at 5-HT(2) serotonin receptors. Bioorg. Med. Chem. Lett., 2002, 12(2), 155-158.
[http://dx.doi.org/10.1016/S0960-894X(01)00713-2] [PMID: 11755343]
[16]
Fisher, T.E.; Kim, B.; Staas, D.D.; Lyle, T.A.; Young, S.D.; Vacca, J.P.; Zrada, M.M.; Hazuda, D.J.; Felock, P.J.; Schleif, W.A.; Gabryelski, L.J.; Anari, M.R.; Kochansky, C.J.; Wai, J.S. 8-Hydroxy-3,4-dihydropyrrolo[1,2-a]pyrazine-1(2H)-one HIV-1 integrase inhibitors. Bioorg. Med. Chem. Lett., 2007, 17, 6511-6515.
[http://dx.doi.org/10.1016/j.bmcl.2007.09.086] [PMID: 17931865]
[17]
Arban, R.; Bianchi, F.; Buson, A.; Cremonesi, S.; Di Fabio, R.; Gentile, G.; Micheli, F.; Pasquarello, A.; Pozzan, A.; Tarsi, L.; Terreni, S.; Tonelli, F. Pyrrolo[1,2-a]pyrazine and pyrazolo[1,5-a]pyrazine: novel, potent, and selective series of Vasopressin 1b receptor antagonists. Bioorg. Med. Chem. Lett., 2010, 20, 5044-5049.
[http://dx.doi.org/10.1016/j.bmcl.2010.07.037] [PMID: 20674355]
[18]
Micheli, F.; Bertani, B.; Bozzoli, A.; Crippa, L.; Cavanni, P.; Di Fabio, R.; Donati, D.; Marzorati, P.; Merlo, G.; Paio, A.; Perugini, L.; Zarantonello, P. Phenylethynyl-pyrrolo[1,2-a]pyrazine: a new potent and selective tool in the mGluR5 antagonists arena. Bioorg. Med. Chem. Lett., 2008, 18, 1804-1809.
[http://dx.doi.org/10.1016/j.bmcl.2008.02.024] [PMID: 18304814]
[19]
Alizadeh, A.; Bagherinejad, A.; Moafi, L.; Zhu, L.G. A catalyst-free synthetic route to thiazolo [3, 4-a]benzimidazole derivatives through a three-component reaction. Synlett, 2016, 27, 1803-1805.
[http://dx.doi.org/10.1055/s-0035-1561612]
[20]
Moradi, L.; Piltan, M.; Rostami, H. One-pot synthesis of novel pyrrolo-1,4-benzoxazines via a three-component reaction of 2-amino phenols, acetylenic esters and nitrostyrene derivatives. Chin. Chem. Lett., 2014, 25, 123-126.
[http://dx.doi.org/10.1016/j.cclet.2013.10.009]
[21]
Maleki, A.; Chalavand, R.; Firouzi Haji, R. Synthesis and characterization of the novel diamine‐functionalized Fe3O4@SiO2 nanocatalyst and its application for one‐pot three component synthesis of chromenes. Appl. Organomet. Chem., 2017, , 31.
[http://dx.doi.org/10.1002/aoc.3916]
[22]
Esmaeili, A.; Kakavand, S. Nanocomposites with different metals as magnetically separable nanocatalysts for oxidation of aldehydes. C. R. Chim., 2016, 19, 936-941.
[http://dx.doi.org/10.1016/j.crci.2016.02.009]
[23]
Zheng, X.; Luo, S.; Zhang, L.; Cheng, J.P. Magnetic nanoparticle supported ionic liquid catalysts for CO2 cycloaddition reactions. Green Chem., 2009, 11, 455-458.
[http://dx.doi.org/10.1039/b823123k]
[24]
Shiri, L.; Narimani, H.; Kazemi, M. Synthesis and characterization of sulfamic acid supported on Fe3O4 nanoparticles: A green, versatile and magnetically separable acidic catalyst for oxidation reactions and Knoevenagel condensation. Appl. Organomet. Chem., 2017, , 32.
[http://dx.doi.org/10.1002/aoc.3927]
[25]
Ghorbani-choghamarani, A.; Shiri, L.; Azadi, G. The first report on eco-friendly synthesis of 5-substituted 1H-tetrazoles in PEG catalyzed by Cu (II) immobilized on Fe3O4@SiO2@L-Arginine as a novel, recyclable and non-corrosive catalyst. RSC Advances, 2016, 6, 32653-32660.
[http://dx.doi.org/10.1039/C6RA03023H]
[26]
Naganaboina, R.T.; Nayak, A.; Peddinti, R.K. Trifluoroacetic acid-promoted Michael addition-cyclization reactions of vinylogous carbamates. Org. Biomol. Chem., 2014, 12, 3366-3370.
[http://dx.doi.org/10.1039/C4OB00437J] [PMID: 24756460]
[27]
Moradi, L.; Piltan, M.; Rostami, H.; Abasi, G. One-pot synthesis of pyrrolo[1,2-a] pyrazines via three component reaction of ethylenediamine, acetylenic esters and nitrostyrene derivatives. Chin. Chem. Lett., 2013, 24, 740-742.
[http://dx.doi.org/10.1016/j.cclet.2013.04.038]

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