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Synthesis and antimicrobial activities of pyrido[2,3-d]pyrimidine, pyridotriazolopyrimidine, triazolopyrimidine, and pyrido[2,3-d:6,5d']dipyrimidine derivatives
Anhar Abdel-Aziem (1)
, Marwa Sayed El-Gendy (2) , Abdou Osman Abdelhamid (3,*) (1) Department of Chemistry, Faculty of Science (Girls), Azhar University, Nasr City, Cairo, 11754, Egypt
(2) Department of Chemistry, Faculty of Science (Girls), Azhar University, Nasr City, Cairo, 11754, Egypt
(3) Department of Chemistry, Faculty of Science, Cairo University, Giza, 12613, Egypt
(*) Corresponding Author
Received: 25 Sep 2012 | Revised: 25 Oct 2012 | Accepted: 30 Oct 2012 | Published: 31 Dec 2012 | Issue Date: December 2012
Abstract
A new series of pyridotriazolopyrimidines were synthesized via reaction of hydrazonoyl halides with pyrido[2,3-d]pyrimidines. The structures of the newly synthesized compounds were established by elemental analysis, spectral data and alternative synthetic routes whenever possible. Some of synthesized compounds were also screened in vitro for their antimicrobial activity against a variety of bacterial and fungal samples.
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DOI: 10.5155/eurjchem.3.4.455-460.683
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[1]. Pankaj Kumar Singh, Shalki Choudhary, Aanchal Kashyap, Himanshu Verma, Swati Kapil, Manoj Kumar, Mohit Arora, Om Silakari
An exhaustive compilation on chemistry of triazolopyrimidine: A journey through decades
Bioorganic Chemistry 88, 102919, 2019
DOI: 10.1016/j.bioorg.2019.102919
[2]. Tariq A. Shah, Zubair Ahmad, Niyaz A. Mir, M. Muneer, Nigam P. Rath, Musheer Ahmad
One step synthesis of highly functionalized thiazolo[3,2-b][1,2,4]triazole, triazolo[1,5-a]pyrimidine and triazolo[3,4-b][1,3,4]thiadiazine
RSC Advances 5(130), 107931, 2015
DOI: 10.1039/C5RA21270G
[3]. Mohamed Abd-Elsabour, Hytham F. Assaf, Ahmed M. Abo-Bakr, Abdulrahman G. Alhamzani, Mortaga M. Abou-Krisha, Aamal A. Al-Mutairi, Hesham M. Alsoghier
Green electro-organic synthesis of a novel catechol derivative based on o-benzoquinone nucleophilic addition
New Journal of Chemistry 47(1), 131, 2023
DOI: 10.1039/D2NJ04530C
[4]. SHOBHANA A. GADARA, KARTIK D. LADVA
Solid Phase Synthesis and Antimicrobial Activity of Novel Triazolo[1,5-a]pyrimidine Derivatives
Asian Journal of Chemistry 32(9), 2298, 2020
DOI: 10.14233/ajchem.2020.22793
[5]. Farhad Shirzaei, Hamid Reza Shaterian
Basic ionic liquid, 2-hydroxyethylammonium formate, catalyzed one-pot synthesis of novel 2-(phenylsulfonyl)-1H-benzo[a]pyrano[2,3-c]phenazin-3-amine derivatives
Research on Chemical Intermediates 48(2), 751, 2022
DOI: 10.1007/s11164-021-04627-z
[6]. Gyeongjin Kim, Boeon Suh, Cheal Kim
A naked-eye sulfonamide-based colorimetric and fluorescent “turn-on” chemosensor for detecting fluoride
Journal of Molecular Structure 1254, 132307, 2022
DOI: 10.1016/j.molstruc.2021.132307
[7]. Iram Batool, Aamer Saeed, Irfan Zia Qureshi, Saima Kalsoom, Ayesha Razzaq
Synthesis, molecular docking and biological evaluation of new thiazolopyrimidine carboxylates as potential antidiabetic and antibacterial agents
Research on Chemical Intermediates 42(2), 1139, 2016
DOI: 10.1007/s11164-015-2078-2
[8]. Yasser H. Zaki, Sobhi M. Gomha, Amany M. G. Mohamed
Utility of 2-thioxo-pyrido[2,3-d]pyrimidinone in synthesis of pyridopyrimido[2,1-b][1,3,5]-thiadiazinones and pyridopyrimido[2,1-b][1,3]thiazinones as antimicrobial agents
Chemistry Central Journal 11(1), , 2017
DOI: 10.1186/s13065-017-0286-0
[9]. Guotai Li, Fanny Trausel, Michelle P. Helm, Benjamin Klemm, Tobias G. Brevé, Susan A. P. Rossum, Muhamad Hartono, Harm H. P. J. Gerlings, Matija Lovrak, Jan H. Esch, Rienk Eelkema
Tuneable Control of Organocatalytic Activity through Host–Guest Chemistry
Angewandte Chemie International Edition 60(25), 14022, 2021
DOI: 10.1002/anie.202102227
[10]. Mohamed M. Hammouda, Khaled M. Elattar, Ayman Y. El-Khateeb, Sahar E. Hamed, Amany M. A. Osman
Developments of pyridodipyrimidine heterocycles and their biological activities
Molecular Diversity , , 2023
DOI: 10.1007/s11030-023-10623-9
[11]. Ranjana Aggarwal, Shilpa Sharma, Mona Hooda, Dionisia Sanz, Rosa M. Claramunt, Brendan Twamley, Isabel Rozas
Visible-light mediated regioselective approach towards synthesis of 7-aroyl-6-methyl-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazines
Tetrahedron 75(50), 130728, 2019
DOI: 10.1016/j.tet.2019.130728
[12]. Guotai Li, Fanny Trausel, Michelle P. Helm, Benjamin Klemm, Tobias G. Brevé, Susan A. P. Rossum, Muhamad Hartono, Harm H. P. J. Gerlings, Matija Lovrak, Jan H. Esch, Rienk Eelkema
Tuneable Control of Organocatalytic Activity through Host–Guest Chemistry
Angewandte Chemie 133(25), 14141, 2021
DOI: 10.1002/ange.202102227
[13]. Nancy George, Gurleen Singh, Riddima Singh, Gurjaspreet Singh, Anita Devi, Harminder Singh, Gurpreet Kaur, Jandeep Singh
Microwave accelerated green approach for tailored 1,2,3–triazoles via CuAAC
Sustainable Chemistry and Pharmacy 30, 100824, 2022
DOI: 10.1016/j.scp.2022.100824
[14]. Kamelia M. El-mahdy, Azza M. El-kazak
A Simple Synthesis and Antimicrobial Activity of Some New 1,2,4-Triazolopyrimidine Derivatives
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DOI: 10.3987/COM-21-14409
[15]. Maha A. Alshubramy, Khalid A. Alamry, Mahmoud A. Hussein
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DOI: 10.1039/D3RA01336G
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Journal of Molecular Structure 1248, 131395, 2022
DOI: 10.1016/j.molstruc.2021.131395
[17]. Milad Masoumi, Mohammad Bayat, Fahimeh Sadat Hosseini
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DOI: 10.1016/j.heliyon.2020.e05047
[18]. Badr Jismy, Hassan Allouchi, Monia Aweli, Mohamed Abarbri, Fatma Allouch
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Journal of Fluorine Chemistry 229, 109390, 2020
DOI: 10.1016/j.jfluchem.2019.109390
[19]. Anhar Abdel-Aziem
Utility of 2-Acetyl Benzofuran for the Synthesis of New Heterocycles as Potential Anticancer Agents
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DOI: 10.1002/jhet.2906
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DOI: 10.1002/ejoc.201300683
[21]. Kamal M. DAWOOD, Eman A. RAGAB, Korany A. ALI
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DOI: 10.3906/kim-1503-75
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DOI: 10.1007/s12633-023-02372-z
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Polycyclic Aromatic Compounds 43(4), 3175, 2023
DOI: 10.1080/10406638.2022.2064885
[24]. Dmitrii Yu. Vandyshev, Oleg N. Burov, Anton V. Lisovin, Daria A. Mangusheva, Mikhail A. Potapov, Tatiana N. Ilyinova, Khidmet S. Shikhaliev, Athina Geronikaki, Domenico Spinelli
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DOI: 10.3390/molecules27103326
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DOI: 10.2174/1385272823666191019111627
[26]. Hong Sun, Zhongyuan Wang, Liyuan Deng, Weiyin Hu, Tianhui Liao, Xin Zhao, Zhixu Zhou, Huifang Chai, Chunshen Zhao
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Molecular Crystals and Liquid Crystals 742(1), 10, 2022
DOI: 10.1080/15421406.2022.2043000
[27]. Rachel L. Beingessner, Yiwen Fan, Hicham Fenniri
Molecular and supramolecular chemistry of rosette nanotubes
RSC Advances 6(79), 75820, 2016
DOI: 10.1039/C6RA16315G
[28]. Mpelegeng Victoria Bvumbi, Anza Imanuel Nemudzivhadi, Musiiwa Victoria Sengane, Simon Mnyakeni Moleele
Reactions of 3-amino-1,2,4-triazine with coupling reagents and electrophiles
Heterocyclic Communications 28(1), 157, 2022
DOI: 10.1515/hc-2022-0149
[29]. Kamal Mohamed Dawood, Hussein Khalaf-Allah Abu-Deif
Synthesis and antimicrobial activity of some new 1,2-bis-[1,3-thiazolidin-3-yl]ethane derivatives
European Journal of Chemistry 4(3), 277, 2013
DOI: 10.5155/eurjchem.4.3.277-284.837
[30]. Biswajita Baruah, Mohit L. Deb
Catalyst-free and additive-free reactions enabling C–C bond formation: a journey towards a sustainable future
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DOI: 10.1039/D0OB02149K
[31]. Basant Farag, Fatimah Agili, Samar El‐Kalyoubi, Said A. Said, Shaker Youssif, Wael Shehta
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ChemistrySelect 7(7), , 2022
DOI: 10.1002/slct.202103834
[32]. Paweł Lenartowicz, Mateusz Psurski, Aleksandra Kotynia, Aleksandra Pieniężna, Monika Cuprych, Klaudia Poniatowska, Justyna Brasuń, Paweł Kafarski
Dipeptides of S-Substituted Dehydrocysteine as Artzyme Building Blocks: Synthesis, Complexing Abilities and Antiproliferative Properties
International Journal of Molecular Sciences 22(4), 2168, 2021
DOI: 10.3390/ijms22042168
[33]. Felipe S. Stefanello, Yuri G. Kappenberg, Juliane N. Araújo, Steffany Z. Franceschini, Marcos A.P. Martins, Nilo Zanatta, Bernardo A. Iglesias, Helio G. Bonacorso
Trifluoromethyl-substituted aryldiazenyl-pyrazolo[1,5-a]pyrimidin-2-amines: Regioselective synthesis, structure, and optical properties
Journal of Fluorine Chemistry 255-256, 109967, 2022
DOI: 10.1016/j.jfluchem.2022.109967
[34]. Elisandra Scapin, Clarissa P. Frizzo, Leticia V. Rodrigues, Geórgia C. Zimmer, Rodrigo A. Vaucher, Michelle R. Sagrillo, Janice L. Giongo, Carlos A. M. Afonso, Patrícia Rijo, Nilo Zanatta, Helio G. Bonacorso, Marcos A. P. Martins
Synthesis, antimicrobial activity and cytotoxic investigation of novel trifluoromethylated tetrazolo[1,5-a]pyrimidines
Medicinal Chemistry Research 26(3), 640, 2017
DOI: 10.1007/s00044-017-1783-3
[35]. Sanae Lahmidi, El Hassane Anouar, Mohamed El Hafi, Mohammed Boulhaoua, Abdelaziz Ejjoummany, Meryem El Jemli, El Mokhtar Essassi, Joel T. Mague
Synthesis, X-ray, spectroscopic characterization, DFT and antioxidant activity of 1,2,4-triazolo[1,5-a]pyrimidine derivatives
Journal of Molecular Structure 1177, 131, 2019
DOI: 10.1016/j.molstruc.2018.09.046
[36]. Wael Shehta, Fatimah Agili, Basant Farag, Said A Said, Shaker Youssif, Mohamed E Abdraboh, Samar El-Kalyoubi
Design, synthesis and antitumor activity of novel pyran-functionalized uracil derivatives: docking studies
Future Medicinal Chemistry 15(5), 421, 2023
DOI: 10.4155/fmc-2022-0279
[37]. Samia M. Sayed, Mohamed A. Raslan, Kamal M. Dawood
Synthesis and Reactivity of Phenylthiourea Derivatives: An Efficient Synthesis of New Thiazole-Based Heterocycles
Journal of Heterocyclic Chemistry 53(2), 508, 2016
DOI: 10.1002/jhet.2327
[38]. Sanae Lahmidi, El Hassane Anouar, Lahcen El Hamdaoui, Younes Ouzidan, Manpreet Kaur, Jerry P. Jasinski, Nada Kheira Sebbar, El Mokhtar Essassi, Mohammed El Moussaouiti
Synthesis, crystal structure, spectroscopic characterization, hirshfeld surface analysis, DFT calculations and antibacterial activity of ethyl 2-(4-vinylbenzyl)-2-(5-methyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-yl)-3-(4-vinylphenyl)propanoate
Journal of Molecular Structure 1191, 66, 2019
DOI: 10.1016/j.molstruc.2019.04.076
[39]. Nadia Abdelriheem, Sayed Ahmad, Abdou Abdelhamid
Synthesis of some new Thieno[2,3-b]pyridines, Pyrimidino[4',5':4,5]thieno[2,3-b]pyridine and Pyridines Incorporating 5-Bromobenzofuran-2-yl Moiety
Molecules 20(1), 822, 2015
DOI: 10.3390/molecules20010822
[40]. Sobhi Mohamed Gomha, Mohamed Gomaa Badrey
Ecofriendly regioselective one-pot synthesis of chromeno[4,3-d][1,2,4]triazolo[4,3-a]pyrimidine derivatives
European Journal of Chemistry 4(2), 180, 2013
DOI: 10.5155/eurjchem.4.2.180-184.767
[41]. Sumit Chaudhary, R.N. Rai, Deeti Jyothi, Umesh Prasad Singh
Solid state synthesis, thermal, spectral, optical, crystal structure and atomic packing studies of 2-(3-Hydroxyphenyl)-2,3-dihydroquinazolin-4(1H)-one
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DOI: 10.1016/j.matlet.2023.134253
[42]. Oluwole Samuel Aremu, Saba Alapour, Neha Manhas, Moganavelli Singh, Parvesh Singh, Neil Anthony Koorbanally
Synthesis, molecular docking and anticancer activity of 5,5'-(phenylmethylene)bis(6-amino-2-thiouracil) derivatives
Phosphorus, Sulfur, and Silicon and the Related Elements 196(10), 920, 2021
DOI: 10.1080/10426507.2021.1946060
[43]. Dongkyun Gil, Boeon Suh, Cheal Kim
A New Reversible Colorimetric Chemosensor Based on Julolidine Moiety for Detecting F−
Journal of Fluorescence 31(6), 1675, 2021
DOI: 10.1007/s10895-021-02801-5
[44]. Sherif M. H. Sanad, Ahmed A. M. Ahmed, Ahmed E. M. Mekky
Efficient synthesis and molecular docking of novel antibacterial pyrimidines and their related fused heterocyclic derivatives
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DOI: 10.1002/jhet.3789
[45]. Abdou O. Abdelhamid, Sobhi M. Gomha, Ahmad S. Shawali
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HETEROCYCLES 91(11), 2126, 2015
DOI: 10.3987/COM-15-13319
References
[1]. Furukawa, K.; Hasegawa, T. Can. Pat. Appl. CA 2,151,871, 1995; Chem. Abstr. 1996, 124, 289568c.
[2]. Yanagihara, Y.; Kasai, H.; Kawashima, T.; Shida, T. Jpn. J. Pharmacol. 1988, 48, 91-101.
http://dx.doi.org/10.1254/jjp.48.91
PMid:2462074
[3]. Ellingboe, J. W. US Pat. 5,466,692, 1995; Chem. Abstr. 1996, 124, 176134q.
[4]. Deyanov, A. B.; Niyazov, R. K.; Nazmetdinov, F. Y.; Syropyatov, B. Y.; Kolla, V. E.; Konshin, M. E. Khim-Farm Zh. 1991, 25, 26-28.
[5]. Heidelberger, C.; Ansfield, F. J. Cancer Res. 1963, 23, 1226-1243.
PMid:14070379
[6]. Baba, M.; Pauwels, R.; Herdewijn, P.; De-Clercq, E.; Desmyster, J.; Vandepulfe, M. Biochem. Biophys. Res. Commun. 1987, 142, 128-134.
http://dx.doi.org/10.1016/0006-291X(87)90460-8
[7]. De Clercq, E. J. Med. Chem. 1986, 29, 1561-1569.
http://dx.doi.org/10.1021/jm00159a001
[8]. De Clercq, E. Anticancer Res. 1986, 6, 549-556.
PMid:3752935
[9]. Parish, H. A.; Gilliom, R. D.; Purcell, W. P.; Browne, R. K.; Spirk, R. F.; White, H. D. J. Med. Chem. 1982, 25, 98-102.
http://dx.doi.org/10.1021/jm00343a022
[10]. Bold, R. J.; Termuhlen, P. M.; McConkey, D. J. Surg. Oncol. 1997, 6, 133-142.
http://dx.doi.org/10.1016/S0960-7404(97)00015-7
[11]. Reed, J. C. Curr. Opin. Oncol. 1999, 11, 68-75.
http://dx.doi.org/10.1097/00001622-199901000-00014
PMid:9914881
[12]. Abdelhamid, A. O.; Ismail, Z. H.; Abdel-Gawad, S. M.; Ghorab, M. M.; Abdel-Aziem, A. Phosphorus Sulfur 2009, 184, 58-75.
http://dx.doi.org/10.1080/10426500802077630
[13]. Abdelhamid, A. O.; Ismail, Z. H.; Abdel-Aziem, A. J. Chem. Res. 2007, 10(8), 609-616.
[14]. Abdelhamid, A. O.; Ismail, Z. H.; Abdel-Azem, A. Phosphorus Sulfur 2008, 183, 1735-1745.
http://dx.doi.org/10.1080/10426500701734190
[15]. Abdelhamid, A. O.; Abdelall, E. K. A.; Zaki, Y. H. J. Heterocycl. Chem. 2010, 47, 477-482.
[16]. Abdelhamid, A. O. J. Heterocycl. Chem. 2009, 46, 680-686.
http://dx.doi.org/10.1002/jhet.141
[17]. Abdelhamid, A. O.; Shokry, A. S.; Tawfiek, S. M. J. Heterocycl. Chem. 2012, 49, 116-124
http://dx.doi.org/10.1002/jhet.699
[18]. Abdelhamid, A. O.; Fahmi, A. A.; Alsheflo, A. A. M. Eur. J. Chem. 2012, 3, 129-137.
http://dx.doi.org/10.5155/eurjchem.3.2.129-137.579
[19]. G. Favrel, G.; Chvz, J. Bull. Soc. Chem. France 1927, 41, 1601-1622.
[20]. Eweiss, N. E.; Osman. A. Tetrahedron Lett. 1979, 13, 1169-1170.
http://dx.doi.org/10.1016/S0040-4039(01)86092-5
[21]. Shawali, A. S.; Abdelhamide, A. O. Bull. Soc. Chim. Jpn. 1976, 49, 321-324.
http://dx.doi.org/10.1246/bcsj.49.321
[22]. Shawali, A. S.; Osman. A. Tetrahedron 1971, 27, 2517-2528.
http://dx.doi.org/10.1016/S0040-4020(01)90753-7
[23]. Abdelhamide, A. O.; Attaby, F. A.; Zaki, M. Y. Phosphorous Sulfur 1990, 53, 403-410.
http://dx.doi.org/10.1080/10426509008038050
[24]. Tayler, C.; Edward, J.; Cheng, C. C. J. Org. Chem. 1960, 25, 148-149
http://dx.doi.org/10.1021/jo01071a611
[25]. Youssif, S.; El-Bahaie, S.; Nabih, E. J. Chem. Res. (S) 1999, (2), 112-113.
[26]. Mosselhi, M. A. N. Mon. Chem. 2002, 133, 1297-1304.
http://dx.doi.org/10.1007/s00706-002-0469-8
[27]. Youssif, S.; El-Bahaie, S.; Nabih. E. Bull. Korean Chem. Soc. 2003, 24, 1429-1432.
[28]. Bauer, A. W; Kirby, W. W. M.; Sherris, J. C.; Turck, M. Amer. J. Clin. Pathol. 1966, 45, 493-496.
PMid:5325707
[29]. Mohamed, M. S.; Awad, S. M.; Sayed, A. I. Molecules 2010, 15, 1882-1890.
http://dx.doi.org/10.3390/molecules15031882
PMid:20336018
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