- Research article
- Open Access
Synthesis and antifungal activities of novel nicotinamide derivatives containing 1,3,4-oxadiazole
© Wu et al.; licensee Chemistry Central Ltd. 2013
- Received: 11 February 2013
- Accepted: 21 March 2013
- Published: 5 April 2013
Pant diseases in agriculture are extremely difficult to control, which bring about for billions of dollars in economic losses worldwide each year; Nicotinamide derivatives has attracted more and more attention in the field of pesticide due to their broad bioactivities. In an effort to discover new molecules with good antifungal activity, a series of nicotinamide derivatives containing 1,3,4-oxadiazole were synthesized and bio-assayed.
Bioassays demonstrated that some of the title compounds exhibited favorable antifungal activities against Gibberella zeae, Fusarium oxysporum, and Cytospora mandshurica. compounds 7b, 7c, 8, 9a, 9b, and 9c displayed 46.4%, 39.6%, 53.0%, 43.2%, 58.3%, 45.6% activities against G. Zeae, respectively; the activities of compounds 7a, 7b, 8, 9a, 9b, and 9c against F. oxysporum were 55.2%, 51.1%, 58.9%, 63.2%, 53.3%, and 47.6%, respectively; whereas inhibitory rates of compounds 7a, 7b, 7c, 8, 9a, 9b, and 9c on C. mandshurica were 53.1%, 49.9%, 44.9%, 52.8%, 59.8%, 54.5%, and 49.3%, respectively.
A series of the novel nicotinamide derivatives containing 1,3,4-oxadiazole were synthesized and bio-assayed. The results of antifungal tests revealed that the synthesized nicotinamide derivatives possessed weakly to moderately antifungal activities against G. zeae, F. oxysporum, and C. mandshurica. Most of the synthesized compounds exhibited similar activities as (or higher than) these of hymexozol on their corresponding fungus, and compounds 7a, 8, 9a, and 9b showed considerable prospects for further optimization. Primary structure-activity relationships revealed that the introduction of the groups of 4-chloro-6-methyl on benzene, the hydrazone group containing N,N-dimethylamino, and acetyl at -NH 2 could enhance the antifungal activity.
- Antifungal Activity
- Fusarium Head Blight
- Structure Activity Relationship
In recently years, plant diseases in agriculture are extremely difficult to control due to the continued moist weather during the crop growing season and the resistance of fungicides in the pathogen population, which bring about for billions of dollars in economic losses worldwide each year . Take fusarium head blight (FHB) as example, it was caused by Gibberella zeae and was endemic in the wheat producing areas of many provinces of China, this kind of disease have caused an estimated 30 to 50% of reduction and even completely failure of harvests in many wheat-producing areas . Therefore, the controlling of plant pathogens (such as G. zeae) has become more and more difficult, and the development of novel fungicidal molecules for these pathogens has been attracted more and more attention.
1,3,4-oxadiazole derivatives, another important heterocyclic derivative, has attracted more and more attention in development of fungicide, in the past few years, a lots of 1,3,4-oxadiazole derivatives with good antifungal activity have been developed by our group, some of the developed compounds processed good prospects for commercialization [19–24]. New fungicidal molecules are developed in the present work on the basis of the following: incorporation of the sub-structural unit of 1,3,4-oxadiazole into the backbone of boscalid and structural variation by the introduction of different kinds of moiety, resulting in nicotinamides containing a 1,3,4-oxadiazole substructure with broad-spectrum activity. Based on this hypothesis, a series of novel nicotinamide derivatives containing 1,3,4-oxadiazole substructure were designed and synthesized. Biological assays revealed that most of the synthesized compounds were provided with weak to moderate activities against G. Zeae, F. oxysporum, and C. mandshurica at 50 mg/L. Some of the synthesized compounds exhibited similar or higher activities as that of hymexozol on their corresponding fungus, compounds 9a, 7a, 8, and 9b showed considerable prospects.
The structures of the synthesized compounds (5–9) were established on the basis of their spectroscopic data. The IR spectra showed absorption bands around near 3230–3400 cm-1, 2990–3150 cm-1for the N-H, and Ar-H stretching vibrations, respectively. The absorption bands near 1670–1710 cm-1 were the presence C = O functional groups, the absorption bands of 1450–1620 cm-1 were the skeletal vibration of benzene ring. In the 1H-NMR spectra of the title compounds, the -CONHAr proton appeared as a broad singlet at 11.88-10.27 ppm range; the -CH = N- proton for compounds 9a-9d mainly appeared as a singlet near the 8.50 ppm; the protons at 6 and 4 positions of pyridine ring were occurred as double-double peaks near 8.57-8.51 and 7.61-8.33, respectively; and the protons at 5 position of pyridine is near the 7.60 ppm. The properties, 1H NMR, 13C NMR, IR, and the elemental analysis data of the title compounds in more detail are also listed in Additional file 1 [see Additional file 1].
Antifungal activity and structure activity relationship
Antifungal activities of the title compounds 5–9 at 50 mg/L
17.9 ± 1.6
10.3 ± 0.9
15.5 ± 0.7
33.2 ± 1.7
21.3 ± 1.1
30.3 ± 1.9
19.0 ± 2.9
55.2 ± 0.6
53.1 ± 1.3
46.4 ± 1.3
51.1 ± 1.0
49.9 ± 1.1
39.6 ± 1.3
31.9 ± 1.4
44.9 ± 0.7
27.9 ± 0.2
12.5 ± 1.7
17.3 ± 1.0
53.0 ± 2.4
58.9 ± 4.3
52.8 ± 1.3
43.2 ± 0.6
63.2 ± 0.9
59.8 ± 1.4
58.3 ± 2.7
53.3 ± 3.9
54.5 ± 1.2
45.6 ± 1.8
47.6 ± 1.0
49.3 ± 1.1
35.4 ± 1.9
17.2 ± 0.3
34.3 ± 0.9
55.54 ± 3.9
56.12 ± 2.1
49.61 ± 3.2
100 ± 3.74
100 ± 4.9
100 ± 5.23
Primary structure activity relationships (SAR) revealed that antifungal activities on the three fungus can be improved to a certain extent by introduction of N,N-dimethylamino. For instance, compound 9a showed much higher activities against both G. Zeae and F. oxysporum than that of 7a, and compounds 9b-9d also showed slightly better activities than these of 7b-7d. In addition, the introduction of acetyl can enhance the antifungal activity when chlorine was at 4-position of benzene, that why compound 8 showed higher activity than that of compound 7b. Moreover, the substituent on benzene play an important role when the group on 1,3,4-oxadiazole was “-NH2”, as we can see that compound 7a (R = 4-chloro-6-methyl) showed higher activity than that of 7b (R = 4-chloro), and compound 7c (R = 6-methyl) showed slightly lower activity, and the activity of 7d (R = H) was the lowest one. So the active order was 7a > 7b > 7c > 7d; a similar case can be found when -NH2 group was changed to –N = CHN (CH3)2 (9a > 9b > 9c > 9d). Finally, the compound with thiol (5) displayed much lower activity than that of the compound with amino group, but the introduction of -CH3 group (compound 6) could increase the activity against all the test fungus. Further structural modification is currently underway basing on the primary SAR to discover the potential nicotinamides containing 1,3,4-oxadiazole.
Unless otherwise stated, all the reagents and reactants were purchased from commercial suppliers; melting points were uncorrected and determined on a XT-4 binocular microscope (Beijing Tech Instrument Co., China). The 1H-NMR and 13C-NMR spectra were recorded on a JEOL ECX 500 NMR spectrometer (JEOL Ltd., Japan) at room temperature operating at 500 MHz for 1H-NMR and 125 MHz for 13C-NMR by using CDCl3 or DMSO as solvents and TMS as an internal standard; infrared spectra were recorded in KBr on a IR Pristige-21 spectrometer (Shimadzu corporation, Japan); elemental analysis was performed on an Elemental Vario-III CHN analyzer (Elementar, German). The course of the reactions was monitored by TLC; analytical TLC was performed on silica gel GF 254. Intermediates 3 and 4 were prepared according to the reported methods  and used without further purifications, the process for preparing of them can be found in Additional file 1.
Antifungal biological assay
All the compounds (5, 6, 7a-7d, 8, 9a-9d) were evaluated for their antifungal activities against G. zeae, F. oxysporium, and C. mandshurica in vitro as described in literature [31, 32]. The results of preliminary bioassays were compared with the experimental data of the commercial agricultural fungicide, hymexazol and carbendazim. All the compounds were dissolved in dimethyl sulfoxide (DMSO, 10 mL) before mixing with potato dextrose agar (PDA, 90 mL). The compounds were tested at a concentration of 50 mg/L. All fungal species were incubated in PDA at 27 ±1°C for 5 days to obtain new mycelium for antifungal assay. Mycelia dishes approximately 4 mm in diameter were cut from the culture medium. One of the specimens was picked up with a sterilized inoculation needle and then inoculated in the center of the PDA plate aseptically. The inoculated plates were incubated at 27 ±1°C for 5 days. DMSO in sterile distilled water served as the control, whereas hymexazol and carbendazim acted as the positive control. Three replicates were conducted for each treatment. The radial growth of the fungal colonies was measured on the sixth day and the data were statistically analyzed. The in vitro inhibiting effects of the test compounds on the fungi were calculated by the formula:
I(%) = [(C-T)/(C-0.4)] × 100, where C represents the diameter of fungal growth on untreated PDA, T represents the diameter of fungi on treated PDA, and I is the inhibitory rate.
In conclusion, a series of the novel nicotinamide derivatives containing 1,3,4-oxadiazole were designed and synthesized. The synthesized compounds were characterized by spectral data (1H NMR, 13C NMR, IR) and elemental analysis. All of the compounds were subjected to fungicidal activities in vitro against G. zeae, F. oxysporum, and C. mandshurica. The results showed that the synthesized nicotinamide derivatives possessed weakly to moderately antifungal activities against the tested fungus. Most of the synthesized compounds exhibited similar activities as (or higher activities than) that of hymexozol on their corresponding fungus, and the compounds 9a, 7a, 8, and 9b showed considerable prospects for further optimization. Primary structure activity relationships revealed that the introduction of the groups of 4-chloro-6-methyl on benzene, the hydrazone group containing N,N-dimethylamino, and acetyl at -NH2 could enhance the antifungal activities against G. zeae, F. oxysporum, and C. mandshurica. However, the structures of the synthesized compounds need to be optimized. Further structural modification and biological evaluation are currently underway to explore the full potential of this kind of nicotinamides containing 1,3,4-oxadiazole.
This work was supported Key Technologies R&D Program (No.2011BAE06B05-6) and the Special Foundation of Governor for Outstanding talents in Guizhou (No.2011-38) the Introduction of Talent Research projects of Guizhou University (No. 2011–24).
- Bai GH, Gregory S: Management and resistance in wheat and barley to fusarium head blight. Annu Rev Phytopathol. 2004, 42: 135-161. 10.1146/annurev.phyto.42.040803.140340.View ArticleGoogle Scholar
- De Wolf ED, Madden LV, Lipps PE: Risk assessment models for wheat Fusarium head blight epidemics based on within-season weather data. Phytopathol. 2003, 93: 428-435. 10.1094/PHYTO.2003.93.4.428.View ArticleGoogle Scholar
- Komori T, Ujita S, Inoue T: Preparation of N-(3-phenoxybenzyl)nicotinamide derivatives as plant fungicides. Chem Abstr. 2010, 154: 64642-Google Scholar
- Kozlevcar B, Leban I, Turel I, Segedin P, Petric M, Pohleven F, White Andrew JP, Williams DJ, Sieler J: Complexes of copper(II) acetate with nicotinamide: preparation, characterization and fungicidal activity; crystal structures of [Cu2(O2CCH3)4(nia)] and [Cu2(O2CCH3)4(nia)2]. Polyhedron. 1999, 18: 755-762. 10.1016/S0277-5387(98)00350-7.View ArticleGoogle Scholar
- Komori T, Ujita S, Inoue T: Preparation of N-(4-phenoxybenzyl)pyridine-3-carboxamide derivatives as plant fungicides. Chem Abstr. 2010, 154: 64641-Google Scholar
- Frackenpohl J, Hense A, Arnold C, Franken EM, Malsam O, Sanwald E, Goergens U: Preparation of Nicotinamides as Agrochemical Insecticides. Chem Abstr. 2008, 152: 287405-Google Scholar
- Yokoi S, Obayashi T, Sato K, Nagai J, Kawagishi A, Mtsuo S: Pest control compositions containing N-heteroaryl-nicotinamides and insecticides, acaricides, or nematocides. Chem Abstr. 2005, 142: 256292-Google Scholar
- Zhu YC, Yuan LP, Cao J, Shen XX, Lu DH, Ni CC, Shen Z, Chen L, Zhang YB: Synthesis and bioactivity of 2-benzylsulfanyl nicotinamide derivatives. Agrichemicals. 2008, 10: 287-291.Google Scholar
- Gesing ERF, Mueller KH, Kysela E, Drewes MW, Dahmen P, Feucht D, Pontzen R: Preparation of N-phenylnicotinamides for use as herbicides. Chem Abstr. 2001, 134: 266207-Google Scholar
- Jeschke P, Lindner W, Bonse G, Santel HJ, Luerssen K, Schmidt RR, Hartwig J: Herbicidal and plant-mematocidal compositions based on mercaptonicotinic acid derivatives. Chem Abstr. 1993, 119: 160137-Google Scholar
- Chung IM, Kim JJ, Chun SC, Ahmad A: Potential herbicidals and growth regulators constituents in rice hulls of oryza sativa. J Chem. 2008, 20: 820-822.Google Scholar
- Thomas AB, Nanda RK, Kothapalli LP, Deshpande AD: Synthesis and antimicrobial activity of N-[2-(aryl/substituted aryl)-4-oxo-1,3-thiazolidin- 3-yl]pyridine-4-carboxamide. J Kor Chem Soc. 2011, 55: 960-968. 10.5012/jkcs.2011.55.6.960.View ArticleGoogle Scholar
- Vijay V, Soni N, Khanna V: Synthesis and antimicrobial activity of 5-arylidine derivatives of N-(2-(4-chlorophenyl)-4-oxo-3-thiazolidinyl)isonicotinamide. Inter J Res Pharm Sci. 2011, 1: 34-43.Google Scholar
- Wu J, Kang SH, Song BA, Hu DY, He M, Jin LH, Song Y: Synthesis and antibacterial activity against ralstonia solanacearum for novel hydrazone derivatives containing a pyridine moiety. Chem Cent J. 2012, 6: 28-10.1186/1752-153X-6-28.View ArticleGoogle Scholar
- Dhore JW, Pethe GB, Wagh SP, Thorat GD: Synthesis, characterization and biological studies of some triazolyl isonicotinamide. Arch Appl Sci Res. 2011, 3: 407-414.Google Scholar
- Liu CL: World Pesticides: Fungicide. 2006, Beijing: Chemical Industry PressGoogle Scholar
- Queron PY, Grosjean-Cournoyer MC, Desbordes P, Genix P, Hartmann B, Mattes A, Kunz K, Fischer R, Gaertzen O, Ort O, Mansfield D, Villier A: N-[4-(pyridin-2-yl)butyl]-carboxamide derivatives as fungicides, their preparation, fungicidal compositions, and use for the control of phytopathogenic fungi. Chem Abstr. 2008, 148: 121597-Google Scholar
- Wen F, Zhang H, Yu ZY, Jin H, Yang Q, Hou TP: Design, synthesis and antifungal/insecticidal evaluation of novel nicotinamide derivatives. Pestic Biochem Phy. 2010, 98: 248-253. 10.1016/j.pestbp.2010.06.015.View ArticleGoogle Scholar
- Xu WM, Yang S, Bhadury P, He J, He M, Gao LL, Hu DY, Song BA: Synthesis and bioactivity of novel sulfone derivatives containing 2,4-dichlorophenyl substituted 1,3,4-oxadiazole/thiadiazole moiety as chitinase inhibitors. Pestic Biochem Phy. 2011, 101: 6-15. 10.1016/j.pestbp.2011.05.006.View ArticleGoogle Scholar
- Jin LH, He J, He M, Xu WM, Yang S: The preliminary study of inhibitory mechanism of sulfone compounds xa202 and xt208 against Gibberella zeae. Afr J Micr Res. 2011, 5: 4889-4895.Google Scholar
- Xu WM, He J, He M, Han FF, Chen XH, Pan ZX, Wang J, Tong MG: Synthesis and antifungal activity of novel sulfone derivatives containing 1,3,4-oxadiazole moieties. Molecules. 2011, 16: 9129-9141. 10.3390/molecules16119129.View ArticleGoogle Scholar
- Xu WM, Han FF, He M, Hu DY, He J, Yang S, Song BA: Inhibition of tobacco bacterial wilt with sulfone derivatives containing an 1,3,4-oxadiazole moiety. J Agric Food Chem. 2012, 60: 1036-1041. 10.1021/jf203772d.View ArticleGoogle Scholar
- Chen CJ, Song BA, Yang S, Xu GF, Bhadury PS, Jin LH, Hu DY, Li QZ, Liu F, Xue W, Chen Z: Synthesis and antifungal activities of 5-(3,4,5-trimethoxyphenyl)-2-sulfonyl-1,3,4-thiadiazole and 5-(3,4,5-trimeth -oxyphenyl)-2-sulfonyl-1,3,4-oxadiazole derivatives. Bioorg Med Chem. 2007, 15: 3981-3989. 10.1016/j.bmc.2007.04.014.View ArticleGoogle Scholar
- Liu F, Luo XQ, Song BA, Bhadury PS, Yang S, Jin LH, Xue W, Hu DY: Synthesis and antifungal activity of novel sulfoxide derivatives containing trimethoxyphenyl substituted 1,3,4-thiadiazole and 1,3,4-oxadiazole moiety. Bioorg Med Chem. 2008, 16: 3632-3640. 10.1016/j.bmc.2008.02.006.View ArticleGoogle Scholar
- Wu J, Song BA, Hu DY, Yue M, Yang S: Design, synthesis and insecticidal activities of novel pyrazole amides containing hydrazone substructures. Pest Manag Sci. 2012, 68: 801-810. 10.1002/ps.2329.View ArticleGoogle Scholar
- Wright SW, Petraitis JJ, Abelman MM, Batt DG, Bostrom LL, Corbett RL, Decicco CP, Di Meo SV, Freimark B, Giannaras JV, Green AM, Jetter JW, Nelson DJ, Orwat MJ, Pinto DJ, Pratta MA, Sherk SR, Williams JM, Magolda RL, Aner EC: Heteroaryl-fused 2-phenylisothiazolone inhibitors of cartilage breakdown. J Med Chem. 1994, 37: 3071-3078. 10.1021/jm00045a012.View ArticleGoogle Scholar
- Pommer EH, Zeeh B, Goetz N, Girgensohn B: Fungicidal compositions containing pyridine carboxylic acid derivatives. Chem Abstr. 1976, 84: 39707-Google Scholar
- Clark DA, Lahm GP, Smith BK, Barry JD, Clagg DG: Synthesis of insecticidal fluorinated anthranilic diamides. Bioorg Med Chem. 2008, 16: 3163-3170. 10.1016/j.bmc.2007.12.017.View ArticleGoogle Scholar
- Rose U: 2-Aryl-substituted 4H-3,1-benzoxazin-4-ones as novel active substances for the cardiovascular system. J Heterocyclic Chem. 1991, 28: 2005-2012. 10.1002/jhet.5570280836.View ArticleGoogle Scholar
- Fallon GD, Francis CL, Johansson K, Liepa AJ, Woodgate RCJ: N, N-Dialkyl-N′-Chlorosulfonylchloroformamidines in Heterocyclic Synthesis. II. Thiazolo-, Thiadiazolo-, and Oxadiazolo- Fused [1,2,4,6] Thiatriazine Dioxides. Austr J Chem. 2005, 58: 891-900. 10.1071/CH05070.View ArticleGoogle Scholar
- Wu J, Wang J, Hu DY, He M, Jin LH, Song BA: Synthesis and antifungal activity of novel pyrazolecarboxamide derivatives containing a hydrazone moiety. Chem Cent J. 2012, 6: 51-10.1186/1752-153X-6-51.View ArticleGoogle Scholar
- Song SQ, Zhou LG, Li D, Tang D, Li JQ, Jiang WB: Antifungal activity of five plants from Xinjiang. Nat Prod Res Dev. 2004, 16: 157-159.Google Scholar
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