部分噻诺[2,3-b]吡啶类、噻诺[3,2-d]嘧啶类和噻诺[3,2-d][1,2,3]三嗪酮类对金蛾的杀虫作用研究

IF 1.1 4区 化学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Etify A. Bakhite, Mohamed A. Gad, Esraa Khamies, Felwa A. Thagfan, Rania Ali El Hadi Mohamed, Moustafa M. S. Bakry
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引用次数: 0

摘要

目的:金Aonidiella aurantii是一种高度多食性害虫,属于金Aonidiella didiae科,对柑橘类植物的危害特别大。这种害虫通过侵害水果和叶子对柑橘生产构成重大威胁。相比之下,杂环化合物已被证明在农药和杀虫剂中是必不可少的,包括杀菌剂、杀虫剂/杀螨剂和除草剂。鉴于此,本课题组重点合成了上述化合物,并对其对金蛾的杀虫活性进行了评价。方法:在实验室合成了以烟酸乙酯支架为亚结构的三个主要系列的熔融杂环化合物。采用番石榴叶浸渍法对合成的化合物进行了对金银蛾若虫和成虫的杀虫活性评价。结果与讨论:用少量过量的无水碳酸钠在乙醇中回流,将4-芳基-5-氰基-2-甲基-6-硫氧基-1,6-二氢吡啶-3-羧酸酯(Ia-Ib)与N-芳基-2-氯乙酰胺进行反应,生成相应的3-氨基-4-芳基-2-[N-(芳基)氨基]-5-乙氧羰基-6-甲基噻吩[2,3-b]吡啶(IIa-IIe),产率很高。在乙酸酐存在下,将化合物(IIb-IId)与原甲酸三乙酯煮沸,得到[3′,2′:4,5]吡啶[3,2-d]噻吩嘧啶(IIIb-IIId)。用亚硝酸钠在冰醋酸中浓溶液处理化合物(IIa-IId),生成吡啶[3′,2′:4,5]噻吩[3,2-d][1,2,3]三嗪酮(IVa-IVd)。所有化合物的结构都通过元素分析和光谱分析得到了证实。结论:含4-氯苯基支架的化合物(Ib)和(IIId)对金Aonidiella aurantii若虫和成虫均有较好的抑制作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Exploration of Some Thieno[2,3-b]pyridines, Thieno[3,2-d]pyrimidinones, and Thieno[3,2-d][1,2,3]triazinones as Insecticidal Agents Against Aonidiella aurantii

Exploration of Some Thieno[2,3-b]pyridines, Thieno[3,2-d]pyrimidinones, and Thieno[3,2-d][1,2,3]triazinones as Insecticidal Agents Against Aonidiella aurantii

Objective: Aonidiella aurantii, a highly polyphagous insect pest belonging to the Diaspididae family, is particularly harmful to citrus plants. This pest poses a significant threat to citrus production by infesting both fruits and foliage. In contrast, heterocycle-based compounds have proven to be essential in agrochemicals and pesticides, including fungicides, insecticides/acaricides, and herbicides. In light of this, our research group focused on the synthesis of the title compounds and the evaluation of their insecticidal activity against Aonidiella aurantii. Methods: Three main series of fused heterocyclic compounds, predominantly featuring the ethyl nicotinate scaffold as a substructure, were synthesized in our laboratory. Most of the synthesized compounds were evaluated for their insecticidal activity against the nymphs and adult females of Aonidiella aurantii using the guava leaf dipping technique. Results and Discussion: The reaction of ethyl 4-aryl-5-cyano-2-methyl-6-thioxo-1,6-dihydropyridine-3-carboxylates (Ia–Ib) with N-aryl-2-chloroacetamides, carried out by refluxing in ethanol with a slight excess of anhydrous sodium carbonate, resulted in the formation of the corresponding 3-amino-4-aryl-2-[N-(aryl)carbamoyl]-5-ethoxycarbonyl-6-methylthieno[2,3-b]pyridines (IIa–IIe) in excellent yields. Upon boiling compounds (IIb–IId) with triethyl orthoformate in the presence of acetic anhydride, pyrido[3',2':4,5]thieno[3,2-d]pyrimidinones (IIIb–IIId) were obtained. Treatment of compounds (IIa–IId) with a concentrated solution of sodium nitrite in glacial acetic acid resulted in the formation of pyrido[3',2':4,5]thieno[3,2-d][1,2,3]triazinones (IVa–IVd). The structures of all compounds were confirmed through elemental and spectral analyses. Conclusions: Compounds containing the 4-chlorophenyl scaffold, such as (Ib) and (IIId), exhibited promising results against both nymphs and adult females of Aonidiella aurantii.

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来源期刊
Russian Journal of Bioorganic Chemistry
Russian Journal of Bioorganic Chemistry 生物-生化与分子生物学
CiteScore
1.80
自引率
10.00%
发文量
118
审稿时长
3 months
期刊介绍: Russian Journal of Bioorganic Chemistry publishes reviews and original experimental and theoretical studies on the structure, function, structure–activity relationships, and synthesis of biopolymers, such as proteins, nucleic acids, polysaccharides, mixed biopolymers, and their complexes, and low-molecular-weight biologically active compounds (peptides, sugars, lipids, antibiotics, etc.). The journal also covers selected aspects of neuro- and immunochemistry, biotechnology, and ecology.
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