Synthesis and biological evaluation of novel pyridylpyrazole amides containing benzothiazole/thiourea/urea motif as pesticidal agents

被引:2
|
作者
Shang, Junfeng [1 ]
Zhang, Yan [1 ]
Yang, Na [1 ]
Xiong, Lixia [1 ]
Bian, Qiang [2 ]
Wang, Baolei [1 ]
机构
[1] Nankai Univ, Coll Chem, State Key Lab Elemento Organ Chem, Tianjin 300071, Peoples R China
[2] Nankai Univ, Coll Chem, Natl Pesticide Engn Res Ctr Tianjin, Tianjin, Peoples R China
基金
中国国家自然科学基金;
关键词
Pyridylpyrazole amides; benzothiazole; thiourea; urea; pesticidal activities; INSECTICIDAL ACTIVITIES; ANTHRANILIC DIAMIDES; LEAD OPTIMIZATION; DESIGN; DERIVATIVES; POTENT; SAR;
D O I
10.1080/10426507.2023.2192935
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A series of novel pyridylpyrazole amide compounds which contain benzothiazole, thiourea, and urea moieties, respectively, were successfully synthesized. Their structures were confirmed by IR, H-1 NMR, C-13 NMR, and HRMS. Some of the compounds were found to have favorable insecticidal potentials; particularly, the insecticidal activities of 3-chloro-1-(3-chloropyridin-2-yl)-N-(6-(trifluoromethyl)benzo[d]thiazol-2-yl)-1H-pyrazole-5-carboxamide (3b), 1-(3-chloropyridin-2-yl)-N-(4,6-dichlorobenzo[d]thiazol-2-yl)-3-(trifluoromethyl)-1H-pyrazole-5-carboxamide (3g), 3-bromo-N-(4-chloro-2-(3-ethylthioureido)phenyl)-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxamide (6e), 3-bromo-N-(4-chloro-2-(3-isopropylthioureido)-6-methylphenyl)-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxamide (6g), 3-bromo-1-(3-chloropyridin-2-yl)-N-(2-(3-isopropylureido)-6-methylphenyl)-1H-pyrazole-5-carboxamide (7c), 3-bromo-N-(4-chloro-2-(3-isopropylureido)phenyl)-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxamide (7d), 3-bromo-N-(4-chloro-2-(3-isopropylureido)-6-methylphenyl)-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxamide (7f), and 3-bromo-N-(2-(3-(tert-butyl)ureido)-4-chloro-6-methylphenyl)-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxamide (7g) were close to and even superior to those of the insecticide triflumuron toward diamondback moth, and can be used as novel insecticidal leading structures for further investigations. Some of the compounds showed good fungicidal potentials against a broad spectrum of tested fungi including Sclerotinia sclerotiorum, Cercospora arachidicola, Physalospora piricala and Rhizoctonia cerealis, and were comparable with the commercial fungicide controls, among others, 3b, 3-bromo-1-(3-chloropyridin-2-yl)-N-(6-(trifluoromethyl)benzo[d]thiazol-2-yl)-1H-pyrazole-5-carboxamide (3d), and N-(4-chloro-2-methyl-6-(3-methylthioureido)phenyl)-1-(3-chloropyridin-2-yl)-3-(trifluoromethyl)-1H-pyrazole-5-carboxamide (6i) could serve as novel fungicidal leading compounds for further research. The structure-activity relationships were analyzed and discussed in detail. This research provides useful information for the design and discovery of novel insecticidal/fungicidal agents.
引用
收藏
页码:659 / 672
页数:14
相关论文
共 50 条
  • [21] Synthesis of Novel Benzothiazole-Piperazine Derivatives and Their Biological Evaluation as Acetylcholinesterase Inhibitors and Cytotoxic Agents
    Gurdal, Enise Ece
    Turgutalp, Bengisu
    Gulcan, Hayrettin Ozan
    Ercetin, Tugba
    Sahin, Mustafa Fethi
    Durmaz, Irem
    Cetin-Atalay, Rengul
    Quoc Dat Nguyen
    Sippl, Wolfgang
    Yarim, Mine
    ANTI-CANCER AGENTS IN MEDICINAL CHEMISTRY, 2017, 17 (13) : 1837 - 1845
  • [22] Synthesis and Insecticidal Evaluation of Novel Anthranilic Diamides Derivatives Containing 4-Chlorine Substituted N-Pyridylpyrazole
    Li, Huangong
    Zhao, Yangyang
    Sun, Pengwei
    Gao, Li
    Li, Yuxin
    Xiong, Lixia
    Yang, Na
    Zhou, Sha
    Li, Zhengming
    CHINESE JOURNAL OF CHEMISTRY, 2021, 39 (01): : 75 - 80
  • [23] Synthesis of novel thiourea-/urea-benzimidazole derivatives as anticancer agents
    Siddig, Lamia A.
    Khasawneh, Mohammad A.
    Samadi, Abdelouahid
    Saadeh, Haythem
    Abutaha, Nael
    Wadaan, Mohammad Ahmed
    OPEN CHEMISTRY, 2021, 19 (01): : 1062 - 1073
  • [24] Synthesis of benzothiazole derivatives and their biological evaluation as anticancer agents
    Caputo, Rosanna
    Calabro, Maria Luisa
    Micale, Nicola
    Schimmer, Aaron D.
    Ali, Moshin
    Zappala, Maria
    Grasso, Silvana
    MEDICINAL CHEMISTRY RESEARCH, 2012, 21 (09) : 2644 - 2651
  • [25] Synthesis and biological activity of acyl thiourea containing difluoromethyl pyrazole motif
    Min, Li-Jing
    Zhai, Zhi-Wen
    Shi, Yan-Xia
    Han, Liang
    Tan, Cheng-Xia
    Weng, Jian-Quan
    Li, Bao-Ju
    Zhang, Yong-Gang
    Liu, Xing-Hai
    PHOSPHORUS SULFUR AND SILICON AND THE RELATED ELEMENTS, 2020, 195 (01) : 22 - 28
  • [26] Synthesis and biological evaluation of terminal functionalized thiourea-containing dipeptides as antitumor agents
    Huang, Ri-Zhen
    Zhang, Bin
    Huang, Xiao-Chao
    Liang, Gui-Bin
    Qin, Jian-Mei
    Pan, Ying-Ming
    Liao, Zhi-Xin
    Wang, Heng-Shan
    RSC ADVANCES, 2017, 7 (15): : 8866 - 8878
  • [27] SYNTHESIS, CHARACTERIZATION AND BIOLOGICAL EVALUATION OF SOME NOVEL BENZOTHIAZOLE ANALOGS AS POTENTIAL ANTITUBERCULAR AGENTS
    Satyadev, Siddhanadham Arun
    Prava, Raj Kumar
    Mantha, Sowmya
    Koduru, Aparna
    Gowtami, Thimmysetty
    INTERNATIONAL JOURNAL OF PHARMACEUTICAL SCIENCES AND RESEARCH, 2021, 12 (01): : 576 - 586
  • [28] Synthesis and biological evaluation of fluoropyrazolesulfonylurea and thiourea derivatives as possible antidiabetic agents
    Faidallah, Hassan M.
    Al-Mohammadi, Manal M.
    Alamry, Khalid A.
    Khan, Khalid A.
    JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, 2016, 31 : 157 - 163
  • [29] Synthesis and Biological Activity of Substituted Urea and Thiourea Derivatives Containing 1,2,4-Triazole Moieties
    Kocyigit-Kaymakcioglu, Bedia
    Celen, Ahmet Ozgur
    Tabanca, Nurhayat
    Ali, Abbas
    Khan, Shabana I.
    Khan, Ikhlas A.
    Wedge, David E.
    MOLECULES, 2013, 18 (03): : 3562 - 3576
  • [30] Design, Synthesis and Biological Evaluation of Novel Rapamycin Benzothiazole Hybrids as mTOR Targeted Anti-cancer Agents
    Xie, Lijun
    Huang, Jie
    Chen, Xiaoming
    Yu, Hui
    Li, Kualiang
    Yang, Dan
    Chen, Xiaqin
    Ying, Jiayin
    Pan, Fusheng
    Lv, Youbing
    Cheng, Yuanrong
    CHEMICAL & PHARMACEUTICAL BULLETIN, 2016, 64 (04) : 346 - 355