Lei Zhang, Jiyong Liu, Liqi Zhou, Chengyi Yan, Daoxin Wu, Minhua Liu
{"title":"含有 1,2,4-三唑分子的新型偏二胺支架的定向合成和杀虫活性","authors":"Lei Zhang, Jiyong Liu, Liqi Zhou, Chengyi Yan, Daoxin Wu, Minhua Liu","doi":"10.1002/jhet.4866","DOIUrl":null,"url":null,"abstract":"<p>In an effort to discover a new insecticide, we designed and synthesized a series of novel <i>meta</i>-diamide compounds containing 1,2,4-triazole with cyproflanilide as a lead compound. All the compounds were characterized by <sup>1</sup>H NMR, <sup>13</sup>C NMR, and HR-MS. Both <i>Plutella xylostella</i> and <i>Mythimna separata</i> were tested for their insecticidal activity at 200 mg/L (<i>P. xylostella</i>: 0%–100%; <i>M. separata</i>: 0%–100%), 20 mg/L (<i>P. xylostella</i>: 0%–97%; <i>M. separata</i>: 0%–100%), and 2 mg/L (<i>P. xylostella</i>: 0%–97%; <i>M. separata</i>: 0%–100%), while <i>Aphis craccivora</i> was tested for its insecticidal activity at 400 mg/L (<i>A. craccivora</i>: 0%–36%). Further studies are needed to investigate the insecticidal activity of <i>A. craccivora</i>. Preliminary bioactivity results showed that most of the compounds had good insecticidal activity at 200 mg/L against <i>P. xylostella</i> and <i>M. separata</i>. Especially, the compound <b>7p</b>, <i>N</i>-(cyclopropylmethyl)-<i>N</i>-(5-((2,6-dibromo-4-(perfluoropropan-2-yl)phenyl) carbamoyl)-2-(1<i>H</i>-1,2,4-triazol-1-yl)phenyl)-6-(trifluoromethyl)nicotinamide (<b>7p</b>), showed good insecticidal activity at even lower doses of 2 mg/L (<i>P. xylostella</i>: 97%; <i>M. separata</i>: 100%), which was equivalent to that of the lead compound cyproflanilide (<i>P. xylostella</i>: 100%; <i>M. separata</i>: 100%), as well as significantly better than the two known compounds <b>I</b><sub><b>a</b></sub> (<i>P. xylostella</i>: 97%; <i>M. separata</i>: 0%) and <b>I</b><sub><b>b</b></sub> (<i>P. xylostella</i>: 60%; <i>M. separata</i>: 0%). Preliminary structure–activity relationship was also discussed based on insecticidal tests. The results indicate that <i>meta</i>-diamide compounds containing 1,2,4-triazole can be developed as novel insecticides.</p>","PeriodicalId":194,"journal":{"name":"Journal of Heterocyclic Chemistry","volume":"61 9","pages":"1411-1416"},"PeriodicalIF":2.0000,"publicationDate":"2024-06-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Oriented synthesis and insecticidal activities of novel meta-diamide scaffolds incorporating with 1,2,4-triazole moiety\",\"authors\":\"Lei Zhang, Jiyong Liu, Liqi Zhou, Chengyi Yan, Daoxin Wu, Minhua Liu\",\"doi\":\"10.1002/jhet.4866\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>In an effort to discover a new insecticide, we designed and synthesized a series of novel <i>meta</i>-diamide compounds containing 1,2,4-triazole with cyproflanilide as a lead compound. All the compounds were characterized by <sup>1</sup>H NMR, <sup>13</sup>C NMR, and HR-MS. Both <i>Plutella xylostella</i> and <i>Mythimna separata</i> were tested for their insecticidal activity at 200 mg/L (<i>P. xylostella</i>: 0%–100%; <i>M. separata</i>: 0%–100%), 20 mg/L (<i>P. xylostella</i>: 0%–97%; <i>M. separata</i>: 0%–100%), and 2 mg/L (<i>P. xylostella</i>: 0%–97%; <i>M. separata</i>: 0%–100%), while <i>Aphis craccivora</i> was tested for its insecticidal activity at 400 mg/L (<i>A. craccivora</i>: 0%–36%). Further studies are needed to investigate the insecticidal activity of <i>A. craccivora</i>. Preliminary bioactivity results showed that most of the compounds had good insecticidal activity at 200 mg/L against <i>P. xylostella</i> and <i>M. separata</i>. Especially, the compound <b>7p</b>, <i>N</i>-(cyclopropylmethyl)-<i>N</i>-(5-((2,6-dibromo-4-(perfluoropropan-2-yl)phenyl) carbamoyl)-2-(1<i>H</i>-1,2,4-triazol-1-yl)phenyl)-6-(trifluoromethyl)nicotinamide (<b>7p</b>), showed good insecticidal activity at even lower doses of 2 mg/L (<i>P. xylostella</i>: 97%; <i>M. separata</i>: 100%), which was equivalent to that of the lead compound cyproflanilide (<i>P. xylostella</i>: 100%; <i>M. separata</i>: 100%), as well as significantly better than the two known compounds <b>I</b><sub><b>a</b></sub> (<i>P. xylostella</i>: 97%; <i>M. separata</i>: 0%) and <b>I</b><sub><b>b</b></sub> (<i>P. xylostella</i>: 60%; <i>M. separata</i>: 0%). Preliminary structure–activity relationship was also discussed based on insecticidal tests. The results indicate that <i>meta</i>-diamide compounds containing 1,2,4-triazole can be developed as novel insecticides.</p>\",\"PeriodicalId\":194,\"journal\":{\"name\":\"Journal of Heterocyclic Chemistry\",\"volume\":\"61 9\",\"pages\":\"1411-1416\"},\"PeriodicalIF\":2.0000,\"publicationDate\":\"2024-06-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Heterocyclic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/jhet.4866\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Heterocyclic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/jhet.4866","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Oriented synthesis and insecticidal activities of novel meta-diamide scaffolds incorporating with 1,2,4-triazole moiety
In an effort to discover a new insecticide, we designed and synthesized a series of novel meta-diamide compounds containing 1,2,4-triazole with cyproflanilide as a lead compound. All the compounds were characterized by 1H NMR, 13C NMR, and HR-MS. Both Plutella xylostella and Mythimna separata were tested for their insecticidal activity at 200 mg/L (P. xylostella: 0%–100%; M. separata: 0%–100%), 20 mg/L (P. xylostella: 0%–97%; M. separata: 0%–100%), and 2 mg/L (P. xylostella: 0%–97%; M. separata: 0%–100%), while Aphis craccivora was tested for its insecticidal activity at 400 mg/L (A. craccivora: 0%–36%). Further studies are needed to investigate the insecticidal activity of A. craccivora. Preliminary bioactivity results showed that most of the compounds had good insecticidal activity at 200 mg/L against P. xylostella and M. separata. Especially, the compound 7p, N-(cyclopropylmethyl)-N-(5-((2,6-dibromo-4-(perfluoropropan-2-yl)phenyl) carbamoyl)-2-(1H-1,2,4-triazol-1-yl)phenyl)-6-(trifluoromethyl)nicotinamide (7p), showed good insecticidal activity at even lower doses of 2 mg/L (P. xylostella: 97%; M. separata: 100%), which was equivalent to that of the lead compound cyproflanilide (P. xylostella: 100%; M. separata: 100%), as well as significantly better than the two known compounds Ia (P. xylostella: 97%; M. separata: 0%) and Ib (P. xylostella: 60%; M. separata: 0%). Preliminary structure–activity relationship was also discussed based on insecticidal tests. The results indicate that meta-diamide compounds containing 1,2,4-triazole can be developed as novel insecticides.
期刊介绍:
The Journal of Heterocyclic Chemistry is interested in publishing research on all aspects of heterocyclic chemistry, especially development and application of efficient synthetic methodologies and strategies for the synthesis of various heterocyclic compounds. In addition, Journal of Heterocyclic Chemistry promotes research in other areas that contribute to heterocyclic synthesis/application, such as synthesis design, reaction techniques, flow chemistry and continuous processing, multiphase catalysis, green chemistry, catalyst immobilization and recycling.