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Oriented synthesis and insecticidal activities of novel meta‐diamide scaffolds incorporating with 1,2,4‐triazole moiety.

Authors :
Zhang, Lei
Liu, Jiyong
Zhou, Liqi
Yan, Chengyi
Wu, Daoxin
Liu, Minhua
Source :
Journal of Heterocyclic Chemistry; Sep2024, Vol. 61 Issue 9, p1411-1416, 6p
Publication Year :
2024

Abstract

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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
0022152X
Volume :
61
Issue :
9
Database :
Complementary Index
Journal :
Journal of Heterocyclic Chemistry
Publication Type :
Academic Journal
Accession number :
180232159
Full Text :
https://doi.org/10.1002/jhet.4866