Title:Combinatorial Synthesis of Indole Derivatives as Anti-oomycetes Agents
Volume: 27
Issue: 19
Author(s): Fei Hai, Ruxue Wei, Yan Li, Ruiguang Wang, Yuee Tian, Shengming Liu, Genqiang Chen and Zhiping Che*
Affiliation:
- Laboratory of Pesticidal Design & Synthesis, Department of Plant Protection, College of Horticulture and
Plant Protection, Henan University of Science and Technology, Luoyang 471023, China
Keywords:
Natural product, indole synthesis, anti-oomycete activity, Phytophthora capsici, indole derivatives, plant secondary metabolites.
Abstract:
Background: Developing high-efficiency and low-risk small-molecule green fungicide
is the key to effective control of the plant pathogenic oomycetes. Indole is an important raw
material for drug synthesis. Due to its unique structural skeleton, indole, and its derivatives have
exhibited a wide range of biological activities. However, a study on the synthesis of novel indole
derivatives as fungicidal agents against Phytophthora capsici has not yet been reported.
Methods: The important intermediates 2a-c and 3a-c were synthesized in high yields by Vilsmeier-
Haack and Knoevenagel reactions with indole as the lead compound. Furthermore, different
substituted benzenesulfonyl groups were introduced into the NH position of the indole ring,
and twelve indole derivatives (I-a-l) were prepared. Their structures were well characterized by
1H NMR, HRMS, and melting point.
Results: The results showed that 2-[(N-(4-nitrobenzenesulfonyl)-indole-3)-methylene]-diethyl
malonate (I-d) and 2-[(N-(4-nitrobenzenesulfonyl)-5-cyanoindole-3)-methylene]-diethyl malonate
(I-l) showed more anti-oomycete activity against P. capsici than the commercialized fungicide
zoxamide, with corresponding EC50 values of 26.53, 23.48 and 28.16 mg/L, respectively,
and the protective effect of the compounds against P. capsici in vivo further confirmed the above
results.
Conclusion: The preliminary structure-activity relationship showed that the formyl group modification
at the C-3 position of the indole ring was acceptable, and the different anti-oomycete activities
of R1 and R2 were significantly different, with R1 being 5-CN > H > 6-Me, and R2 being
4-NO2 > 3-NO2, H > 4-Me.