Synthesis, Crystal Structure and Bioactivities of N-(5-(4-chlorobenzyl)-1,3,5-Triazinan-2-Ylidene)Nitramide

• Published in: Crystals (Basel) 2020-04, Vol.10 (4), p.245
• Main Authors: Qin, Yao-Guo, Yang, Zhao-Kai, Fan, Jia, Jiang, Xin, Yang, Xin-Ling, Chen, Ju-Lian
• Format: Article
• Language: English
• Subjects: antifungal activity; aphicidal activity; Benzene; Bonding strength; Crystal structure; Fungicides; Hydrocarbons; Hydrogen; Hydrogen atoms; Hydrogen bonding; Insects; Methods; Molecular structure; nitramide; NMR; Nuclear magnetic resonance; Single crystals; Solvents; Synthesis
• ISSN: 2073-4352; 2073-4352
• DOI: 10.3390/cryst10040245

The compound N-(5-(4-chlorobenzyl)-1,3,5-triazinan-2-ylidene)nitramide (C10H12ClN5O2, M = 269.70) was synthesized and structurally confirmed by 1H NMR, 13C NMR, HRMS and single-crystal x-ray diffraction. The crystal belongs to the monoclinic system with space group P21/c. The title compound consisted of a benzene ring and a 1,3,5-triazine ring. All carbon atoms in the benzene ring were nearly coplanar with a dihedral (C6–C5–C10 and C7–C8–C9) angle of 1.71°and all non-hydrogen atoms of the 1,3,5-triazine ring were not planar, but exhibited a half-chair conformation. The crystal structure was stabilized by a strong intramolecular hydrogen bonding interaction N(3)–H(3)···O(2) and three intermolecular hydrogen bonding interactions, N(2)–H(2)···O(1), N(2)–H(2)···N(4) and N(3)–H(3)···Cl(1). The preliminary bioassay showed that the title compound showed not only aphicidal activity against Sitobion miscanthi (inhibition rate: 74.1%) and Schizaphis graminum (77.5%), but also antifungal activities against Pythium aphanidermatum (62.0%). These results provide valuable guidelines for the design and synthesis of novel aphid control agents and fungicides.