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Design, Synthesis, and Biological Evaluation of Novel 1,3,4‐Thiadiazolylpyrazolines Compounds Containing Ferrocene

Liqin ChenKey Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, College of Chemistry & Materials Science Northwest University Xi'an 710127 ChinaHui‐Hui DuanKey Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, College of Chemistry & Materials Science Northwest University Xi'an 710127 ChinaXinyu ZhangKey Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, College of Chemistry & Materials Science Northwest University Xi'an 710127 ChinaQiong ZhangKey Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, College of Chemistry & Materials Science Northwest University Xi'an 710127 ChinaHailian HuangKey Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, College of Chemistry & Materials Science Northwest University Xi'an 710127 ChinaJunlong ZhaoKey Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, College of Chemistry & Materials Science Northwest University Xi'an 710127 ChinaBang ChenKey Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, College of Chemistry & Materials Science Northwest University Xi'an 710127 ChinaChengwen HuaKey Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, College of Chemistry & Materials Science Northwest University Xi'an 710127 ChinaXiao‐Feng GouKey Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, College of Chemistry & Materials Science Northwest University Xi'an 710127 China
2018en
ABI

Аннотация

The synthesis of 1,3,4‐thiadiazole skeleton compounds exhibiting high fungicidal activities has been demonstrated. Thirteen novel 1,3,4‐thiadiazolyl‐pyrazolines compounds containing ferrocene were designed and synthesized from the ferrocenylchalcones intermediates 3a – 3m and the 2‐hydrazino‐5‐phenyl‐1,3,4‐thiadiazole intermediate 8 . All compounds were characterized by 1 H NMR, 13 C NMR, FT‐IR spectra, and HR‐MS, and the structure of one of the new compounds N ‐(4‐phenyl‐1,3,4‐thiadiazol‐2‐yl)‐3‐ferrocenyl‐5‐phenyl‐pyrazoline 9a was further determined by X‐ray diffraction analysis. The preliminary results of a biological activity assay indicated that all the title compounds exhibited significant fungicidal activities against Pythium solani , Gibberella saubinetii , and Gibberella nicotiancola . Furthermore, compounds 9e and 9h displayed even higher fungicidal activities against the three fungal species compared with the control drug pyraclostrobin.

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