Synthesis, Crystal Structure and Biological Activity of Diethyl 1,4-dihydro-2,6-dimethyl-4-(4-methyl-1,2,3-thiadi azol-5-yl)pyridine-3,5-dicarboxylate

被引:0
|
作者
李娟娟 [1 ,2 ]
华学文 [2 ,3 ]
范志金 [2 ,3 ]
姬晓恬 [2 ,3 ]
宗广宁 [2 ,3 ]
李凤云 [2 ,3 ]
黄云 [1 ]
宋海滨 [2 ]
刘超伦 [2 ,3 ]
Yury Yu. Morzherin [4 ]
Nataliya P. Belskaya [4 ]
Vasiliy A. Bakulev [4 ]
机构
[1] Department of Plant Pathology, Sichuan Agricultural University
[2] State Key Laboratory of Elemento-organic Chemistry, Nankai University
[3] Collaborative Innovation Center of Chemical Science and Engineering(Tianjin)
[4] The Ural Federal University Named after the First President of Russia B. N. Yeltsin,Yeltsin UrFU 620002, Ekaterinburg, Russia
关键词
1; 4-dihydropyridine; 2; 3-thiadiazole; crystal structure; biological activity;
D O I
10.14102/j.cnki.0254-5861.2014.04.022
中图分类号
TQ460.1 [基础理论];
学科分类号
1007 ;
摘要
The title compound diethyl 1,4-dihydro-2,6-dimethyl-4-(4-methyl-1,2,3-thiadiazol-5-yl) pyridine-3,5-dicarboxylate(C16H21N3O4S, Mr = 351.42) was prepared by the Hantszch reaction with 4-methyl-1,2,3-thiadiazole-5-formaldehyde, ethyl acetoacetate and ammonium acetate in the presence of aluminum chloride in alcohol, and its structure was characterized by IR spectra, 1H-NMR, EA, and single-crystal X-ray diffraction. The crystal of the title compound belongs to monoclinic system, space group P21/n with a = 11.300(2), b = 12.771(3), c = 12.826(3) ?, β = 96.55(3)o, V = 1839.0(6) ?3, Z = 4, Dc = 1.296 g/cm3, μ(MoKa) = 0.71073 mm-1, F(000) = 744, R = 0.0981 and wR = 0.1994. X-ray diffraction result shows that the torsion angles of N(1)–C(2)– C(3)–C(4) and C(2)–C(3)–C(4)–C(8) are 178.9(3)° and –130.3(3)°, respectively. All rings in the title compound are non-planar. The bioassay results indicate that the title compound has good fungicidal activity, good antivirus activity against tobacco mosaic virus and certain extent of insecticidal activity against Mythimna separata.
引用
收藏
页码:535 / 543
页数:9
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