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.
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收藏
页码:535 / 543
页数:9
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