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新型 3-[(5-芳基-1,3,4-恶二唑-2-基)甲基]苯并[d]噻唑-2(3H)-酮的合成、结构和抗真菌活性。

Synthesis, structure and antifungal activity of new 3-[(5-aryl-1,3,4-oxadiazol-2-yl)methyl]benzo[d]thiazol-2(3H)-ones.

机构信息

College of Chemical Engineering and Materials Science, Zhejiang University of Technology, Hangzhou 310014, China.

出版信息

Molecules. 2012 Jan 18;17(1):989-1001. doi: 10.3390/molecules17010989.

Abstract

A series of new 3-[(5-aryl-1,3,4-oxadiazol-2-yl)methy])benzo[d]thiazol-2(3H)-ones were synthesized by reaction of (5-substituted-2-oxobenzothiazolin-3-yl)-acetohydrazide with various aromatic acids in POCl(3) under reflux conditions. The structures of the title compounds were confirmed by ¹H-NMR, ¹³C-NMR, IR, MS and elemental analysis. Furthermore, the structure of compound 4i was determined by single-crystal X-ray diffraction. The preliminary bioassy results indicated that some of them showed moderate inhibition activity against Colletotrichum orbiculare, Botrytis cinerea and Rhizoctonia solani.

摘要

一系列新的 3-[(5-芳基-1,3,4-恶二唑-2-基)甲基]苯并[d]噻唑-2(3H)-酮是通过(5-取代-2-氧代苯并噻唑啉-3-基)乙酰肼与各种芳酸在 POCl(3)中回流条件下反应合成的。标题化合物的结构通过 ¹H-NMR、¹³C-NMR、IR、MS 和元素分析得到确认。此外,化合物 4i 的结构通过单晶 X 射线衍射确定。初步的生物测定结果表明,其中一些对炭疽菌、灰葡萄孢和立枯丝核菌表现出中等抑制活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00f5/6268515/314ba2441409/molecules-17-00989-g003.jpg

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