摘要
本文利用3-芳基-4-氨基-5-巯基-1,2,4-均三唑和苯甲酰异硫氰酸酯在无水丙酮中反应,得到一系列3-芳基-6-苯甲酰氨基均三唑并[3,4-b]-1,3,4-噻二唑,用元素分析、IR、1HNMR和MS确定了其结构,提出了可能的反应机制。并对其代表产物2h进行了初步的抗菌和除草实验。
S-triazolo[3,4-b]-1,3,4-thiadiazoles are fused heterocyclic derivatives showing various biological effect, such as antifungal, antibacterial, hypotensive and CNS depressant. In view of the pharmacological and synthetic interests of this kind of fused heterocycles, we investigate the reaction of 3-aryl-4-amino-5-mercapto-1,2,4-s-triazoles 1a-j with benzoyl isothiocyanate in the presence of absolute acetone and obtained a series of 3-aryl-6-benzoylamino-s-triazolo[3,4-b]-1,3,4-thiadiazoles,2a-j, whose structures were determined by elemental analysis, IR,  ̄1H NMR and MS. The possible mechanism of this reaction has been suggested in the meantime.It was found that the representative compound2h has moderate herbicidal activity.
出处
《高等学校化学学报》
CSCD
北大核心
1994年第2期220-223,共4页
Chemical Journal of Chinese Universities
基金
国家自然科学基金
关键词
均三唑
噻二唑
芳基
稠杂环化合物
S-triazolo[3
4-b]-1
3
4-thiadiazoles
Synthesis
Mechanism
Biological activity