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首页> 外文期刊>Bulletin of the Korean Chemical Society >Heterocyclic Systems Containing Bridgehead Nitrogen Atom: Synthesis and Evaluation of Biological Activity of Imidazo[2,1-b]-1,3,4-thiadiazolo [2,3-c] -s-triazoles, s-Triazolo [3,4-b] -1,3,4-thiadiazolo [3,2-6] imidazo [4,5-b] quinoxaline and bis-(s-Triazolo[3,4-b]-1,3,4-thiadiazolo[3,2-b][imidazo[4,5-b]-cyclohexane]-5a,6a-diene)
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Heterocyclic Systems Containing Bridgehead Nitrogen Atom: Synthesis and Evaluation of Biological Activity of Imidazo[2,1-b]-1,3,4-thiadiazolo [2,3-c] -s-triazoles, s-Triazolo [3,4-b] -1,3,4-thiadiazolo [3,2-6] imidazo [4,5-b] quinoxaline and bis-(s-Triazolo[3,4-b]-1,3,4-thiadiazolo[3,2-b][imidazo[4,5-b]-cyclohexane]-5a,6a-diene)

机译:含桥头氮原子的杂环系统:咪唑并[2,1-b] -1,3,4-噻二唑[2,3-c] -s-三唑,s-三唑[3,4-]的合成和生物活性评估b] -1,3,4-噻二唑[3,2-6]咪唑并[4,5-b]喹喔啉和bis-(s-Triazolo [3,4-b] -1,3,4-噻二唑[3 ,2-b] [咪唑并[4,5-b]-环己烷] -5a,6a-二烯)

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摘要

Condensation of 4-amino-5-mercapto-3-(α-naphthyl)-s-triazole (1) with cyanogen bromide gives 6-arnino-3-(α-naph-thyl)-s-triazolo[3,4-b]-1,3,4-thiadiazole (2) which on condensation with chloranil yields 3,9-di-(α-naphthyl)-6,14-dioxo-bis-(s-triazolo[3,4-b]-1,3,4-thiadiazolo[3,2-b]imidazo[4,5-b)]cyclohexane]-5a,6a-diene) (3). 3-(α-naphthyl)-s-triazolo[3,4-b-1,3,4-thiadiazolo[3,2-b]imidazo[4,5-b]quinoxaline (4) is obtained by a similar condensation of (2) with 2,3-dichloroquinoxaline. The reaction of (2) with α-haloketones followed by bromination affords 7-aryl-3-(α-naphthyl)-imidazo[2,1-b)]-1,3,4-thiadiazolo[2,3-c]-s-triazoles (5) and their 6-bromo analogues 6 respectively. The structures of all newly synthesized compounds were established on the basis of elemental analyses, IR,~1H-NMR. The antibacterial and antifungal activities of all newly synthesized compounds have also been evaluated.
机译:4-氨基-5-巯基-3-(α-萘基)-s-三唑(1)与溴化氰的缩合得到6-氨基--3-(α-萘基)-s-三唑[3,4- b] -1,3,4-噻二唑(2),与氯甲腈缩合后可生成3,9-二-(α-萘基)-6,14-二氧代双-(s-三唑[3,4-b] -1,3,4-噻二唑并[3,2-b]咪唑并[4,5-b)]环己烷] -5a,6a-二烯)(3)。通过类似的缩合获得3-(α-萘基)-s-三唑并[3,4-b-1,3,4-噻二唑并[3,2-b]咪唑并[4,5-b]喹喔啉(4)。 (2)用2,3-二氯喹喔啉。 (2)与α-卤代酮反应,然后溴化,得到7-芳基-3-(α-萘基)-咪唑并[2,1-b)]-1,3,4-噻二唑[2,3-c] -s-三唑(5)和它们的6-溴类似物6。所有新合成的化合物的结构都是在元素分析,IR,〜1H-NMR的基础上建立的。还对所有新合成的化合物的抗菌和抗真菌活性进行了评估。

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