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Synthesis and Antimicrobial Activity of Furochromone, Benzofuran and Furocoumarin Derivatives Bearing Sulfonyl Moiety

机译:具有磺酰基部分的呋喃苯醌,苯并呋喃和呋喃香豆素衍生物的合成及抑菌活性

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摘要

New visnagin-9-sulfonamide derivatives 3 and 4a−c were synthesized through the reaction of visnagin-9-sulfonyl chloride 2 with amino compounds. Acetylation of compounds 4b and 4c gave the monoacetyl and diacetyl derivatives 5 and 6, respectively. Diazotization reaction of compound 4b afforded the corresponding benzotriazole derivative 8. Pyrazole and thiopyrimidine derivatives 9 and 10 were obtained via the opening of pyrone ring upon reaction of compound 3 with hydrazine hydrate and thiourea, respectively. In addition, hydrolysis of compound 3 with potassium hydroxide furnished the visnaginone derivative 11 which used as starting material for synthesize benzofuran derivatives 12−14 and bergaptene derivatives 15−17. The synthesized compounds were tested for antimicrobial activity. Furochromone derivatives 3, 4a−c, 5, 6 and 8 (visnagin-9-sulfonamide derivatives) demonstrate moderate antibacterial and antifungal activities compared with the antibacterial and antifungal activites of the standard drugs. Benzofuran derivatives 11−14 (visnaginone derivatives) showed the lowest antimicrobial activity among all the compounds investigated in this study. Furocoumarin derivatives 15a,b, 16 and 17 (furobenzopyransulfonamide [bergaptensulfonamides]) are moderately active against all the tested strains. This work is licensed under a Creative Commons Attribution 4.0 International License.
机译:通过visnagin-9-磺酰氯2与氨基化合物的反应合成了新的visnagin-9-磺酰胺衍生物3和4a-c。化合物4b和4c的乙酰化分别得到单乙酰基和二乙酰基衍生物5和6。化合物4b的重氮化反应得到相应的苯并三唑衍生物8。当化合物3分别与水合肼和硫脲反应时,通过打开吡咯环获得吡唑和硫代嘧啶衍生物9和10。另外,化合物3用氢氧化钾的水解提供了visnaginone衍生物11,其用作合成苯并呋喃衍生物12-14和香菜烯衍生物15-17的原料。测试合成的化合物的抗微生物活性。与标准药物的抗菌和抗真菌活性相比,呋喃苯甲酮衍生物3、4a-c,5、6和8(visnagin-9-磺酰胺衍生物)显示出中等的抗菌和抗真菌活性。在本研究中所有研究的化合物中,苯并呋喃衍生物11-14(维吉纳酮衍生物)显示出最低的抗菌活性。呋喃香豆素衍生物15a,b,16和17(呋喃苯并吡喃磺酰胺[bergaptensulfonamides])对所有测试菌株均具有中等活性。本作品已根据知识共享署名4.0国际许可协议获得许可。

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