{"title":"微波辐射下Suzuki偶联反应高效合成5-(4-(取代[1,1 ' -联苯]-4-酰基甲氧基)苄基)噻唑烷-2,4-二酮及其生物筛选","authors":"Mitesh B. Vekariya, Tejal D. Bhatt, H. Joshi","doi":"10.14233/ajomc.2022.ajomc-p388","DOIUrl":null,"url":null,"abstract":"In present study, an efficient and greener protocol is developed for the synthesis of 5-(4-(substituted [1,1′-biphenyl]-4-yl-methoxy)benzyl)-thiazolidine-2,4-diones by using microwave irradiations. Here, a one-pot reaction between 5-(4-((4-bromobenzyl)oxy)benzyl)thiazolidine-2,4-dione, substituted aryl boronic acid and K2CO3 in the presence of toluene:water:ethanol solvents under conventional heating methods and microwave irradiation methods is reported. All the final compounds were characterized by FT-IR, 1H NMR, 13C NMR and mass spectroscopic analysis. The antimicrobial evaluation studies show moderate activities against used microbes.","PeriodicalId":8544,"journal":{"name":"Asian Journal of Organic & Medicinal Chemistry","volume":"57 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Efficient Synthesis of 5-(4-(Substituted [1,1′-Biphenyl]-4-yl-methoxy)benzyl)thiazolidine-\\n2,4-diones under Microwave Irradiation using Suzuki Coupling Reaction\\nand their Biological Screening\",\"authors\":\"Mitesh B. Vekariya, Tejal D. Bhatt, H. Joshi\",\"doi\":\"10.14233/ajomc.2022.ajomc-p388\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In present study, an efficient and greener protocol is developed for the synthesis of 5-(4-(substituted [1,1′-biphenyl]-4-yl-methoxy)benzyl)-thiazolidine-2,4-diones by using microwave irradiations. Here, a one-pot reaction between 5-(4-((4-bromobenzyl)oxy)benzyl)thiazolidine-2,4-dione, substituted aryl boronic acid and K2CO3 in the presence of toluene:water:ethanol solvents under conventional heating methods and microwave irradiation methods is reported. All the final compounds were characterized by FT-IR, 1H NMR, 13C NMR and mass spectroscopic analysis. The antimicrobial evaluation studies show moderate activities against used microbes.\",\"PeriodicalId\":8544,\"journal\":{\"name\":\"Asian Journal of Organic & Medicinal Chemistry\",\"volume\":\"57 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Asian Journal of Organic & Medicinal Chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.14233/ajomc.2022.ajomc-p388\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Asian Journal of Organic & Medicinal Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.14233/ajomc.2022.ajomc-p388","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Efficient Synthesis of 5-(4-(Substituted [1,1′-Biphenyl]-4-yl-methoxy)benzyl)thiazolidine-
2,4-diones under Microwave Irradiation using Suzuki Coupling Reaction
and their Biological Screening
In present study, an efficient and greener protocol is developed for the synthesis of 5-(4-(substituted [1,1′-biphenyl]-4-yl-methoxy)benzyl)-thiazolidine-2,4-diones by using microwave irradiations. Here, a one-pot reaction between 5-(4-((4-bromobenzyl)oxy)benzyl)thiazolidine-2,4-dione, substituted aryl boronic acid and K2CO3 in the presence of toluene:water:ethanol solvents under conventional heating methods and microwave irradiation methods is reported. All the final compounds were characterized by FT-IR, 1H NMR, 13C NMR and mass spectroscopic analysis. The antimicrobial evaluation studies show moderate activities against used microbes.