B. Prasanna, B. Srinivas, Y. Jagannadham, Sumangala Rao
{"title":"An Efficient Synthesis of Thiazolo and Thiadiazolo Quinoxaline Derivatives in Ionic Liquid","authors":"B. Prasanna, B. Srinivas, Y. Jagannadham, Sumangala Rao","doi":"10.1155/2012/865414","DOIUrl":null,"url":null,"abstract":"A series of 3-substitutedphenyl-1-thia-tetrazopentaleno[1,2-b] naphthalene 4(a-d) and 2-substitutedphenyl-1-thia-pentazopentaleno[1,2-b] naphthalene 5(a-d) were synthesized via., the reaction of 2-aminothiazoles 2(a-d) and 2-aminothiadiazoles 3(a-d) with 2,3-dichloro quinoxaline 1 in ionic liquid without using any catalyst. This protocol has the advantages of easier workup, milder reaction conditions, high yields, and environmentally benign procedure over traditional methods. The synthesized compounds 4(a-d) and 5(a-d) tested for their anti-fungal activity and these compounds were characterized by IR, NMR and Mass spectral analysis.","PeriodicalId":11519,"journal":{"name":"E-journal of Chemistry","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2012-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2012/865414","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"E-journal of Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/2012/865414","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2
Abstract
A series of 3-substitutedphenyl-1-thia-tetrazopentaleno[1,2-b] naphthalene 4(a-d) and 2-substitutedphenyl-1-thia-pentazopentaleno[1,2-b] naphthalene 5(a-d) were synthesized via., the reaction of 2-aminothiazoles 2(a-d) and 2-aminothiadiazoles 3(a-d) with 2,3-dichloro quinoxaline 1 in ionic liquid without using any catalyst. This protocol has the advantages of easier workup, milder reaction conditions, high yields, and environmentally benign procedure over traditional methods. The synthesized compounds 4(a-d) and 5(a-d) tested for their anti-fungal activity and these compounds were characterized by IR, NMR and Mass spectral analysis.