Hayam Mohammed, Eman A. Ahmed, B. Hussein, Omran Abdellah
{"title":"One-pot Multicomponent Synthesis of Novel Polyfunctionalized Pyridines","authors":"Hayam Mohammed, Eman A. Ahmed, B. Hussein, Omran Abdellah","doi":"10.21608/sjsci.2023.227734.1111","DOIUrl":null,"url":null,"abstract":": In this work, we synthesized a novel arylidene malononitrile 3 via the treatment of o -alkyl vanillin derivative 1 with malononitrile 2 in the presence of triethylamine (TEA) as a catalyst. The arylidene malononitrile 3 was subjected to react under one-pot multicomponent reaction (MCR) condition with respective methylarylketones 4a-f and sodium ethoxide 5 in ethanol to afford a new series of 2-(4-(6-aryl-3-cyano-2-ethoxypyridin-4-yl)-2-methoxyphenoxy)- N -phenylacetamides 6a-f . The structure of the new products was assured via spectral and elemental analysis. The reaction mechanism was suggested.","PeriodicalId":146413,"journal":{"name":"Sohag Journal of Sciences","volume":"39 13","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Sohag Journal of Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21608/sjsci.2023.227734.1111","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
: In this work, we synthesized a novel arylidene malononitrile 3 via the treatment of o -alkyl vanillin derivative 1 with malononitrile 2 in the presence of triethylamine (TEA) as a catalyst. The arylidene malononitrile 3 was subjected to react under one-pot multicomponent reaction (MCR) condition with respective methylarylketones 4a-f and sodium ethoxide 5 in ethanol to afford a new series of 2-(4-(6-aryl-3-cyano-2-ethoxypyridin-4-yl)-2-methoxyphenoxy)- N -phenylacetamides 6a-f . The structure of the new products was assured via spectral and elemental analysis. The reaction mechanism was suggested.