V. G. Shtamburg, V. Shtamburg, A. A. Anishchenko, A. Mazepa
{"title":"The peculiarities of the 4-carboxyphenylglyoxal and N-alkoxy-N’-arylureas interaction","authors":"V. G. Shtamburg, V. Shtamburg, A. A. Anishchenko, A. Mazepa","doi":"10.17628/ecb.2020.9.339-344","DOIUrl":null,"url":null,"abstract":"It was found that 3-alkoxy-4,5-dihydroxyimidazolidin-2-ones are the only products of interaction of N-alkoxyureas with arylglyoxals which have strong electronegative substituent in the forth position of the aryl moiety. The possibility of obtaining such products as 3-alkoxy-1aryl-5-(4-carboxyphenyl)-4,5-dihydroxyimidazolidin-2-ones, 3-alkoxy-1-alkyl-5-(4-carboxyphenyl)-4,5-dihydroxyimidazolidin-2-ones and 3-alkoxy-1-phenyl-4,5-dihydroxy-5-(4-nitrophenyl)-imidazolidin-2-ones has been verified in the experimental way. In most the cases 3alkoxy-4,5-dihydroxyimidazolidin-2-ones were produced as a mixture of diastereomers.","PeriodicalId":11880,"journal":{"name":"European Chemical Bulletin","volume":"9 1","pages":"339"},"PeriodicalIF":0.0000,"publicationDate":"2020-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"6","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Chemical Bulletin","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.17628/ecb.2020.9.339-344","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Chemistry","Score":null,"Total":0}
引用次数: 6
Abstract
It was found that 3-alkoxy-4,5-dihydroxyimidazolidin-2-ones are the only products of interaction of N-alkoxyureas with arylglyoxals which have strong electronegative substituent in the forth position of the aryl moiety. The possibility of obtaining such products as 3-alkoxy-1aryl-5-(4-carboxyphenyl)-4,5-dihydroxyimidazolidin-2-ones, 3-alkoxy-1-alkyl-5-(4-carboxyphenyl)-4,5-dihydroxyimidazolidin-2-ones and 3-alkoxy-1-phenyl-4,5-dihydroxy-5-(4-nitrophenyl)-imidazolidin-2-ones has been verified in the experimental way. In most the cases 3alkoxy-4,5-dihydroxyimidazolidin-2-ones were produced as a mixture of diastereomers.