1,4二氢嘧啶[1,2 -a]苯并咪唑的合成与结构解析

Kaushik Joshi, Vikas Chauhan, Hardik Bhatt, Nikunj Dave
{"title":"1,4二氢嘧啶[1,2 -a]苯并咪唑的合成与结构解析","authors":"Kaushik Joshi, Vikas Chauhan, Hardik Bhatt, Nikunj Dave","doi":"10.9734/ajocs/2022/v11i119112","DOIUrl":null,"url":null,"abstract":"Considering various biomedical significance & with a view of pharmacological actions of compound belong to this class, new series of N-(substituted phenyl)-2-methyl-4-(2-(6-oxo-1-phenyl-1-6-dihydro-[2-3-bipyridin]-5-yl)phenyl)-1-4-dihydro pyrimido [1, 2-a] benzimidazole-3-carboxamide ware prepared. The formation of the compound was accomplished by cyclocondensation of 2-(1, 2-dihydro-2-oxo-1-phenyl-5-(pyridin-2-yl)pyridin-3-yl) benzaldehyde and N-(substituted phenyl)-3-oxobutanamide, 2-amino-benzimidazole under acid catalyzed conditions. The structures of pyrimidobenzimidazoles were determined by MASS, IR, 1H NMR spectroscopic techniques & Elemental analysis technique.","PeriodicalId":8505,"journal":{"name":"Asian Journal of Chemical Sciences","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2022-01-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthesis and Structural Elucidation of 1, 4 Dihydropyrimido [1, 2-a] Benzimidazole\",\"authors\":\"Kaushik Joshi, Vikas Chauhan, Hardik Bhatt, Nikunj Dave\",\"doi\":\"10.9734/ajocs/2022/v11i119112\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Considering various biomedical significance & with a view of pharmacological actions of compound belong to this class, new series of N-(substituted phenyl)-2-methyl-4-(2-(6-oxo-1-phenyl-1-6-dihydro-[2-3-bipyridin]-5-yl)phenyl)-1-4-dihydro pyrimido [1, 2-a] benzimidazole-3-carboxamide ware prepared. The formation of the compound was accomplished by cyclocondensation of 2-(1, 2-dihydro-2-oxo-1-phenyl-5-(pyridin-2-yl)pyridin-3-yl) benzaldehyde and N-(substituted phenyl)-3-oxobutanamide, 2-amino-benzimidazole under acid catalyzed conditions. The structures of pyrimidobenzimidazoles were determined by MASS, IR, 1H NMR spectroscopic techniques & Elemental analysis technique.\",\"PeriodicalId\":8505,\"journal\":{\"name\":\"Asian Journal of Chemical Sciences\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-01-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Asian Journal of Chemical Sciences\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.9734/ajocs/2022/v11i119112\",\"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 Chemical Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.9734/ajocs/2022/v11i119112","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

考虑到这类化合物的多种生物医学意义和药理作用,制备了N-(取代苯基)-2-甲基-4-(2-(6-氧-1-苯基-1-6-二氢-[2-3-联吡啶]-5-基)苯基-1-4-二氢嘧啶[1,2 -a]苯并咪唑-3-羧酰胺新系列。该化合物由2-(1,2 -二氢-2-氧-1-苯基-5-(吡啶-2-基)吡啶-3-基)苯甲醛和N-(取代苯基)-3-氧丁酰胺,2-氨基苯并咪唑在酸催化条件下环缩合而成。采用质谱、红外光谱、核磁共振氢谱及元素分析技术对嘧啶苯并咪唑的结构进行了表征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis and Structural Elucidation of 1, 4 Dihydropyrimido [1, 2-a] Benzimidazole
Considering various biomedical significance & with a view of pharmacological actions of compound belong to this class, new series of N-(substituted phenyl)-2-methyl-4-(2-(6-oxo-1-phenyl-1-6-dihydro-[2-3-bipyridin]-5-yl)phenyl)-1-4-dihydro pyrimido [1, 2-a] benzimidazole-3-carboxamide ware prepared. The formation of the compound was accomplished by cyclocondensation of 2-(1, 2-dihydro-2-oxo-1-phenyl-5-(pyridin-2-yl)pyridin-3-yl) benzaldehyde and N-(substituted phenyl)-3-oxobutanamide, 2-amino-benzimidazole under acid catalyzed conditions. The structures of pyrimidobenzimidazoles were determined by MASS, IR, 1H NMR spectroscopic techniques & Elemental analysis technique.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信