铜催化单锅合成 N,N-4-三苯基噻唑-2-胺

IF 3.3 2区 化学 Q1 CHEMISTRY, ORGANIC
Jia-Hao Weng, Xiao-Hu Xu, Zhi-Peng Guan* and Zhi-Bing Dong*, 
{"title":"铜催化单锅合成 N,N-4-三苯基噻唑-2-胺","authors":"Jia-Hao Weng,&nbsp;Xiao-Hu Xu,&nbsp;Zhi-Peng Guan* and Zhi-Bing Dong*,&nbsp;","doi":"10.1021/acs.joc.4c0141710.1021/acs.joc.4c01417","DOIUrl":null,"url":null,"abstract":"<p >Herein, we reported an efficient copper-catalyzed strategy for the synthesis of <i>N</i>,<i>N</i>-4-triphenylthiazol-2-amines from bromoacetophenone, phenylthiourea and iodobenzene. This method features good functional group tolerance, easy availability of starting materials and simplicity of operation, which provides an alternative method for the synthesis of 2-aminothiazoles.</p>","PeriodicalId":57,"journal":{"name":"The Journal of Organic Chemistry","volume":"89 22","pages":"16390–16400 16390–16400"},"PeriodicalIF":3.3000,"publicationDate":"2024-10-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Copper-Catalyzed One-Pot Synthesis of N,N-4-Triphenylthiazol-2-amines\",\"authors\":\"Jia-Hao Weng,&nbsp;Xiao-Hu Xu,&nbsp;Zhi-Peng Guan* and Zhi-Bing Dong*,&nbsp;\",\"doi\":\"10.1021/acs.joc.4c0141710.1021/acs.joc.4c01417\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Herein, we reported an efficient copper-catalyzed strategy for the synthesis of <i>N</i>,<i>N</i>-4-triphenylthiazol-2-amines from bromoacetophenone, phenylthiourea and iodobenzene. This method features good functional group tolerance, easy availability of starting materials and simplicity of operation, which provides an alternative method for the synthesis of 2-aminothiazoles.</p>\",\"PeriodicalId\":57,\"journal\":{\"name\":\"The Journal of Organic Chemistry\",\"volume\":\"89 22\",\"pages\":\"16390–16400 16390–16400\"},\"PeriodicalIF\":3.3000,\"publicationDate\":\"2024-10-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Journal of Organic Chemistry\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.joc.4c01417\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Organic Chemistry","FirstCategoryId":"1","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.joc.4c01417","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0

摘要

在此,我们报告了一种以溴苯乙酮、苯基硫脲和碘苯为原料合成 N,N-4-三苯基噻唑-2-胺的高效铜催化策略。该方法具有官能团耐受性好、起始原料易得、操作简单等特点,为 2-氨基噻唑的合成提供了另一种方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Copper-Catalyzed One-Pot Synthesis of N,N-4-Triphenylthiazol-2-amines

Copper-Catalyzed One-Pot Synthesis of N,N-4-Triphenylthiazol-2-amines

Herein, we reported an efficient copper-catalyzed strategy for the synthesis of N,N-4-triphenylthiazol-2-amines from bromoacetophenone, phenylthiourea and iodobenzene. This method features good functional group tolerance, easy availability of starting materials and simplicity of operation, which provides an alternative method for the synthesis of 2-aminothiazoles.

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
The Journal of Organic Chemistry
The Journal of Organic Chemistry 化学-有机化学
CiteScore
6.20
自引率
11.10%
发文量
1467
审稿时长
2 months
期刊介绍: The Journal of Organic Chemistry welcomes original contributions of fundamental research in all branches of the theory and practice of organic chemistry. In selecting manuscripts for publication, the editors place emphasis on the quality and novelty of the work, as well as the breadth of interest to the organic chemistry community.
×
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