{"title":"底物和试剂依赖的脒和2-叔氨基苯甲醛的选择性环化。","authors":"Yi Zhang , Renchao Ma , Yongmin Ma , Weiwei Fang","doi":"10.1039/d5ob00424a","DOIUrl":null,"url":null,"abstract":"<div><div>Herein, we present an efficient and substrate/reagent-dependent annulation of amidines with 2-<em>tert</em>-amino benzaldehydes. When <em>N</em>-alkyl benzimidamides are employed, amidines undergo self-annulation to generate a hydrotriazine skeleton. In contrast, <em>N</em>-aryl benzimidamides yield quinazolines/hydroquinazolines under similar conditions. Additionally, the coupling of 2-<em>tert</em>-amino benzaldehydes with amidines under basic conditions yields 1,3,5-triazine derivatives.</div></div>","PeriodicalId":96,"journal":{"name":"Organic & Biomolecular Chemistry","volume":"23 21","pages":"Pages 5111-5115"},"PeriodicalIF":2.9000,"publicationDate":"2025-04-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Substrate- and reagent-dependent selective annulation of amidines and 2-tert-amino benzaldehydes†\",\"authors\":\"Yi Zhang , Renchao Ma , Yongmin Ma , Weiwei Fang\",\"doi\":\"10.1039/d5ob00424a\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Herein, we present an efficient and substrate/reagent-dependent annulation of amidines with 2-<em>tert</em>-amino benzaldehydes. When <em>N</em>-alkyl benzimidamides are employed, amidines undergo self-annulation to generate a hydrotriazine skeleton. In contrast, <em>N</em>-aryl benzimidamides yield quinazolines/hydroquinazolines under similar conditions. Additionally, the coupling of 2-<em>tert</em>-amino benzaldehydes with amidines under basic conditions yields 1,3,5-triazine derivatives.</div></div>\",\"PeriodicalId\":96,\"journal\":{\"name\":\"Organic & Biomolecular Chemistry\",\"volume\":\"23 21\",\"pages\":\"Pages 5111-5115\"},\"PeriodicalIF\":2.9000,\"publicationDate\":\"2025-04-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic & Biomolecular Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S1477052025003532\",\"RegionNum\":3,\"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":"Organic & Biomolecular Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S1477052025003532","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Substrate- and reagent-dependent selective annulation of amidines and 2-tert-amino benzaldehydes†
Herein, we present an efficient and substrate/reagent-dependent annulation of amidines with 2-tert-amino benzaldehydes. When N-alkyl benzimidamides are employed, amidines undergo self-annulation to generate a hydrotriazine skeleton. In contrast, N-aryl benzimidamides yield quinazolines/hydroquinazolines under similar conditions. Additionally, the coupling of 2-tert-amino benzaldehydes with amidines under basic conditions yields 1,3,5-triazine derivatives.
期刊介绍:
Organic & Biomolecular Chemistry is an international journal using integrated research in chemistry-organic chemistry. Founded in 2003 by the Royal Society of Chemistry, the journal is published in Semimonthly issues and has been indexed by SCIE, a leading international database. The journal focuses on the key research and cutting-edge progress in the field of chemistry-organic chemistry, publishes and reports the research results in this field in a timely manner, and is committed to becoming a window and platform for rapid academic exchanges among peers in this field. The journal's impact factor in 2023 is 2.9, and its CiteScore is 5.5.