Literature DB >> 27112949

Synthesis of Novel Imidazo[1,2-a]pyridin-2-amines from Arylamines and Nitriles via Sequential Addition and I2 /KI-Mediated Oxidative Cyclization.

Xianhai Tian1, Lina Song1, Manman Wang1, Zhigang Lv1, Jie Wu1, Wenquan Yu2, Junbiao Chang3,4.   

Abstract

A novel and practical strategy for the construction of imidazo[1,2-a]pyridin-2-amine frameworks has been developed. The present sequential approach involves addition of arylamines to nitriles and I2 /KI-mediated oxidative C-N bond formation without purification of the intermediate amidines. This operationally simple synthetic process provides a facile access to a variety of new 2-amino substituted imidazo[1,2-a]pyridines and related heterocyclic compounds in an efficient and scalable fashion.
© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  C−N bond formation; imidazo[1,2-a]pyridin-2-amine; iodine; oxidative cyclization; sequential synthesis

Year:  2016        PMID: 27112949     DOI: 10.1002/chem.201600849

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  2 in total

1.  Superparamagnetic nanoparticle-catalyzed coupling of 2-amino pyridines/pyrimidines with trans-chalcones.

Authors:  Oanh T K Nguyen; Pha T Ha; Ha V Dang; Yen H Vo; Tung T Nguyen; Nhan T H Le; Nam T S Phan
Journal:  RSC Adv       Date:  2019-02-13       Impact factor: 4.036

2.  Direct intramolecular double cross-dehydrogentive-coupling (CDC) cyclization of N-(2-pyridyl)amidines under metal-free conditions.

Authors:  Fengping Yi; Chao Fu; Qihui Sun; Huazhen Wei; Genfa Yu; Weiyin Yi
Journal:  RSC Adv       Date:  2019-12-19       Impact factor: 3.361

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.