4.6 Article

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

Journal

CHEMISTRY-A EUROPEAN JOURNAL
Volume 22, Issue 22, Pages 7617-7622

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201600849

Keywords

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

Funding

  1. National Natural Science Foundation of China [81302637, 81330075]

Ask authors/readers for more resources

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 I-2/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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available