Volume 55, Issue 10 pp. 2325-2333
Article

A Consecutive Condensation, Cyclization, and Dehydration for the Synthesis of Benzimidazopyrroloquinazolines Catalyzed by TsOH

Yi-Ping Wang

Yi-Ping Wang

School of Chemistry and Materials Science, Jiangsu Key Laboratory of Green Synthetic Chemistry for Functional Materials, Jiangsu Normal University, Xuzhou, Jiangsu, 221116 People's Republic of China

These authors contributed equally to this work.Search for more papers by this author
Xue-Rong Ou

Xue-Rong Ou

School of Chemistry and Materials Science, Jiangsu Key Laboratory of Green Synthetic Chemistry for Functional Materials, Jiangsu Normal University, Xuzhou, Jiangsu, 221116 People's Republic of China

These authors contributed equally to this work.Search for more papers by this author
Yue Wang

Yue Wang

School of Chemistry and Materials Science, Jiangsu Key Laboratory of Green Synthetic Chemistry for Functional Materials, Jiangsu Normal University, Xuzhou, Jiangsu, 221116 People's Republic of China

Search for more papers by this author
Jian-Quan Liu

Jian-Quan Liu

School of Chemistry and Materials Science, Jiangsu Key Laboratory of Green Synthetic Chemistry for Functional Materials, Jiangsu Normal University, Xuzhou, Jiangsu, 221116 People's Republic of China

Search for more papers by this author
Xiang-Shan Wang

Corresponding Author

Xiang-Shan Wang

School of Chemistry and Materials Science, Jiangsu Key Laboratory of Green Synthetic Chemistry for Functional Materials, Jiangsu Normal University, Xuzhou, Jiangsu, 221116 People's Republic of China

E-mail: [email protected]Search for more papers by this author
First published: 17 August 2018
Citations: 2

Abstract

A consecutive condensation, cyclization, and dehydration of 2-(1H-benzo[d]imidazol-2-yl) anilines and ketonic acid in toluene catalyzed by TsOH gave a series of benzo[4,5]imidazo [1,2-c]pyrrolo[1,2-a]quinazolin-3(2H)-one derivatives in good to high yields. The structure of 3e was further confirmed unambiguously by X-ray diffraction analysis.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.