One-pot regioselective C–H activation iodination–cyanation of 2,4-diarylquinazolines using malononitrile as a cyano source

Author:

Yan Ziqiao12345,Ouyang Banlai6789,Mao Xunchun12345,Gao Wei12345,Deng Zhihong12345,Peng Yiyuan12345ORCID

Affiliation:

1. Key Laboratory of Functional Small Organic Molecule

2. Ministry of Education

3. Jiangxi Province's Key Laboratory of Green Chemistry

4. Jiangxi Normal University

5. Nanchang

6. Department of Chemistry

7. Nanchang Normal University

8. Nanchang 330032

9. China

Abstract

A one-pot cyanation of 2,4-arylquinazoline with NIS and malononitrile has been developed.

Funder

National Natural Science Foundation of China

Jiangxi Provincial Department of Science and Technology

Jiangxi Normal University

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Reference90 articles.

1. A. J.Fatiadi in Preparation and Synthetic Applications of Cyano Compounds , ed. S. Patai and Z. Rappoport , Wiley , New York , 1983 , vol. 2 , pp. 1057–1303

2. Z.Rappoport , The Chemistry of the Cyano Group , Interscience , New York , 1970

3. R. C.Larock , Comprehensive Organic Transformations , VCH , New York , 1989

4. 5-Amidinobenzo[b]thiophenes as dual inhibitors of factors IXa and Xa

5. Catalytic reactions involving the cleavage of carbon–cyano and carbon–carbon triple bonds

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