105
Views
1
CrossRef citations to date
0
Altmetric
Research Articles

An Efficient One-Pot Synthesis of 6,9-Dihydrofuro[3,2-f]Quinoline-8-Carbonitrile Derivatives under Catalyst-Free Conditions

, , & ORCID Icon
Pages 6696-6704 | Received 16 Jun 2021, Accepted 28 Sep 2021, Published online: 07 Oct 2021
 

Abstract

A new series of 6,9-dihydrofuro[3,2-f]quinoline-8-carbonitrile derivatives were prepared, via one-pot reaction of ethyl 5-aminobenzofuran-2-carboxylate, aromatic aldehydes and 3-oxo-3-phenylpropanenitrile in ethanol as a solvent at reflux. The advantages of this protocol include mild reaction conditions, easy purification, high yields, and catalyst-free approach. IR, 1H NMR, 13C NMR and HRMS spectras were used to identify the structures of all the synthesized compounds.

Graphical Abstract

Acknowledgement

We are grateful to the Natural Science Foundation for Colleges and Universities of Jiangsu Province (18KJB150024), Science and Technology Development Fund of Kangda College of Nanjing Medical University (KD2020KYJJZD072) and Innovation training program projects for the students of Kangda College of Nanjing Medical University for financial support.

Disclosure statement

No potential conflict of interest was reported by the author(s).

Scheme 1. The model reaction of 1, 2a, and 3.

Scheme 1. The model reaction of 1, 2a, and 3.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.