Issue 43, 2022

Formal [4+1] cyclization of (thio/imido)hydrazides and ethyl 3,3,3-trifluoropropanoate: unified synthesis of 1,3,4-oxadiazoles, 1,3,4-thiadiazoles and 1,2,4-triazoles

Abstract

Here we report an efficient and practical one-step synthesis of a series of 1,3,4-oxadiazoles with ethyl ester decoration, which was accomplished by the formal [4+1] cyclization of hydrazides and commercially available ethyl 3,3,3-trifluoropropanoate. In contrast to previously reported synthetic processes, this method features operational simplicity, easy scalability and good substrate tolerability. Furthermore, the present synthetic method can be generalized to access 1,3,4-thiadiazoles and 1,2,4-triazoles.

Graphical abstract: Formal [4+1] cyclization of (thio/imido)hydrazides and ethyl 3,3,3-trifluoropropanoate: unified synthesis of 1,3,4-oxadiazoles, 1,3,4-thiadiazoles and 1,2,4-triazoles

Supplementary files

Article information

Article type
Paper
Submitted
19 Aug 2022
Accepted
03 Oct 2022
First published
04 Oct 2022

New J. Chem., 2022,46, 20755-20759

Formal [4+1] cyclization of (thio/imido)hydrazides and ethyl 3,3,3-trifluoropropanoate: unified synthesis of 1,3,4-oxadiazoles, 1,3,4-thiadiazoles and 1,2,4-triazoles

L. Zhao, J. Xu, J. Ma, G. Yin, F. Li, T. Suo and C. Wang, New J. Chem., 2022, 46, 20755 DOI: 10.1039/D2NJ04147B

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