Issue 48, 2022

Regioselective synthesis of N1-substituted-4-nitropyrazole-5-carboxylates via the cyclocondensation of ethyl 4-(dimethylamino)-3-nitro-2-oxobut-3-enoate with substituted hydrazines

Abstract

A simple and expeditious method for the regioselective synthesis of N1-substituted-4-nitropyrazole-5-carboxylates was developed. The method involves cyclocondensation of ethyl 4-(dimethylamino)-3-nitro-2-oxobut-3-enoate with a series of monosubstituted hydrazines to give N1-substituted-4-nitropyrazole-5-carboxylates with excellent regioselectivity and good yields. Solvent effects on regioselectivity of the cyclocondensation were examined.

Graphical abstract: Regioselective synthesis of N1-substituted-4-nitropyrazole-5-carboxylates via the cyclocondensation of ethyl 4-(dimethylamino)-3-nitro-2-oxobut-3-enoate with substituted hydrazines

Supplementary files

Article information

Article type
Paper
Submitted
03 Nov 2022
Accepted
21 Nov 2022
First published
22 Nov 2022

Org. Biomol. Chem., 2022,20, 9746-9752

Regioselective synthesis of N1-substituted-4-nitropyrazole-5-carboxylates via the cyclocondensation of ethyl 4-(dimethylamino)-3-nitro-2-oxobut-3-enoate with substituted hydrazines

R. Zhao, Z. Hong, B. Wang, J. Kempson, L. Cornelius, J. Li, Y. Li and A. Mathur, Org. Biomol. Chem., 2022, 20, 9746 DOI: 10.1039/D2OB02006H

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