Synthesis of pyrazolo[1,5-a]quinoxalin-4(5H)-ones via one-pot amidation/N-arylation reactions under transition metal-free conditions

Author:

Wiethan Carson1234,Franceschini Steffany Z.1234,Bonacorso Helio G.1234,Stradiotto Mark5678

Affiliation:

1. Departamento de Química

2. Universidade Federal de Santa Maria

3. 97105-900 Santa Maria

4. Brazil

5. Department of Chemistry

6. Dalhousie University

7. Halifax

8. B3H 4R2 Canada

Abstract

An efficient one-pot procedure for the synthesis of new pyrazolo[1,5-a]quinoxalin-4(5H)-ones from easily prepared 1-(2-chlorophenyl-5-ethylcarboxylate)pyrazoles and various primary alkylamines is described.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Reference20 articles.

1. A. R. Katritzky , C. A.Ramsden, E. F. V.Scriven and R. J. K.Taylor, Comprehensive Heterocyclic Chemistry III, Pergamon, Oxford, 2008

2. A. Ricci , Amino Group Chemistry: From Synthesis to the Life Sciences, Wiley-VCH, Weinheim, 2008

3. C–N bond forming cross-coupling reactions: an overview

4. Dialkylbiaryl phosphines in Pd-catalyzed amination: a user's guide

5. Diversification of edaravone via palladium-catalyzed hydrazine cross-coupling: Applications against protein misfolding and oligomerization of beta-amyloid

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