A Novel Synthesis of Substituted Benzo[1,2,4]triazine Derivatives via Copper-Catalyzed Intermolecular N-Arylation of 2-Iodoaniline and Hydrazonoyl Chlorides

Abstract In this contribution, a speedy and direct approach for the synthesis of benzo[1,2,4]triazine derivatives via a copper-catalyzed intermolecular N-arylation of 2-iodoaniline and hydrazonoyl chlorides is described. The reaction proceeds in THF at room temperature with no need for any ligand. The use of simple and readily available starting materials, mild copper-catalytic reaction conditions, and good yields (72–92%) are remarkable specifications of this protocol.

Authors

Publication Details

Journal
Synlett
Published
2024-09-30
DOI
https://doi.org/10.1055/s-0043-1775402
Citations
4
Primary Topic
Synthesis and Characterization of Heterocyclic Compounds
Type
article
Field-Weighted Citation Impact
1.00

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article

A Novel Synthesis of Substituted Benzo[1,2,4]triazine Derivatives via Copper-Catalyzed Intermolecular N-Arylation of 2-Iodoaniline and Hydrazonoyl Chlorides

Manijeh Nematpour, Reihane Nouri
4 citations
Synlett
Synthesis and Characterization of Heterocyclic Compounds
1.00
article

A Novel Synthesis of Substituted Benzo[1,2,4]triazine Derivatives via Copper-Catalyzed Intermolecular N-Arylation of 2-Iodoaniline and Hydrazonoyl Chlorides

Manijeh Nematpour, Reihane Nouri
article en
4 citations

Abstract

Abstract In this contribution, a speedy and direct approach for the synthesis of benzo[1,2,4]triazine derivatives via a copper-catalyzed intermolecular N-arylation of 2-iodoaniline and hydrazonoyl chlorides is described. The reaction proceeds in THF at room temperature with no need for any ligand. The use of simple and readily available starting materials, mild copper-catalytic reaction conditions, and good yields (72–92%) are remarkable specifications of this protocol.

SynlettVol. 36(06)
Farhangian University
Openalex Percentile: Top 27%
Synthesis and Characterization of Heterocyclic Compounds
1.00
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