Synthesis of Fused Pyrrolo-napthridinone via Ligand-free Copper Catalysed Ullmann (C-N coupling) Type Reaction

Fused pyrrole, pyridine with pyridinone components are known to possess many biological and pharmaceutical properties. Fused pyrrole with naptharidinone also has many potentials. A tandem approach of intramolecular lactamization and N-arylation using a copper catalyst to obtain a fused pyrrolo- naptharidinone has been developed. A ligand-free method has been proposed for cyclization and Ullmann (C-N coupling) type reaction in a single step. This approach will make it possible to synthesise pyrrolo- naphthyridinone N-aryl substituted natural product compounds without the need for extra additives.

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Publication Details

Journal
Letters in Organic Chemistry
Published
2024-10-08
DOI
https://doi.org/10.2174/0115701786328544240924041302
Primary Topic
Synthesis and Characterization of Pyrroles
Type
article
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article

Synthesis of Fused Pyrrolo-napthridinone via Ligand-free Copper Catalysed Ullmann (C-N coupling) Type Reaction

Malempati Srimannarayana, M. N. V. Ramesh
Letters in Organic Chemistry
Synthesis and Characterization of Pyrroles
article

Synthesis of Fused Pyrrolo-napthridinone via Ligand-free Copper Catalysed Ullmann (C-N coupling) Type Reaction

Malempati Srimannarayana, M. N. V. Ramesh
article en

Abstract

Fused pyrrole, pyridine with pyridinone components are known to possess many biological and pharmaceutical properties. Fused pyrrole with naptharidinone also has many potentials. A tandem approach of intramolecular lactamization and N-arylation using a copper catalyst to obtain a fused pyrrolo- naptharidinone has been developed. A ligand-free method has been proposed for cyclization and Ullmann (C-N coupling) type reaction in a single step. This approach will make it possible to synthesise pyrrolo- naphthyridinone N-aryl substituted natural product compounds without the need for extra additives.

Letters in Organic ChemistryVol. 22(4)
GITAM University (IN)
Openalex Percentile: Top 87%
Synthesis and Characterization of Pyrroles
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