Transition-Metal-Free Sequential Two-Step Synthesis of Pyrido[3,2-c]pyridazin-4(1H)-ones via Intramolecular Cyclization of α-Keto Hydrazones

Abstract Sequential two-step protocol for the construction of pyrido[3,2-c]pyridazin-4(1H)-one fused system under metal-free conditions has been developed. The condensation cascade between β-keto-ester/nitrile (pyridine derivative) and diazonium salts derived from aniline analogues to obtain diaza compounds, which undergo intramolecular cyclization with high regioselectivity to furnish pyrido[3,2-c]pyridazin-4(1H)-one heterocycles with moderate to good yields.

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Publication Details

Journal
Synlett
Published
2026-11-10
DOI
https://doi.org/10.1055/a-2981-9333
Primary Topic
Synthesis of heterocyclic compounds
Type
article
Field-Weighted Citation Impact
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article

Transition-Metal-Free Sequential Two-Step Synthesis of Pyrido[3,2-c]pyridazin-4(1H)-ones via Intramolecular Cyclization of α-Keto Hydrazones

Suresh Kumar Suthar, Ganesh Tatya Kamble
Synlett
Synthesis of heterocyclic compounds
article

Transition-Metal-Free Sequential Two-Step Synthesis of Pyrido[3,2-c]pyridazin-4(1H)-ones via Intramolecular Cyclization of α-Keto Hydrazones

Suresh Kumar Suthar, Ganesh Tatya Kamble
article en

Abstract

Abstract Sequential two-step protocol for the construction of pyrido[3,2-c]pyridazin-4(1H)-one fused system under metal-free conditions has been developed. The condensation cascade between β-keto-ester/nitrile (pyridine derivative) and diazonium salts derived from aniline analogues to obtain diaza compounds, which undergo intramolecular cyclization with high regioselectivity to furnish pyrido[3,2-c]pyridazin-4(1H)-one heterocycles with moderate to good yields.

Synlett
Bhupal Nobles University (IN), The Institute of Scientific and Industrial Research, The University of Osaka (JP), The University of Osaka (JP)
Synthesis of heterocyclic compounds
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