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Synthesis of 3-Amino-substituted <i>N</i>-Alkylindazoles via Palladium(II)-catalyzed Intramolecular N-Arylation of Tosylhydrazines
28
Citations
14
References
2007
Year
Combinatorial ChemistryDiversity Oriented Synthesis3-Amino-substituted N-alkyl Indazoles3-Amino-substituted N-alkylindazolesEngineeringNatural SciencesIntramolecular N-arylationDiversity-oriented SynthesisOrganic ChemistryCatalysisEfficient SynthesisChemistrySynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
Abstract An efficient synthesis of 3-amino-substituted N-alkyl indazoles is described. Reaction of readily available o-halo aryl hydrazines with palladium(II) acetate and cupper(I) iodide in the presence of a base afforded the corresponding 3-substituted N-tosylindazoles in excellent yields. These products were further functionalized after detosylation with Na–Hg, followed by alkylation to afford 3-amino-substituted N-alkylindazoles.
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