4-[18F]Fluorophenylpiperazines by Improved Hartwig-Buchwald N-Arylation of 4-[18F]fluoroiodobenzene, Formed via Hypervalent λ3-Iodane Precursors: Application to Build-Up of the Dopamine D4 Ligand [18F]FAUC 316

Molecules

Fabian Kügler²  Johannes Ermert¹  Peter Kaufholz²  Heinz H. Coenen² 

[1] Institute of Neuroscience and Medicine, INM-5: Nuclear Chemistry, Forschungszentrum Jülich, 52425 Jülich, Germany;

关键词: fluorine-18;    Hartwig-Buchwald N-arylation;    dopamine D₄ radioligand;    iodophenyl-iodonium compounds;    iodonium ylides;   

DOI  :  10.3390/molecules20010470

来源: mdpi

【 摘 要 】

Substituted phenylpiperazines are often neuropharmacologically active compounds and in many cases are essential pharmacophores of neuroligands for different receptors such as D₂-like dopaminergic, serotoninergic and other receptors. Nucleophilic, no-carrier-added (n.c.a.) ¹⁸F-labelling of these ligands in an aromatic position is desirable for studying receptors with in vivo molecular imaging. 1-(4-[¹⁸F]Fluorophenyl)piperazine was synthesized in two reaction steps starting by ¹⁸F-labelling of a iodobenzene-iodonium precursor, followed by Pd-catalyzed N-arylation of the intermediate 4-[¹⁸F]fluoro-iodobenzene. Different palladium catalysts and solvents were tested with particular attention to the polar solvents dimethylformamide (DMF) and dimethylsulfoxide (DMSO). Weak inorganic bases like potassium phosphate or cesium carbonate seem to be essential for the arylation step and lead to conversation rates above 70% in DMF which is comparable to those in typically used toluene. In DMSO even quantitative conversation was observed. Overall radiochemical yields of up to 40% and 60% in DMF and DMSO, respectively, were reached depending on the labelling yield of the first step. The fluorophenylpiperazine obtained was coupled in a third reaction step with 2-formyl-1H-indole-5-carbonitrile to yield the highly selective dopamine D₄ ligand [¹⁸F]FAUC 316.

【 授权许可】

CC BY   
© 2014 by the authors; licensee MDPI, Basel, Switzerland.