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2,3-Dihydroimidazo[1,2-b]ferroceno[d]pyridazines and a 3,4-dihydro-2H-pyrimido[1,2-b]ferroceno[d]pyridazine: Synthesis, structure and in vitro antiproliferation activity on selected human cancer cell lines

2013; Elsevier BV; Volume: 750; Linguagem: Inglês

10.1016/j.jorganchem.2013.10.057

1872-8561

Dániel Csókás, Benedek Imre Károlyi, Szilvia Bősze, Ildikó Szabó, Gábor Báti, László Drahos, Antal Csámpai,

Synthesis and Biological Evaluation

Abstract Starting from (Sp)-ferroceno[d]pyridazin-1(2H)-one a series of novel ferrocene-fused heterocycles with planar- and central chirality were synthesised. The thione analogue of the precursor obtained by treatment with Lawesson reagent underwent facile mercury-mediated aminations with a selection of aminoalcohols. The resulted intermediates were subjected to cyclisations by Appel- and Mitsunobu protocols. Two diastereomers carrying phenyl group in endo- and exo positions, respectively, in the fused metallocene scaffold underwent spontaneous oxidation affording the same planar chiral imidazo[1,2-b]ferroceno[d]pyridazine isolated as side product. The structures of the new compounds including diastereomers of different central chirality were confirmed by IR, 1H, 13C and 15N NMR spectroscopy. The in vitro antitumour activity of the fused ferrocene derivatives was investigated against HepG2 hepatoma and HT-29 colorectal adenocarcinoma cell cultures by the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT)-assay. The measured 50% inhibitory concentration (IC50) values indicate that synthesised metallocene bases can be regarded as lead structures for the development of a novel class of heavy metal-free drug candidates with promising activity.