Abstract
The condensation of 1-(ferrocenylalkyl)pyrazole-3-carbaldehydes with 4′-aminotetraphenylporphyrin, followed by reduction with NaBH(OAc)3 in 1,2-dichloroethane, provides a convenient method for the synthesis of 5-{4-[({1-[1-(ferrocen-1-yl)alkyl]-5-methyl-1H-pyrazol-3-yl}methyl)amino]phenyl}-10,15,20-triphenylporphyrins which exhibit pronounced cytotoxicity against Staphylococcus aureus under ultrasonic irradiation.
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Original Russian Text © E.Yu. Osipova, A.N. Rodionov, Yu.A. Belousov, M.M. Il’in, A.L. Nikolaev, A.V. Gopin, S.E. Mazina, A.A. Simenel, 2016, published in Zhurnal Organicheskoi Khimii, 2016, Vol. 52, No. 1, pp. 133–136.
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Osipova, E.Y., Rodionov, A.N., Belousov, Y.A. et al. Synthesis of ferrocenyl-containing heterocyclic derivatives of 5-(4-aminophenyl)-10,15,20-triphenylporphyrin for sonodynamic therapy. Russ J Org Chem 52, 127–130 (2016). https://doi.org/10.1134/S1070428016010243
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DOI: https://doi.org/10.1134/S1070428016010243