Reaction of chlorobutanoylferrocene with 2,4 dinitrophenylhydrazine
Анотація
To date, important compounds incorporating a substituted 1,4,5,6-tetrahydropyridazine moiety include agents such as the natural antibacterial drugs, as well as a progesterone receptor ligands and a cannabinoid receptor antagonists CB1 [1]. On the other hand, a recent review [2] shows the structures of dozens of promising ferrocene-containing drug candidates against various types of cancer, malaria, pathogenic bacteria and fungi, viral diseases, and much more. In our work, we found a way to combine such important pharmacophore fragments as ferrocene and tetrahydropyridazine in one molecule.
Посилання
Diastereoselective synthesis of functionalized tetrahydropyridazines containing indole scaffolds via an inverse-electron-demand aza-Diels–Alder reaction / T. Chen, C. Che, Z. Guo, X.-Q. Dong, C.-J. Wang // Org. Chem. Front. 2021. Vol. 8, № 16. Р. 4392–4398.
Ferrocene-based drugs, delivery nanomaterials and fenton mechanism: state of the art, recent developments and prospects / C. Ornelas, D. Astruc // Pharmaceutics. 2023. Vol. 15, № 8. article № 2044.