Abstract
Digitoxin and digoxin 4'''-(3-carboxypropanoates)(4'''-hemisuccinates) III and X were prepared by an indirect method, using dicyclohexylcarbodiimide-induced condensation of the cardioglycoside with 4-(2,2,2-trichloroethoxy)-4-oxobutanoic acid in dichloromethane in the presence of 4-dimethylaminopyridine or pyridine followed by removal of the 2,2,2-trichloroethyl group with zinc in a mixture of tetrahydrofuran, acetic acid and water. The hemisuccinates III and X were condensed with L-tyrosine methyl ester in tetrahydrofuran, using N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline as the coupling reagent. Structure of the products was proved by 1H NMR and 13C NMR spectra. The conjugates IV and XI were labelled with [125I] in the L-tyrosine moiety. The obtained radioligands V and XII are designed as a part of the RIA system for cardioglycoside analyses.
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