Abstract The invention relates to the method of preparation of N-glycosyl compounds of anthracyclin antibiotics of formula I <IMAGE> I where R1 is the hydrogen atom or hydroxylic group, whereas R2 is the residue of a mono- or oligosaccharide of a series of aldeses and ketoses or the derivatives reacted with the amine group of the antibiotic. The invention depends upon the reaction of the antibiotic, which is converted into the form of base, in an organic solvent by treatment with molar excess of the saccharide or its derivative at temperature from 20 DEG up to 60 DEG C., for several hours, in the presence of a catalyst, under continuous stirring. The product is precipitated from the reaction mixture upon the addition of a nonpolar solvent and subsequently is purified by known methods.
Anthracycline antibiotics selected from the group consisting of daunorubicin and adriamycin, of the formula ##STR3## where R 1 is hydrogen or a hydroxyl group and where R 2 is selected from the group consisting of ribose, glucose, fructose residues and the glucuronamide residues formed with N-octylamide, N-butylamide and the methyl ester of glucuronic acid.
Claim 2
Dependent Claim
54 words
Anthracycline antibiotics selected from the group consisting of daunorubicin and adriamycin, of the formula ##STR3## where R 1 is hydrogen or a hydroxyl group and where R 2 is selected from the group consisting of ribose, glucose, fructose residues and the glucuronamide residues formed with N-octylamide, N-butylamide and the methyl ester of glucuronic acid.
Claim 3
Dependent Claim
117 words
The method of preparation of the N-glycosyl compounds of anthracycline antibiotics according to claim 1 of the formula I comprising the steps of reacting the selected anthracycline antibiotic free-base in an organic solvent selected from the group consisting of dimethylacetamide and dimethylformamide with a molar excess of a saccharide or its derivative selected from the group consisting of ribose, glucose, fructose, the glucuronic acid N-octylamide, the glucuronic acid N-butylamide and the glucuronic acid methyl ester; at a temperature from 20° to 60° C., for at least about 12 hours in the presence of an acidic catalyst, under continuous stirring and the product is precipitated from the reaction mixture upon addition of non-polar solvent and subsequently is purified.
Claim 4
Dependent Claim
21 words
The method according to claim 2, wherein the catalyst is selected from the group consisting of acetic acid and Lewis acids.