FIELD: molecular biology, gene engineering. SUBSTANCE: deoxythionucleotide derivatives of the general formula , wherein R1 is 4,4-dimethoxytrityl; R2-H is H or N=C-(CH2)2; B is thymine residue, N4 is benzoylcytosine, N6 is benzoyladenine and N2 is isobutyrylguanidineare prepared from 5′-O-dimethoxytrityl-N-acyl-2-deoxynucleosides and S-methyl-thiodichlorophosphate used in 1.5-2-fold molar excess in pyridine at temperature of 0-5 C in presence of 4-10-fold excess of 1,2,4-triazole, and the reaction mixture, if required, is treated with ethylene cyanohydrin. Thereafter, the resulting solution is neutralized with triethyl-ammonium bicarbonate, extracted with chloroform, the extract is dried, and solvent is evaporated. The yield of the end product is up to 85-95 % . EFFECT: simplified production process.
Authors
Dates
1994-02-28—Published
1987-10-27—Filed