Synthesis of 5-oxymethyl-1,2,4-triazole-3-carboxamides

نویسندگان

چکیده

Objectives . A key step in the synthesis of natural nucleoside analogs is formation a glycosidic bond between carbohydrate fragment and heterocyclic base. Glycosylation methods differ terms regio- stereoselectivity. promising method for highly specific new pharmacologically active compounds involves an enzymatic reaction catalyzed by genetically engineered phosphorylases. This study devoted to library bases—5-oxymethyl-1,2,4-triazole- 3-carboxamides—in order investigate substrate specificity Methods cyclization acylamidrazones obtained from single synthetic precursor β-N-tert-butyloxycarbonyl-oxalamidrazone was used parallel-synthesize 5-alkoxy/ aryloxymethyl-1,2,4-triazole-3-carboxamides. Silica gel column chromatography isolate purify synthesized compounds. complex physicochemical analysis (nuclear magnetic resonance spectroscopy, chromatography, mass spectrometry) confirmed structure work. Results 5-alkoxy/aryloxymethyl-1,2,4-triazole-3-carboxamides were The possibility obtaining chemico-enzymatic demonstrated on basis preliminary assessment results. Conclusions characteristics series novel 5-alkoxy/aryloxymethyl- 1,2,4-triazole-3-carboxamides studied along with their potential act as substrates transglycosylation

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ژورنال

عنوان ژورنال: ?????? ?????????? ??????????

سال: 2022

ISSN: ['2410-6593', '2686-7575']

DOI: https://doi.org/10.32362/2410-6593-2022-17-4-311-322