https://www.selleckchem.com/pr....oducts/filgotinib.ht
Glycosyl heterocycles, being as nucleoside analogs with modified glycon and hybrid heterocycle motifs, are of considerable interest and thus the targeted compounds were synthesized via convenient and efficient approach. New indolyl-thiadiazolyl thioglycosides scaffolds were synthesized starting with the reaction of indole-3-carbaldehyde with 2- aminothiadiazole-5-thiole followed by glycosylation and deprotection. Likewise, new molecular hybrids comprising indole, thiadiazole, triazole and glycosyl moieties were synthesized utilizing
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