1-(tert-butyl) 3-methyl 3-(2-(benzylthio)-1-hydroxyethyl)azetidine-1,3-dicarboxylate
The benzylthio group acts as a protected thiol, while the hydroxyethyl moiety provides a reactive site for further functionalization, including etherification, esterification, or coupling reactions.



![2-amino-6-phenyl-4-(3,4,5-trimethoxyphenyl)thieno[2,3-b]pyridine-3-carboxylic acid](https://navyachempharma.com/wp-content/uploads/2025/08/16-7.png)

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