Synthesis of 9-[1-(1 -hydroxyethyl)-3-(phosphonomethoxy)propyl]adenine and prodrug as possible antiviral agents
Related Experiment Video
Updated: Aug 13, 2026

Synthesis of Antiviral Tetrahydrocarbazole Derivatives by Photochemical and Acid-catalyzed C-H Functionalization via Intermediate Peroxides (CHIPS)
Published on: June 20, 2014
Ajit Ghosh1, Yahya El-Kattan, Minwan Wu
1BioCryst Pharmaceuticals Inc., Birmingham, AL 35244, USA.
Abstract:
The appropriately protected C-1'-hydroxyethyl-3-hydroxypropyl-N9-adenine nucleoside was prepared from 1-pivaloyloxy-5-tert-butyldiphenylsilyloxy-3-pentanol and adenine through the Mitsunobu reaction. One of the terminal hydroxyls was converted to the phosphonomethoxy derivative and the prodrug.
Related Concept Videos
Antiviral Nucleoside Inhibitors
DNA Base Pairing
Inhibitors of Viral Protein Synthesis
Preparation of 1° Amines: Gabriel Synthesis
Strong bases like NaOH or KOH deprotonate the phthalimide to form the corresponding anion, which acts as a nucleophile. Further, the anion attacks an...
Inhibitors of Virion Maturation and Assembly
Inhibitors Of Virion Release

