1.
European Journal of Organic Chemistry
; 2022(25), 2022.
Article
in English
| ProQuest Central | ID: covidwho-1919275
ABSTRACT
A convergent route for the synthesis of BCX‐1777 and BCX‐4430 from a Boc‐protected 2‐pyrrolidinone, derived from 2,3,5‐tri‐O‐benzyl‐d‐ribonolactone, and a dihalogenated pyrrolopyrimidine as the key starting materials is reported. A chemoselective cross‐coupling was achieved from the two key starting materials in 79 % yield. Luche reduction and mesylation resulted in the stereoselective formation of an advanced intermediate in 77 % yield over two steps, which served as a precursor for synthesizing BCX‐1777 and BCX‐4430 in 38 % (over 10 steps) and 32 % (over 11 steps) overall yields, respectively, from 2,3,5‐tri‐O‐benzyl‐d‐ribonolactone.Dedicated to the students in my lab for their perseverance during the COVID-19 pandemic