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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1392005Generated: October 30, 2026

Ammonium fluoride → Sonedenoson

https://huagongshe.com/reaction/1392005

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium fluorideHCID 25516—
Reactant6-amino-2-[2-(4-chlorophenyl)ethoxy]-9-(2,3,5-tri-O-tert-butyldimethyl-beta-D-ribofuranosyl)purineHCID 131726800—
SolventMethanolHCID 887—
ProductSonedenosonHCID 991009859.9%

Reaction Steps

To a solution of 3438.4 g (4.51 mol) of 6-amino-2-[2-(4-chlorophenyl)ethoxy]-9-(2,3,5-tri-O-tert-butyldimethyl-β-D-ribofuranosyl)purine in 48.4 L of methanol was added 1.679 g (45.32 mol) of ammonium fluoride. The solution was heated to reflux and monitored by HPLC to determine completion. The reaction was allowed to cool to room temperature and the solvent was concentrated under reduced pressure. The reaction mixture was partitioned between water (17.3 L) and ethyl acetate (17.3 L). The aqueous layer was washed again with ethyl acetate (17.4 L). The combined organic layers were dried over magnesium sulfate (1000 g), filtered and removed under reduced pressure. The resultant solid was recrystallized from ethanol (9.87 L) to yield an off-white solid (1139 g, 59.8% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07342003B2
Source datasetuspto-grants-2008_03
ORD IDord-a24ccedc7beb4d729a02c600fa3809c3
Source noteuspto-grants-2008_03