Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593931Generated: October 25, 2026

2-Fluorothiophenol → HCID 10434433, compound

https://huagongshe.com/reaction/1593931

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-FluorothiophenolHCID 520216—
Reactant2-{6-[((1R,2R)-2-hydroxycyclopentyl)amino]-purin-9-yl}(4S,5S,3R)-5-(chloromethyl)oxolane-3,4-diolHCID 67189486—
SolventDimethylformamideHCID 6228—
SolventSodium HydroxideHCID 14798—
ProductHCID 10434433HCID 1043443385.4%

Reaction Steps

To a solution of 2-fluorothiophenol (38 mL, 406 mmol) in 2N sodium hydroxide (100 mL) was added 2-{6-[((1R,2R)-2-hydroxycyclopentyl)amino]purin-9-yl}(4S,5S,3R)-5-(chloromethyl)oxolane-3,4-diol (15.0 g, 40.6 mmol) in N,N-dimethylformamide (120 mL). The mixture was warmed to 100 C for 4 hours, following the progress of the reaction by TLC. The N,N-dimethylformamide was removed under reduced pressure, and the remaining mixture was diluted with water (200 mL), neutralized with acetic acid, extracted with ethyl acetate (3×125 mL), and the combined organic layers were dried over MgSO4. After removing the solvent under reduced pressure the residue was triturated with diethyl ether and filtered, to afford 16 grams of 2-{6-[((1R,2R)-2-hydroxycyclopentyl)amino]purin-9-yl}(4S,5S,3R)-5-[(2-fluorophenylthio)methyl]oxolane-3,4-diol as a white powder (85% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07300923B2
Source datasetuspto-grants-2007_11
ORD IDord-a2e76e5625634c26b1d422c5be5c866c
Source noteuspto-grants-2007_11