Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1793796Generated: November 3, 2026

Triethylamine → HCID 10254259, compound

https://huagongshe.com/reaction/1793796

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzene, 1-iodo-2-(trifluoromethyl)-HCID 67957—
ReactantHCID 10131507HCID 10131507—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10254259HCID 10254259—

Reaction Steps

To a solution of (4S,2R,3R,5R)-2-[6-(cyclopentylamino)purin-9-yl]-5-ethynyloxolane-3,4-diol (40 mg, 0.12 mmol) in tetrahydrofuran (4 mL) under nitrogen was added catalytic amounts (3 mg) of (4S,2R,3R,5R)-2-[6-(cyclopentylamino)purin-9-yl]-5-ethynyloxolane-3,4-diol (II) and copper (I) iodide, followed by 1-iodo-2-trifluoromethylbenzene (0.042 mL). Triethylamine (0.4 mL) was then added, and the mixture was stirred for 15 minutes at room temperature. The solvent was removed under reduced pressure, and the residue was purified by preparative TLC, eluting with methanol:methylene chloride (6.5:1), to yield (4S,2R,3R,5R)-2-[6-(cyclopentylamino)purin-9-yl]-5-{2-[2-(trifluoromethyl)phenyl]ethynyl}-oxolane-3,4-diol, a compound of Formula I.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07022681B2
Source datasetuspto-grants-2006_04
ORD IDord-d2a0f5cfdcd44dc9883f896fcc688efa
Source noteuspto-grants-2006_04