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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1793795Generated: November 4, 2026

Triethylamine → HCID 58618547, compound

https://huagongshe.com/reaction/1793795

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzene, 1-iodo-2-(trifluoromethyl)-HCID 67957—
ReactantHCID 58618539HCID 58618539—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58618547HCID 58618547—

Reaction Steps

To a solution of [9-((1R,2R,4R,5R)-4-ethynyl-7,7-dimethyl-3,6,8-trioxabicyclo[3.3.0]oct-2-yl)purin-6-yl]cyclopentylamine (40 mg, 0.12 mmol), a compound of formula (5), in tetrahydrofuran (4 ml) under nitrogen was added catalytic amounts (3 mg) of dichlorobis(triphenylphosphine)palladium(II) and copper(II)iodide, followed by 1-iodo-2-trifluoromethylbenzene (0.25 ml, 0.3 mmol). Triethylamine (0.4 ml) was then added, and the mixture 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 [9-((1R,2R,4R,5R)-7,7-dimethyl-4-{2-[2-(trifluoromethyl)-phenyl]ethynyl}-3,6,8-trioxabicyclo[3.3.0]oct-2-yl)purin-6-yl]cyclopentylamine, a compound of formula (6).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07022681B2
Source datasetuspto-grants-2006_04
ORD IDord-1518cf6339854ca9831a3ed3ec3e5a15
Source noteuspto-grants-2006_04