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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535382Generated: October 25, 2026

Tetrahydrofuran → 5-Bromo-6-(2-phenylethynyl)pyridin-2-amine

https://huagongshe.com/reaction/535382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantPhenylacetyleneHCID 10821—
Reactant5,6-Dibromopyridin-2-amineHCID 13692781—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product5-Bromo-6-(2-phenylethynyl)pyridin-2-amineHCID 86694367—

Reaction Steps

A mixture of 5,6-dibromopyridin-2-amine (80 g, 318 mmol), ethynylbenzene (78 ml, 698 mmol), copper(I) iodide (1.51 g, 7.94 mmol), Dichlorobis(triphenylphosphine)-palladium(II) (5.79 g, 7.94 mmol) and triethylamine (110 ml, 794 mmol) is stirred under argon atmosphere in ACN (500 ml) with THF (250 ml) for 21 h at 50° C. The mixture is diluted with water and extracted with DCM. The combined organic layers are dried over MgSO4, concentrated in vacuo and the product purified by NP chromatography. Yield: 82 g (94%). HPLC-MS: M+H=273/275; tR=1.34 min (*Method—1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859541B2
Source datasetuspto-grants-2014_10
ORD IDord-78e017eace924fb999574e5f0b82d9bc
Source noteuspto-grants-2014_10