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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 923664Generated: October 30, 2026

Tetrahydrofuran → 4-Chloro-6-(2-phenylethynyl)pyridin-2-amine

https://huagongshe.com/reaction/923664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantPhenylacetyleneHCID 10821—
Reactant2-Amino-4,6-dichloropyridineHCID 5316649—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product4-Chloro-6-(2-phenylethynyl)pyridin-2-amineHCID 86694368—

Reaction Conditions

Temperature90 °C

Reaction Steps

Dichlorobis(triphenylphosphine)palladium(II) (2.5 g, 3.06 mmol) is added to a mixture of 2-amino-4,6-dichloropyridine (5 g, 30.7 mmol), ethynylbenzene (7.05 g, 69 mmol), copper(I) iodide (0.58 g, 3.07 mmol), triethylamine (10.8 ml, 78 mmol), THF (25 ml) and ACN (50 ml) under argon atmosphere and is stirred at 90° C. for 17 h. The mixture is diluted with water (100 ml) and extracted with EtOAc. The combined organic layers are dried over MgSO4 and concentrated in vacuo. The product is purified by NP chromatography. Yield: 3.52 g (50%). HPLC-MS: M+H=229; tR=1.85 min (METHOD—1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278978B2
Source datasetuspto-grants-2016_03
ORD IDord-63ead371f50e48648c7e70d8155a9b9f
Source noteuspto-grants-2016_03