Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 923659Generated: October 26, 2026

Tetrahydrofuran → 4-Bromo-6-[2-[tris(propan-2-yl)silyl]ethynyl}pyridin-2-amine

https://huagongshe.com/reaction/923659

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
Reactant(Triisopropylsilyl)acetyleneHCID 2734682—
Reactant4,6-Dibromopyridin-2-amineHCID 53440006—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product4-Bromo-6-[2-[tris(propan-2-yl)silyl]ethynyl}pyridin-2-amineHCID 123389078—

Reaction Conditions

Temperature50 °C

Reaction Steps

Under argon atmosphere dichlorobis(triphenylphosphine)palladium(II) (1.6 g, 2.2 mmol) is added to a mixture of 2-amino-4,6-dibromopyridine (5.44 g, 21.6 mmol), ethynyl-tri(propan-2-yl)silane (5.1 g, 28.1 mmol), copper(I) iodide (0.44 g, 2.3 mmol) and triethylamine (9 ml, 64 mmol) in ACN (32 ml) with THF (16 ml). After stirring at 50° C. for 17 h the mixture is diluted with water and extracted with EtOAc. The combined organic layers are dried over MgSO4 and concentrated in vacuo. The product is purified by NP chromatography. Yield: 4.7 g (62%). HPLC-MS: M+H=353/355; tR=1.80 min (METHOD—1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278978B2
Source datasetuspto-grants-2016_03
ORD IDord-c8c290959038463abdda31a65883c50f
Source noteuspto-grants-2016_03