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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1402707Generated: October 31, 2026

Chloride → 1-(2-(Pyridin-2-ylethynyl)pyridin-3-yl)ethanone

https://huagongshe.com/reaction/1402707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
ReactantTriethylamineHCID 8471—
ReactantEthynylpyridineHCID 137268—
Reactant1-(2-Bromopyridin-3-yl)ethan-1-oneHCID 9990369—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product1-(2-(Pyridin-2-ylethynyl)pyridin-3-yl)ethanoneHCID 71238330—

Reaction Conditions

Temperature25 °C

Reaction Steps

750 mg 3-Acetyl-2-bromopyridin, 550 μL 2-ethynyl-pyridine, 765 μL triethylamin, 255 mg triphenylphosphinpalladium(II) chlorid, 17 mg Cu(I)I were suspended in 10 mL DMF under argon atmosphere and stirred for 2 h at 25° C. The mixture was diluted with DCM and extracted with diluted aq. NH3 and saturated NH4Cl solution. The organic phase was concentrated and the mixture separated via FCC (100 g SiO2, cyclohexane→cyclohexane/ethylacetate 35:65) to yield 455 mg 1-(2-(pyridin-2-ylethynyl)pyridin-3-yl)ethanone as solid. Analysis: HPLC-MS: Rt=0.88 min (method E) M+H=223.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912173B2
Source datasetuspto-grants-2014_12
ORD IDord-0e60fbdeb892424081bbd0e76f74e87a
Source noteuspto-grants-2014_12