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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892231Generated: November 1, 2026

N,N-Dimethylpropargylamine → HCID 58476641, compound

https://huagongshe.com/reaction/1892231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylpropargylamineHCID 81643—
Reactant3,5-dibromo-2,6-dimethylpyridineHCID 817217—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventDiethylamineHCID 8021—
SolventEthyl AcetateHCID 8857—
SolventSodium CarbonateHCID 10340—
ProductHCID 58476641HCID 5847664151%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a mixture of 3,5-dibromo-2,6-dimethlpyridine (605 mg, 2.54 mmol), copper iodide (22 mg, 0.11 mmol) and bis(triphenylphosphine)palladium(II) chloride (41 mg, 0.058 mmol) in diethylamine (3.0 mL) was added propargyl(dimethylamine) (0.27 mL, 2.50 mmol). The reaction mixture was allowed to stir for 15 h at 50° C. and was then allowed to cool to rt. The resulting mixture was diluted with EtOAc (30 mL) and 1M aqueous Na2CO3 (20 mL). After stirring for 30 min, the organic solution was separated and the aqueous solution was extracted with EtOAc (2×15 mL). The organic solutions were combined, washed with water and brine, dried over Na2SO4, filtered and concentrated. The residue was purified by column chromatography to give 3-(5-bromo-2,6-dimethylpyridin-3-yl)-N,N-dimethylprop-2-yn-1-amine (313 mg, 51%) as a dark oil. LCMS (AA): Rt=1.47 min, m/z=267.1 (M−H), 269.1 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507667B2
Source datasetuspto-grants-2013_08
ORD IDord-2dd48e155cae469ab52418e10f6d3b19
Source noteuspto-grants-2013_08