Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2388004Generated: November 1, 2026

N,N-Dimethylpropargylamine → N,N-dimethyl-3-(6-methyl-5-nitropyridin-3-yl)prop-2-yn-1-amine

https://huagongshe.com/reaction/2388004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylpropargylamineHCID 81643—
Reactant5-Bromo-2-methyl-3-nitropyridineHCID 25067266—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventDiethylamineHCID 8021—
SolventEthyl AcetateHCID 8857—
SolventSodium CarbonateHCID 10340—
ProductN,N-dimethyl-3-(6-methyl-5-nitropyridin-3-yl)prop-2-yn-1-amineHCID 5847657291%

Reaction Steps

To a mixture of 5-bromo-2-methyl-3-nitropyridine (6.50 g, 30.0 mmol), copper iodide (280 mg, 1.5 mmol) and bis(triphenylphosphine)palladium(II) chloride (520 mg, 0.75 mmol) in diethylamine (17 mL) was added propargyl(dimethylamine) (4.04 mL, 37.5 mmol). The reaction mixture was allowed to stir for 15 h at rt. The resulting mixture was diluted with EtOAc (200 mL) and 1M aqueous Na2CO3 (150 mL). After stirring for 30 min, the organic solution was separated and the aqueous solution was extracted with EtOAc (2×100 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 N,N-dimethyl-3-(6-methyl-5-nitropyridin-3-yl)prop-2-yn-1-amine (5.98 g, 91%) as a dark oil. LCMS (FA): Rt=0.77 min, m/z=220.1 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268992B2
Source datasetuspto-grants-2012_09
ORD IDord-c0d2e0154db84b77b2e6f1365eeea44c
Source noteuspto-grants-2012_09