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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672213Generated: October 30, 2026

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

https://huagongshe.com/reaction/1672213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylpropargylamineHCID 81643—
Reactant5-Bromo-2-methyl-3-nitropyridineHCID 25067266—
CatalystCopper iodideHCID 83717—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
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 numberUS07998952B2
Source datasetuspto-grants-2011_08
ORD IDord-5538065ae6b0483c83f67b1cfdb6bd73
Source noteuspto-grants-2011_08