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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2406724Generated: November 1, 2026

Triethylamine → n-Butyl 3-(2-(methylamino)-5-nitropyridin-3-yl)acrylate

https://huagongshe.com/reaction/2406724

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantButyl AcrylateHCID 8846—
Reactant3-bromo-N-methyl-5-nitropyridin-2-amineHCID 16477216—
ReactantTri(o-toluoyl)phosphineHCID 19696886—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Productn-Butyl 3-(2-(methylamino)-5-nitropyridin-3-yl)acrylateHCID 77522859—

Reaction Conditions

Temperature100 °C

Reaction Steps

Triethylamine (32 μl), n-butyl acrylate (33 μl), tri(o-toluoyl)phosphine (24 mg), and palladium acetate (5 mg) were added to a tube containing a DMF (3 ml) solution containing 3-bromo-N-methyl-5-nitropyridin-2-amine (45 mg) and the tube was sealed, followed by stirring at 100° C. for 8 hours. The reaction solution was adjusted to room temperature, and n-butyl acrylate (33 μl), tri(o-toluoyl)phosphine (24 mg), and palladium acetate (5 mg) were added again to the tube and the tube was sealed, followed by stirring at 100° C. for 9 hours. Further, the reaction solution was adjusted to room temperature, and water was added, followed by extraction with ethyl acetate. The resultant was washed with saturated saline and dried over anhydrous sodium sulfate. Subsequently, the solvent was distilled away under reduced pressure, the obtained residue was purified by silica gel chromatography (n-hexane:ethyl acetate=16:1 to 3:1), and a yellow solid of n-butyl 3-(2-(methylamino)-5-nitropyridin-3-yl)acrylate (44 mg) was thus obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809371B2
Source datasetuspto-grants-2014_08
ORD IDord-573a1bf762174e0b869f3b49e97d5531
Source noteuspto-grants-2014_08