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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910764Generated: November 2, 2026

N-(2-aminoethyl)-N-(4-nitrophenyl)amine → HCID 66850960, compound

https://huagongshe.com/reaction/1910764

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2-aminoethyl)-N-(4-nitrophenyl)amineHCID 236318—
Reactant2-Trifluoromethanesulfonyloxy-4,6-dimethylpyridineHCID 57668797—
SolventDiglymeHCID 8150—
ProductHCID 66850960HCID 6685096056.5%

Reaction Conditions

Temperature165 °C

Reaction Steps

To a solution of trifluoro-methanesulfonic acid 4,6-dimethyl-pyridin-2-yl ester (0.6 g, 2.35 mmol) in diglyme (2 mL) was added N*1*-(4-nitro-phenyl)-ethane-1,2-diamine (0.51 g, 2.82 mmol). The reaction mixture was heated to 165° C. for 24 h. The resulting reaction mixture was concentrated under reduced pressure and the residue diluted with chloroform. The organic layer was washed with brine and water and dried over sodium sulfate. The solvent was evaporated and the crude residue was purified by column chromatography (60-120 mesh) using 20% ethyl acetate/petroleum ether as eluent to afford N-(4,6-dimethyl-pyridin-2-yl)-N′-(4-nitro-phenyl)-ethane-1,2-diamine (0.38 g, 55%) as a cream solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604029B2
Source datasetuspto-grants-2013_12
ORD IDord-ab5c2889ae8d49f9836ee31df11b37fc
Source noteuspto-grants-2013_12