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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443803Generated: November 2, 2026

N-(2-aminoethyl)acetamide → N-{2-[(2-Chloro-5-nitropyrimidin-4-yl)amino]ethyl}acetamide

https://huagongshe.com/reaction/1443803

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2-aminoethyl)acetamideHCID 66082—
ReactantDiisopropylethylamineHCID 81531—
Reactant2,4-Dichloro-5-nitropyrimidineHCID 521266—
SolventTetrahydrofuranHCID 8028—
ProductN-{2-[(2-Chloro-5-nitropyrimidin-4-yl)amino]ethyl}acetamideHCID 21081032—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 5.8 g (30 mmol) 2,4-dichloro-5-nitropyrimidine in 120 mL of tetrahydrofuran (THF) at −78° C. under Argon atmosphere was added 5.2 mL (30 mmol) of N,N-diisopropylethylamine followed by 3.1 mL (30 mmol) of N-acetylethylenediamine. The mixture was stirred at −78° C. for 30 min, allowed to warm to room temperature, and stirred for an additional 3 hours. The solvent was removed in vacuo and the residue purified by flash chromatography eluting with EtOAc to provide the compound of formula (2), N-(2-(2-chloro-5-nitropyrimidin-4-ylamino)ethyl)acetamide as pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662819B2
Source datasetuspto-grants-2010_02
ORD IDord-57703b16a929487f860dc7c2afda1fe5
Source noteuspto-grants-2010_02