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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068804Generated: October 30, 2026

2-(4-Aminophenyl)ethylamine → HCID 21190172, compound

https://huagongshe.com/reaction/1068804

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Aminophenyl)ethylamineHCID 72895—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 15472383HCID 15472383—
SolventAcetonitrileHCID 6342—
ProductHCID 21190172HCID 2119017233.6%

Reaction Steps

To a solution of 1.63 g (12.0 mmol) of 2-[4-(amino)phenyl]ethylamine and 1.68 g (13 mmol) of N,N-diisopropylethylamine in 40 ml of acetonitrile was added a solution of 3.50 g (10.0 mmol) of 5-ethoxycarbonyl-3-trichloroacetylimidazo[1,2-a]pyridine in 10 ml of acetonitrile. The mixture was stirred for one hour at room temperature. The resulting crystalline precipitates were collected by filtration, washed with acetonitrile and dried to afford 1.03 g of the desired compound (33.6%, a yellow crystals). The filtrate was concentrated. The residne was crystallized from acetonitrile-methylene chloride. Crystalline precipitatse were collected by filtration, washed with acetonitrile to afford 1.60 g of the desired compound (52.1%, a yellow crystals).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06251905B1
Source datasetuspto-grants-2001_06
ORD IDord-1ce0dc9bb6c34fcb8aee204f94cab4a5
Source noteuspto-grants-2001_06