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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1794376Generated: November 2, 2026

p-Aminophenylacetic acid ethyl ester → HCID 22221045, compound

https://huagongshe.com/reaction/1794376

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Aminophenylacetic acid ethyl esterHCID 225219—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant3-(5-(4-Chlorophenyl)-4-isoxazolyl]propionic acidHCID 22221291—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 22221045HCID 2222104593%

Reaction Steps

A mixture of ethyl 4-aminophenylacetate (0.32 g), 3-[5-(4-chlorophenyl)-4-isoxazolyl]propionic acid (0.37 g), 1-hydroxy-1H-1,2,3-benzotriazole hydrate (0.28 g), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (0.35 g) and N,N-dimethylformamide (15 ml) was stirred at room temperature overnight. The reaction mixture was poured into water and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with dilute hydrochloric acid, saturated aqueous sodium hydrogencarbonate and then saturated brine, dried (MgSO4) and concentrated. The residue was subjected to silica gel column chromatography, and N-(4-ethoxycarbonylmethylphenyl)-3-[5-(4-chlorophenyl)-4-isoxazolyl]propionamide (0.56 g, yield 93%) was obtained as colorless crystals from a fraction eluted with ethyl acetate-hexane (1:1, volume ratio). The crystals were recrystallized from ethyl acetate-hexane. melting point: 117–118° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07022725B2
Source datasetuspto-grants-2006_04
ORD IDord-1c2330c705dc4f058a0f61cb593dc3d4
Source noteuspto-grants-2006_04