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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 60060Generated: October 29, 2026

Phenylacetic Acid → N-[1-(4-ethyloxazol-2-yl)-2-(4-nitrophenyl)ethyl]-2-phenylacetamide

https://huagongshe.com/reaction/60060

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetic AcidHCID 999—
ReactantTriethylamineHCID 8471—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant(S)-(4-ethyloxazol-2-yl)-2-(4-nitrophenyl)ethanamineHCID 59464675—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductN-[1-(4-ethyloxazol-2-yl)-2-(4-nitrophenyl)ethyl]-2-phenylacetamideHCID 66694986—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (S)-1-(4-ethyloxazol-2-yl)-2-(4-nitrophenyl)ethanamine, 65, (2.9 g, 11 mmol), phenylacetic acid (1.90 g, 14 mmol) and 1-hydroxybenzotriazole (HOBt) (0.94 g, 7.0 mmol) in DMF (100 mL) at 0° C., is added 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (EDCI) (2.68 g, 14 mmol) followed by triethylamine (6.0 mL, 42 mmol). The mixture is stirred at 0° C. for 30 minutes then at room temperature overnight. The reaction mixture is diluted with water and extracted with EtOAc. The combined organic phase is washed with 1 N aqueous HCl, 5% aqueous NaHCO3, water and brine, and dried over Na2SO4. The solvent is removed in vacuo to afford the desired product which is used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440963B2
Source datasetuspto-grants-2016_09
ORD IDord-97e156dfd0de4ee28cf3612a4dbe6750
Source noteuspto-grants-2016_09