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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271437Generated: November 2, 2026

Triethylamine → 2-[2-(4-Trifluoromethyl-phenyl)-vinyl]-oxazole-4-carboxylic acid [4-(4-[1,2,3]triazol-1-yl-butyl)-phenyl]-amide

https://huagongshe.com/reaction/1271437

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant4-(4-[1,2,3]Triazol-1-yl-butyl)-phenylamineHCID 18453532—
Reactant2-{2-[4-(Trifluoromethyl)phenyl]ethenyl}-1,3-oxazole-4-carboxylic acidHCID 69487434—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product2-[2-(4-Trifluoromethyl-phenyl)-vinyl]-oxazole-4-carboxylic acid [4-(4-[1,2,3]triazol-1-yl-butyl)-phenyl]-amideHCID 72787656—

Reaction Steps

2-[2-(4-Trifluoromethyl-phenyl)-vinyl]-oxazole-4-carboxylic acid (100 mg, 0.35 mmol), N-ethyl-N′-(3-dimethyl-aminopropyl)carbodiimide hydrochloride (101 mg, 0.53 mmol), 1-Hydroxybenzotriazole hydrate (73 mg, 0.53 mmol) and triethylamine (71 mg, 0.71 mmol) are suspended in dichloromethane (5 ml). After stirring at room temperature for 15 min 4-(4-[1,2,3]Triazol-1-yl-butyl)-phenylamine (84 mg, 0.39 mmol) is added and stirring is continued for 20 h. Ethyl acetate (10 ml) is added and the mixture washed with aq. HCl (1N, 10 ml), sat. NaHCO3, (10 ml), dried over sodium sulfate and concentrated in vacuo. The crude product is purified by flash column chromatography (ethyl acetate/heptane 9:1) yielding 2-[2-(4-trifluoromethyl-phenyl)-vinyl]-oxazole-4-carboxylic acid [4-(4-[1,2,3]triazol-1-yl-butyl)-phenyl]-amide 11 as a colorless solid. Yield 109 mg (64%); m.p. 183–185° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07205326B2
Source datasetuspto-grants-2007_04
ORD IDord-cceee2bdfecf4a319ff162115d84d0bc
Source noteuspto-grants-2007_04