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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2421184Generated: November 2, 2026

Triethylamine → HCID 67215335, compound

https://huagongshe.com/reaction/2421184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-chloro-1,3-dimethyl-1H-imidazol-3-ium chlorideHCID 11126651—
Reactant3-(3-Chlorophenyl)-5-methyl-1,2-oxazole-4-carboxylic acidHCID 24259594—
ReactantHCID 67215710HCID 67215710—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 67215335HCID 6721533562%

Reaction Steps

To a solution of 3-(3-chloro-phenyl)-5-methyl-isoxazole-4-carboxylic acid (200 mg, 0.85 mmol) in dichloromethane (4 mL) was added 2-methoxy-4-morpholin-4-yl-benzoic acid hydrazide (266 mg, 0.85 mmol) and 2-chloro-1,3-dimethylimidazolium chloride (313 mg, 1.85 mmol). After the solution was stirred for 15 min at ambient temperature triethylamine (0.59 ml, 4.21 mmol) was added over a period of 2 min and the reaction mixture was stirred for 18 h at this temperature. It was diluted with ethyl acetate (20 mL 1) and washed with aqueous sodium carbonate (half saturated). The aqueous layers were extracted with ethyl acetate. Drying over sodium sulfate and purification by chromatography (SiO2, heptane:ethyl acetate:dichloromethane=60:20:20 to 0:80:20) afforded the title compound (235 mg, 62%) as a white solid. MS: m/e=453.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07956074B2
Source datasetuspto-grants-2011_06
ORD IDord-e9a797ff4f454310adcb7392f18b8504
Source noteuspto-grants-2011_06