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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262962Generated: November 3, 2026

Triethylamine → HCID 68775699, compound

https://huagongshe.com/reaction/2262962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant3-Acetoxybenzoic acidHCID 238669—
Reactant1-(3-Phenyl-(1,2,4)thiadiazol-5-yl)-piperazineHCID 2777760—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 68775699HCID 6877569922.3%

Reaction Steps

To a solution of 3-acetoxybenzoic acid (180 mg, 1.00 mmol) and triethylamine (0.293 ml, 2.10 mmol) in toluene (10 ml) was added diphenylphosphoryl azide (0.226 ml, 1.05 mmol) at room temperature, and the mixture was stirred at room temperature for 30 minutes, followed by elevating the temperature to 90° C. and stirring for 1.5 hour. The resulting mixture was cooled to room temperature, 1-(3-phenyl-1,2,4-thiadiazol-5-yl)piperazine (172 mg, 0.700 mmol) was added thereto, and the mixture was stirred at room temperature for 2 hours and half. Water was poured to the reaction mixture, and the resulting solution was extracted with ethyl acetate. The extract was washed with water and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:1) and recrystallized from a mixed solvent of hexane and tetrahydrofuran to give 66 mg (22.3%) of the desired product as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851473B2
Source datasetuspto-grants-2010_12
ORD IDord-daf98b9cbb604e6082dc12e750503664
Source noteuspto-grants-2010_12