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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262978Generated: November 2, 2026

Triethylamine → HCID 68779810, compound

https://huagongshe.com/reaction/2262978

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant2-Methoxynicotinic acidHCID 708093—
Reactant1-(3-Phenyl-(1,2,4)thiadiazol-5-yl)-piperazineHCID 2777760—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 68779810HCID 6877981021.7%

Reaction Steps

To a solution of 2-methoxynicotinic acid (153 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 hour and half. The resulting mixture was cooled to room temperature, 1-(3-phenyl-1,2,4-thiadiazol-5-yl)piperazine (172 mg, 0.70 mmol) was added thereto, and the mixture was stirred at room temperature for 3 hours. 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 60.2 mg (21.7%) of the desired product as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851473B2
Source datasetuspto-grants-2010_12
ORD IDord-dcb9a9fdf7e6407c924a10f50b739c65
Source noteuspto-grants-2010_12