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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2263044Generated: October 26, 2026

Water → N-[6-(Acetylamino)pyridin-3-yl]-4-(3-phenyl-1,2,4-thiadiazol-5-yl)piperazine-1-carboxamide

https://huagongshe.com/reaction/2263044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-(3-Phenyl-(1,2,4)thiadiazol-5-yl)-piperazineHCID 2777760—
Reactant2,2,2-Trichloroethyl[6-(acetylamino)pyridin-3-yl]carbamateHCID 86245259—
SolventDimethyl SulfoxideHCID 679—
ProductN-[6-(Acetylamino)pyridin-3-yl]-4-(3-phenyl-1,2,4-thiadiazol-5-yl)piperazine-1-carboxamideHCID 6877694947.5%

Reaction Steps

A mixed solution of 2,2,2-trichloroethyl [6-(acetylamino)pyridin-3-yl]carbamate (241 mg, 0.738 mmol), 1-(3-phenyl-1,2,4-thiadiazol-5-yl)piperazine (200 mg, 0.812 mmol) and diisopropylethylamine (0.129 ml, 0.738 mmol) in dimethyl sulfoxide (2.5 ml) was stirred at 70° C. for 15 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 (ethyl acetate) and recrystallized from a mixed solvent of hexane and tetrahydrofuran to give 148 mg (47.5%) of the desired product as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851473B2
Source datasetuspto-grants-2010_12
ORD IDord-ca0ff9ec77a84e86b5f76a3c1bf1a8ec
Source noteuspto-grants-2010_12