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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262986Generated: October 31, 2026

Water → 4-[3-(3-Furyl)-1,2,4-thiadiazol-5-yl]-N-pyridin-3-ylpiperazine-1-carboxamide

https://huagongshe.com/reaction/2262986

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropylethylamineHCID 81531—
Reactant2,2,2-Trichloroethyl pyridin-3-ylcarbamateHCID 68575380—
Reactant1-[3-(3-Furyl)-1,2,4-thiadiazol-5-yl]piperazineHCID 68777843—
SolventDimethyl SulfoxideHCID 679—
Product4-[3-(3-Furyl)-1,2,4-thiadiazol-5-yl]-N-pyridin-3-ylpiperazine-1-carboxamideHCID 6877742228.5%

Reaction Steps

A mixed solution of 2,2,2-trichloroethyl pyridin-3-ylcarbamate (311 mg, 1.15 mmol), 1-[3-(3-furyl)-1,2,4-thiadiazol-5-yl]piperazine (300 mg, 1.27 mmol) and diisopropylethylamine (0.221 ml, 1.27 mmol) in dimethyl sulfoxide (3.8 ml) was stirred at 80° C. for 1 hour 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 (ethyl acetate) and recrystallized from a mixed solvent of hexane and tetrahydrofuran to give 117 mg (28.3%) of the desired product as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851473B2
Source datasetuspto-grants-2010_12
ORD IDord-898154617e2343afafc2c9107717f9cd
Source noteuspto-grants-2010_12