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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2263019Generated: October 29, 2026

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

https://huagongshe.com/reaction/2263019

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropylethylamineHCID 81531—
Reactant2,2,2-Trichloroethyl pyridin-4-ylcarbamateHCID 14257294—
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-4-ylpiperazine-1-carboxamideHCID 6878201730.8%

Reaction Steps

A mixed solution of 2,2,2-trichloroethyl pyridin-4-ylcarbamate (207 mg, 0.770 mmol), 1-[3-(3-furyl)-1,2,4-thiadiazol-5-yl]piperazine (200 mg, 0.846 mmol) and diisopropylethylamine (0.134 ml, 0.846 mmol) in dimethyl sulfoxide (2.5 ml) was stirred at 80° C. 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 (ethyl acetate) and recrystallized from a mixed solvent of hexane and tetrahydrofuran to give 84.5 mg (30.8%) of the desired product as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851473B2
Source datasetuspto-grants-2010_12
ORD IDord-debbd1bacb3747469b526ff26c86f440
Source noteuspto-grants-2010_12