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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262985Generated: November 1, 2026

Hydrochloric Acid → 1-[3-(3-Furyl)-1,2,4-thiadiazol-5-yl]piperazine

https://huagongshe.com/reaction/2262985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHexaneHCID 8058—
ReactantTert-butyl 4-[3-(3-furyl)-1,2,4-thiadiazol-5-yl]piperazine-1-carboxylateHCID 68778731—
SolventEthyl AcetateHCID 8857—
Product1-[3-(3-Furyl)-1,2,4-thiadiazol-5-yl]piperazineHCID 68777843—

Reaction Steps

tert-Butyl 4-[3-(3-furyl)-1,2,4-thiadiazol-5-yl]piperazine-1-carboxylate (3.30 g, 9.81 mmol) was dissolved in ethyl acetate (50 ml), and a solution of 4 N hydrogen chloride in ethyl acetate (25 ml) was added thereto, followed by stirring at room temperature for 18 hours. Hexane (120 ml) was poured to the reaction mixture, and a solid was separated by filtration. The obtained solid was dissolved in an aqueous saturated sodium hydrogen carbonate solution, followed by stirring at room temperature for 2 hours. Water was poured to the reaction mixture, and the resulting solution was extracted with a mixed solution of ethyl acetate/tetrahydrofuran (1:1). The extract was washed with water and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. Hexane was added to the residue, and 1.30 g (56.0%) of the desired product as a solid was separated by filtration.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851473B2
Source datasetuspto-grants-2010_12
ORD IDord-f3b0c4480cd7449dbce89e37572746b2
Source noteuspto-grants-2010_12