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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1264873Generated: October 30, 2026

Piperazine → 5-Amino-2-(2-furyl)-7-piperazinyl[1,2,4]triazolo[1,5-c]pyrimidine

https://huagongshe.com/reaction/1264873

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant5-Amino-7-chloro-2-(2-furyl)[1,2,4]triazolo[1,5-c]pyrimidineHCID 9942767—
SolventDimethyl SulfoxideHCID 679—
Product5-Amino-2-(2-furyl)-7-piperazinyl[1,2,4]triazolo[1,5-c]pyrimidineHCID 1861369878%

Reaction Conditions

Temperature150 °C

Reaction Steps

Into 180 mL of DMSO, 10.5 g (44.6 mmol) of Compound E and 19.2 g (223 mmol) of piperazine were dissolved, followed by stirring at 150° C. for about 2 hours. After completion of the reaction, the solvent was evaporated under reduced pressure, water was added to the residue, and the mixture was extracted with chloroform. The organic layer was washed with water and brine, and then dried over anhydrous magnesium sulfate. After evaporation of the solvent, the resulting residue was purified by silica gel column chromatography (23% aqueous ammonia/methanol/chloroform=1/10/90) and then recrystallized from ethyl acetate to obtain 9.91 g of Compound F as a white solid (yield: 78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06545000B1
Source datasetuspto-grants-2003_04
ORD IDord-4ed4e073b107416ca31cf42e55bf4ca8
Source noteuspto-grants-2003_04