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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2242798Generated: November 2, 2026

Piperazine → HCID 178517383, compound

https://huagongshe.com/reaction/2242798

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantPotassium HydroxideHCID 14797—
Reactant4-Pyrrolidin-1-yl-2,6,7-trichloropteridineHCID 13799884—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178517383HCID 178517383—

Reaction Conditions

Temperature-10 °C

Reaction Steps

a)+b) 460 μl (0.82 mmol) of a 10% solution of potassium hydroxide in water is added dropwise to a solution of 250 mg (0.82 mmol) 4-pyrrolidin-1-yl-2,6,7-trichloro-pteridine in 15 ml of tetrahydrofuran cooled to −10° C. The mixture is stirred for one hour at −10° C., slowly allowed to come up to ambient temperature and stirred for approx. another 16 hours. Then a solution of 318 mg (3.69 mmol) piperazine in 10 ml of tetrahydrofuran is added and the mixture is refluxed for approx. 16 hours. Then the solvent is eliminated in vacuo, the residue is mixed with water and extracted with dichloromethane. The organic phase is dried on sodium sulphate and the solvent is eliminated in vacuo. The residue is purified by chromatography. Yield 50 mg (14% of theoretical)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674788B2
Source datasetuspto-grants-2010_03
ORD IDord-99553d901e164e6da0bf9ddc237fb610
Source noteuspto-grants-2010_03