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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330847Generated: October 30, 2026

Piperazine → HCID 178517383, compound

https://huagongshe.com/reaction/330847

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 numberUS08877756B2
Source datasetuspto-grants-2014_11
ORD IDord-328cd6c9d5bf4080855c6d50cf864177
Source noteuspto-grants-2014_11