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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330851Generated: October 31, 2026

Piperazine → 6-Chloro-7-(4-hydroxypiperidin-1-yl)-2-piperazin-1-yl-4-pyrrolidin-1-yl-pteridine

https://huagongshe.com/reaction/330851

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantPiperidin-4-olHCID 79341—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Pyrrolidin-1-yl-2,6,7-trichloropteridineHCID 13799884—
Solvent1,4-DioxaneHCID 31275—
Product6-Chloro-7-(4-hydroxypiperidin-1-yl)-2-piperazin-1-yl-4-pyrrolidin-1-yl-pteridineHCID 86616763—

Reaction Conditions

Temperature40 °C

Reaction Steps

a)+b) 80 mg (0.26 mmol) 4-pyrrolidin-1-yl-2,6,7-trichloro-pteridine are dissolved in 5 ml dioxane and combined with 29 mg (0.29 mmol) 4-hydroxypiperidin and 49 μl (0.37 mmol) diisopropylethylamine. The mixture is stirred for approx. 16 h at 40° C. The reaction mixture is then slowly added dropwise to a solution of 113 mg (1 mmol) piperazine in 15 ml dioxane at a temperature of 80° C. The mixture is stirred for approx. 16 h at 80° C., cooled to ambient temperature and then poured onto ice water. It is extracted with dichloromethane, the organic phase is dried on sodium sulphate and the solvent is eliminated in vacuo. The residue is taken up in some dichloromethane and combined with petroleum ether, the precipitate formed is suction filtered. Yield 58 mg (53% of theoretical).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877756B2
Source datasetuspto-grants-2014_11
ORD IDord-c7ac017b0edf477ea885dc502f2b3938
Source noteuspto-grants-2014_11