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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522652Generated: October 28, 2026

1,4-Dioxane hydrochloride → Phenyl[2-(1-piperazinyl)-5-pyrimidinyl]methanone hydrochloride

https://huagongshe.com/reaction/522652

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-Dioxane hydrochlorideHCID 20443148—
ReactantTert-butyl 4-(5-benzoylpyrimidin-2-yl)piperazine-1-carboxylateHCID 118022456—
Solvent1,4-DioxaneHCID 31275—
ProductPhenyl[2-(1-piperazinyl)-5-pyrimidinyl]methanone hydrochlorideHCID 11802263690%

Reaction Steps

To a solution of tert-butyl 4-(5-benzoylpyrimidin-2-yl)piperazine-1-carboxylate (1 g, 2.7 mmol) in dioxane (20 mL) was added 4 M HCl-dioxane (20 mL), and the reaction mixture was stirred at room temperature overnight. LCMS showed the reaction was completed. The mixture was directly concentrated to give phenyl(2-(piperazin-1-yl)pyrimidin-5-yl)methanone HCl salt as a yellowish solid (0.95 g, 90%). MS (ES+) C15H16N4O requires: 268, found: 269 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334263B2
Source datasetuspto-grants-2016_05
ORD IDord-99c7400e40b640e8bd6222be1b684379
Source noteuspto-grants-2016_05