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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044654Generated: October 25, 2026

Water → 5-Chloro-4,6-dimorpholino-2-(4-phenylpiperazin-1-yl)pyrimidine

https://huagongshe.com/reaction/1044654

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChlorosuccinimideHCID 31398—
Reactant4,6-Dimorpholino-2-(4-phenylpiperazin-1-yl)pyrimidineHCID 44250437—
CatalystBenzoyl PeroxideHCID 7187—
SolventChloroformHCID 6212—
Product5-Chloro-4,6-dimorpholino-2-(4-phenylpiperazin-1-yl)pyrimidineHCID 4425132346%

Reaction Steps

The synthesis method shall be explained concretely, and in order, below. 4,6-dimorpholino-2-(4-phenylpiperazin-1-yl)pyrimidine (300 mg, 0.73 mmol) was dissolved in chloroform solution (5 ml), benzoyl peroxide (0.3 mg, 0.0014 mmol) and N-chlorosuccinimide (117 mg, 0.87 mmol) was added, and refluxed under heating for 1 hour. Water was added, and extraction was done with dichloromethane. After washing the organic layer with saturated saline, drying was done with MgSO4, and the solvent was distilled away under reduced pressure. Purification was done by silica gel chromatography (hexane:ethyl acetate=4:1), and 142 mg of 5-chloro-4,6-dimorpholino-2-(4-phenylpiperazin-1-yl)pyrimidine was obtained (yield 46%). The melting point measurement result, the MS measurement result, and the NMR data for the obtained Compound 130 are shown below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563715B2
Source datasetuspto-grants-2013_10
ORD IDord-3d3ce296a70b40cfa29cb59e45f92637
Source noteuspto-grants-2013_10