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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044653Generated: October 25, 2026

Water → 4,6-Dimorpholino-5-fluoro-2-(4-phenylpiperazin-1-yl)pyrimidine

https://huagongshe.com/reaction/1044653

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-Fluoro-2,4,6-trimethylpyridinium Trifluoromethanesulfonate [Fluorinating Reagent]HCID 2724575—
Reactant4,6-Dimorpholino-2-(4-phenylpiperazin-1-yl)pyrimidineHCID 44250437—
SolventDichloromethaneHCID 6344—
Product4,6-Dimorpholino-5-fluoro-2-(4-phenylpiperazin-1-yl)pyrimidineHCID 4425050031%

Reaction Steps

The synthesis method shall be explained concretely, and in order, below. 4,6-dimorpholino-2-(4-phenylpiperazin-1-yl)pyrimidine (380 mg, 0.926 mmol) was dissolved in dichloromethane (5 ml), and N-fluoro-2,4,6-trimethylpyridinium triflate (402 mg, 1.39 mmol) was added. After agitation for 30 minutes at room temperature, 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 122 mg of 4,6-dimorpholino-5-fluoro-2-(4-phenylpiperazin-1-yl)pyrimidine was obtained (yield 31%). The melting point measurement result, the MS measurement result, and the NMR data for the obtained Compound 82 are shown below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563715B2
Source datasetuspto-grants-2013_10
ORD IDord-76a6e3b911c34f25b31dba654b45452f
Source noteuspto-grants-2013_10