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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234117Generated: October 25, 2026

2-[4-(5-Bromo-2-methoxybenzyl)-1-piperazinyl]pyrimidine → 4-Phenyl-2-[(4-(2-pyrimidinyl)-piperazinyl)methyl]anisole

https://huagongshe.com/reaction/234117

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-[4-(5-Bromo-2-methoxybenzyl)-1-piperazinyl]pyrimidineHCID 1240303—
ReactantHCID 178418255HCID 178418255—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
Product4-Phenyl-2-[(4-(2-pyrimidinyl)-piperazinyl)methyl]anisoleHCID 9845721—

Reaction Steps

A solution of 182 mg 2-[(4-(2-pyrimidinyl)-piperazinyl)methyl]-4- bromoanisole in 1 mL of tetrahydrofuran heated to 60° C. and 6 mg of Pd(PPh3)4 was added. To this mixture 0.5 mL of a 1M solution of phenylmagnesium bromide in tetrahydrofuran was added dropwise. The reaction mixture was heated at relux temperature under nitrogen for 1 hr, cooled to room temperature and the solvent removed by evaporation under reduced pressure to yield 4-phenyl-2-[(4-(2-pyrimidinyl)-piperazinyl)methyl]anisole which was purified by chromatography on silica gel using 5% methanol in dichloromethane as eluent. Evaporation of the solvent yielded 140 mg of a solid which was treated with ethyl acetate-HCl to give 50 mg of 4-phenyl-2-[(4-(2-pyrimidinyl)piperazinyl)methyl]anisole dihydrochloride (Compound 1 ), mp 205°-207° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05594141
Source datasetuspto-grants-1997_01
ORD IDord-4919be748fa34c228f15b152956edf7a
Source noteuspto-grants-1997_01