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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282179Generated: November 3, 2026

Water → n-(4-((4-(4,6-Diethoxypyrimidin-2-yl)piperazin-1-yl)methyl)-phenylmethyl)acetamide

https://huagongshe.com/reaction/1282179

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantN-((4-(chloromethyl)phenyl)methyl)acetamideHCID 15550682—
Reactant1-(4,6-Diethoxypyrimidin-2-yl)piperazineHCID 18423168—
SolventDimethylformamideHCID 6228—
Productn-(4-((4-(4,6-Diethoxypyrimidin-2-yl)piperazin-1-yl)methyl)-phenylmethyl)acetamideHCID 18423001115.5%

Reaction Steps

A solution of N-(4-chloromethylphenylmethyl)acetamide (1.2 g), 1-(4,6-diethoxypyrimidin-2-yl)piperazine (1.7 g) and potassium carbonate (1.3 g) in dimethylformamide (20 ml) was stirred at 80° C. for 4.5 hr. The reaction mixture was poured into water(150 ml) and extracted with ethyl acetate. The extract was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated to give a brown oil (2.9 g). The obtained brown oil was purified by silica gel column chromatography to give a pale-yellow oil (2.4 g). The obtained pale-yellow oil was crystallized from ethyl acetate/hexane (2:1, 30 ml) to give the title compound (1.7 g) as white crystals, m.p.=119-120° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06455528B1
Source datasetuspto-grants-2002_09
ORD IDord-fd766baa0f114d35803b8229213d5240
Source noteuspto-grants-2002_09