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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1477698Generated: October 31, 2026

Methyl iodide → 1-{4-[(4-chlorobenzyl)oxy]benzyl}-4-[4-(4-fluorophenyl)piperazin-yl]-6-methoxy-1,3,5-triazin-2(1H)-one

https://huagongshe.com/reaction/1477698

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant3-{4-[(4-Chlorobenzyl)oxy]benzyl}-6-[4-(4-fluorophenyl)piperazin-1-yl]-1,3,5-triazine-2,4(1H,3H)-dioneHCID 117839829—
SolventDimethylformamideHCID 6228—
Product1-{4-[(4-chlorobenzyl)oxy]benzyl}-4-[4-(4-fluorophenyl)piperazin-yl]-6-methoxy-1,3,5-triazin-2(1H)-oneHCID 1178397737%

Reaction Steps

To an N,N-dimethylformamide solution (4 mL) of a crude product (0.69 mmol) of 3-{4-[(4-chlorobenzyl)oxy]benzyl}-6-[4-(4-fluorophenyl)piperazin-1-yl]-1,3,5-triazine-2,4(1H,3H)-dione, potassium carbonate (332 mg, 2.40 mmol) and methyl iodide (137 μL, 2.20 mmol) were added at room temperature and the resultant mixture was stirred at room temperature for 1 day. After the completion of the reaction, the reaction solution was concentrated under reduced pressure and the resultant residue was purified by silica gel column chromatography to obtain the title compound (26 mg, two step yield: 7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403798B2
Source datasetuspto-grants-2016_08
ORD IDord-5698fc973458407b8bcccda1bfa7cbbc
Source noteuspto-grants-2016_08