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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1477577Generated: October 30, 2026

Sodium Iodide → 3-(4-Chlorobenzyl)-6-[4-(4-fluorophenyl)piperazin-1-yl]-1,3,5-triazine-2,4(1H,3H)-dione

https://huagongshe.com/reaction/1477577

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant1-Chloro-4-(chloromethyl)benzeneHCID 7723—
ReactantLithium hydrideHCID 62714—
Reactant6-[4-(4-Fluorphenyl)piperazin-1-yl]-1,3,5-triazine-2,4(1H,3H)-dioneHCID 117839334—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product3-(4-Chlorobenzyl)-6-[4-(4-fluorophenyl)piperazin-1-yl]-1,3,5-triazine-2,4(1H,3H)-dioneHCID 11783934616.3%

Reaction Steps

To an N,N-dimethylformamide solution of 6-[4-(4-fluorophenyl)piperazin-1-yl]-1,3,5-triazine-2,4(1H,3H)-dione (1.20 g, 4.12 mmol) synthesized in Reference Synthesis Example 18, lithium hydride (75 mg, 4.94 mmol), 4-chlorobenzyl chloride (0.70 g, 4.12 mmol), and sodium iodide (catalytic amount) were added at room temperature and the resultant solution was stirred at 50° C. for 8 hours. After completion of the reaction, the reaction solution was poured into water and the resultant mixture was washed with ethyl acetate. Diluted hydrochloric acid was added to the water phase to adjust pH to 3 and the obtained solid was collected by filtration. Extraction with a mixed solution of ethyl acetate and tetrahydrofuran from the filtrate was performed and the organic layer was concentrated under reduced pressure. The residue and the solid collected by filtration were combined to obtain the title compound (280 mg, yield 15%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403798B2
Source datasetuspto-grants-2016_08
ORD IDord-65e621a028094e45bb7d8aa12bdbaf79
Source noteuspto-grants-2016_08