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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1477708Generated: October 29, 2026

Potassium Carbonate → 1-(4-Chlorobenzyl)-4-{[1-(4-fluorophenyl)piperidin-4-yl]amino}-1,3,5-triazin-2(1H)-one

https://huagongshe.com/reaction/1477708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-(4-Fluorophenyl)piperidin-4-amineHCID 19693945—
ReactantHCID 117839620HCID 117839620—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
Product1-(4-Chlorobenzyl)-4-{[1-(4-fluorophenyl)piperidin-4-yl]amino}-1,3,5-triazin-2(1H)-oneHCID 11783994052.5%

Reaction Steps

To a chloroform solution (1.1 mL) of 4-chloro-1-(4-chlorobenzyl)-1,3,5-triazin-2(1H)-one (59 mg, 0.23 mmol) synthesized in Reference Synthesis Example 11, potassium carbonate (80 mg, 0.58 mmol) and 1-(4-fluorophenyl)piperidine-4-amine (66 mg, 0.34 mmol) synthesized in Reference Synthesis Example 83 were added and the resultant mixture was stirred at room temperature for 30 minutes. After the completion of the reaction, water was added to the reaction solution and extraction with chloroform from the resultant reaction solution was performed. The organic layer was concentrated under reduced pressure and the resultant residue was purified by silica gel column chromatography (hexane/ethyl acetate=1/5→0/1 and next, ethyl acetate/methanol=19/1 (v/v)) to obtain the title compound (50 mg, yield: 52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403798B2
Source datasetuspto-grants-2016_08
ORD IDord-a2885db1740048438308962a4049e313
Source noteuspto-grants-2016_08