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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1477704Generated: November 2, 2026

Triethylamine → HCID 117839832, compound

https://huagongshe.com/reaction/1477704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-Fluorobenzoyl chlorideHCID 67879—
ReactantHCID 117839396HCID 117839396—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 117839832HCID 11783983263.1%

Reaction Steps

To an N,N-dimethylformamide solution (1 mL) of 1-(4-chlorobenzyl)-4-(piperazin-1-yl)-1,3,5-triazin-2(1H)-one (31 mg, 0.10 mmol) synthesized in Reference Synthesis Example 9, triethylamine (28 μL, 0.20 mmol) and 4-fluorobenzoyl chloride (18 μL, 0.15 mmol) were added at room temperature and the resultant mixture was stirred at room temperature for 4 hours. After the completion of the reaction, saturated ammonium chloride aqueous solution was added to the reaction solution and extraction with ethyl acetate 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=1/4→0/1 (v/v)) to obtain the title compound (27 mg, yield: 63%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403798B2
Source datasetuspto-grants-2016_08
ORD IDord-a5b3ac9781f440cb9f0517c5aab4ac3c
Source noteuspto-grants-2016_08