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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1064876Generated: October 31, 2026

1-(2-Hydroxyethyl)piperazine → HCID 22272640, compound

https://huagongshe.com/reaction/1064876

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Hydroxyethyl)piperazineHCID 7677—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 22272849HCID 22272849—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 22272640HCID 22272640100.2%

Reaction Steps

To a solution of this acetamide (498 mg, 1.57 mmol) in acetonitrile (10 ml) were added 1-(2-hydroxyethyl)piperazine (371 mg, 2.85 mmol) and potassium carbonate (469 mg, 3.39 mmol) successively with ice-cooling, and stirred at room temperature for 12 hours. The reaction solution was diluted with water and extracted with chloroform. The organic layer was washed with a saturated sodium chloride solution, dried over anhydrous sodium sulfate and concentrated in vacuo. The resulting reside was purified by a silica gel column chromatography (silica gel 50 g, developing solvent; chloroform:methanol=25:1 10:1) and recrystallized from ether-hexane to provide 575 mg (yield 99%) of 2-[4-(2-hydroxyethyl)piperazin-1-yl]-N-(2,6-diisopropyl-3-fluorophenyl)acetamide as colorless needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06969711B2
Source datasetuspto-grants-2005_11
ORD IDord-a5c2c13b317c4c1daef7bdc3775c4faf
Source noteuspto-grants-2005_11