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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272925Generated: October 31, 2026

Potassium Carbonate → HCID 53482797, compound

https://huagongshe.com/reaction/2272925

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Fluorophenethyl bromideHCID 573153—
ReactantHCID 71224372HCID 71224372—
SolventEthanolHCID 702—
ProductHCID 53482797HCID 5348279734.4%

Reaction Steps

A solution containing 2-(piperidin-4-yl-methyl)-3,4-dihydropyrazino[1,2-b]indazol-1(2H)-one hydrochloride (528 mg; 1.64 mmol), potassium carbonate (610 mg; 4.4 mmol), 4-fluorophenethyl bromide (450 mg; 2.2 mmol) in ethanol (10 ml) was kept stirred under reflux for 24 h. The reaction was then stopped by cooling the mixture at room temperature and concentrating the solvent under reduced pressure. The residue was taken up with DCM (30 ml) and washed respectively with a saturated solution of NaHCO3 (2×20 ml), water (2×15 ml) and a saturated solution of NaCl (10 ml). The organic phase was then dried with Na2SO4 and the solvent was removed by evaporation at reduced pressure. The solid raw product was then purified by flash chromatography on silica gel, using as eluent a mixture of chloroform:methanol in a ratio of 9:1. The product thus purified was dissolved in a mixture of diethyl ether:ethanol in a ratio of 10:1 (10 ml) and treated at room temperature with 3M hydrochloric ethanol (0.33 ml). The solid thus formed was filtered and crystallized by a mixture isopropanol:diisopropyl ether in a ratio of 3:7. Thus, 250 mg of 2-({1-[2-(4-fluorophenyl)ethyl]piperidin-4-yl}methyl)-3,4-dihydropyrazino[1,2-b]-indazol-1(2H)-one hydrochloride were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120801B2
Source datasetuspto-grants-2015_09
ORD IDord-8f919d6df7d54a3fb0d06cab6980137f
Source noteuspto-grants-2015_09