Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852104Generated: October 30, 2026

Hydrochloric Acid → HCID 17906331, compound

https://huagongshe.com/reaction/852104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(4-Fluorophenyl)piperidineHCID 2759136—
ReactantHCID 17906318HCID 17906318—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventChloroformHCID 6212—
SolventAcetonitrileHCID 6342—
ProductHCID 17906331HCID 1790633148%

Reaction Steps

Add 4-(4-fluoro-phenyl)-piperidine (133 mg, 0.744 mol) (See Table No.1, SM 2) to a suspension of 3-[4-(2-bromo-ethoxy)-phenyl]-6-fluoro-benzo[d]isoxazole (250 mg, 0.744 mol) in a mixture of water:acetonitrile (0.1 mL:2.5 mL). Then add potassium carbonate (164 mg, 1.63 mmol) and potassium iodide (12 mg, 1.07 mmol) and heat at reflux for 8 hours. Stir at room temperature for 72 hours, filter the suspension and wash the solid thoroughly with dichloromethane. Dilute the resulting solution with dichloromethane (5 mL) and wash with water (5 mL), 10% HCl (5 mL), water (5 mL), saturated sodium chloride (5 mL), dry (MgSO4), filter and evaporate to give a white solid. Dissolve the solid in a minimum amount of chloroform and add 1.0 M HCl in ether and stir under a nitrogen atmosphere for 1 hour. Collect the solid by vacuum filtration, wash thoroughly with ether and dry to give the title compound (168 mg, 48% Yield). Microanalysis (C, H, N) is consistent with the final, desired compound. mp-235-239° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253165B2
Source datasetuspto-grants-2007_08
ORD IDord-9dcd964128d34be3abefa55e5793302d
Source noteuspto-grants-2007_08