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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166546Generated: October 27, 2026

Potassium Carbonate → 6-(5-Phenyl-1,3,4-oxadiazol-2-yl)methoxy-2-piperidinomethyltetralin hydrochloride

https://huagongshe.com/reaction/1166546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-(Chloromethyl)-5-phenyl-1,3,4-oxadiazoleHCID 314941—
Reactant6-Hydroxy-2-piperidinomethyltetralinHCID 21939861—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product6-(5-Phenyl-1,3,4-oxadiazol-2-yl)methoxy-2-piperidinomethyltetralin hydrochlorideHCID 2299855369.2%

Reaction Steps

To a solution of 6-hydroxy-2-piperidinomethyltetralin (141 mg, free form of Reference Example 19) and 2-chloromethyl-5-phenyl-1,3,4-oxadiazole (148 mg) in DMF (3 ml) was added potassium carbonate (143 mg) and the reaction mixture was stirred at room temperature for 24 hr. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic layer was washed with water and saturated aqueous sodium chloride, dried, and concentrated. The residue was purified by silica gel column chromatography (eluent: ethyl acetate: methanol=10:1) and alumina column chromatography (eluent:ethyl acetate: hexane=1:4), and then converted into its hydrochloride, which was further recrystallized from methanol-diethyl ether to obtain the titled compound (175 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06613805B2
Source datasetuspto-grants-2003_09
ORD IDord-b052644c32754254b323cd18657f9d00
Source noteuspto-grants-2003_09