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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1983126Generated: October 30, 2026

Piperidine → HCID 16722802, compound

https://huagongshe.com/reaction/1983126

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantHCID 16722749HCID 16722749—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 16722802HCID 1672280280.1%

Reaction Conditions

Temperature170 °C

Reaction Steps

To a solution of 2-(4-fluoro-phenyl)-5-(5-methyl-3-phenyl-isoxazol-4-yl)-[1,3,4]oxadiazole (200 mg, 0.62 mmol) in DMSO (2 mL) was added piperidine (307 μL, 3.11 mmol) and the resulting mixture stirred for 5 h at 170° C. After cooling to ambient temperature the reaction mixture was extracted with aqueous hydrochloric acid (1 N, 20 mL) and ethyl acetate (20 mL). The aqueous layer was extracted with ethyl acetate (20 mL) and the combined organic layers were washed with brine (half-saturated, 20 mL) and aqueous sodium carbonate (saturated, 20 mL). Drying over sodium sulfate and purification by chromatography (SiO2, heptane:ethyl acetate:dichloromethane=80:0:20 to 50:30:20) afforded the title compound (192 mg, 80%) as a white solid. MS: m/e=387.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07541372B2
Source datasetuspto-grants-2009_06
ORD IDord-a532a8e929fc4691a96c1bc70fb10df0
Source noteuspto-grants-2009_06