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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2396495Generated: October 29, 2026

N-(2-Aminoethyl)piperidine → HCID 18987437, compound

https://huagongshe.com/reaction/2396495

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2-Aminoethyl)piperidineHCID 33944—
ReactantHCID 18987424HCID 18987424—
ProductHCID 18987437HCID 18987437—

Reaction Conditions

Temperature120 °C

Reaction Steps

5-Trichloromethyl-3-[1-methyl-1H-indol-3-yl]-1,2,4-oxadiazole (0.100 g, 0.316 mmol) (D8) was dissolved with stirring in 1-(2-aminoethyl) piperidine (0.8 ml) and heated to 120° C. After 0.5 h, the reaction mixture was allowed to cool and was partitioned between EtOAc and water. The organic layer was then washed with water (1×), dried (Na2SO4) and evaporated under reduced pressure to give a yellow oil which was purified by silica gel chromatography (10% MeOH in EtOAc as eluant) to give the title compound as a colourless oil that crystallised on standing (0.095 g, 93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05492919
Source datasetuspto-grants-1996_02
ORD IDord-dc6c0ada4cc34ef9b2e4027dede478f0
Source noteuspto-grants-1996_02