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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2396494Generated: October 30, 2026

4-Methylpiperidine → HCID 86749263, compound

https://huagongshe.com/reaction/2396494

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylpiperidineHCID 69381—
ReactantHCID 14773942HCID 14773942—
SolventMethanolHCID 887—
ProductHCID 86749263HCID 86749263—

Reaction Steps

5-Ethenyl-3-(1-methyl-1-H-indol-3-yl)-1,2,4-oxadiazole (D2)(0.0254 g, 1.13 mmol) was dissolved in methanol (5 ml) and 4-methyl piperidine (0.167 ml, 1.69 mmol) was added. The mixture was left standing at room temperature for 16 hours, before being evaporated under reduced pressure to give a colourless oil, which was purified by silica-gel chromatography, eluting with ethyl acetate to afford the title compound as a colourless oil that crystallised on standing. The material was then converted to its hydrochloride salt, mp 192°-192° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05492919
Source datasetuspto-grants-1996_02
ORD IDord-7a66bda427fa45d6adfccc36c96fb49a
Source noteuspto-grants-1996_02