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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397640Generated: October 29, 2026

N'1-[((2S)-1-[(4-fluorophenyl)sulfonyl]-2-piperidylcarbonyl)oxy]ethanimidamide → (2S)-1-[(4-fluorophenyl)sulfonyl]-2-(3-methyl-1,2,4-oxadiazol-5-yl)piperidine

https://huagongshe.com/reaction/397640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN'1-[((2S)-1-[(4-fluorophenyl)sulfonyl]-2-piperidylcarbonyl)oxy]ethanimidamideHCID 86759129—
SolventO-XyleneHCID 7237—
Product(2S)-1-[(4-fluorophenyl)sulfonyl]-2-(3-methyl-1,2,4-oxadiazol-5-yl)piperidineHCID 52104633—

Reaction Steps

The title compound was prepared by a similar method to Preparation 6 from N′1-[((2S)-1-[(4-fluorophenyl)sulfonyl]-2-piperidylcarbonyl)oxy]ethanimidamide [see Preparation 82] and xylene. The crude product was purified by column chromatography on silica gel eluting with a solvent gradient of 100:0 changing to 80:20, by volume, hexane:ethyl acetate in 10% increments, to afford (2S)-1-[(4-fluorophenyl)sulfonyl]-2-(3-methyl-1,2,4-oxadiazol-5-yl)piperidine as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610707B1
Source datasetuspto-grants-2003_08
ORD IDord-4ac1838502054db385a382963e4a11aa
Source noteuspto-grants-2003_08