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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221372Generated: October 25, 2026

tert-Butyl 4-sulfanylpiperidine-1-carboxylate → 4-(3-Pyridin-4-yl-[1,2,4]oxadiazol-5-ylmethylsulfanyl)piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/221372

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-sulfanylpiperidine-1-carboxylateHCID 21906090—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantMethanesulfonic acid 3-pyridin-4-yl-[1,2,4]oxadiazol-5-ylmethyl esterHCID 57954388—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product4-(3-Pyridin-4-yl-[1,2,4]oxadiazol-5-ylmethylsulfanyl)piperidine-1-carboxylic acid tert-butyl esterHCID 57954409—

Reaction Steps

t-BuOK (92 mg, 823 μmol) and methanesulfonic acid 3-pyridin-4-yl-[1,2,4]oxadiazol-5-ylmethyl ester (Preparation 12, 150 mg, 588 μmol) were added to a stirred solution of 4-mercaptopiperidine-1-carboxylic acid tert-butyl ester (191 mg, 881 mol) in anhydrous THF (10 ml). After 100 min, the reaction mixture was diluted with Et2O, before being washed with NaHCO3 and brine. The organic layer was dried (MgSO4), filtered, and concentrated, then the residue was purified by column chromatography (IH-EtOAc, 3:2) to afford the title compound: RT=3.77 min; m/z (ES+)=377.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207147B2
Source datasetuspto-grants-2012_06
ORD IDord-bad805c3d4a949ff81a3f21fa38fd134
Source noteuspto-grants-2012_06