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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2063402Generated: November 1, 2026

Triethylamine → 4-(5-Methanesulfonyloxymethyl-[1,2,4]oxadiazol-3-yl)-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/2063402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant4-(5-Hydroxymethyl-[1,2,4]oxadiazol-3-yl)-piperidine-1-carboxylic acid tert-butyl esterHCID 57986906—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product4-(5-Methanesulfonyloxymethyl-[1,2,4]oxadiazol-3-yl)-piperidine-1-carboxylic acid tert-butyl esterHCID 57986850—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-(5-hydroxymethyl-[1,2,4]oxadiazol-3-yl)-piperidine-1-carboxylic acid tert-butyl ester (0.2 g, 0 7 mmol) in methylene chloride (5 mL) was added methanesulfonyl chloride (0.1 g, 0.9 mmol) and triethyl amine (0.14 g, 1.4 mmol) at 0° C. After stirred at 0° C. for 1 hour, the mixture was diluted with EtOAc and washed with H2O, brine. After drying (Na2SO4), the solvent was removed in vacuo, and the residue was purified by silica column chromatography with EtOAc/hexanes to afford the desired product

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288384B2
Source datasetuspto-grants-2012_10
ORD IDord-6ed7a5efd1da4c28a321ccdd0a2ad557
Source noteuspto-grants-2012_10