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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850796Generated: October 30, 2026

Potassium Carbonate → 2-((1S,2R)-2-(1-(5-isopropyl-1,2,4-oxadiazol-3-yl)piperidin-4-yl)cyclopropyl)ethanol

https://huagongshe.com/reaction/1850796

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantIsobutyryl chlorideHCID 62325—
ReactantHCID 178513430HCID 178513430—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
Product2-((1S,2R)-2-(1-(5-isopropyl-1,2,4-oxadiazol-3-yl)piperidin-4-yl)cyclopropyl)ethanolHCID 70818991—

Reaction Conditions

Temperature80 °C

Reaction Steps

N-hydroxy-4-((1R,2S)-2-(2-hydroxyethyl)cyclopropyl)piperidine-1-carboximidamide (4.8 g, 21.10 mmol) was dissolved in Pyridine (60 ml) and isobutyryl chloride (18.44 ml, 176 mmol) was added. The mixture was stirred at 80° C. for 3 h and the solvent was evaporated to dryness. The residue was dissolved in MeOH (100 ml) and potassium carbonate (24.32 g, 176 mmol) was added. The mixture was stirred at 50° C. for 2 h. Another potassium carbonate (24.32 g, 176 mmol) was added and the mixture was stirred at 50° C. for another 2 h. The mixture was cooled down and diluted with EtOAc (100 mL), washed with water, sat. NH4Cl, dried over MgSO4, evaporated. The crude material was purified by silica gel column eluting with 20-70% EtOAc in hexane to afford the desired product. LC/MS (m/z): 280 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957062B2
Source datasetuspto-grants-2015_02
ORD IDord-413a6e42cec94a3dbd24893ce86d6740
Source noteuspto-grants-2015_02