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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 421825Generated: November 1, 2026

Methanol → 2,2-Dimethylpropyl 4-[4-(5-methoxy-1,2,4-oxadiazol-3-yl)pyridin-2-yl]-1-piperazinecarboxylate

https://huagongshe.com/reaction/421825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant2,2-Dimethylpropyl 4-{4-[5-(trichloromethyl)-1,2,4-oxadiazol-3-yl]pyridin-2-yl}-1-piperazinecarboxylateHCID 11992708—
Product2,2-Dimethylpropyl 4-[4-(5-methoxy-1,2,4-oxadiazol-3-yl)pyridin-2-yl]-1-piperazinecarboxylateHCID 11992801—

Reaction Steps

2,2-Dimethylpropyl 4-[4-(5-trichloromethyl-1,2,4-oxadiazol-3-yl)pyridin-2-yl]-1-piperazinecarboxylate (106 mg) obtained in Example 32 was dissolved in methanol (2 mL), and oily sodium hydride (10 mg) was added thereto and stirred at room temperature for 15 minutes, and then aqueous saturated ammonium chloride solution was added to it and extracted with ethyl acetate. The organic layer was washed with saturated saline water, and dried with anhydrous sodium sulfate. The solvent was evaporated away, and the resulting residue was isolated and purified through thin-layer silica gel chromatography (hexane/ethyl acetate=1/1) to obtain 2.5 mg of the entitled compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101618B2
Source datasetuspto-grants-2012_01
ORD IDord-0044f945fa32425784d6b6404fd567fb
Source noteuspto-grants-2012_01