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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 421822Generated: October 25, 2026

Sodium hydride → 2,2-dimethylpropyl 4-(4-[5-[(1S)-1-hydroxyethyl]-1,2,4-oxadiazol-3-yl]pyridin-2-yl)-1-piperazinecarboxylate

https://huagongshe.com/reaction/421822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactantmethyl (S)-lactateHCID 94386—
Reactant2,2-Dimethylpropyl 4-{4-[amino(hydroxyimino)methyl]pyridin-2-yl}-1-piperazinecarboxylateHCID 136381718—
SolventTetrahydrofuranHCID 8028—
Product2,2-dimethylpropyl 4-(4-[5-[(1S)-1-hydroxyethyl]-1,2,4-oxadiazol-3-yl]pyridin-2-yl)-1-piperazinecarboxylateHCID 11992703—

Reaction Conditions

Temperature60 °C

Reaction Steps

2,2-Dimethylpropyl 4-{4-[amino(hydroxyimino)methyl]pyridin-2-yl}-1-piperazinecarboxylate (657 mg) was dissolved in tetrahydrofuran (10 mL), oily sodium hydride (82.6 mg) was added thereto and stirred at 60° C. for 15 minutes, then methyl (S)-lactate (0.333 mL) was added thereto and heated under reflux for 1 hour. Aqueous saturated ammonium chloride solution was added to the reaction liquid, 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 silica gel column chromatography (hexane/ethyl acetate=1/1) to obtain 402 mg of the entitled compound as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101618B2
Source datasetuspto-grants-2012_01
ORD IDord-1c7c403979834b1bba20428783564d99
Source noteuspto-grants-2012_01