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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368108Generated: November 3, 2026

Hydrochloric Acid → HCID 178461776, compound

https://huagongshe.com/reaction/2368108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTrimethyl borateHCID 8470—
ReactantSodium HydroxideHCID 14798—
ReactantHydrogen peroxide waterHCID 449047—
ReactantHCID 86658702HCID 86658702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178461776HCID 178461776—

Reaction Steps

To a solution of tert-butyl [(1S)-2-{[1-(5-bromo[1,3]oxazolo[5,4-b]pyridin-2-yl)piperidin-4-yl]oxy}-1-methylethyl]carbamate (484 mg) in THF (3 mL) was added 1.6M n-butyllithium-hexane solution (1.70 mL) at −78° C., and the mixture was stirred at the same temperature for 20 min. Trimethyl borate (0.355 mL) was added to the reaction mixture, and the mixture was allowed to warm to room temperature and stirred for 30 min. 30% Hydrogen peroxide water (3 mL) and 8M aqueous sodium hydroxide solution (1 mL) were added to the reaction mixture, and the mixture was stirred at room temperature for 30 min. The reaction mixture was neutralized with 1M hydrochloric acid, and extracted with ethyl acetate, and the extract was dried over magnesium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (68.1 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703758B2
Source datasetuspto-grants-2014_04
ORD IDord-e243a8368f5e4c60bd2a2b178bce3c19
Source noteuspto-grants-2014_04