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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368077Generated: October 30, 2026

Hydrochloric Acid → HCID 58484014, compound

https://huagongshe.com/reaction/2368077

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant3-IsoxazolamineHCID 1810216—
ReactantHCID 67448291HCID 67448291—
ReactantHCID 178419135HCID 178419135—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 58484014HCID 58484014—

Reaction Steps

To a solution of 1-({1-[6-(cyclopropylmethoxy)-1,3-benzoxazol-2-yl]piperidin-4-yl}oxy)propan-2-one (400 mg) and isoxazol-3-amine (0.129 mL) in methanol (6 mL) and acetic acid (0.300 mL) was added decaborane (213 mg), and the mixture was stirred at room temperature for 3 hr. 1M Hydrochloric acid was added to the reaction mixture, and the mixture was stirred at room temperature for 30 min, and extracted with ethyl acetate. The extract was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel chromatography (hexane/ethyl acetate). The obtained residue was applied to preparative HPLC (C18, mobile phase: water/acetonitrile (containing 0.1% TFA)). Saturated aqueous sodium hydrogen carbonate solution was added to the obtained fraction, and the mixture was extracted with ethyl acetate and the extract was dried over anhydrous sodium sulfate. The residue was concentrated under reduced pressure to give the title compound (126 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703758B2
Source datasetuspto-grants-2014_04
ORD IDord-8e4e4bb52c954f8bb543fe7c83bf27db
Source noteuspto-grants-2014_04