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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 265282Generated: October 30, 2026

Pyridine → HCID 86751066, compound

https://huagongshe.com/reaction/265282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-(O-aminooxy)ethylamine dihydrochlorideHCID 14362326—
ReactantHCID 19078362HCID 19078362—
SolventEthanolHCID 702—
ProductHCID 86751066HCID 86751066105.3%

Reaction Steps

A mixture of 1-{1-[4-oxo-4-(4-chlorophenyl)butyl]-4-piperidinyl}-1,3-dihydro-2-benzimidazolone (3.00 g), O-(2-aminoethyl)hydroxylamine dihydrochloride (1.35 g), 3 equivalents of pyridine, and absolute ethanol (75 ml) was heated under reflux, under nitrogen, with stirring, for three hrs. The reaction mixture was partitioned between 10% sodium hydroxide solution and ethyl acetate. The layers were separated and the aqueous phase extracted with ethyl acetate. The combined organic extracts were dried over anhydrous sodium sulfate, filtered, and the filtrate was evaporated. The residue was taken up in toluene and evaporated. The residue was purified by flash chromatography (180:19:1 dichloromethane/methanol/ammonium hydroxide). The appropriate fractions were collected and evaporated. The residue was dissolved in absolute ethanol and treated with ethereal hydrogen chloride. The solvent was evaporated, and the residue was taken up in hot 2-propanol and chilled. The precipitate was collected and recrystallized twice from absolute ethanol/ether to give 2.1 g (53%) of product, mp 140°-145° C. (dec).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05648367
Source datasetuspto-grants-1997_07
ORD IDord-ad4ebdd453e94b9ca0d46d32a376ddc0
Source noteuspto-grants-1997_07