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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 265283Generated: October 29, 2026

Pyridine → HCID 73474168, compound

https://huagongshe.com/reaction/265283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-(O-aminooxy)ethylamine dihydrochlorideHCID 14362326—
ReactantHCID 19078339HCID 19078339—
SolventEthanolHCID 702—
ProductHCID 73474168HCID 7347416847.8%

Reaction Steps

A mixture of 1-[1-(4-oxo-4-phenylbutyl)-4-piperidinyl]-1,3-dihydro-2-benzimidazolone (3.85 g), O-(2-aminoethyl)hydroxylamine dihydrochloride (1.89 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 from 2-propanol and then twice from ethanol/ether to give 1.5 g (29%) of product, mp 175°-180° C. (dec).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05648367
Source datasetuspto-grants-1997_07
ORD IDord-f746a2537a3045279acd5c193212c0e1
Source noteuspto-grants-1997_07