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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2299696Generated: October 30, 2026

3-(Oxiran-2-yl)pyridine → HCID 18007277, compound

https://huagongshe.com/reaction/2299696

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Oxiran-2-yl)pyridineHCID 13319561—
ReactantHCID 18007303HCID 18007303—
SolventEthanolHCID 702—
ProductHCID 18007277HCID 18007277—

Reaction Steps

Under nitrogen, a solution of 3-oxiranylpyridine (1.9 g) and N-benzyl-(3-methoxy-6,7,8,9-tetrahydro-5H-benzocyclohepten-6-yl)amine (3.3 9) in ethanol (15 ml) was refluxed for 5 hours. After removal of ethanol in vacuo, the residue was dissolved into a mixture of aqueous sodium hydrogencarbonate and ethyl acetate. After separation, the organic layer was washed with brine, dried over anhydrous magnesium sulfate and evaporated in vacuo. The residue was purified by column chromatography on silica gel (chloroform:methanol=20:1) to give 2-[N-benzyl-N-(3-methoxy-6,7,8,9-tetrahydro-5H-benzocyclohepten-6-yl) amino]-1-(pyridin-3-yl)ethanol (520 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06495546B1
Source datasetuspto-grants-2002_12
ORD IDord-21ab8396476b43d48480b0713040dfc9
Source noteuspto-grants-2002_12