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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351909Generated: October 31, 2026

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

https://huagongshe.com/reaction/1351909

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Oxiran-2-yl)pyridineHCID 13319561—
ReactantHCID 18007303HCID 18007303—
SolventEthanolHCID 702—
ProductHCID 18007277HCID 1800727711%

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 g) 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 numberUS07217706B2
Source datasetuspto-grants-2007_05
ORD IDord-14a3cf1a75444593bdbd099c522bf0cd
Source noteuspto-grants-2007_05