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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1454168Generated: November 5, 2026

(R)-5-(Oxiran-2-ylmethoxy)quinoline → HCID 10146651, compound

https://huagongshe.com/reaction/1454168

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-5-(Oxiran-2-ylmethoxy)quinolineHCID 11735808—
ReactantHCID 18727491HCID 18727491—
SolventEthanolHCID 702—
ProductHCID 10146651HCID 1014665167%

Reaction Steps

1-(Piperidine-3-carbonyl)-piperidine-3-carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amide (79) (243.4 mg; 0.497 mmol) is dissolved in ethanol (12 mL) at ambient temperature. (R)-5-Oxiranylmethoxy-quinoline (2) (100.0 mg; 0.497 mmol) is added, then the mixture is refluxed for 17 hours. After cooling to ambient temperature, the solution is concentrated in vacuo at 40° C. The residue is purified via silica gel chromatography with gradient elution (50%→100% acetone in hexanes, then 5%→20% ethanol in acetone) affording the desired product (230 mg) as a white solid. ESMS: MH+ 691.6

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07476680B2
Source datasetuspto-grants-2009_01
ORD IDord-9a4921f56db147a0aa34432fb9e5017e
Source noteuspto-grants-2009_01