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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720923Generated: October 30, 2026

N-(piperidine-4-carbonyl)-3-(3-pridyl)-alanine [4-phenyl-1-(3-phenyl-propyl)-butyl]-amide → N-{1-[2-(R)-hydroxy-3-(quinolin-5-yloxy)-propyl]-piperidine-4-carbonyl}-3-(3-pyridyl)-alanine [4-phenyl-1-(3-phenyl-propyl)-butyl]-amide

https://huagongshe.com/reaction/720923

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(piperidine-4-carbonyl)-3-(3-pridyl)-alanine [4-phenyl-1-(3-phenyl-propyl)-butyl]-amideHCID 10208518—
Reactant(R)-5-(Oxiran-2-ylmethoxy)quinolineHCID 11735808—
SolventEthanolHCID 702—
ProductN-{1-[2-(R)-hydroxy-3-(quinolin-5-yloxy)-propyl]-piperidine-4-carbonyl}-3-(3-pyridyl)-alanine [4-phenyl-1-(3-phenyl-propyl)-butyl]-amideHCID 5988559252.5%

Reaction Steps

N-(Piperidine-4-carbonyl)-3-(3-pyridyl)-alanine [4-phenyl- 1-(3-phenyl-propyl)-butyl]-amide (87) (261.8 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 25 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 (190 mg) as a white solid. ESMS:MH+ 728.6

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135483B2
Source datasetuspto-grants-2006_11
ORD IDord-017d43c661d54381a032be5afd9c76d4
Source noteuspto-grants-2006_11