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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33922Generated: October 26, 2026

Piperidine → 4-(4-((Quinolin-2-yl)methoxy)phenyl)-3-(pyridin-4-yl)but-3-en-2-one

https://huagongshe.com/reaction/33922

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant4-PyridinylacetoneHCID 80552—
Reactant4-(2-quinolinylmethoxy)BenzaldehydeHCID 14578960—
SolventTolueneHCID 1140—
Product4-(4-((Quinolin-2-yl)methoxy)phenyl)-3-(pyridin-4-yl)but-3-en-2-oneHCID 68578495—

Reaction Steps

A mixture of 4-((quinolin-2-yl)methoxy)benzaldehyde (2.5 g, 9.5 mmol), 1-(pyridin-4-yl)propan-2-one (1.3 g, 9.5 mmol) and piperidine (162 mg, 1.9 mmol) in toluene (50 mL) was heated at reflux for 18 h, concentrated, and the residue chromatographed on silica eluting with a gradient of ethyl acetate in hexanes giving impure title substance (2.4 g) as a yellow solid which was chromatographed again on silica eluted with 1% and 2% methanol in dichloromethane containing 0.5% concentrated ammonium hydroxide giving a 3:1 mixture of the title substance contaminated with the pyridyl starting material. Yield 2.0 g, 55%. The title substance appeared to be a 10:1 mixture of two isomers by NMR. 1H NMR (CDCl3, 400 mHz, partial) δ 2.35 (s, 3H, major isomer), 2.23 (s, 3H, minor isomer). HPLC-MS 6.09 min, m/e 381 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429665B2
Source datasetuspto-grants-2008_09
ORD IDord-cdc2826d4e884d9da32a0d7456f0a126
Source noteuspto-grants-2008_09