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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166273Generated: November 3, 2026

1,4'-Bipiperidine → 3-[1,4']Bipiperidinyl-1'-ylmethyl-2-phenyl-quinoline-4-carboxylic Acid Methyl Ester

https://huagongshe.com/reaction/1166273

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4'-BipiperidineHCID 78607—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Quinolinecarboxylic acid, 3-(bromomethyl)-2-phenyl-, methyl esterHCID 10498448—
SolventTetrahydrofuranHCID 8028—
Product3-[1,4']Bipiperidinyl-1'-ylmethyl-2-phenyl-quinoline-4-carboxylic Acid Methyl EsterHCID 1081314956.4%

Reaction Conditions

Temperature50 °C

Reaction Steps

5 g (14 mmol) of 3-bromomethyl-2-phenyl-quinoline-4-carboxylic acid methyl ester (compound of Description 2), 2.9 g, (15.4 mmol) of 90% [1,4′]Bipiperidinyl (Aldrich), 2.7 ml (15.4 mmol) of ethyl-diisopropyl-amine were dissolved in 100 ml of dry THF and the mixture was stirred for one night at 50° C. The solvent was concentrated, the residue was dissolved in CH2Cl2, washed with water, and the organic phase was dried over MgSO4. After concentration of the solvent, the residue was purified by flash chromatography over 160 g of silicagel (eluting with CH2Cl2/MeOH/NH4OH:95/5/0.5) affording 3.5 g (yield 56%) of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06613770B1
Source datasetuspto-grants-2003_09
ORD IDord-24c88c5e2f9c48b6b9c7b44b15e597e6
Source noteuspto-grants-2003_09