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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266149Generated: October 30, 2026

ethyl 6-(N,N-diethylamino)-3-oxohexanoate → ethyl 2-[3-(N,N-diethylamino)propyl]-4-(3,4-dimethoxyphenyl)-6,7-dimethoxyquinoline-3-carboxylate

https://huagongshe.com/reaction/266149

Reaction equation

Participants

RoleNameHCIDCharge
Reactantethyl 6-(N,N-diethylamino)-3-oxohexanoateHCID 19032338—
Reactant2-Amino-3',4',4,5-tetramethoxybenzophenone hydrochlorideHCID 21466134—
SolventEthanolHCID 702—
Productethyl 2-[3-(N,N-diethylamino)propyl]-4-(3,4-dimethoxyphenyl)-6,7-dimethoxyquinoline-3-carboxylateHCID 1903236314%

Reaction Steps

A mixture of 2-amino-4,5,3',4'-tetramethoxybenzophenone hydrochloride (7.7 g), ethyl 6-(N,N-diethylamino)-3-oxohexanoate (5.0 g) and ethanol (100 ml) was stirred under reflux for 4 hours. The reaction mixture was concentrated under reduced pressure, and the residue was dissolved in chloroform. The chloroform layer was washed with an aqueous saturated solution of sodium bicarbonate and water and dried over magnesium sulfate, and the solvent was evaporated. The residue was subjected to column chromatography on silica gel. The fractions eluted with chloroform-methanol (20:1, v/v) gave ethyl 2-[3-(N,N-diethylamino)propyl]-4-(3,4-dimethoxyphenyl)-6,7-dimethoxyquinoline-3-carboxylate (1.51 g, 14%). This compound was recrystallized from ethanol-hexane. Colorless prisms, mp. 96°-98° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05650410
Source datasetuspto-grants-1997_07
ORD IDord-b2f55d19a0fb4d078104a328740f906a
Source noteuspto-grants-1997_07