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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244841Generated: October 28, 2026

3-{2-(2-methoxyethyl)-1-[3-(2-oxopyrrolidin-1-yl)propyl]-1H-imidazo[4,5-c]quinolin-8-yl}-N,N-dimethylprop-2-enamide → 3-{2-(2-methoxyethyl)-1-[3-(2-oxopyrrolidin-1-yl)propyl]-1H-imidazo[4,5-c]quinolin-8-yl}-N,N-dimethylpropanamide

https://huagongshe.com/reaction/244841

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-{2-(2-methoxyethyl)-1-[3-(2-oxopyrrolidin-1-yl)propyl]-1H-imidazo[4,5-c]quinolin-8-yl}-N,N-dimethylprop-2-enamideHCID 69082294—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product3-{2-(2-methoxyethyl)-1-[3-(2-oxopyrrolidin-1-yl)propyl]-1H-imidazo[4,5-c]quinolin-8-yl}-N,N-dimethylpropanamideHCID 69082300108.5%

Reaction Conditions

Temperature50 °C

Reaction Steps

A glass Parr vessel was charged with 10% palladium on carbon (0.07 g), methanol (50 mL) and 3-{2-(2-methoxyethyl)-1-[3-(2-oxopyrrolidin-1-yl)propyl]-1H-imidazo[4,5-c]quinolin-8-yl}-N,N-dimethylprop-2-enamide (0.66 g, 1.47 mmol). The vessel was evacuated and charged with hydrogen gas (40 psi, 2.8×105 Pa). The mixture was shaken at 50° C. for approximately 72 hours. The reaction mixture was cooled to ambient temperature and filtered. The filtrate was concentrated under reduced pressure to provide 720 mg of crude 3-{2-(2-methoxyethyl)-1-[3-(2-oxopyrrolidin-1-yl)propyl]-1H-imidazo[4,5-c]quinolin-8-yl}-N,N-dimethylpropanamide as a white semi-solid. MS (ESI) m/z 452 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658666B2
Source datasetuspto-grants-2014_02
ORD IDord-05921736f5d54d52afacd06e9e1ab7ae
Source noteuspto-grants-2014_02