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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440709Generated: October 26, 2026

8-Aminoquinoline → 1-Acetyl-N-(quinolin-8-yl)-4-piperidinecarboxamide

https://huagongshe.com/reaction/1440709

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-AminoquinolineHCID 11359—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Acetylpiperidine-4-carbonyl chloride hydrochlorideHCID 53430810—
SolventDimethylformamideHCID 6228—
Product1-Acetyl-N-(quinolin-8-yl)-4-piperidinecarboxamideHCID 1941984258.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 8-aminoquinoline (48.50 g) in dimethylformamide (300 ml) was stirred at 80° C., under nitrogen, as a mixture of 1-acetylpiperidine-4-carbonyl chloride hydrochloride (106.30 g) and potassium carbonate (93.0 g) was added in portions. The slurry was stirred at 80° C. overnight, quenched with water (1200 ml) and extracted with dichloromethane. The extracts were dried over anhydrous magnesium sulfate, filtered, and the filtrate was evaporated. The residue was purified first by high performance liquid chromatography (silica; 25:1 dichloromethane-methanol), followed by flash chromatography (silica; 50:1 dichloromethane-methanol). The appropriate fractions were collected and evaporated to give 58.5 g (58.6%) of product, as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05500423
Source datasetuspto-grants-1996_03
ORD IDord-32b67ffd99d94f81a0c82546cf166794
Source noteuspto-grants-1996_03