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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911772Generated: November 1, 2026

Water → 2-((Cyclobutylmethyl)(ethyl)amino)-8-methylquinoline-3-carbaldehyde

https://huagongshe.com/reaction/1911772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-8-methylquinoline-3-carboxaldehydeHCID 689082—
Reactant(Cyclobutylmethyl)(ethyl)amineHCID 23366322—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product2-((Cyclobutylmethyl)(ethyl)amino)-8-methylquinoline-3-carbaldehydeHCID 5748684275%

Reaction Steps

Potassium carbonate (0.62 g, 4.5 mmol) was added to a solution of 2-chloro-8-methyl-quinoline-3-carbaldehyde (0.45 g, 2.2 mmol) and cyclobutylmethyl-ethyl-amine (0.47 g, 4.1 mmol) in anhydrous dimethyl formamide (5 mL) under nitrogen. After stirring for 0.5 h at RT, the reaction mixture was heated for 20 h at 80-95° C. Thereafter, the reaction was cooled to RT, water (30 mL) and ethyl acetate (30 mL) were added, and the organic layer was separated from the aqueous mixture. The organic extract was washed with brine, dried over sodium sulfate and the solvent was evaporated in vacuo. The residue was purified by chromatography using silica gel to afford the title compound as a pale yellow liquid (0.46 g, 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604055B2
Source datasetuspto-grants-2013_12
ORD IDord-bdfbe09040d94836af576c32d8a12371
Source noteuspto-grants-2013_12