Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917675Generated: October 25, 2026

Acetic Acid → 1-(6-Methylpyridin-2-YL)-2-(quinolin-6-YL)ethanone

https://huagongshe.com/reaction/917675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant6-ChloroquinolineHCID 69163—
Reactant2-Acetyl-6-methylpyridineHCID 138872—
ReactantPotassium tert-butoxideHCID 23665647—
Catalystpalladium(II) acetateHCID 167845—
Catalyst2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 2734217—
SolventTetrahydrofuranHCID 8028—
Product1-(6-Methylpyridin-2-YL)-2-(quinolin-6-YL)ethanoneHCID 6888420378.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 6-chloro-quinoline (2.08 g, 12.3 mmol) in tetrahydrofuran (50 mL) was added 1-(6-methyl-pyridin-2-yl)-ethanone (2.0 g, 14.8 mmol, 1.1 equiv), palladium acetate (0.055 g, 0.25 mmol, 0.02 equiv), 2-dicyclohexylphosphino-2′-(N,N-dimethylamino)biphenyl (0.197 g, 0.50 mmol, 0.04 equiv), and potassium tert-butoxide (3.76 g, 30.75 mmol, 2.2 equiv). The resulting reaction mixture was heated to 80° C. for 18 hours, then cooled down to 20° C., and slowly treated with acetic acid (3 mL). The resulting solids were filtered off, and the mother liquor was concentrated in vacuo. Silica gel chromatography (3:1 hexane/acetone) yielded 1-(6-Methyl-pyridin-2-yl)-2-quinolin-6-yl-ethanone (2.52 g, 78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07273936B2
Source datasetuspto-grants-2007_09
ORD IDord-aded6d5236e449bebd3106f19a3e1ef9
Source noteuspto-grants-2007_09