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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795753Generated: October 27, 2026

Triethylamine → 2-[(8-Difluoromethoxyquinolin-5-yl)carbonyl]-4,4,6,6-tetramethylcyclohexane-1,3,5-trione

https://huagongshe.com/reaction/1795753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,2,4,4-Tetramethylcyclohexane-1,3,5-trioneHCID 11769166—
Reactant8-Difluoromethoxy-5-quinolinecarboxylic acidHCID 22179190—
CatalystTrimethylsilyl cyanideHCID 82115—
SolventAcetonitrileHCID 6342—
Product2-[(8-Difluoromethoxyquinolin-5-yl)carbonyl]-4,4,6,6-tetramethylcyclohexane-1,3,5-trioneHCID 22179179—

Reaction Conditions

Temperature25 °C

Reaction Steps

0.4 g (1.7 mmol) of 8-difluoromethoxy-5-quinolinecarboxylic acid was dissolved in 20 ml of acetonitrile, 0.4 g (1.9 mmol) of N,N-dicyclohexylcarbodiimide and 0.3 g (1.7 mmol) of 2,2,4,4-tetramethylcyclohexane-1,3,5-trione were added and the mixture was stirring at 25° C. for 20 hours. 0.4 g (4.0 mmol) of triethylamine and 2 drops of trimethylsilyl cyanide were then added, and stirring was continued at 30–35° C. for a further 3 hours. The precipitate was filtered off, and the filtrate was concentrated, 20 ml of 5% strength potassium carbonate solution were added and the mixture was washed with methyl tert-butyl ether. The aqueous phase was subsequently adjusted to pH 3 using concentrated hydrochloric acid and extracted with ethyl acetate. The solvent was removed and the residue was chromatographed over silica gel (mobile phase: methylene chloride/methanol). This gave 0.2 g of a colorless powder;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07030063B1
Source datasetuspto-grants-2006_04
ORD IDord-0d8b37eaa90146c9a1e1735757c7949d
Source noteuspto-grants-2006_04