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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966293Generated: October 29, 2026

Methyl iodide → 6-(2-Methoxyphenyl)-5-[(pyrrolidin-1-yl)carbonyl]-2,2,4-trimethyl-1,2-dihydroquinoline

https://huagongshe.com/reaction/1966293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant6-(2-Hydroxyphenyl)-5-[(pyrrolidin-1-yl)carbonyl]-2,2,4-trimethyl-1,2-dihydroquinolineHCID 58026934—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product6-(2-Methoxyphenyl)-5-[(pyrrolidin-1-yl)carbonyl]-2,2,4-trimethyl-1,2-dihydroquinolineHCID 5802711863.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 6-(2-hydroxyphenyl)-5-[(pyrrolidin-1-yl)carbonyl]-2,2,4-trimethyl-1,2-dihydroquinoline (Compound No. 8-1, 65.0 mg, 0.179 mmol), methyl iodide (11.1 μL, 0.178 mmol) and potassium carbonate (49.5 mg, 0.358 mmol) was suspended in anhydrous N,N-dimethylformamide (1.5 mL), and the reaction mixture was stirred at 50° C. overnight. After cooling down, it was diluted with ethyl acetate (100 mL). The whole was washed with water (100 mL) and saturated brine (50 mL) successively, dried over anhydrous magnesium sulfate, and then the solvent was removed under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give the titled compound (42.5 mg) as a colorless solid. (Yield 63%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420635B2
Source datasetuspto-grants-2013_04
ORD IDord-3175e5b434e5469583ef10be1463f28d
Source noteuspto-grants-2013_04