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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678340Generated: October 30, 2026

Diisopropylethylamine → 6-[2-Methoxy-4-(2-methylpyridin-3-ylcarbonyloxy)phenyl]-5-(2-methoxyphenylaminomethyl)-2,2,4-trimethyl-1,2-dihydroquinoline

https://huagongshe.com/reaction/1678340

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Methylnicotinic acidHCID 643373—
ReactantHCID 25015626HCID 25015626—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product6-[2-Methoxy-4-(2-methylpyridin-3-ylcarbonyloxy)phenyl]-5-(2-methoxyphenylaminomethyl)-2,2,4-trimethyl-1,2-dihydroquinolineHCID 2479879965%

Reaction Steps

A mixture of 6-(4-hydroxy-2-methoxyphenyl)-5-(2-methoxyphenylaminomethyl)-2,2,4-trimethyl-1,2-dihydroquinoline (Reference Compound No. 4-1, 25.0 mg, mmol), 2-methylnicotinoic acid (8.0 mg, 0.058 mmol), N,N-diisopropylethylamine (20.2 μL, 0.116 mmol) and O-(7-azabenzotriazol-1-yl)-N,N,N,N-tetramethyluronium hexafluorophosphate (24.3 mg, mmol) was dissolved in anhydrous N,N-dimethylformamide (0.5 mL), and then the reaction mixture was stirred at room temperature overnight. The reaction mixture was diluted with ethyl acetate (70 mL). The mixture was washed with water (70 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 (20.7 mg) as a colorless solid. (Yield 65%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008498B2
Source datasetuspto-grants-2011_08
ORD IDord-b81692b0fd704e8ea28516374865cfcf
Source noteuspto-grants-2011_08