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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387867Generated: October 31, 2026

Diisopropylethylamine → [4-(3-Fluoro-4-nitrophenoxy)-7-methoxyquinolin-6-yl]carbamic acid benzyl ester

https://huagongshe.com/reaction/387867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Fluoro-4-nitrophenolHCID 520948—
Reactant(4-Chloro-7-methoxyquinolin-6-yl)carbamic acid benzyl esterHCID 58931435—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product[4-(3-Fluoro-4-nitrophenoxy)-7-methoxyquinolin-6-yl]carbamic acid benzyl esterHCID 589312618.8%

Reaction Conditions

Temperature130 °C

Reaction Steps

(4-Chloro-7-methoxyquinolin-6-yl)carbamic acid benzyl ester (1.58 g) was added to 1-methyl-2-pyrrolidone (5 ml), and then 3-fluoro-4-nitrophenol (0.87 g) and N,N-diisopropylethylamine (1.2 ml) were added and the mixture was heated and stirred at 130° C. for 6 hours. The reaction solution was poured into saturated aqueous sodium bicarbonate and extracted with ethyl acetate, and the organic layer was washed with saturated saline and dried over magnesium sulfate. The organic layer was concentrated and the obtained residue was subjected to NH silica gel column chromatography for elution with a solvent (ethyl acetate) to obtain the title compound (188 mg) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372981B2
Source datasetuspto-grants-2013_02
ORD IDord-b593e303039b460299f8abd9dfe29e23
Source noteuspto-grants-2013_02