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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721178Generated: October 31, 2026

Ethyl Acetate → 4-[3-(7-Bromo-2-quinolinylmethoxy)phenylamino]-2,2-diethyl-4-oxobutanoic acid

https://huagongshe.com/reaction/1721178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant3-AminophenolHCID 11568—
ReactantSodium hydrideHCID 24758—
Reactant7-Bromo-2-(chloromethyl)quinolineHCID 22416915—
Reactant3-(7-Bromo-2-quinolinylmethoxy)anilineHCID 22416920—
SolventDimethylformamideHCID 6228—
Product4-[3-(7-Bromo-2-quinolinylmethoxy)phenylamino]-2,2-diethyl-4-oxobutanoic acidHCID 22416879—

Reaction Steps

3-(7-bromo-2-quinolinylmethoxy)aniline: 0.32 g of NaH (95%) is added at 0° to a solution of 1.38 g of 3-aminophenol in 30 ml of DMF and then the batch is stirred for 30 min. at 0°. 3.2 g of 2-chloromethyl-7-bromo-quinoline in solid form are then added thereto and the batch is stirred for a further one hour at 0° and for another hour at 20°. It is then diluted with ethyl acetate, washed with water, dried over Na2SO4 and concentrated by evaporation. The evaporation residue is chromatographed on 250 g of silica gel. The product-containing fractions eluted with toluene/ethyl acetate 95:5 are combined and concentrated by evaporation to give the title compound which is further purified by crystallisation from CH2Cl2 /ether/hexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05508408
Source datasetuspto-grants-1996_04
ORD IDord-4a3012371141420d9b0a407a16e1fab2
Source noteuspto-grants-1996_04