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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1470323Generated: November 2, 2026

N-Ethylaniline → Laquinimod

https://huagongshe.com/reaction/1470323

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-EthylanilineHCID 7670—
ReactantTriphenylphosphine dichlorideHCID 260420—
Reactant5-Chloro-4-hydroxy-1-methyl-2-oxo-1,2-dihydroquinoline-3-carboxylic acidHCID 54720227—
SolventChloroformHCID 6212—
ProductLaquinimodHCID 5467794692.1%

Reaction Conditions

Temperature27.5 °C

Reaction Steps

N-Ethyl aniline (5.2 gm) was taken in chloroform (100 ml) and stirred for 10 minutes at 25-30° C. under nitrogen atmosphere. The resulting mass was followed by the addition of dichlorotriphenyl phosphorane (26.6 gm) at 25-30° C. and the reaction mixture was stirred for 15 minutes. 1,2-Dihydro-4-hydroxy-5-chloro-1-methyl-2-oxo-quinoline-3-carboxylic acid (10 gm) was added to the resulting mass at 25-30° C. followed by heating to reflux (40-45° C.) and then stirred for 3 hours at reflux. Chloroform was distilled out from the reaction mass under vacuum at below 55° C. The resulting residue was cooled to 25-30° C., followed by the addition of ethyl acetate (50 ml) and water (50 ml) at 25-30° C. and the resulting mixture was stirred for 30 minutes at 25-30° C. The separated solid was filtered, washed with water and then dried to yield 12.95 gm of laquinimod (HPLC purity: 99.24%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006443B2
Source datasetuspto-grants-2015_04
ORD IDord-c84554338c0c4479b5e19cc8f1e7397e
Source noteuspto-grants-2015_04