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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1363462Generated: October 30, 2026

N-Ethylaniline → Laquinimod

https://huagongshe.com/reaction/1363462

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-EthylanilineHCID 7670—
ReactantHeptaneHCID 8900—
ReactantHCID 54680901HCID 54680901—
SolventMethanolHCID 887—
ProductLaquinimodHCID 5467794698%

Reaction Steps

Laquinimod acid was prepared according to the method described in U.S. Pat. No. 6,875,869: 5-Chloro-1,2-dihydro-4-hydroxy-1-methyl-2-oxo-quinoline-3-carboxylic acid methyl ester (3.0 g), N-ethylaniline (2 eq 2-2.88 ml), and heptane (60 ml) were heated and the volatiles, mainly heptane and formed methanol, (32 ml) distilled off during 6 hours and 35 minutes. After cooling to room temperature the crystalline suspension was filtered and the crystals were washed with heptane and dried in vacuum to yield laquinimod acid (3.94 g, 98%) as white to off-white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07884208B2
Source datasetuspto-grants-2011_02
ORD IDord-d9b14485551f40dc8eb5b258169096c9
Source noteuspto-grants-2011_02