Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 395294Erstellt: 26. Oktober 2026

Triethylamine → Tasquinimod

https://huagongshe.com/reaction/395294

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktThionyl ChlorideHCID 24386—
EduktN-Methyl-4-(trifluoromethyl)anilineHCID 15099755—
Edukt3-Quinolinecarboxylic acid, 1,2-dihydro-4-hydroxy-5-methoxy-1-methyl-2-oxo-HCID 54703582—
LösungsmittelDichloromethaneHCID 6344—
ProduktTasquinimodHCID 5468287665,4%

Reaktionsschritte

To an ice-cold solution of 1,2-dihydro-4-hydroxy-5-methoxy-1-methyl-2-oxo-quinoline-3-carboxylic acid (8 g, 0.032 mol), triethylamine (15.5 ml, 0.11 mol) and 4-trifluoromethyl-N-methylaniline (6.1 g, 0.035 mol) in 150 ml of dichloromethane, a solution of thionyl chloride (3.0 ml, 0.042 mol) in 10 ml of dichloromethane was added dropwise during 0.5 hours. The stirring was continued at 4° C. for 4 hours. The solution was diluted with 10 ml of dichloromethane, washed with cold 1 M sulfuric acid and then extracted with 1 M sodium hydroxide. The pH of the aqueous phase was adjusted to 8-8.5, and the aqueous solution was clarified by filtration and then acidified with hydrochloric acid to pH 4. On standing a crystalline precipitate was formed which was filtered off, washed with water and dried to give the title compound (8.5 g), yield 65%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06605616B1
Quelldatensatzuspto-grants-2003_08
ORD IDord-8fb59ffbbf8c4d6fbc1decf11f051f76
Quellennotizuspto-grants-2003_08