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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 49884Erstellt: 24. Oktober 2026

3-Chloro-4-fluoroaniline → 1-(3-Chloro-4-fluoroanilino)-4-(4-pyridylmethyl)phthalazine

https://huagongshe.com/de/reaction/49884

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Chloro-4-fluoroanilineHCID 9708—
EduktTriethylamine hydrochlorideHCID 11130—
EduktSodium HydroxideHCID 14798—
EduktPhosphorus oxide (P4O10)HCID 14812—
Edukt4-(4-Pyridylmethyl)-1(2H)-phtalazinoneHCID 789954—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produkt1-(3-Chloro-4-fluoroanilino)-4-(4-pyridylmethyl)phthalazineHCID 9799193—

Reaktionsbedingungen

Temperatur200 °C

Reaktionsschritte

A mixture of 1.42 g (10 mmol) phosphorus pentoxide, 1.38 g (10 mmol) triethylamine hydrochloride, and 1.46 g (10 mmol) 3-chloro-4-fluoroaniline is heated and stirred in a nitrogen atmosphere at 200° C. until a homogeneous melt has formed. To the melt, 0.593 g (2.5 mmol) 4-(4-pyridylmethyl)-1(2H)-phthalazinone is added and the reaction mixture stirred for a further 3 h at 200° C. After cooling to RT, the hyalinocrystalline reaction mixture is distributed between 150 ml dichloromethane and a mixture of 10 ml water and 20 ml 2N sodium hydroxide solution with intensive stirring and sonication. The organic phase washed with water and dried over sodium sulfate is concentrated by evaporation and the residue recrystallized from acetate. Title compound is obtained after a second recrystallization from methanol/water and drying under HV (8 h at 100° C.); m.p. 185-187° C.; ESI-MS: (M+H)+=365.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06710047B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-8dbc3bce22d84d228a83e727e949ad00
Quellennotizuspto-grants-2004_03