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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 49891Erstellt: 24. Oktober 2026

4-Aminobiphenyl → N-(4-phenylphenyl)-4-(pyridin-4-ylmethyl)phthalazin-1-amine

https://huagongshe.com/de/reaction/49891

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-AminobiphenylHCID 7102—
EduktTriethylamine hydrochlorideHCID 11130—
EduktPhosphorus oxide (P4O10)HCID 14812—
EduktCarbonate IonHCID 19660—
Edukt4-(4-Pyridylmethyl)-1(2H)-phtalazinoneHCID 789954—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethane methanolHCID 21226129—
ProduktN-(4-phenylphenyl)-4-(pyridin-4-ylmethyl)phthalazin-1-amineHCID 6419389—

Reaktionsbedingungen

Temperatur200 °C

Reaktionsschritte

A mixture of 2.41 g (16.98 mmol) phosphorus pentoxide, 2.32 g (16.85 mmol) triethylamine hydrochloride, 3 g (17.73 mmol) 4-aminobiphenyl, and 1 g (4.21 mmol) 4-(4-pyridylmethyl)-1(2H)-phthalazinone is stirred for 20 h at 200° C. under a nitrogen atmosphere. After cooling to RT, the hyalinocrystalline melt is distributed between a dichloromethane/methanol mixture (99:1) and a mixture of water and saturated aqueous carbonate solution on (1:1) with intensive stirring and the use of an ultrasonic bath. The organic phase dried over sodium sulfate is evaporated under vacuum and the residue purified by means of flash chromatography on silica gel with particle size 0.04-0.06 mm, using a dichloromethane/methanol mixture (49:1). Title compound is obtained after evaporation of the product-containing fractions under vacuum and recrystallization of the residue from acetonitrile; m.p. 189-191 °C.; ESI-MS: (M+H)+=389.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06710047B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-68d8d685ff174f3fb8764293eccc5175
Quellennotizuspto-grants-2004_03