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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1057722Erstellt: 26. Oktober 2026

Ammonia → 1-(3-Phenoxyanilino)-4-(4-pyridylmethyl)phthalazine

https://huagongshe.com/reaction/1057722

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniaHCID 222—
Edukt(4-Aminophenoxy)benzeneHCID 8764—
Edukt1-Chloro-4-(4-pyridinylmethyl)phthalazineHCID 1944609—
LösungsmittelDichloromethane methanolHCID 21226129—
Produkt1-(3-Phenoxyanilino)-4-(4-pyridylmethyl)phthalazineHCID 22742003—

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

A mixture of 256 mg (1.00 mmol) 1-chloro-4-(4-pyridylmethyl)phthalazine and 556 mg (3.00 mmol) 4-phenoxyaniline (Aldrich) is heated for 2 h at 90° C. The melt is cooled and stirred with 6 ml NH3 solution (10% in water: or 10 ml sat. NaHCO3 solution) and 15 ml dichloromethane/methanol 50:1 for 30 min. The aqueous phase is then separated off and extracted again with dichloromethane. The organic phase is dried (Na2SO4), concentrated by evaporation, and chromatographed (SiO2; ethyl acetate→ethyl acetate/CH3OH, 19:1→10:1). Crystallization from acetonitrile yields the title compound: m.p.: 186-189° C.; Anal. calc. (C26H21N4O) C, 77.02%; H, 5.22%; N, 13.82%; found C, 77.2%; H, 4.9%; N, 13.8%. The starting material is prepared as follows:

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06514974B2
Quelldatensatzuspto-grants-2003_02
ORD IDord-ae489a8ae65d4ef0bb4ec17145bf7e5a
Quellennotizuspto-grants-2003_02