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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1057681Erstellt: 25. Oktober 2026

3-Aminophenol → 1-(3-Hydroxyanilino)-4-(4-pyridylmethyl)phthalazine

https://huagongshe.com/reaction/1057681

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-AminophenolHCID 11568—
Edukt1-Chloro-4-(4-pyridinylmethyl)phthalazineHCID 1944609—
LösungsmittelAcetateHCID 175—
LösungsmittelMethanolHCID 887—
LösungsmittelPotassium CarbonateHCID 11430—
Produkt1-(3-Hydroxyanilino)-4-(4-pyridylmethyl)phthalazineHCID 6419391—

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

A mixture of 0.384 g (1.5 mmol) 1-chloro-4-(4-pyridylmethyl)phthalazine and 0.491 g (4.5 mmol) 3-aminophenol is heated under nitrogen atmosphere for 1 h at 90° C. and for 3 h at 120° C. The reaction mixture is then taken up in a mixture of 30 ml acetate and 20 ml 20% aqueous potassium carbonate solution while stirring for about 4 h, and the filtration material is digested for 20 min in 20 ml of boiling methanol. After cooling to RT, filtration, washing of the filter residue with methanol, and drying under HV (8 h, 130° C.), title compound is obtained with a water content of 1.94%; m.p. 217-219° C.; ESI-MS: (M+H)+=329.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06514974B2
Quelldatensatzuspto-grants-2003_02
ORD IDord-b8048b229dce442895d6fce30d189c6a
Quellennotizuspto-grants-2003_02