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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 432619Erstellt: 26. Oktober 2026

3,4-Bis(4-methoxyphenyl)-6-chloropyridazine → 3,4-Bis(4-methoxyphenyl)-6-phenylpyridazine

https://huagongshe.com/reaction/432619

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3,4-Bis(4-methoxyphenyl)-6-chloropyridazineHCID 12568084—
EduktWater methylene chlorideHCID 21908982—
EduktHCID 178418255HCID 178418255—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelBenzeneHCID 241—
Produkt3,4-Bis(4-methoxyphenyl)-6-phenylpyridazineHCID 1211384236,9%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

3,4-Bis(4-methoxyphenyl)-6-chloropyridazine [Eur. J. Med. Chem.-Chimica Therapeutica, 14, 53-60 (1979)] (309.3 mg, 0.95 mmol) was dissolved in benzene (2 ml). Tetrakis(triphenylphosphine)palladium [Pd(Ph3P)4] (90.6 mg, 0.08 mmol) and phenylmagnesium bromide (1.0 M tetrahydrofuran solution) (1.5 ml) were then added successively, followed by stirring at 60° C. for 75 minutes. After water-methylene chloride was added to the reaction mixture, the mixture was extracted with methylene chloride and the organic layer was dried over anhydrous sodium sulfate. The solvent was distilled off and the residue was then separated and purified by chromatography on a silica gel column [silica gel (40 g), hexane/ethyl acetate (2/1)], whereby the title compound was obtained as a pale yellow amorphous solid (129 mg, 36.9%)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06664256B1
Quelldatensatzuspto-grants-2003_12
ORD IDord-b3638a0bd3904b26a3442cfa33b7aabb
Quellennotizuspto-grants-2003_12