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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 407628Erstellt: 25. Oktober 2026

Cesium carbonate → 3-Bromo-5-(6-tert-butyl-8-fluoro-1-oxo-1,2-dihydrophthalazin-2-yl)pyridine-4-carbaldehyde

https://huagongshe.com/reaction/407628

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCesium carbonateHCID 10796—
Edukt3,5-Dibromo-4-pyridinecarboxaldehydeHCID 2762998—
Edukt4,7-Dimethoxy-1,10-phenanthrolineHCID 10462298—
Edukt6-(tert-Butyl)-8-fluorophthalazin-1(2H)-oneHCID 59473765—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt3-Bromo-5-(6-tert-butyl-8-fluoro-1-oxo-1,2-dihydrophthalazin-2-yl)pyridine-4-carbaldehydeHCID 8668392529,3%

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

A sealed tube equipped with a magnetic stirrer was charged with 6-tert-butyl-8-fluoro-1,2-dihydrophthalazin-1-one 101h (220 mg, 1.0 mmol), 3,5-dibromopyridine-4-carbaldehyde (530 mg, 2.0 mmol), CuI (190 mg, 1.0 mmol), 4,7-dimethoxy-1,10-phenanthroline (244 mg, 1.0 mmol), Cs2CO3 (652 mg, 2.0 mmol) and dioxane (8 mL). After three cycles of vacuum/argon flush, the mixture was heated at 110° C. for 5 h. It was then filtered and the filtrate was evaporated in vacuo. The residue was purified by silica gel column chromatography eluting with ethyl acetate/petroleum ether (1:3, V/V) to afford 109a (118 mg, 29.3%) as a solid. LCMS: [M+H]+ 406

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08754077B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-7f64fb5af8364cc8b54c3244a78fad26
Quellennotizuspto-grants-2014_06