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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 407607Erstellt: 25. Oktober 2026

Cesium carbonate → 2-(6-(tert-butyl)-8-fluoro-1-oxophthalazin-2(1H)-yl)-6-chlorobenzaldehyde

https://huagongshe.com/reaction/407607

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCesium carbonateHCID 10796—
EduktEthoxytrimethylsilaneHCID 15772—
Edukt2-Chloro-6-fluorobenzaldehydeHCID 67847—
Edukt6-(tert-Butyl)-8-fluorophthalazin-1(2H)-oneHCID 59473765—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-(6-(tert-butyl)-8-fluoro-1-oxophthalazin-2(1H)-yl)-6-chlorobenzaldehydeHCID 5947382852%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

To a 10 mL round bottom flask were added 6-tert-butyl-8-fluoro-2H-phthalazin-1-one 101h (640 mg, 2.9 mmol), 2-chloro-6-fluorobenzaldehyde (506 mg, 3.2 mmol), and cesium carbonate (488 mg, 1.5 mmol). The flask was evacuated and backfilled with nitrogen three times then ethoxytrimethylsilane (684 mg, 5.8 mmol) and DMF (5 mL) were added to the reaction flask. The resulting mixture was heated to 60° C. After 4 h of stirring, the solution was allowed to cool down to ambient temperature and the reaction was quenched by addition of 2 mL of H2O drop-wise. The desired product started to precipitate from the DMF and water mixture. The solid was collected by filtration after cooling down to 5° C., and washed with DMF/water (2/1, 2 mL, pre-cooled to 6° C.) and H2O (2 mL). The filter cake was dried under vacuum oven at 65° C. for overnight to afford 519 mg (52%) of 101i as a yellow solid. MS: [M+H]+: 359

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08754077B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-3593461688bb4cb6901edf0687b528aa
Quellennotizuspto-grants-2014_06