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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 561832Erstellt: 25. Oktober 2026

Sodium Carbonate → N-Cyclopropyl-2-methoxy-6-[(1E)-3-methoxyprop-1-en-1-yl]isonicotinamide

https://huagongshe.com/reaction/561832

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CarbonateHCID 10340—
EduktTriphenylphosphineHCID 11776—
Edukt2-[(1E)-3-methoxyprop-1-en-1-yl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 16217443—
Edukt2-Chloro-N-cyclopropyl-6-methoxyisonicotinamideHCID 84580935—
KatalysatorPalladium bromide (PdBr2)HCID 83469—
LösungsmittelDimethylformamideHCID 6228—
ProduktN-Cyclopropyl-2-methoxy-6-[(1E)-3-methoxyprop-1-en-1-yl]isonicotinamideHCID 66760917—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a solution of 2-chloro-N-cyclopropyl-6-methoxyisonicotinamide from the previous step (1 eq.) in DMF (0.3 M) was added (2-[(1E)-3-methoxyprop-1-en-1-yl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (1 eq.), palladium bromide (5% loading), triphenylphosphine (10% loading) and sodium carbonate (2 M aqueous solution, 3 eq.). The resulting suspension was heated at 100° C. for 7 h. The reaction mixture was quenched with water and extracted with ether. The combined organic extracts were washed with sat. aq. NaHCO3 and brine. Drying over Na2SO4, filtration and concentration of the filtrate in vacuo afforded the crude product as a brown tar. Purification by way of column chromatography (SiO2, 1:1 (v/v) Hex:EtOAc) followed by recrystallization from Hex:ether afforded the title compound as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08063105B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-b9f2faf003814cd486e079bdd716ec80
Quellennotizuspto-grants-2011_11