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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 561834Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/561834

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—
Edukt2,6-Dichloro-N-cyclopropylisonicotinamideHCID 21510026—
KatalysatorPalladium bromide (PdBr2)HCID 83469—
LösungsmittelDimethylformamideHCID 6228—
ProduktN-Cyclopropyl-2,6-bis[(1E)-3-methoxyprop-1-en-1-yl]isonicotinamideHCID 66761510—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a solution of 2,6-dichloro-N-cyclopropylisonicotinamide from Amine 41, Step 1 (I eq.) in DMF (0.08 M) was added (2-[(1E)-3-methoxyprop-1-en-1-yl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (2.7 eq.), palladium bromide (5% loading), triphenylphosphine (10% loading) and sodium carbonate (2 M aqueous solution, 5 eq.). The resulting suspension was heated at 100° C. for 8 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 red oil. Purification by way of column chromatography (SiO2, 1:1 (v/v) Hex:EtOAc) afforded the title compound as a yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08063105B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-577ce0bfa216420d91f2772d3771d42c
Quellennotizuspto-grants-2011_11