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HRID 1774722Erstellt: 25. Oktober 2026

Dimethylformamide → 2,2-Dimethyl-N-[5-(1-methyl-2-oxo-1,2,3,4-tetrahydro-quinolin-6-yl)-pyridin-3-yl]-propionamide

https://huagongshe.com/reaction/1774722

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktSodium CarbonateHCID 10340—
EduktN-(5-Bromo-pyridin-3-yl)-2,2-dimethyl-propionamideHCID 24229189—
Edukt1-methyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroquinolin-2(1H)-oneHCID 72208233—
KatalysatorDichlorobis(triphenylphosphine)palladiumHCID 6102075—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2,2-Dimethyl-N-[5-(1-methyl-2-oxo-1,2,3,4-tetrahydro-quinolin-6-yl)-pyridin-3-yl]-propionamideHCID 8667910474,3%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

A microwave vial was charged with N-(5-bromopyridin-3-yl)pivalamide (0.2 g, 0.778 mmol), 1-methyl-6-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-3,4-dihydro-1H-quinolin-2-one (intermediate A-1) (0.246 g, 0.856 mmol) and DMF (4 mL). The reaction mixture was purged with Argon; then, bis(triphenylphosphine)palladium(II)chloride (0.055 g, 0.078 mmol), followed by 1N aqueous Na2CO3 solution (2.33 mL, 2.33 mmol) were added and the reaction was heated in the microwave at 120° C. for 5 min. The reaction mixture was diluted with EtOAc, filtered through Dicalite and washed with EtOAc (2×20 mL). The resulting filtrate was washed with brine, dried over Na2SO4, filtered and evaporated to dryness. The residue was purified by silica gel flash chromatography eluting with a 0 to 5% MeOH-DCM gradient to give the title compound (0.195 g, 74%) as a white solid. MS: 338.2 (M+H+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09260408B2
Quelldatensatzuspto-grants-2016_02
ORD IDord-332363a642e24ff38ae63dd309fe91f7
Quellennotizuspto-grants-2016_02