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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 271963Erstellt: 23. Oktober 2026

Diisopropylamine → 5-(2,3-Difluorophenyl)-1-(2-methoxyethyl)-3-nitropyridin-2(1H)-one

https://huagongshe.com/de/reaction/271963

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylamineHCID 7912—
Edukt(2,3-Difluorophenyl)boronic acidHCID 2734333—
EduktTrisodium 3,3',3''-phosphinetriyltris(benzene-1-sulphonate)HCID 6099338—
Edukt5-Bromo-1-(2-methoxyethyl)-3-nitropyridin-2(1H)-oneHCID 22293279—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkt5-(2,3-Difluorophenyl)-1-(2-methoxyethyl)-3-nitropyridin-2(1H)-oneHCID 2229317359,7%

Reaktionsschritte

Palladium acetate (41.0 mg, 0.18 mmol) was added to a solution of 5-bromo-1-(2-methoxyethyl)-3-nitropyridin-2(1H)-one (500 mg, 1.81 mmol), 2,3-difluorophenyl boronic acid (570 mg, 3.61 mmol), diisopropylamine (0.759 mL, 5.41 mmol) and 3,3′,3″-phosphinidynetris(benzenesulfonic acid) trisodium salt (310 mg, 0.541 mmol), in N,N-dimethylformamide (15 mL) and water (5 mL) and heated to 80° C. After 2 h, the mixture was allowed to cool to ambient temperature and filtered. Purification by reverse phase HPLC (C-18, 95% water/acetonitrile→5% water/acetonitrile with 0.1% trifluoroacetic acid) gave the title compound (335mg). MS 311 (M+1). 1H NMR (500 MHz, CDCl3) δ 8.56 (d, J=2.7 Hz, 1H), 8.03 (d, J=2.4 Hz, 1H), 7.23-7.18 (m, 2H), 7.15-7.12 (m, 1H), 4.33 (t, J=4.8 Hz, 2H), 3.74 (t, J=4.8 Hz, 2H), 3.35 (s, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07452903B2
Quelldatensatzuspto-grants-2008_11
ORD IDord-f6745fbe17ca470d8269988cd63aae8a
Quellennotizuspto-grants-2008_11