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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1029139Erstellt: 27. Oktober 2026

Potassium Carbonate → N-(2-Hydroxy-ethyl)-4-(6-oxo-5,6-dihydro-benzo[c][1,8]naphthyridin-1-yl)-benzenesulfonamide

https://huagongshe.com/reaction/1029139

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
Edukt(4-(N-(2-Hydroxyethyl)sulfamoyl)phenyl)boronic acidHCID 44119332—
Edukt1-Chlorobenzo[C][1,8]naphthyridin-6(5H)-oneHCID 58168008—
Katalysatorpalladium(II) acetateHCID 167845—
Lösungsmittel1,4-Dioxane--water (1/1)HCID 21886435—
LösungsmittelWater ethylacetateHCID 22728543—
ProduktN-(2-Hydroxy-ethyl)-4-(6-oxo-5,6-dihydro-benzo[c][1,8]naphthyridin-1-yl)-benzenesulfonamideHCID 698154934%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

Compound 83 (100 mg, 0.43 mmol), 4-(2-hydroxyethylsulfamoyl)phenylboronic acid (212 mg, 0.87 mmol), Pd(OAc)2 (5 mg, 0.02 mmol), S-Phos (18 mg, 0.04 mmol), and K2CO3 (299 mg, 2.17 mmol) were dissolved in dioxane/H2O (2.2 mL, 10/1, v/v), and stirred overnight at 100° C. The reaction mixture was diluted with H2O/EtOAc, and filtered through an Extrelut column. The column was washed with EtOAc, and the filtrate was concentrated. The crude product was purified via Biotage eluting with a gradient of 0 to 10% MeOH in CH2Cl2. The resulting material was triturated with MeOH, filtered, and dried under vacuum to provide 174 (6 mg, 4% yield) as a light-yellow solid. LC-MS (M+H=396, obsd.=396).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08735584B2
Quelldatensatzuspto-grants-2014_05
ORD IDord-56f590d7ee3541859663f9c58e2073c2
Quellennotizuspto-grants-2014_05