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HRID 1029138Erstellt: 25. Oktober 2026

Hydrochloric Acid → 2,3-Dichloro-N-[4-(6-oxo-5,6-dihydro-benzo[c][1,8]naphthyridin-1-yloxy)-phenyl]-benzenesulfonamide

https://huagongshe.com/reaction/1029138

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktTriethylamineHCID 8471—
Edukt2,3-Dichlorobenzene-1-sulfonyl chlorideHCID 2734222—
Edukt1-(4-Amino-phenoxy)-5H-benzo[c][1,8]naphthyridin-6-oneHCID 58168367—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt2,3-Dichloro-N-[4-(6-oxo-5,6-dihydro-benzo[c][1,8]naphthyridin-1-yloxy)-phenyl]-benzenesulfonamideHCID 4420528917,1%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

Compound 137 (50 mg, 0.16 mmol), 2,3-dichloro-benzenesulfonyl chloride (45 mg, 0.18 mmol), and Et3N (0.07 mL, 0.49 mmol) were suspended in dioxane (2 mL), and stirred overnight at 80° C. The reaction mixture was acidified with 1M HCl, 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 25 to 100% EtOAc in hexanes to provide 173 (14 mg, 17% yield) as a white solid. LC-MS (M+H=512, obsd.=512).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08735584B2
Quelldatensatzuspto-grants-2014_05
ORD IDord-5a82d64b1cd24b8099be0897252ba853
Quellennotizuspto-grants-2014_05