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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 749253Erstellt: 25. Oktober 2026

Diisopropylethylamine → 3-(4-{[6-({2-Hydroxy-2-[5-hydroxy-6-(hydroxymethyl)pyridin-2-yl]ethyl}amino)hexyl]oxy}butyl)benzenesulfonamide formate

https://huagongshe.com/reaction/749253

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
EduktBenzenesulfonamide, 3-[4-[(6-bromohexyl)oxy]butyl]-HCID 21895438—
Edukt2-amino-1-(2-phenyl-4H-[1,3]dioxino[5,4-b]pyridin-6-yl)ethanolHCID 68866033—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-(4-{[6-({2-Hydroxy-2-[5-hydroxy-6-(hydroxymethyl)pyridin-2-yl]ethyl}amino)hexyl]oxy}butyl)benzenesulfonamide formateHCID 6932146922,1%

Reaktionsschritte

A stirred solution of 2-amino-1-(2-phenyl-4H-[1,3]dioxino[5,4-b]pyridin-6-yl)ethanol (100 mg) (EP220054A2), diisopropylethylamine (0.08 ml) and 3-{4-[(6-bromohexyl)oxy]butyl}benzenesulfonamide (120 mg) in N,N-dimethylformamide (2 ml) under nitrogen was heated to 50° for 18 h. The mixture was cooled to 20° and the solvent evaporated in vacuo. The residue was dissolved in acetic acid (4 ml) and water (2 ml) and was heated to 70° for 18 h. The mixture was cooled to 20°, the solvent evaporated in vacuo and the residue purified by mass-directed autopreparative HPLC to give the title compound (22 mg). LCMS RT=2.23 min, ES+ve 496 (MH)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07402598B2
Quelldatensatzuspto-grants-2008_07
ORD IDord-d11b74b3a7094aacb354d613d9c0fa96
Quellennotizuspto-grants-2008_07