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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 658193Erstellt: 23. Oktober 2026

Stannous Chloride → 6-Amino-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzofuran-2-carboxamide

https://huagongshe.com/de/reaction/658193

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktStannous ChlorideHCID 24479—
EduktN-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-6-nitro-1-benzofuran-2-carboxamideHCID 59341358—
LösungsmittelDimethylformamideHCID 6228—
Produkt6-Amino-N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzofuran-2-carboxamideHCID 59341434—

Reaktionsschritte

15.0 ml (30 mmol) of a 2 M tin(II) chloride solution in DMF are added to N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-6-nitro-1-benzofuran-2-carboxamide (1550 mg, 4.92 mmol). The mixture is stirred overnight. The solvent is removed under reduced pressure using a rotary evaporator. The crude product is taken up in methanol and, together with acidic ion exchange resin (Dowex WX2-200), shaken for about 1 h. The loaded ion exchanger is washed with methanol, then with water, DMF, again with methanol, with dichloromethane and finally again with methanol. The product is eluted with methanol/triethylamine 95:5. The solvent is removed under reduced pressure using a rotary evaporator. The crude product is purified on silica gel 60 (mobile phase: dichloromethane/triethylamine 100:1→dichloro-methane/methanol/triethylamine 100:1:1→dichloromethane/methanol/triethylamine 90:10:1). 643 mg (46% of theory) of the title compound are isolated.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08076355B2
Quelldatensatzuspto-grants-2011_12
ORD IDord-6281bb043fa5453c8000b70327066ec7
Quellennotizuspto-grants-2011_12