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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 400496Erstellt: 25. Oktober 2026

3-[(2-Fluorophenyl)sulfamoyl]benzoic acid → N-(2-fluorophenyl)-3-[(8aR)-hexahydropyrrolo[1,2-a]pyrazin-2(1H)-ylcarbonyl]benzenesulfonamide

https://huagongshe.com/reaction/400496

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-[(2-Fluorophenyl)sulfamoyl]benzoic acidHCID 2318073—
Edukt(8aR)-Octahydropyrrolo(1,2-a)pyrazineHCID 7004239—
Lösungsmittel2-MethyltetrahydrofuranHCID 7301—
LösungsmittelDimethylacetamideHCID 31374—
ProduktN-(2-fluorophenyl)-3-[(8aR)-hexahydropyrrolo[1,2-a]pyrazin-2(1H)-ylcarbonyl]benzenesulfonamideHCID 46853381—

Reaktionsschritte

To a mixture of 3-{[(2-fluorophenyl)amino]sulfonyl}benzoic acid (800 mg, 2.71 mmol) and 2-(3H-[1,2,3]triazolo[4,5-h]pyridin-3-yl)-1,1,3,3-tetramethylisouronium hexafluorophosphate(V) (1133 mg, 2.98 mmol) in N,N-dimethylacetamide (6.5 mL) and 2-methyltetrahydrofuran (19.5 mL) was added (R)-octahydropyrrolo[1,2-a]pyrazine (479 mg, 3.79 mmol). The reaction was stirred at room temperature for 3 hours, diluted with 2-methyltetrahydrofuran (5 mL), and washed with saturated bicarbonate (2×25 mL). The combined aqueous layers were adjusted to pH 7 with buffer and re-extracted with 2-methyltetrahydrofuran (3×15 mL). The combined organic layers were concentrated under reduced pressure. The residue was taken up in ethanol (25 mL) and concentrated to give the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08741899B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-6e4348d19e1f49dea3c43bce0d0e1878
Quellennotizuspto-grants-2014_06