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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 537662Erstellt: 25. Oktober 2026

Sulfathiazole → Succinylsulfathiazole

https://huagongshe.com/reaction/537662

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfathiazoleHCID 5340—
EduktSuccinic anhydrideHCID 7922—
EduktTriethylamineHCID 8471—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktSuccinylsulfathiazoleHCID 531567%

Reaktionsschritte

Compound 27j was synthesized by the method outlined in FIG. 1. Briefly, Compound 27j was synthesized by first complexing succinic anhydride with sulfathiazole by reacting these compounds at room temperature for 6 hours in tetrahydrofuran (THF) in the presence of triethylamine (TEA) to produce succinylsulfathiazole as a white solid (67% yield). The succinylsulfathiazole was then reacted for 2 hours at room temperature with O—(N-succinimidyl)-1,1,3,3-tetramethyluronium tetrafluoroborate (TSTU) in dichloromethane in the presence of TEA to produce the corresponding succinimidyl ester, which was reacted with 1-(4-aminobutyl)-2-{1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl}acetamide in dichloromethane in the presence of TEA at room temperature for 16 hours to produce Compound 27j as a yellow gummy mass (45% yield). Compound 27j was characterized by NMR, two-dimensional NMR, and mass spectroscopy.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08865130B2
Quelldatensatzuspto-grants-2014_10
ORD IDord-8fd6deb09784415188ca734f94fbc50f
Quellennotizuspto-grants-2014_10