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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1401902Erstellt: 24. Oktober 2026

Trifluoroacetic acid → 4-(2-azetidin-3-yl-4-chlorophenoxy)-5-chloro-N-(5-chloro-1,3-thiazol-2-yl)-2-fluorobenzenesulfonamide

https://huagongshe.com/de/reaction/1401902

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrifluoroacetic acidHCID 6422—
EduktTert-butyl 3-(5-chloro-2-hydroxyphenyl)azetidine-1-carboxylateHCID 59436608—
Edukt5-Chloro-N-(5-chloro-1,3-thiazol-2-yl)-N-(2,4-dimethoxybenzyl)-2,4-difluorobenzenesulfonamideHCID 59436622—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-(2-azetidin-3-yl-4-chlorophenoxy)-5-chloro-N-(5-chloro-1,3-thiazol-2-yl)-2-fluorobenzenesulfonamideHCID 46840815—

Reaktionsschritte

5-Chloro-N-(5-chloro-1,3-thiazol-2-yl)-N-(2,4-dimethoxybenzyl)-2,4-difluorobenzenesulfonamide (Preparation 655) and tert-butyl 3-(5-chloro-2-hydroxyphenyl)azetidine-1-carboxylate (Preparation 237) were stirred in dichloromethane (2 ml) and trifluoroacetic acid (1 ml) to prepare the title compound using Method F above but where the N,N-dimethylformamide was replaced with dimethyl sulphoxide. The crude product was concentrated in vacuo and purified by preparative HPLC to afford the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08907101B2
Quelldatensatzuspto-grants-2014_12
ORD IDord-49ffe7d70dc34548b50de0b608ca6430
Quellennotizuspto-grants-2014_12