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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 133402Erstellt: 23. Oktober 2026

4-Bromobenzenesulfonamide → 2-Phenylbenzene-1-sulfonamide

https://huagongshe.com/de/reaction/133402

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-BromobenzenesulfonamideHCID 69696—
KatalysatorPalladiumHCID 23938—
Produkt2-Phenylbenzene-1-sulfonamideHCID 12371520—

Reaktionsschritte

In Scheme 1 the compounds of the invention, 1, are prepared in 4 steps. Sulfonylation of valine methyl ester with 4-bromo-benzenesulfonyl chloride was carried out in the presence of Hunig base to give sulfonamide Intermediate 1. This 4-bromo-benzenesulfonamide was furthered coupled with boronate ester using Palladium catalyst under Suzuki coupling condition to provide biphenyl sulfonamide Intermediate 2. Biphenyl sulfonamide Intermediate 2 was then alkylated with various alkylating reagents to provide biphenyl sulfonamide ester (Intermediate 3). Hydrolysis of Intermediate 3 was carried out using bases such as NaOH, or LiOH to form the final product 1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07390833B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-68ca173bd40c4077ab21cedd0d8e35de
Quellennotizuspto-grants-2008_06