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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 18881Erstellt: 27. Oktober 2026

2-Amino-5-bromobenzophenone → N-(2-Benzoyl-4-bromo-phenyl)-4-oxazol-5-yl-benzenesulfonamide

https://huagongshe.com/reaction/18881

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Amino-5-bromobenzophenoneHCID 99677—
Edukt4-(1,3-Oxazol-5-yl)benzenesulphonyl chlorideHCID 2776415—
ProduktN-(2-Benzoyl-4-bromo-phenyl)-4-oxazol-5-yl-benzenesulfonamideHCID 11329171—

Reaktionsschritte

The title compound was prepared according to the general procedure for the synthesis of N-Aryl-benzenesulfonamides previously described using 138 mg of (2-amino-5-bromo-phenyl)-phenyl-methanone and 121 mg of 4-oxazol-5-yl-benzenesulfonyl chloride. 1H-NMR (400 MHz, CDCl3): δ 7.25-7.35 (m, 5H), 7.45-7.49 (m, 4H), 7.63-7.71 (m, 4H), 7.95 (s, 1H), 9.67 (s, 1H). MS: m/z 484.3 (M++1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07741519B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-0d4dbbcaee7544ed93eacefc6c2d97e4
Quellennotizuspto-grants-2010_06