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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 39159Erstellt: 24. Oktober 2026

Water → 3'-amino-N-methylbiphenyl-4-sulfonamide

https://huagongshe.com/de/reaction/39159

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktPotassium CarbonateHCID 11430—
Edukt3-Aminophenylboronic acidHCID 92269—
Edukt4-bromo-N-methylbenzene-1-sulfonamideHCID 101215—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelDimethylformamideHCID 6228—
Produkt3'-amino-N-methylbiphenyl-4-sulfonamideHCID 5920619150%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

To a solution of 4-bromo-N-methyl-benzene sulfonamide (2.49 g, 10 mmol) in DMF (20 mL) was added 3-amino-phenyl boronic acid (1.51 g, 11 mmol), Pd(PPh3)4 (90 mg, 0.30 mmol), potassium carbonate (1.52 g, 11 mmol) and water (5 mL). The resulting mixture was degassed by gently bubbling argon through the solution for 5 minutes at 20° C. The reaction mixture was then heated at 80° C. overnight. The reaction was filtered through a pad of silica gel, which was washed with CH2Cl2 (50 mL×3). The combined organics were concentrated under reduced pressure to give crude product, which was washed with EtOAc to give pure 3′-amino-N-methylbiphenyl-4-sulfonamide (C-3) (1.3 g, 50%). NMR (300 MHz, CDCl3) δ 7.85 (d, J=8.7 Hz, 2H), 7.75 (d, J=8.7 Hz, 2H), 7.19 (t, J=7.8 Hz, 1H), 6.95-7.01 (m 2H), 6.73-6.77 (m, 1H), 2.54 (s, 3H). MS (ESI) m/e (M+H+) 263.0.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524767B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-c4df9bd19f31462292cf31d960a25ce6
Quellennotizuspto-grants-2013_09