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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 239846Erstellt: 24. Oktober 2026

Dichloromethane → 4'-Methoxy-biphenyl-4-sulfonic acid (2-benzoyl-4-chloro-phenyl)-amide

https://huagongshe.com/de/reaction/239846

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
EduktCesium carbonateHCID 10796—
Edukt(4-Methoxyphenyl)boronic acidHCID 201262—
EduktN-(2-benzoyl-4-chloro-phenyl)-4-iodo-benzenesulfonamideHCID 10028837—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
LösungsmittelTriethylamineHCID 8471—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
Produkt4'-Methoxy-biphenyl-4-sulfonic acid (2-benzoyl-4-chloro-phenyl)-amideHCID 11294528—

Reaktionsbedingungen

Temperatur55 °C

Reaktionsschritte

To a magnetically stirred mixture of N-(2-Benzoyl-4-chloro-phenyl)-4-iodo-benzenesulfonamide (497 mg, 1.0 mmol), [1,1′ Bis(diphenylphosphino)-ferrocene]dichloropalladium(II) complex with dichloromethane (1:1) (30 mg, 0.037 mmol) and dry cesium carbonate (511 mg, 1.57 mmol) in NMP (3 mL), was added DME (3 mL) and dry triethylamine (3 mL) under dry nitrogen. To this stirred mixture was added (4-methoxyphenyl)boronic acid (202 mg) and the mixture was stirred at 55° C. overnight. The reaction was worked up by addition to crushed ice and extracted with ethyl acetate (3×75 mL), and the organic layer was dried (MgSC4), filtered and concentrated. The crude product was chromatographed on silica gel using 10-30% EtOAc/Hexane. 1H NMR (CDCl3) δ 9.64 (br s, 1H, NH), 7.75 (dm, 1H), 7.75 (dm, 2H, J=8.8 Hz), 7.48 (m, 3H), 7.56 (dm, 2H, J=8.4 Hz), 7.51 (m), 7.32 (d 1H, J=2.2 Hz), 7.26 (d, 1H, J=7 Hz), 7.09 (d, 2H, J=8.4 Hz), 3.65 (s, 3H). MS: m/z 478.0 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08642808B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-592736e1a81240459e7130027c172419
Quellennotizuspto-grants-2014_02