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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 29253Erstellt: 25. Oktober 2026

Sodium Carbonate → N-{3-[2-(2,4-Dichloro-benzoyl)-3-methoxy-benzofuran-6-yl]-benzyl}-methanesulfonamide

https://huagongshe.com/reaction/29253

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CarbonateHCID 10340—
EduktN-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)methanesulfonamideHCID 59298860—
Edukt(6-Bromo-3-methoxybenzofuran2-yl)(2,4-dichloro-phenyl)methanoneHCID 59788953—
KatalysatorBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelToluene ethanolHCID 21863594—
ProduktN-{3-[2-(2,4-Dichloro-benzoyl)-3-methoxy-benzofuran-6-yl]-benzyl}-methanesulfonamideHCID 5978891930,3%

Reaktionsschritte

(6-Bromo-3-methoxybenzofuran2yl)(2,4-dichloro-phenyl)-methanone (110 mg, 0.264 mmol), prepared as described above was dissolved in toluene/ethanol (1:1 8 mL). To this solution was added N-[3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzyl]-methanesulfonamide (99 mg, 0.317 mmol) and aqueous sodium carbonate (2M, 1.59 mmol). The mixture was degassed with nitrogen for 30 minutes and then Pd(dppf)2Cl2 (19.32 mg, 0.03 mmol) was added. The resultant mixture was heated at 85 deg C. for 18 hours at which time it was cooled to ambient and concentrated via rotary evaporation. The oil thus obtained was diluted with EtOAc and washed with water and brine and dried over MgSO4. The organic layer was filtered and concentrated and purified by HPLC to give the desired compound (40.4 mg, 29%) 1H-NMR (CDCl3): δ 7.84 (d, 1H), 7.63-7.25 (m, 9H), 4.85 (br t, 1H), 4.40 (d, 2H), 4.24 (s, 3H), 2.95 (s, 3H). (M+H) 506.1 RT=3.66 min.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07420066B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-10ab920ac66a43ff9698d3ce4cff3707
Quellennotizuspto-grants-2008_09