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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 68616Erstellt: 25. Oktober 2026

4-Fluorobenzenesulfonyl chloride → N-(4-(4-methoxybenzyloxy)-3-bromobenzyl)-4-fluoro-N-methylbenzenesulfonamide

https://huagongshe.com/reaction/68616

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Fluorobenzenesulfonyl chlorideHCID 9588—
EduktDiisopropylethylamineHCID 81531—
Edukt(4-(4-methoxybenzyloxy)-3-bromophenyl)-N-methylmethanamineHCID 63045147—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-(4-(4-methoxybenzyloxy)-3-bromobenzyl)-4-fluoro-N-methylbenzenesulfonamideHCID 6686919463%

Reaktionsschritte

To a solution of intermediate 33 (2.7 g, 8.0 mmol, 1 eq) in DCM (10 mL) was added 4-fluorobenzene-1-sulfonyl chloride (1.9 g, 9.6 mmol, 1.2 eq) and DIEA (2.8 mL, 16.0 mmol, 2 eq). After stirring at room temperature for 1 h, the reaction was washed with saturated NaHCO3 and brine, dried (Na2SO4), and concentrated in vacuo. The crude product was purified via silica gel chromatography (0-40% EtOAc/hexane) to give 2.48 g (63%) of N-(4-(4-methoxybenzyloxy)-3-bromobenzyl)-4-fluoro-N-methylbenzenesulfonamide (34).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08822467B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-b2e061bbd6374298b51da5dc80af701b
Quellennotizuspto-grants-2014_09