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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 492097Erstellt: 25. Oktober 2026

Methanesulfonyl chloride → N-[5-(Methanesulfonylamino-methyl)-naphthalen-2-yl]-benzenesulfonamide

https://huagongshe.com/reaction/492097

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanesulfonyl chlorideHCID 31297—
EduktN-(5-aminomethyl-5,6,7,8-tetrahydro-naphthalen-2-yl)-benzenesulfonamideHCID 57678964—
LösungsmittelPyridineHCID 1049—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-[5-(Methanesulfonylamino-methyl)-naphthalen-2-yl]-benzenesulfonamideHCID 57678989—

Reaktionsschritte

N-(5-Aminomethyl-5,6,7,8-tetrahydro-naphthalen-2-yl)-benzenesulfonamide is dissolved in methylene chloride and pyridine, and the mixture is cooled in an ice bath. Methanesulfonyl chloride is added dropwise, and the reaction mixture is stirred at ice bath temperature, then allowed to warm to room temperature. The reaction mixture is quenched by addition of water and extracted with methylene chloride. The organic layer is washed with water, dried (MgSO4), filtered and concentrated under reduced pressure to give N-[5-(Methanesulfonylamino-methyl)-naphthalen-2-yl]-benzenesulfonamide. 5-(Methanesulfonylamino-methyl)-naphthalene-2-sulfonic acid phenylamide may be similarly prepared.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07531577B2
Quelldatensatzuspto-grants-2009_05
ORD IDord-1f95af295ef4496ea09dfb8cac524b85
Quellennotizuspto-grants-2009_05