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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 583482Erstellt: 25. Oktober 2026

N-Trimethylsilyl-N-methylacetamide → N-[(4-sulfamoylphenyl)methyl]-2-[[2-[(4-sulfamoylphenyl)methylcarbamoyl]phenyl]disulfanyl]benzamide

https://huagongshe.com/reaction/583482

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-Trimethylsilyl-N-methylacetamideHCID 81953—
Edukt2,2'-Dithiodibenzoyl chlorideHCID 88164—
Edukt4-(Aminomethyl)benzenesulfonamide hydrochloride hydrateHCID 21584567—
LösungsmittelPyridineHCID 1049—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-[(4-sulfamoylphenyl)methyl]-2-[[2-[(4-sulfamoylphenyl)methylcarbamoyl]phenyl]disulfanyl]benzamideHCID 46536935,4%

Reaktionsschritte

A slurry of 4-(aminomethyl)benzenesulfonamide hydrochloride hydrate (6.5 gf 29 mmol) in 100 mL pyridine was allowed to stir with N-methyl-N-(trimethylsilyl)acetamide (13.4 mL, 83.0 mmol) until a homogenous solution occurred. The solution was cooled to 0° C. to 5° C. and a solution of 2,2'-dithiobisbenzoyl chloride (4.0 g, 16.0 mmol) in 20 mL dichloromethane was added dropwise. The resulting solution was allowed to stir for 18 hours and the dichloromethane was removed in vacuo. The crude product was precipitated with the addition of water and the resulting solid was collected by filtration. The crude product was recrystallized from a mixture of dimethylformamide, ethanol, and water to yield 3.3 g of the title compound, mp 267-269° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05929114
Quelldatensatzuspto-grants-1999_07
ORD IDord-5aad2cea920c49739b25da5c2dc544c4
Quellennotizuspto-grants-1999_07