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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 321971Erstellt: 26. Oktober 2026

Benzenesulfonamide → 5-Benzenesulfonylcarbamoyl-2-benzyl-1-(2-chlorobenzyl)benzimidazole

https://huagongshe.com/reaction/321971

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzenesulfonamideHCID 7370—
Edukt2-Benzyl-5-carboxy-1-(2-chlorobenzyl) benzimidazoleHCID 18681056—
Edukt3-(Cycloundecen-1-yl)-1,2-diazacycloundec-2-eneHCID 53630274—
LösungsmittelDimethylformamideHCID 6228—
Produkt5-Benzenesulfonylcarbamoyl-2-benzyl-1-(2-chlorobenzyl)benzimidazoleHCID 982788770,1%

Reaktionsschritte

N,N′-carbonyldiimidazole (0.401 g) is added all at once to an N,N-dimethylformamide (20 ml) solution of 2-benzyl-5-carboxy-1-(2-chlorobenzyl) benzimidazole (0.466 g), and the solution is stirred for one hour at room temperature. Subsequently, a N,N-dimethylformamide (5 ml) solution of benzenesulfonamide (0.389 g) and diazabicycloundecene (0.377 g) is added, and the solution is stirred for 48 hours at 100° C. The reaction solution is cooled, and the solvent is removed through evaporation under reduced pressure. This material is dissolved in a mixture solution of methanol and water. The pH is adjusted to pH 5˜6 using 10% hydrochloric acid. Precipitated crystals are separated through filtration, and are dried. Thus, 5-benzenesulfonylcarbamoyl-2-benzyl-1-(2-chlorobenzyl)benzimidazole (0.447 g) is obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06211177B1
Quelldatensatzuspto-grants-2001_04
ORD IDord-39f4988d685d46ebb28951e8b58776a3
Quellennotizuspto-grants-2001_04