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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1699618Erstellt: 26. Oktober 2026

4-Nitrobenzenesulfonamide → 1-(2-Chlorobenzyl)-2-methyl-6-(4-nitrobenzenesulfonylcarbamoyl)benzimidazole

https://huagongshe.com/reaction/1699618

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-NitrobenzenesulfonamideHCID 22784—
Edukt6-Carboxy-1-(2-Chlorobenzyl)-2-MethylbenzimidazoleHCID 18680817—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-(2-Chlorobenzyl)-2-methyl-6-(4-nitrobenzenesulfonylcarbamoyl)benzimidazoleHCID 1868100343,1%

Reaktionsschritte

N,N′-carbonyldiimidazole (0.432 g) is added all at once to an N,N-dimethylformamide (15 ml) solution of 6-carboxy-1-(2-chlorobenzyl)-2-methylbenzimidazole (0.432 g) (example 75), and the solution is stirred for one hour at room temperature. Subsequently, an N,N-dimethylformamide (5 ml) solution of 4-nitrobenzenesulfonamide (0.538 g) and diazabicyclotindecene (0.405 g) is added, and the solution is stirred for 84 hours at 100° C. The reaction solution is cooled and the solvent is removed through evaporation under reduced pressure. When chloroform and hydrochloric acid are added to the residue and the solution is stirred, crystals precipitated. The crystals are separated through filtration, dried, and thus, 1-(2-chlorobenzyl)-2-methyl-6-(4-nitrobenzenesulfonylcarbamoyl)benzimidazole (0.300 g) is obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06348032B1
Quelldatensatzuspto-grants-2002_02
ORD IDord-08d94b7200534d1ab77db94f0a2fe645
Quellennotizuspto-grants-2002_02