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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1276908Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1276908

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-NitrobenzenesulfonamideHCID 22784—
Edukt6-Carboxy-1-(2-Chlorobenzyl)-2-MethylbenzimidazoleHCID 18680817—
Edukt3-(Cycloundecen-1-yl)-1,2-diazacycloundec-2-eneHCID 53630274—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-(2-Chlorobenzyl)-2-methyl-6-(4-nitrobenzenesulfonylcarbamoyl)benzimidazoleHCID 1868100346,5%

Reaktionsschritte

N,N'-carbodiimidazole (0.432 g) was added at a time to a solution of 0.400 g of 6-carboxy-1-(2-chlorobenzyl)-2-methylbenzimidazole in 15 ml of N,N-dimethylformamide, and the solution was stirred at room temperature for 1 hour. Subsequently, a solution of 0.538 g of 4-nitrobenzenesulfonamide and 0.405 g of diazabicycloundecene in 5 ml of N,N-dimethylformamide, and the mixture was stirred at 100° C. for 84 hours. The reaction solution was cooled, and the solvent was distilled off under reduced pressure. Chloroform and hydrochloric acid were added to the residue, and the mixture was stirred to precipitate the crystals. The crystals precipitated were separated through filtration, and were dried to give 0.300 g of 1-(2-chlorobenzyl)-2-methyl-6-(4-nitrobenzenesulfonylcarbamoyl)benzimidazole (220).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06166219
Quelldatensatzuspto-grants-2000_12
ORD IDord-86bedd3ec8fe4d2b909a2f1c6b7011a6
Quellennotizuspto-grants-2000_12