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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Nitrobenzenesulfonamide | HCID 22784 | — |
| Edukt | 6-Carboxy-1-(2-Chlorobenzyl)-2-Methylbenzimidazole | HCID 18680817 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 1-(2-Chlorobenzyl)-2-methyl-6-(4-nitrobenzenesulfonylcarbamoyl)benzimidazole | HCID 18681003 | 43,1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US06348032B1 |
|---|
| Quelldatensatz | uspto-grants-2002_02 |
|---|
| ORD ID | ord-08d94b7200534d1ab77db94f0a2fe645 |
|---|
| Quellennotiz | uspto-grants-2002_02 |
|---|