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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Benzenesulfonamide | HCID 7370 | — |
| Edukt | 2-Benzyl-5-carboxy-1-(2-chlorobenzyl) benzimidazole | HCID 18681056 | — |
| Edukt | 3-(Cycloundecen-1-yl)-1,2-diazacycloundec-2-ene | HCID 53630274 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 5-Benzenesulfonylcarbamoyl-2-benzyl-1-(2-chlorobenzyl)benzimidazole | HCID 9827887 | 70,1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06211177B1 |
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| Quelldatensatz | uspto-grants-2001_04 |
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| ORD ID | ord-39f4988d685d46ebb28951e8b58776a3 |
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| Quellennotiz | uspto-grants-2001_04 |
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