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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1072934Erstellt: 26. Oktober 2026

1-Butanesulfonamide → 6-(1-n-Butanesulfonylcarbamoyl)-1-(2,4-dichlorobenzyl)-3-methyl-2-benzimidazolone

https://huagongshe.com/reaction/1072934

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-ButanesulfonamideHCID 18460—
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Edukt6-Carboxy-1-(2,4-dichlorobenzyl)-3-methyl-2-benzimidazoloneHCID 22387851—
LösungsmittelDimethylformamideHCID 6228—
Produkt6-(1-n-Butanesulfonylcarbamoyl)-1-(2,4-dichlorobenzyl)-3-methyl-2-benzimidazoloneHCID 2238775729,2%

Reaktionsschritte

In the same manner as in Example 1, N,N′-carbonyldiimidazole (0.290 g) was added to a mixture of 6-carboxy-1-(2,4-dichlorobenzyl)-3-methyl-2-benzimidazolone (0.314 g) and N,N-dimethylformamide (9 ml), and the mixture was stirred at room temperature for 1 hr. 1-n-Butanesulfonamide (0.246 g) and DBU (0.273 g) were added and the mixture was stirred at 100° C. for 16 hr. The solvent was evaporated and the resulting mixture was extracted with chloroform and water. The organic layer was concentrated and the residue was purified by preparative thin layer chromatography to give 6-(1-n-butanesulfonylcarbamoyl)-1-(2,4-dichlorobenzyl)-3-methyl-2-benzimidazolone (0.123 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06911469B2
Quelldatensatzuspto-grants-2005_06
ORD IDord-8b93bcaac0704066b3b7b120e0d3fb05
Quellennotizuspto-grants-2005_06