HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1166462Erstellt: 23. Oktober 2026
Chlorosulfonic acid → N-methanesulfonyl-5-chlorosulfonyl-2-aminobenzimidazole
https://huagongshe.com/de/reaction/1166462
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Chlorosulfonic acid | HCID 24638 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | 1-(Methylsulfonyl)-1H-Benzimidazol-2-Amine | HCID 22997045 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | N-methanesulfonyl-5-chlorosulfonyl-2-aminobenzimidazole | HCID 22997216 | — |
Reaktionsschritte
To 9.5 mL (20 eq., 142 mmol) of well stirred chlorosulfonic acid at ˜25° C. was added N-methanesulfonyl-2-aminobenzimidazole (1.5 g, 7.1 mmol) in small portions over 1C minutes with slight exotherming. The solution was stirred at ˜25° C. for 3.5 hours, then was added dropwise to a well stirred mixture of ice and water. The aqueous solution was slowly basified to pH ˜7.5 with solid sodium bicarbonate and extracted with EtOAc. A precipitate formed in the organic phase which was filtered off and was washed with H20 and dried on the filter to yield 1.23 g of N-methanesulfonyl-5-chlorosulfonyl-2-aminobenzimidazole. HPLC, single peak, ret. time=7.61 min. MS: Obs. M +H@ 310.0 amu.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US06613743B2 |
|---|
| Quelldatensatz | uspto-grants-2003_09 |
|---|
| ORD ID | ord-4e5339decb32429eadc0cf684119054e |
|---|
| Quellennotiz | uspto-grants-2003_09 |
|---|