Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | 2,6-Dichlorobenzenesulfonylchloride | HCID 522183 | — |
| Edukt | HCID 178496032 | HCID 178496032 | — |
| Lösungsmittel | Sodium Hydroxide | HCID 14798 | — |
| Produkt | HCID 178496035 | HCID 178496035 | — |
Reaktionsschritte
To a solution of 175 mg of 1-(5-hydroxy-1H-benzimidazol-2-yl)-3-(2-methoxyethyl)urea in 15 cm3 of 0.1N aqueous sodium hydroxide solution are added 189 mg of finely ground 2,6-dichlorobenzenesulfonyl chloride. The suspension is stirred for about 20 hours at a temperature in the region of 20° C., 10 cm3 of water are then added and the mixture is cooled to about 5° C. for about 15 minutes. The precipitate is filtered off by suction, washed with three times 2 cm3 of water and dried under reduced pressure (13 kPa) over phosphorus pentoxide. After flash chromatography on a column of silica [eluent: dichloromethane/methanol/acetonitrile (95/3/2 by volume)], 65 mg of 2-{[(2-methoxyethyl)carbamoyl]amino}-1H-benzimidazol-5-yl 2,6-dichlorobenzenesulfonate are obtained in the form of a cream-coloured powder, the characteristics of which are as follows:
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08110571B2 |
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| Quelldatensatz | uspto-grants-2012_02 |
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| ORD ID | ord-9a2bdd8081fe4db59f67a899490d994e |
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| Quellennotiz | uspto-grants-2012_02 |
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