HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1184652Erstellt: 24. Oktober 2026
Dimethyl Sulfoxide → 7-chloro-1-[2-methyl-4-(2-methyl-benzoylamino)-benzoyl]-5-methylthiomethoxy-2,3,4,5-tetrahydro-1H-benzo[b]azepine
https://huagongshe.com/de/reaction/1184652
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Dimethyl Sulfoxide | HCID 679 | — |
| Edukt | Acetic Anhydride | HCID 7918 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Tolvaptan | HCID 216237 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 7-chloro-1-[2-methyl-4-(2-methyl-benzoylamino)-benzoyl]-5-methylthiomethoxy-2,3,4,5-tetrahydro-1H-benzo[b]azepine | HCID 25134215 | — |
Reaktionsschritte
Dimethylsulfoxide (DMSO) (3 ml), acetic anhydride (1.5 ml), and acetic acid (1.5 ml) were added to tolvaptan (1.0 g, 2.2 mmol), and the mixture was stirred at 70° C. for 4 hours. Water and 1N aqueous sodium hydroxide solution were added to the reaction mixture, and the mixture was extracted with ethyl acetate, washed with an aqueous saturated sodium chloride solution, dried over anhydrous sodium sulfate. After filtration and concentration under reduced pressure, the residue was purified by silica gel flash chromatography (n-hexane:ethyl acetate=80:20→20:80). The purified product was concentrated under reduced pressure to obtain 0.62 g of 7-chloro-1-[2-methyl-4-(2-methyl-benzoylamino)-benzoyl]-5-methylthiomethoxy-2,3,4,5-tetrahydro-1H-benzo[b]azepine as white amorphous solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08669229B2 |
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| Quelldatensatz | uspto-grants-2014_03 |
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| ORD ID | ord-13aec5ad380546a894ea2d1be06e15f3 |
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| Quellennotiz | uspto-grants-2014_03 |
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