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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfoxideHCID 679—
EduktAcetic AnhydrideHCID 7918—
EduktSodium HydroxideHCID 14798—
EduktTolvaptanHCID 216237—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelWaterHCID 962—
Produkt7-chloro-1-[2-methyl-4-(2-methyl-benzoylamino)-benzoyl]-5-methylthiomethoxy-2,3,4,5-tetrahydro-1H-benzo[b]azepineHCID 25134215—

Reaktionsbedingungen

Temperatur70 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08669229B2
Quelldatensatzuspto-grants-2014_03
ORD IDord-13aec5ad380546a894ea2d1be06e15f3
Quellennotizuspto-grants-2014_03