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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1184652Generated: October 25, 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/reaction/1184652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium HydroxideHCID 14798—
ReactantTolvaptanHCID 216237—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product7-chloro-1-[2-methyl-4-(2-methyl-benzoylamino)-benzoyl]-5-methylthiomethoxy-2,3,4,5-tetrahydro-1H-benzo[b]azepineHCID 25134215—

Reaction Conditions

Temperature70 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08669229B2
Source datasetuspto-grants-2014_03
ORD IDord-13aec5ad380546a894ea2d1be06e15f3
Source noteuspto-grants-2014_03