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HRID 1184652作成日:2026年10月26日

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

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfoxideHCID 679—
反応物Acetic AnhydrideHCID 7918—
反応物Sodium HydroxideHCID 14798—
反応物TolvaptanHCID 216237—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
生成物7-chloro-1-[2-methyl-4-(2-methyl-benzoylamino)-benzoyl]-5-methylthiomethoxy-2,3,4,5-tetrahydro-1H-benzo[b]azepineHCID 25134215—

反応条件

温度70 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08669229B2
出典データセットuspto-grants-2014_03
ORD IDord-13aec5ad380546a894ea2d1be06e15f3
出典メモuspto-grants-2014_03