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HRID 65206作成日:2026年10月25日

Dimethyl Sulfoxide → 5-[5-[4-(2-Methoxyphenyl)-1-piperazinyl]valeryl]-2-methoxy-benzenesulfonamide dihydrochloride

https://huagongshe.com/reaction/65206

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1-(2-Methoxyphenyl)piperazineHCID 1346—
反応物Sodium CarbonateHCID 10340—
反応物5-(5-Chloropentanoyl)-2-methoxybenzenesulfonamideHCID 21886980—
溶媒WaterHCID 962—
生成物5-[5-[4-(2-Methoxyphenyl)-1-piperazinyl]valeryl]-2-methoxy-benzenesulfonamide dihydrochlorideHCID 20233947123.2%

反応条件

温度90 °C

反応手順

A mixture of 2.6 g of 5-(5-chlorovaleryl)-2-methoxy-benzenesulfonamide, 1.8 g of 1-(2-methoxyphenyl)piperazine, 1 g of sodium carbonate and 20 ml of dimethyl sulfoxide was stirred at 90° C. for 3 hours. After the reaction was finished, water was added to the reaction mixture and then the mixture was extracted with ethyl acetate. The extract was washed with water saturated with sodium chloride and dried over anhydrous sodium sulfate. The solvent was distilled away and the residue was dissolved in acetone followed by adding concentrated hydrochloric acid in required amount to produce crystals. The thus-produced crystals were recrystallized from methanol to obtain 2.8 g of the titled compound (yield: 61%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04613598
出典データセットuspto-grants-1986_09
ORD IDord-851a04a25f894117b3242313f905eb84
出典メモuspto-grants-1986_09