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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dimethyl Sulfoxide | HCID 679 | — |
| 反応物 | 1-(2-Methoxyphenyl)piperazine | HCID 1346 | — |
| 反応物 | Sodium Carbonate | HCID 10340 | — |
| 反応物 | 5-(5-Chloropentanoyl)-2-methoxybenzenesulfonamide | HCID 21886980 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 5-[5-[4-(2-Methoxyphenyl)-1-piperazinyl]valeryl]-2-methoxy-benzenesulfonamide dihydrochloride | HCID 20233947 | 123.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04613598 |
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| 出典データセット | uspto-grants-1986_09 |
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| ORD ID | ord-851a04a25f894117b3242313f905eb84 |
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| 出典メモ | uspto-grants-1986_09 |
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