Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 65206생성일: 2026년 10월 24일
Dimethyl Sulfoxide → 5-[5-[4-(2-Methoxyphenyl)-1-piperazinyl]valeryl]-2-methoxy-benzenesulfonamide dihydrochloride
https://huagongshe.com/ko/reaction/65206
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethyl Sulfoxide | HCID 679 | — |
| 반응물 | 1-(2-Methoxyphenyl)piperazine | HCID 1346 | — |
| 반응물 | Sodium Carbonate | HCID 10340 | — |
| 반응물 | 5-(5-Chloropentanoyl)-2-methoxybenzenesulfonamide | HCID 21886980 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 5-[5-[4-(2-Methoxyphenyl)-1-piperazinyl]valeryl]-2-methoxy-benzenesulfonamide dihydrochloride | HCID 20233947 | 123.2% |
반응 단계
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%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04613598 |
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| 출처 데이터셋 | uspto-grants-1986_09 |
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| ORD ID | ord-851a04a25f894117b3242313f905eb84 |
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| 출처 메모 | uspto-grants-1986_09 |
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