Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1863013생성일: 2026년 10월 26일
Triethylamine → 1-Piperazinesulfonamide, N,N-dimethyl-4-(4-((7-(trifluoromethyl)-4-quinolinyl)amino)benzoyl)-
https://huagongshe.com/reaction/1863013
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Dimethylsulphamoyl chloride | HCID 83372 | — |
| 반응물 | 1-Piperazinyl(4-((7-(trifluoromethyl)-4-quinolinyl)amino)phenyl)methanone | HCID 3055243 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 1-Piperazinesulfonamide, N,N-dimethyl-4-(4-((7-(trifluoromethyl)-4-quinolinyl)amino)benzoyl)- | HCID 3055246 | 88.3% |
반응 단계
Dimethylsulfamoyl chloride (0.72 g, 0.54 ml, 0.005 mol) is added dropwise to a solution of 2.00 g (0.005 mol) of 4-[4-[[7-(trifluoromethyl)-4-quinolinyl]amino]benzoyl]piperazine and 2 ml of triethylamine in 20 ml of dimethylformamide. The reaction is stirred for 19 hours and then partitioned with chloroform-aqueous sodium carbonate. The organic phase is dried over anhydrous sodium sulfate, concentrated, and chromatographed with methylene chloride to 1% methanol/chloroform on silica gel to give 2.24 g of 1-[(dimethylamino)sulfonyl]-4-[4-[[7-(trifluoromethyl)-4-quinolinyl]amino]benzoyl]piperazine. This is crystallized from methylene chloride-cyclohexane to give 1.60 g of 1-[(dimethylamino)sulfonyl]-4-[4-[[-7-(trifluoromethyl)-4-quinolinyl]amino]benzoyl]piperazine of melting point 223°-224.5° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04167567 |
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| 출처 데이터셋 | uspto-grants-1979_09 |
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| ORD ID | ord-99a38c6ca69b49cf937942d68aef5a69 |
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| 출처 메모 | uspto-grants-1979_09 |
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