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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

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Dimethylsulphamoyl chlorideHCID 83372—
반응물1-Piperazinyl(4-((7-(trifluoromethyl)-4-quinolinyl)amino)phenyl)methanoneHCID 3055243—
용매DimethylformamideHCID 6228—
생성물1-Piperazinesulfonamide, N,N-dimethyl-4-(4-((7-(trifluoromethyl)-4-quinolinyl)amino)benzoyl)-HCID 305524688.3%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04167567
출처 데이터셋uspto-grants-1979_09
ORD IDord-99a38c6ca69b49cf937942d68aef5a69
출처 메모uspto-grants-1979_09