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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 492093생성일: 2026년 10월 25일

1H-Imidazole, 4,5-dihydro-2-(methylthio)-, hydriodide (1:1) → N-{5-[(4,5-Dihydro-1H-imidazol-2-ylamino)-methyl]-5,6,7,8-tetrahydro-naphthalen-2-yl}-benzenesulfonamide

https://huagongshe.com/reaction/492093

반응식

참여 물질

역할이름HCID투입량
반응물1H-Imidazole, 4,5-dihydro-2-(methylthio)-, hydriodide (1:1)HCID 12221228—
반응물N-(5-aminomethyl-5,6,7,8-tetrahydro-naphthalen-2-yl)-benzenesulfonamideHCID 57678964—
용매DichloromethaneHCID 6344—
생성물N-{5-[(4,5-Dihydro-1H-imidazol-2-ylamino)-methyl]-5,6,7,8-tetrahydro-naphthalen-2-yl}-benzenesulfonamideHCID 57678992—

반응 조건

온도150 °C

반응 단계

N-(5-Aminomethyl-5,6,7,8-tetrahydro-naphthalen-2-yl)-benzenesulfonamide and 2-methylsulfanyl-4,5-dihydro-1H-imidazole hydroiodide were added to methylene chloride and the reaction mixture was heated to reflux until all of the solvent evaporates. The reaction mixture is heated to 150° C. and then cooled. The resulting mixture is basified by dropwise addition of aqueous NaOH solution, and then purified by preparative liquid chromatography to give N-{5-[(4,5-Dihydro-1H-imidazol-2-ylamino)-methyl]-5,6,7,8-tetrahydro-naphthalen-2-yl}-benzenesulfonamide. 5-[(4,5-Dihydro-1H-imidazol-2-ylamino)-methyl]-5,6,7,8-tetrahydro-napthalene-2-sulfonic acid phenylamide may be similarly prepared.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07531577B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-6ade000977d04fdc804334d334413ba1
출처 메모uspto-grants-2009_05