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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2117911생성일: 2026년 10월 27일

Water → N-{4-(2-{4-[(aminocarbonothioyl)amino]phenyl}ethyl)-5-[4-(methylsulfonyl)benzyl]-1,3-thiazol-2-yl}acetamide

https://huagongshe.com/reaction/2117911

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Benzoyl isothiocyanateHCID 68284—
반응물N-(4-[2-(4-aminophenyl)ethyl]-5-[4-(methylsulfonyl)benzyl]-1,3-thiazol-2-yl)acetamideHCID 21914845—
용매AcetoneHCID 180—
생성물N-{4-(2-{4-[(aminocarbonothioyl)amino]phenyl}ethyl)-5-[4-(methylsulfonyl)benzyl]-1,3-thiazol-2-yl}acetamideHCID 21914747103.2%

반응 단계

To a ice-cold solution of N-{4-[2-(4-aminophenyl)ethyl]-5-[4-(methylsulfonyl)benzyl]-1,3-thiazol-2-yl}acetamide (247.6 mg) in acetone (4.8 ml) was added benzoyl isothiocyanate (94.1 mg), and the mixture was stirred at r.t. for 1 hour. Water was added to the mixture, and the mixture was extracted with AcOEt. The organic layer was washed with water and brine, dried over anhydrous MgSO4, and concentrated in vacuo. The residual amorphous substance was dissolved in EtOH (5 ml), and 6N—NaOH (0.288 ml) was added to the solution at 0° C. The reaction mixture was stirred at r.t. for 2 hours, and neutralized with 1N—HCl at 0° C. The mixture was extracted with AcOEt. The organic layer was washed with water and brine, dried over anhydrous MgSO4, and concentrated in vacuo. The residue was solidified with ethyl ether to give N-{4-(2-{4-[(aminocarbonothioyl)amino]phenyl}ethyl)-5-[4-(methylsulfonyl)benzyl]-1,3-thiazol-2-yl}acetamide (290.7 mg) as an off-white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07442715B2
출처 데이터셋uspto-grants-2008_10
ORD IDord-0f5b7567643b4051a0f7d4c28f440a66
출처 메모uspto-grants-2008_10