돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 412351생성일: 2026년 10월 25일

4-Chlorobenzenesulfonyl chloride → 4-Chloro-N-[2-(4-[2-[4-(2,4-dioxothiazolidin-5-ylmethyl)phenoxymethyl]-1-methyl-1H-benzimidazol-6-yloxy]phenyl)ethyl]benzenesulfonamide hydrochloride

https://huagongshe.com/reaction/412351

반응식

참여 물질

역할이름HCID투입량
반응물4-Chlorobenzenesulfonyl chlorideHCID 7398—
반응물DiisopropylethylamineHCID 81531—
반응물5-[4-[6-[4-(2-aminoethyl)phenoxy]-1-methyl-1H-benzimidazol-2-ylmethoxy]benzyl]thiazolidine-2,4-dione dihydrochlorideHCID 86587773—
용매DimethylformamideHCID 6228—
생성물4-Chloro-N-[2-(4-[2-[4-(2,4-dioxothiazolidin-5-ylmethyl)phenoxymethyl]-1-methyl-1H-benzimidazol-6-yloxy]phenyl)ethyl]benzenesulfonamide hydrochlorideHCID 18537606118.3%

반응 단계

To a mixture of 5-[4-[6-[4-(2-aminoethyl)phenoxy]-1-methyl-1H-benzimidazol-2-ylmethoxy]benzyl]thiazolidine-2,4-dione dihydrochloride (0.4 g), N,N-diisopropylethylamine (0.27 g) and anhydrous N,N-dimethylformamide (15 ml) was added 4-chlorobenzenesulfonyl chloride (0.15 g) and the mixture was stirred at room temperature for 3.5 hours. The reaction mixture was concentrated and diluted with water and tetrahydrofuran and then extracted with ethyl acetate. The extract was washed with saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate and then concentrated. To a solution of the residue in tetrahydrofuran (10 ml) was added 4N hydrogen chloride in ethyl acetate (5 ml) and the mixture was stirred at room temperature for 1.5 hours. To the reaction mixture was added diethyl ether (10 ml) and this mixture was stirred at room temperature for 30 minutes and then was irradiated with ultrasound for 30 minutes. The precipitate was isolated by filtration and washed with acetone, ethyl acetate and n-hexane to afford the title compound (0.3 g, mp 155-160° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06562849B1
출처 데이터셋uspto-grants-2003_05
ORD IDord-7b6de217c5484cfaac502bfb85a7fa7f
출처 메모uspto-grants-2003_05