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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 412359생성일: 2026년 10월 24일

Phenylsulphonyl isocyanate → 1-Benzenesulfonyl-3-(7-[2-[4-(2,4-dioxothiazolidin-5-ylmethyl)phenoxymethyl]-1-methyl-1H-benzimidazol-6-yloxy]naphthalen-1-yl)urea

https://huagongshe.com/ko/reaction/412359

반응식

참여 물질

역할이름HCID투입량
반응물Phenylsulphonyl isocyanateHCID 76096—
반응물5-[4-[6-(8-aminonaphthalen-2-yloxy)-1-methyl-1H-benzimidazol-2-ylmethoxy]benzyl]thiazolidine-2,4-dioneHCID 9832711—
용매TetrahydrofuranHCID 8028—
생성물1-Benzenesulfonyl-3-(7-[2-[4-(2,4-dioxothiazolidin-5-ylmethyl)phenoxymethyl]-1-methyl-1H-benzimidazol-6-yloxy]naphthalen-1-yl)ureaHCID 1853767210.2%

반응 단계

To a solution of 5-[4-[6-(8-aminonaphthalen-2-yloxy)-1-methyl-1H-benzimidazol-2-ylmethoxy]benzyl]thiazolidine-2,4-dione (0.4 g) in anhydrous tetrahydrofuran (8 ml) was added benzenesulfonyl isocyanate (0.22 g) and the mixture was stirred at room temperature for 3 hours. The reaction mixture was concentrated. The residue was chromatographed on a silica gel column using ethyl acetate:n-hexane=3:1 as the eluant. The product was recrystallized from n-hexane to afford the title compound (55 mg, mp 199-205° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06562849B1
출처 데이터셋uspto-grants-2003_05
ORD IDord-b6593c22746346db8367215a0b03631b
출처 메모uspto-grants-2003_05