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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1994748생성일: 2026년 10월 24일

Triethylamine → ethyl {4-[(2-{7-[(2-thienylsulfonyl)amino]-1H-indol-2-yl}-1,3-thiazol-5-yl)methyl]piperazin-1-yl}acetate

https://huagongshe.com/ko/reaction/1994748

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Ammonium ChlorideHCID 25517—
반응물Ethyl piperazine-1-acetateHCID 207112—
반응물HCID 57476122HCID 57476122—
용매DimethylformamideHCID 6228—
생성물ethyl {4-[(2-{7-[(2-thienylsulfonyl)amino]-1H-indol-2-yl}-1,3-thiazol-5-yl)methyl]piperazin-1-yl}acetateHCID 5913601783%

반응 단계

To a solution of N-{2-[5-(chloromethyl)-1,3-thiazol-2-yl]-1H-indol-7-yl}thiophene-2-sulfonamide (0.460 g) in N,N-dimethylformamide (12 ml) were added ethyl piperazin-1-ylacetate (0.385 g) and triethylamine (0.31 ml), and the mixture was stirred at room temperature for 15 hr. Saturated aqueous ammonium chloride solution was added to the reaction solution, and the mixture was extracted with ethyl acetate. The extract was washed successively with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was recrystallized from tetrahydrofuran-hexane to give the title compound (0.507 g, yield 83%) as colorless crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07652133B2
출처 데이터셋uspto-grants-2010_01
ORD IDord-118e0c154ca845e29829a6f936038e57
출처 메모uspto-grants-2010_01