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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 28397생성일: 2026년 10월 24일

4-Carboxyphenylboronic Acid → 4-({4-[(5-chloro-1H-indol-2-yl)sulphonyl]piperazin-1-yl}carbonyl)phenyl boronic acid

https://huagongshe.com/ko/reaction/28397

반응식

참여 물질

역할이름HCID투입량
반응물4-Carboxyphenylboronic AcidHCID 312183—
반응물O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
반응물5-chloro-2-(piperazine-1-sulfonyl)-1H-indoleHCID 22710571—
용매DimethylformamideHCID 6228—
생성물4-({4-[(5-chloro-1H-indol-2-yl)sulphonyl]piperazin-1-yl}carbonyl)phenyl boronic acidHCID 6930738956%

반응 단계

5-Chloro-2-(piperazin-1-ylsulphonyl)-1H-indole (5.42 g, 18.1 mmol) was added to a solution of 4-carboxyphenyl boronic acid (3.00 g, 18.1 mmol) N,N-diisopropylethylamine (2.34 g, 18.1 mmol) and O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium tetrafluoroborate (5.81 g, 18.1 mmol) in 80 mL N,N-dimethylformamide, the mixture was stirred for 2 hours at room temperature. N,N-Dimethylformamide was removed in vacuo and the crude was purified by flash chromatography three times (dichloromethane/methanol, 100-98/2) to give 4-({4-[(5-chloro-1H-indol-2-yl)sulphonyl]piperazin-1-yl}carbonyl)phenyl boronic acid as a colourless solid (56% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07419979B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-4b86f7cb244e4996a5c483f75e27e621
출처 메모uspto-grants-2008_09