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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 736604생성일: 2026년 10월 24일

Water → (4-((4-Methylpiperazin-1-yl)sulfonyl)phenyl)boronic acid

https://huagongshe.com/ko/reaction/736604

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Triisopropyl borateHCID 21531—
반응물1-(4-Bromophenylsulfonyl)-4-methylpiperazineHCID 710729—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물(4-((4-Methylpiperazin-1-yl)sulfonyl)phenyl)boronic acidHCID 1042398258%

반응 조건

온도-78 °C

반응 단계

Triisopropyl borate (0.64 mL, 2.8 mmol) was added to a solution of 1-[(4-bromophenyl)sulfonyl]-4-methylpiperazine (0.602 g, 1.9 mmol; described: in Keasling, H. H. et el. J. Med. Chem. 1965, 8, 548-550) in anhydrous tetrahydrofuran (7 mL) at −78° C. under a nitrogen atmosphere followed by dropwise addition of n-butyllithium (1.4 mL, 2.2 mmol). The resulting mixture was stirred at −78° C. for 2 h and at room temperature for another 16 h. Water (2.0 mL) was added and the mixture stirred for 30 min and evaporated to dryness. The residue was pre-adsorbed onto silica and purified by column chromatography using methylene chloride/methanol, (9:1 to 1:9), as the eluent. The product was re-crystallized from water to give 311 mg (58% yield) of the title compound as white crystals: mp 215-218° C.; 1H NMR (DMSO-d6, 400 MHz) δ 10.89 (br s, 1H), 8.47 (br s, 2H), 8.05 (d, J=8 Hz, 2H), 7.73 (d, J=8 Hz, 2H), 3.77 (m, 2H), 3.40 (m, 2H), 3.13 (m, 2H), 2.71 (s, 3H), 2.65 (m, 2H); 13C NMR (DMSO-d6, 100 MHz) δ 133.7, 133.3, 124.7, 49.8, 41.6, 41.4; MS (TSP) m/z 285 (M++1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07595319B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-e7c0a36263374cefa9478608e05d64a6
출처 메모uspto-grants-2009_09