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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 63245생성일: 2026년 10월 24일

Potassium Carbonate → 1-Chloro-7-(1H-indol-5-yl)-isoquinoline

https://huagongshe.com/ko/reaction/63245

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물5-Indolylboronic acidHCID 2734361—
반응물7-Bromo-1-ChloroisoquinolineHCID 6502024—
용매DimethylformamideHCID 6228—
생성물1-Chloro-7-(1H-indol-5-yl)-isoquinolineHCID 5751684025%

반응 단계

A mixture of 7-bromo-1-chloroisoquinoline (0.50 g, 2.1 mmol), 5-indoleboronic acid (0.40 g, 2.5 mmol), tetrakis(triphenylphosphene)palladium (0.035 g, 0.08 mmol), potassium carbonate (2.1 mL, 2 M, 4.1 mmol), N,N-dimethylformamide (11 mL) was stirred while purging the headspace with argon for 30 min. The mixture was then brought to reflux for 16 h before being allowed to cool to RT. The mixture was filtered through a bed of silica gel, diluted with water (50 mL), and extracted with ethyl acetate (50 mL). The organic layer was separated and washed with NaOH (2×20 mL, 10% aq.), water (5×30 mL, until refractive changes were no longer seen at the organic-aqueous interface), and ammonium chloride (20 mL, sat.). The organic layer was then adsorbed onto silica gel and flash-chromatographed (ethyl acetate/hexanes) to afford 0.14 g (25%) of a yellow solid. MS (ESI): calculated for C17H11ClN2, 278.1. found 301.0 [M+Na]+. 1H NMR (300 MHz, DMSO-d6) δ 6.56-6.58 (m, 1H), 7.44 (t, J=2.77 Hz, 1H), 7.57-7.59 (m, 2H), 7.93 (m, 1H), 8.04 (s, 1H), 8.13-8.20 (m, 1H), 8.27-8.31 (m, 2H), 8.43 (m, 1H), 11.25 (brs, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09447049B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-01d251adb4af45f19b68e80ee76c7def
출처 메모uspto-grants-2016_09