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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 552172생성일: 2026년 10월 24일

Water → 7-Fluoro-2,3,4,9-tetrahydro-1H-beta-carboline

https://huagongshe.com/ko/reaction/552172

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium CarbonateHCID 11430—
반응물7-fluoro-2,3,4,9-tetrahydro-1H-beta-carboline-1-carboxylic acidHCID 60015835—
용매Hydrochloric AcidHCID 313—
용매MethanolHCID 887—
생성물7-Fluoro-2,3,4,9-tetrahydro-1H-beta-carbolineHCID 1507755079%

반응 단계

7-fluoro-2,3,4,9-tetrahydro-1H-β-carboline-1-carboxylic acid (5 g, 21.36 mmol) was suspended in 130 ml of 3N HCl in a 500 ml round-bottom flask and refluxed overnight (16 hr) with stirring. Upon cooling, a light brown solid precipitated out, which was collected by filtration and washed with H2O. The salt obtained by filtration above was then dissolved in hot methanol (200 ml) and treated with 3M K2CO3 (5-10 ml) such that the pH is around 9. 100 ml of H2O was added to this mixture, which was then allowed to stir at RT. The methanol was evaporated on a rotary evaporator to give a white aqueous suspension of the desired free base, which was collected by filtration (3.2 g, 79% yield). 1H-NMR (300 MHz, methanol-d4): δ 2.73 (t, 2H), 3.11 (t, 2H), 3.94 (s, 2H), 6.73 (m, 1H), 6.94 (m, 1H), 7.30 (dd, 1H). Retention Time (LC, method: ammonium acetate standard): 1.25 min. MS (M+H+): 191.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07951801B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-da90186f74fa49cba918a8942482c36a
출처 메모uspto-grants-2011_05