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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 591585생성일: 2026년 10월 25일

Potassium Carbonate → 2'-(1H-pyrazol-1-yl)-9-(pyridin-2-yl)-9H-2,9'-bicarbazole

https://huagongshe.com/reaction/591585

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물L-ProlineHCID 145742—
반응물2-bromo-9-(pyridin-2-yl)-9H-carbazoleHCID 70654852—
반응물2-(1H-pyrazol-1-yl)-9H-carbazoleHCID 71060270—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
생성물2'-(1H-pyrazol-1-yl)-9-(pyridin-2-yl)-9H-2,9'-bicarbazoleHCID 7106045660%

반응 조건

온도90 °C

반응 단계

Under a nitrogen atmosphere, 10 mmol of 2-(1H-pyrazol-1-yl)-9H-carbazole, 10 mmol of 2-bromo-9-(pyridin-2-yl)-9H-carbazole, 1 mmol of copper(I)iodide, 25 mmol of potassium carbonate, and 2 mmol of L-proline were combined in stirring degassed dimethyl sulfoxide. The mixture was heated to 90° C. for 3 days before being cooled and separated between dichloromethane and water. The water layer was washed twice with dichloromethane and the organics were combined and washed once with brine. The organic fraction was dried with magnesium sulfate and concentrated under reduced pressure and subjected to column chromatography of silica with dichloromethane/ethyl acetate as the eluent. After concentrating under reduced pressure, 2′-(1H-pyrazol-1-yl)-9-(pyridin-2-yl)-9H-2,9′-bicarbazole was isolated in a 60% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09238668B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-2f1e30e93aea45c69aacf49e48edc458
출처 메모uspto-grants-2016_01