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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 244409생성일: 2026년 10월 25일

Pyridine → 5-bromo-1-pyridin-3-yl-1H-indazole

https://huagongshe.com/reaction/244409

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물5-bromo-1H-indazoleHCID 761929—
반응물3-Pyridinylboronic acidHCID 2734378—
촉매Cupric acetateHCID 8895—
용매DichloromethaneHCID 6344—
생성물5-bromo-1-pyridin-3-yl-1H-indazoleHCID 5943730111.1%

반응 단계

A mixture of 2.0 g (10.15 mmol) of 5-bromoindazole, 2.49 g (20.30 mmol) of 3-pyridyl boronic acid, 2.77 g (15.25 mmol) of copper acetate, and 2.4 mL of pyridine were dissolved in dry dichloromethane and stirred at room temperature. Oxygen gas was bubbled into the solution for 3 min and the mix was stirred in a screw top reaction vial in open atmosphere. After stirring overnight at room temperature, the reaction was monitored by LCMS which indicated ˜10-15% conversion. The mixture was then warmed to 70° C. After 24 hours, the mixture was cooled to room temperature, diluted with brine and extracted with EtOAc. The organic was washed with brine, dried over sodium sulfate, and concentrated in vacuo onto silica gel. The crude was then purified by Combiflash chromatography using a 0-70% EtOAc/hexanes gradient (product eluted at 35% EtOAc). The product containing fractions were combined and concentrated in vacuo to afford 0.31 g (11%) of 5-bromo-1-pyridin-3-yl-1H-indazole.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08658637B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-69dc3ec10f73440aa4bfbedf448431d6
출처 메모uspto-grants-2014_02