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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15990생성일: 2026년 10월 27일

Cesium fluoride → 6-((6-(4-methyl-1H-imidazol-1-yl)-1H-[1,2,3]triazolo[4,5-b]pyrazin-1-yl)methyl)quinoline

https://huagongshe.com/reaction/15990

반응식

참여 물질

역할이름HCID투입량
반응물Cesium fluorideHCID 25953—
반응물6-((6-bromo-1H-[1,2,3]triazolo[4,5-b]pyrazin-1-yl)methyl)quinolineHCID 54775608—
반응물HCID 178418800HCID 178418800—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
생성물6-((6-(4-methyl-1H-imidazol-1-yl)-1H-[1,2,3]triazolo[4,5-b]pyrazin-1-yl)methyl)quinolineHCID 2485183856%

반응 조건

온도160 °C

반응 단계

A mixture of 6-((6-bromo-1H-[1,2,3]triazolo[4,5-b]pyrazin-1-yl)methyl)quinoline (50 mg, 0.15 mmol), 4-methyl-1H-imidazole (36 mg, 0.44 mmol) and CsF (25 mg, 0.16 mmol) in acetonitrile (1.45 mL) was heated in a microwave to 160° C. for 20 minutes. The reaction was diluted with water (5 mL) and the resulting suspension was filtered. The precipitate was washed with water and then purified by column chromatography using gradient elution with methanol and dichloromethane to afford 6-((6-(4-methyl-1H-imidazol-1-yl)-1H-[1,2,3]triazolo[4,5-b]pyrazin-1-yl)methyl)quinoline (28 mg, yield 56%)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732604B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-c0952ee84e994226b7dcb2797003c9a7
출처 메모uspto-grants-2010_06