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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1892318생성일: 2026년 10월 25일

3-Bromo-6-chloroimidazo(1,2-b)pyridazine → (6-Chloroimidazo[1,2-b]pyridazin-3-yl)(5,7-difluoroquinolin-6-yl)methanol

https://huagongshe.com/reaction/1892318

반응식

참여 물질

역할이름HCID투입량
반응물3-Bromo-6-chloroimidazo(1,2-b)pyridazineHCID 12872323—
반응물5,7-Difluoroquinoline-6-carbaldehydeHCID 57917282—
반응물HCID 178461630HCID 178461630—
용매TetrahydrofuranHCID 8028—
생성물(6-Chloroimidazo[1,2-b]pyridazin-3-yl)(5,7-difluoroquinolin-6-yl)methanolHCID 5814751997%

반응 단계

To a solution of 3-bromo-6-chloro-imidazo[1,2-b]pyridazine (2.40 g, 10.35 mmol) in 30 mL of THF was added EtMgBr (1M in THF, 12.43 mL, 12.42 mmol) solution at rt. The solution was stirred for 30 min and a solution of 5,7-difluoroquinoline-6-carbaldehyde (2.0 g, 10.35 mmol) in 10 mL of THF was added. The resulting mixture was stirred at rt for additional 2 h and then quenched with 50 mL of NH4Cl solution. The solution was extracted with EtOAc and the combined organic layers were washed with water, brine, dried over Na2SO4 and concentrated in vacuo to afford 3.48 g (97%) of the title compound. LCMS (method B): [MH]+=347, tR=1.23 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08507676B2
출처 데이터셋uspto-grants-2013_08
ORD IDord-e51f20782c284a36bcfcb3c8c727a239
출처 메모uspto-grants-2013_08