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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 69201생성일: 2026년 10월 24일

Imidazo[1,2-a]pyridine-6-carbaldehyde → 5-Fluoro-6-[6-(1-methyl-1H-pyrazol-4-yl)-imidazo[1,2-b]pyridazin-3-ylmethyl]-quinoline

https://huagongshe.com/ko/reaction/69201

반응식

참여 물질

역할이름HCID투입량
반응물Imidazo[1,2-a]pyridine-6-carbaldehydeHCID 7164582—
반응물5-Fluoroquinoline-6-carbaldehydeHCID 57917315—
반응물3-Bromo-6-(1-methyl-1h-pyrazol-4-yl)-imidazo[1,2-b]pyridazineHCID 68632486—
생성물5-Fluoro-6-[6-(1-methyl-1H-pyrazol-4-yl)-imidazo[1,2-b]pyridazin-3-ylmethyl]-quinolineHCID 57917488—

반응 단계

(rac)-(5-Fluoro-quinolin-6-yl)-[6-(1-methyl-1H-pyrazol-4-yl)-imidazo[1,2-b]pyridazin-3-yl]-methanol was obtained analogously to Stage 9.1 by replacing 3-bromo-6-chloro-imidazo[1,2-b]pyridazine with 3-bromo-6-(1-methyl-1h-pyrazol-4-yl)-imidazo[1,2-b]pyridazine (Stage 8.1) and imidazo[1,2-a]pyridine-6-carbaldehyde with 5-fluoro-quinoline-6-carbaldehyde (Intermediate A) (tR 0.90 min (conditions 1), (MH+=375).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822468B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-439889cdcf884be28c6710a5346c474e
출처 메모uspto-grants-2014_09