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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 80736생성일: 2026년 10월 23일

4-(1-Pyrrolidinyl)piperidine → 2-Phenyl-3-pyrid-4-yl-6-(4-pyrrolidin-1-ylpiperid-1-yl)imidazo[1,2-b]pyridazine

https://huagongshe.com/ko/reaction/80736

반응식

참여 물질

역할이름HCID투입량
반응물4-(1-Pyrrolidinyl)piperidineHCID 78703—
반응물6-Chloro-2-phenyl-3-pyrid-4-ylimidazo[1,2-b]pyridazineHCID 59406954—
용매EthanolHCID 702—
생성물2-Phenyl-3-pyrid-4-yl-6-(4-pyrrolidin-1-ylpiperid-1-yl)imidazo[1,2-b]pyridazineHCID 59406955—

반응 조건

온도155 °C

반응 단계

A mixture of 4.03 g (13.1 mmol) of 6-chloro-2-phenyl-3-pyrid-4-ylimidazo[1,2-b]pyridazine and 4.4 g (29 mmol) of 4-pyrrolidin-1-ylpiperidine in 50 mL of ethanol is heated at 155° C. for 4 hours. After cooling, the solvent is evaporated off under reduced pressure and the residue is chromatographed on silica gel, eluting with a mixture of dichloromethane and methanol (93:7).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846676B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-c2eb2d7b1f2042a3af4bc5b0db2ec5b6
출처 메모uspto-grants-2014_09