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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 219083생성일: 2026년 10월 26일

1,8-Diazabicyclo(5.4.0)undec-7-ene → 7-Methoxy-4-((5-phenyl-[1,2,3]triazolo[1,5-a]pyridin-3-yl)methoxy)quinoline

https://huagongshe.com/reaction/219083

반응식

참여 물질

역할이름HCID투입량
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물4-Acetamidobenzenesulfonyl azideHCID 5129185—
반응물Methyl 2-(4-phenylpyridin-2-yl)acetateHCID 67503470—
반응물5-Phenyl-[1,2,3]triazolo[1,5-a]pyridine-3-carboxylateHCID 86630264—
용매AcetonitrileHCID 6342—
생성물7-Methoxy-4-((5-phenyl-[1,2,3]triazolo[1,5-a]pyridin-3-yl)methoxy)quinolineHCID 57691340—

반응 단계

5-Phenyl-[1,2,3]triazolo[1,5-a]pyridine-3-carboxylate. To a solution of methyl 2-(4-phenylpyridin-2-yl)acetate (see Lohse, O.; Thevenin, P.; Waldvogel, E. Synlett 1999, 1, 45-48) (0.504 g, 2.22 mmol) in 12 mL CH3CN was added DBU (0.501 ml, 3.33 mmol) and the mixture cooled in an ice bath. To the solution, 4-acetamidobenzenesulfonyl azide (0.533 g, 2.22 mmol) was added and the mixture allowed to warm to rt. The mixture was stirred at rt for 5 h then evaporated. The residue was diluted with CH2Cl2, washed with water, brine, dried over Na2SO4, and filtered. The title compound was obtained after purification via flash chromatography.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08198448B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-9777b9de91304c46a43ed3a49353da7b
출처 메모uspto-grants-2012_06