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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 455127생성일: 2026년 10월 25일

1-Vinylimidazole → 2-(4-chlorophenyl)-3-((1-vinyl-1H-imidazol-2-yl)methyl)imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/455127

반응식

참여 물질

역할이름HCID투입량
반응물1-VinylimidazoleHCID 66171—
반응물2-(4-Chlorophenyl)imidazo[1,2-a]pyridine-3-carbaldehydeHCID 2757793—
반응물6-fluoro-2-(4-fluorophenyl)-3-((1-methyl-1H-imidazol-2-yl)methyl)imidazo[1,2-a]pyridineHCID 67029064—
생성물2-(4-chlorophenyl)-3-((1-vinyl-1H-imidazol-2-yl)methyl)imidazo[1,2-a]pyridineHCID 67028933—

반응 단계

The title compound was prepared according to Method C and the experimentals described for compound 199 from 2-(4-chlorophenyl)imidazo[1,2-a]pyridine-3-carbaldehyde and 1-vinyl-1H-imidazole. (34 mg, 18%). m/e+=335 (M+H+). 1H-NMR (400 MHz, CDCl3, δ): 8.28 (d, 1H, D, J=7.0 Hz), 7.66 (d, 2H, D, J=10.2 Hz), 7.61 (d, 1H, D, J=9.2 Hz), 7.46 (d, 2H, D, J=8.5 Hz), 7.19 (t, 1H, D, J=7.9 Hz), 7.08 (d, 1H), 6.96 (d, 1H), 6.80 (t, 1H, D, J=7.0 Hz), 6.46 (m, 1H), 5.03 (m, 1H), 4.62 (m, 1H), 4.56 (s, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08497278B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-bd0adb78bd4140ecbb4124bda0ccbd24
출처 메모uspto-grants-2013_07