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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 455122생성일: 2026년 10월 25일

2-Methyl-1,3,4-oxadiazole → 2-((2-(4-Chlorophenyl)-6-methylimidazo[1,2-a]pyridin-3-yl)methyl)-5-methyl-1,3,4-oxadiazole

https://huagongshe.com/reaction/455122

반응식

참여 물질

역할이름HCID투입량
반응물2-Methyl-1,3,4-oxadiazoleHCID 558447—
반응물2-(4-Chlorophenyl)-6-methylimidazo[1,2-a]pyridine-3-carbaldehydeHCID 2757806—
반응물6-fluoro-2-(4-fluorophenyl)-3-((1-methyl-1H-imidazol-2-yl)methyl)imidazo[1,2-a]pyridineHCID 67029064—
생성물2-((2-(4-Chlorophenyl)-6-methylimidazo[1,2-a]pyridin-3-yl)methyl)-5-methyl-1,3,4-oxadiazoleHCID 67027492—

반응 단계

The title compound was prepared according to Method C and the experimentals described for compound 199 from 2-(4-chlorophenyl)-6-methylimidazo[1,2-a]pyridine-3-carbaldehyde and 2-methyl-1,3,4-oxadiazole. M/e+ 339 for C18H16ClN4O (M+H)+; 1H-NMR (400 MHz, CDCl3) δ 7.95 (s, 1H), 7.76 (d, J=8.4 Hz, 2H), 7.56 (d, J=9.1 Hz, 1H), 7.45 (d, J=8.4 Hz, 2H), 7.10 (dd, J=9.1, 1.4 Hz, 1H), 4.54 (s, 2H), 2.49 (s, 3H), 2.35 (s, 3H) ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08497278B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-01079419ffa9439db91c9810754c18a5
출처 메모uspto-grants-2013_07