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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 455124Generated: October 25, 2026

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

https://huagongshe.com/reaction/455124

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-1,3,4-oxadiazoleHCID 558447—
Reactant6-Chloro-2-phenylimidazo[1,2-a]pyridine-3-carbaldehydeHCID 2757792—
Reactant6-fluoro-2-(4-fluorophenyl)-3-((1-methyl-1H-imidazol-2-yl)methyl)imidazo[1,2-a]pyridineHCID 67029064—
Product2-((6-Chloro-2-phenylimidazo[1,2-a]pyridin-3-yl)methyl)-5-methyl-1,3,4-oxadiazoleHCID 67029111—

Reaction Steps

The title compound was prepared according to Method C and the experimentals described for compound 199 from 6-chloro-2-phenylimidazo[1,2-a]pyridine-3-carbaldehyde and 2-methyl-1,3,4-oxadiazole. M/e+ 325 for C17H14ClN4O (M+H)+; 1H-NMR (400 MHz, CDCl3) δ 8.25 (d, J=1.4 Hz, 1H), 7.81 (d, J=8.4 Hz, 2H), 7.61 (d, J=9.5 Hz, 1H), 7.51 (d, J=8.4 Hz, 2H), 7.43 (d, J=7.3 Hz, 1H), 7.22 (dd, J=9.5, 1.8 Hz, 1H), 4.58 (s, 2H), 2.52 (s, 3H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08497278B2
Source datasetuspto-grants-2013_07
ORD IDord-2860dbaa1471475c910e5ae2c3f1e83d
Source noteuspto-grants-2013_07