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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 455123Generated: October 25, 2026

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

https://huagongshe.com/reaction/455123

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-1,3,4-oxadiazoleHCID 558447—
Reactant2-(4-Chlorophenyl)imidazo[1,2-a]pyridine-3-carbaldehydeHCID 2757793—
Reactant6-fluoro-2-(4-fluorophenyl)-3-((1-methyl-1H-imidazol-2-yl)methyl)imidazo[1,2-a]pyridineHCID 67029064—
Product2-((2-(4-Chlorophenyl)imidazo[1,2-a]pyridin-3-yl)methyl)-5-methyl-1,3,4-oxadiazoleHCID 67028791—

Reaction Steps

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 2-methyl-1,3,4-oxadiazole. M/e+ 325 for C17H14ClN4O (M+H)+; 1H-NMR (400 MHz, CDCl3) δ 8.22 (d, J=6.6 Hz, 1H), 7.80 (d, J=8.4 Hz, 2H), 7.67 (d, J=9.1 Hz, 1H), 7.47 (d, J=8.4 Hz, 2H), 7.27 (t, J=6.9 Hz, 1H), 6.91 (d, J=6.6 Hz, 1H), 4.58 (s, 2H), 2.50 (s, 3H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08497278B2
Source datasetuspto-grants-2013_07
ORD IDord-234c3edc7b3d4e87be8758fda64ff2a4
Source noteuspto-grants-2013_07