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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 985534Generated: October 27, 2026

Imidazo[1,2-a]pyridine-7-methanol → Imidazo[1,2-A]pyridine-7-carbaldehyde

https://huagongshe.com/reaction/985534

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazo[1,2-a]pyridine-7-methanolHCID 11051824—
CatalystHCID 178418406HCID 178418406—
Solvent1,2-DichloroethaneHCID 11—
ProductImidazo[1,2-A]pyridine-7-carbaldehydeHCID 1102997269%

Reaction Conditions

Temperature50 °C

Reaction Steps

Imidazo[1,2-α]pyridin-7-ylmethanol (1.35 g, 9.38 mmol) was suspended in 1,2-dichloroethane (40 ml), manganese(IV) oxide (4.07 g, 46.9 mmol) added and the mixture heated at 50° C. for 16 h. The mixture was cooled to ambient temperature, filtered through Celite® and evaporated to dryness to give imidazo[1,2-α]pyridine-7-carboxaldehyde (0.92 g, 69%) as a yellow solid. 1H NMR (400 MHz, CDCl3) δH 7.34 (1H, dd, J 7 and 1), 7.75 (1H, s), 7.87 (1H, s), 8.13 (1H, s), 8.21 (1H, d, J 7), 10.00 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06872731B2
Source datasetuspto-grants-2005_03
ORD IDord-05dc5a6338e4474ba606d3fb4495e89e
Source noteuspto-grants-2005_03