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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Imidazo[1,2-a]pyridine-7-methanol | HCID 11051824 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | Imidazo[1,2-A]pyridine-7-carbaldehyde | HCID 11029972 | 69% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06872731B2 |
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| Source dataset | uspto-grants-2005_03 |
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| ORD ID | ord-05dc5a6338e4474ba606d3fb4495e89e |
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| Source note | uspto-grants-2005_03 |
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