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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456046Generated: October 30, 2026

(6-Chloroimidazo(1,2-b)pyridazin-3-yl)methanol → 6-Chloroimidazo[1,2-b]pyridazine-3-carbaldehyde

https://huagongshe.com/reaction/456046

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(6-Chloroimidazo(1,2-b)pyridazin-3-yl)methanolHCID 57352521—
CatalystManganese dioxideHCID 14801—
SolventDichloromethaneHCID 6344—
Product6-Chloroimidazo[1,2-b]pyridazine-3-carbaldehydeHCID 1144670254.3%

Reaction Steps

To a solution of (6-chloro-imidazo[1,2-b]pyridazin-3-yl)-methanol (1.3 g, 7.1 mmol) in DCM (50 mL) was added active MnO2 (3 g, 34.5 mmol). The mixture was stirred at rt overnight and then filtered. The filtrate was concentrated under vacuum and the residue was washed with EtOAc to afford 6-chloro-imidazo[1,2-b]pyridazine-3-carbaldehyde (0.7 g) in 54% yield. 1H-NMR (400 MHz, CDCl3) δ 10.36 (s, 1H), 8.42 (s, 1H), 8.08 (d, 1H), 7.38 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08497368B2
Source datasetuspto-grants-2013_07
ORD IDord-62cc9408a3114ab9a8048bd5cae8609b
Source noteuspto-grants-2013_07