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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892300Generated: November 1, 2026

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

https://huagongshe.com/reaction/1892300

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%

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 filtered. The filtrate was concentrated under vacuum and the residue was washed with EtOAc to affrode 6-chloro-imidazo[1,2-b]pyridazine-3-carbaldehyde (0.7 g) in 54% yield. 1H-NMR (400 MHz, CDCl3) δ ppm 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 numberUS08507676B2
Source datasetuspto-grants-2013_08
ORD IDord-fd711083ba844007a5cc9d47dcf65385
Source noteuspto-grants-2013_08