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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1959637Generated: November 4, 2026

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

https://huagongshe.com/reaction/1959637

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 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 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 numberUS08410264B2
Source datasetuspto-grants-2013_04
ORD IDord-321f4162416247a99731eee8cde3ba02
Source noteuspto-grants-2013_04