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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2205194Generated: November 3, 2026

N-Iodosuccinimide → 6-Chloro-3-iodoimidazo[1,2-b]pyridazine

https://huagongshe.com/reaction/2205194

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
ReactantImidazo(1,2-b)pyridazine, 6-chloro-HCID 138828—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
Product6-Chloro-3-iodoimidazo[1,2-b]pyridazineHCID 5324989790.8%

Reaction Steps

6-chloroimidazo[1,2-b]pyridazine (2.0 g, 13.0 mmol, 1.0 equiv) in chloroform (20 mL) at room temperature was added N-iodosuccinimide (2.9 g, 13.0 mmol, 1.0 equiv) then stirred vigorously overnight. The reaction mixture was diluted in water and extracted with ethyl acetate. Purification using column chromatography gave 3.3 g of the yellow solid, 90%: 1H NMR δ 8.21 (d, J=7.6 Hz, 1H), 7.96 (s, 1H), 7.41 (d, J=7.6 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09370515B2
Source datasetuspto-grants-2016_06
ORD IDord-4e5dce4404514e6b9c769ccd44b63504
Source noteuspto-grants-2016_06