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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 407002Generated: October 29, 2026

N-Iodosuccinimide → 7-Chloro-3-iodoimidazo[1,2-b]pyridazine

https://huagongshe.com/reaction/407002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
Reactant7-Chloroimidazo(1,2-b)pyridazineHCID 67980259—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product7-Chloro-3-iodoimidazo[1,2-b]pyridazineHCID 6798058877.9%

Reaction Steps

N-Iodosuccinimide (2.17 g, 9.65 mmol) was added to a solution of 7-chloroimidazo[1,2-b]pyridazine (0.988 g, 6.43 mmol) in N,N-dimethylformamide (25 mL). The reaction mixture was stirred at r.t. overnight. The mixture was diluted with ethyl acetate, washed with water and brine. The organic layer was dried over MgSO4, filtered, and concentrated under reduced pressure. The residue was purified by flash chromatography on a silica gel column with ethyl acetate in hexane (gradient: 0-50%) to afford the desired product (1.40 g, 77.9%). LCMS (M+H)+: m/z=279.9/281.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754114B2
Source datasetuspto-grants-2014_06
ORD IDord-a375889df9424b4bb56a380b9e738cfd
Source noteuspto-grants-2014_06