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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1798706Generated: October 31, 2026

Chlorosuccinimide → 3-Chloro-2-(chloromethyl)imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1798706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
Reactant2-Chloromethyl-imidazo(1,2-A)pyridineHCID 957614—
SolventDichloromethaneHCID 6344—
Product3-Chloro-2-(chloromethyl)imidazo[1,2-a]pyridineHCID 5958016690.4%

Reaction Steps

N-Chloro succinimide (329 g, 2.46 mmol) was added to a solution of 2-(chloromethyl)imidazo[1,2-a]pyridine (450 mg, 2.2 mmol) in DCM (15 ml) at RT under an atmosphere of nitrogen. Stirring was continued for 2 h (reaction was monitored by TLC) upon which the reaction mixture was diluted with DCM and washed with water and brine solution. The organic layer was dried over sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by flash column chromatography using 10% ethyl acetate in n-hexane and silica gel (230-400 mesh) to afford 3-chloro-2-(chloromethyl)imidazo[1,2-a]pyridine (400 mg, 76%) as Off-white solid. 1H NMR: 200 MHz, CDCl3: δ 8.4 (d, 1H), 7.7 (d, 1H), 7.5 (t, 1H), 7.1 (t, 1H), 4.85 (s, 2H). MS: [M+H]+: m/z=201.8. HPLC: (98.3%, Condition-A).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343973B2
Source datasetuspto-grants-2013_01
ORD IDord-226fcdff754340c88de6574d7d5f3b79
Source noteuspto-grants-2013_01