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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1842420Generated: November 3, 2026

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

https://huagongshe.com/reaction/1842420

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 numberUS08946222B2
Source datasetuspto-grants-2015_02
ORD IDord-21a1575dc7684ab8ad9b412918e22e09
Source noteuspto-grants-2015_02