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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1048698Generated: October 30, 2026

N-Iodosuccinimide → HCID 71484324, compound

https://huagongshe.com/reaction/1048698

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
Reactant2-Chloromethyl-imidazo(1,2-A)pyridineHCID 957614—
SolventAcetonitrileHCID 6342—
ProductHCID 71484324HCID 7148432496.4%

Reaction Steps

5 g (30 mmol) of 2-(chloromethyl)imidazo[1,2-a]pyridine were solubilised in 60 ml of acetonitrile with magnetic stirring, 7.31 g (31.5 mmol) of N-iodosuccinimide were added and the mixture was stirred at r.t. for 15 min. The solid formed was isolated by filtration, washed with 30 ml of water and dried in a vacuum bell jar. 8.46 g (yield=95%) of 2-(chloromethyl)-3-iodoimidazo[1,2-a]pyridine were obtained as a white solid. LC-MS: m/z=293 (MH+); UV purity at 254 nm=99%. 1H NMR (300 MHz, DMSO) δ 8.31 (d, J=6.9 Hz, 1H), 7.58 (d, J=9.1 Hz, 1H), 7.46-7.29 (m, 1H), 7.07 (td, J=6.8, 1.0 Hz, 1H), 4.81 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09381191B2
Source datasetuspto-grants-2016_07
ORD IDord-e6339090121c43e08b00139ee7fb0028
Source noteuspto-grants-2016_07