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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1048688Generated: November 1, 2026

N-Iodosuccinimide → HCID 118195270, compound

https://huagongshe.com/reaction/1048688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
ReactantHCID 118195252HCID 118195252—
SolventAcetonitrileHCID 6342—
ProductHCID 118195270HCID 11819527067.2%

Reaction Steps

0.45 g (1.921 mmol) of ethyl 2-(imidazo[1,2-a]pyridin-2-ylmethoxy)acetate were solubilised in 6 ml of acetonitrile with magnetic stirring, to this solution were added 0.475 g (2.113 mmol) of N-iodosuccinimide. The mixture was stirred at r.t. for 16 h. A solid was removed by filtration and the obtained filtrate was concentrated in vacuo. The residue was triturated with 10 ml of diisopropyl ether and a precipitate was isolated by filtration. 0.465 g (yield=67%) ethyl 2-((3-iodoimidazo[1,2-a]pyridin-2-yl)methoxy)acetate were obtained as a yellow solid. LC-MS: m/z=361 (MH+); UV purity at 254 nm=75%. 1H NMR (300 MHz, DMSO) δ 8.34 (d, J=6.9 Hz, 1H), 7.59 (d, J=8.1 Hz, 1H), 7.47-7.28 (m, 1H), 7.07 (d, J=5.7 Hz, 1H), 4.67 (s, 2H), 4.14 (t, J=10.7 Hz, 4H), 1.22 (d, J=1.9 Hz, 3H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09381191B2
Source datasetuspto-grants-2016_07
ORD IDord-47002306bab44f7d9d903b6422fd5e8b
Source noteuspto-grants-2016_07