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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394651Generated: November 2, 2026

Methyl imidazo(1,2-a)pyridine-6-carboxylate → Methyl 3-iodoimidazo[1,2-a]pyridine-6-carboxylate

https://huagongshe.com/reaction/1394651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl imidazo(1,2-a)pyridine-6-carboxylateHCID 2764326—
ReactantN-IodosuccinamideHCID 21864724—
SolventAcetonitrileHCID 6342—
ProductMethyl 3-iodoimidazo[1,2-a]pyridine-6-carboxylateHCID 1641317095%

Reaction Conditions

Temperature0 °C

Reaction Steps

N-iodosuccinamide (1.55 g, 6.89 mmol) was added to a solution of imidazo[1,2-a]pyridine-6-carboxylic acid methyl ester (1.1 g, 6.24 mmol) in acetonitrile (50 mL) which had been cooled to 0° C. under a nitrogen atmosphere. The reaction stirred for 1 hr, then concentrated in vaccuo to a residue. The residue was dissolved in ethyl acetate (50 mL) and washed with 10% sodium bisulfate (2×10 ml) and brine (1×20 mL), then the organic layers were dried over MgSO4 and evaporated to give 3-iodo-imidazo[1,2-a]pyridine-6-carboxylic acid methyl ester as a pale yellow solid (1.79 g, 95%). 1H NMR (250 MHz, CDCl3): δ 8.91 (s, 1H), 7.85 (dd, 1H, J=2.5, J=10), 7.80 (s, 1H), 7.69 (d, 1H, J=10), 4.01 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07348359B2
Source datasetuspto-grants-2008_03
ORD IDord-5e49c718ddbe42b087c700108fb1ba47
Source noteuspto-grants-2008_03