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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1468280Generated: October 29, 2026

N-Iodosuccinimide → HCID 86710085, compound

https://huagongshe.com/reaction/1468280

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86710086HCID 86710086—
SolventDimethylformamideHCID 6228—
ProductHCID 86710085HCID 8671008566%

Reaction Steps

Butyl 5-methyl-2-(1-methylcyclopropyl)imidazo[1,2-a]pyridine-7-carboxylate (370 mg, 1.29 mmol) obtained in step 1 was dissolved in DMF (3.0 mL), and the solution was stirred at room temperature for 3 hours after adding N-iodosuccinimide (320 mg, 1.42 mmol). Then, a saturated sodium hydrogen carbonate aqueous solution was added to the reaction mixture, and the mixture was filtered through a Presep (registered trademark; diatomaceous earth, granular type M, 4.5 g/25 mL). The solvent was then evaporated under reduced pressure. The residue was purified by silica gel column chromatography (heptane/ethyl acetate=80/20) to give butyl 3-iodo-5-methyl-2-(1-methylcyclopropyl)imidazo[1,2-a]pyridine-7-carboxylate (351 mg, yield 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09000186B2
Source datasetuspto-grants-2015_04
ORD IDord-855d71f57d5e4973ad5a1ec55999287e
Source noteuspto-grants-2015_04