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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743810Generated: November 1, 2026

Sodium Iodide → Methyl 5-amino-6-chloro-2-methylimidazo[1,2-a]pyridine-8-carboxylate

https://huagongshe.com/reaction/1743810

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantBromoacetoneHCID 11715—
ReactantMethyl 2,6-Diamino-5-chloronicotinateHCID 12088100—
SolventMethanolHCID 887—
ProductMethyl 5-amino-6-chloro-2-methylimidazo[1,2-a]pyridine-8-carboxylateHCID 1208809659%

Reaction Steps

A mixture of methyl 2,6-diamino-5-chloronicotinate (EXAMPLE 1, Step 3, 15 g, 74.4 mmol), bromoacetone (10.4 mL, 112 mmol) and sodium iodide (16.7 g, 112 mmol) in methanol (700 mL) was stirred under reflux for 22 h. Another 2.5 mL (33 mmol) of bromoacetone was added and the stirring was continued for 24 h. The reaction mixture was quenched with saturated aqueous sodium carbonate and removed methanol in vacuo. The residue was extracted with ethyl acetate (250 mL×10) adding a small amount of methanol to dissolve the organic solid. The organic extracts were dried over sodium sulfate and concentrated. Purification by column chromatography on silica gel eluting with dichloromethane/methanol (20:1) gave a dark brown solid, which was washed with ethyl acetate and filtered to afford 10.5 g (43.9 mmol, 59%) of the title compound as a pale brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07012080B2
Source datasetuspto-grants-2006_03
ORD IDord-aa1f2e8d9e3e4254bf49cbfb3aa60b9c
Source noteuspto-grants-2006_03