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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890185Generated: October 26, 2026

Water → 2-[4'-(2''-Fluoroethoxy)phenyl]-6-iodoimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1890185

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Fluoroethyl p-ToluenesulfonateHCID 256019—
Reactant2-(4'-Hydroxyphenyl)-6-iodoimidazo[1,2-a]pyridineHCID 24757011—
SolventChloroformHCID 6212—
Product2-[4'-(2''-Fluoroethoxy)phenyl]-6-iodoimidazo[1,2-a]pyridineHCID 2475692952.7%

Reaction Steps

368 mg (corresponding to 1.1 mmol) of 2-(4′-hydroxyphenyl)-6-iodoimidazo[1,2-a]pyridine that was sufficiently dried to remove moisture was dissolved in 15 mL of N,N-dimethylformamide, and 453 mg (corresponding to 3.3 mmol) of potassium carbonate was added thereto. The mixture was supplemented with 280 μL (corresponding to 1.6 mmol) of 2-fluoroethyl-p-toluenesulfonate, and then the solution was stirred at room temperature for 22 hours. After the completion of the reaction, the reaction solution was poured into water and extracted three times with chloroform. The combined chloroform layer was washed with water and a saturated sodium chloride solution, dried over anhydrous sodium sulfate, filtered and concentrated. The resulting crude product was purified by flash silica gel column chromatography (elution solvent: hexane/ethyl acetate=1/1), and further by recycle preparative HPLC (HPLC apparatus: LC-908 (under trade name; manufactured by Japan Analytical Industry Co., Ltd.); column: two JAIGEL 2H (under trade name; manufactured by Japan Analytical Industry Co., Ltd.) connected together; mobile phase: chloroform), to obtain 222 mg (corresponding to 0.580 mmol) of 2-[4′-(2″-fluoroethoxy)phenyl]-6-iodoimidazo[1,2-a]pyridine (FIG. 1-7, Step 3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08506930B2
Source datasetuspto-grants-2013_08
ORD IDord-d18d759f63a64d2092475934509e357a
Source noteuspto-grants-2013_08