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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889472Generated: October 28, 2026

Iodine → 3-((6-Chloro-3-cyanoimidazo[1,2-b]pyridazin-8-yl)(4-methoxybenzyl)amino)benzoic acid

https://huagongshe.com/reaction/889472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantWaterHCID 962—
Reactanttert-Butyl 3-((6-chloro-3-cyanoimidazo[1,2-b]pyridazin-8-yl)(4-methoxybenzyl)amino)benzoateHCID 59314053—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product3-((6-Chloro-3-cyanoimidazo[1,2-b]pyridazin-8-yl)(4-methoxybenzyl)amino)benzoic acidHCID 5931400666.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 253B (100 mg, 0.20 mmol) in acetonitrile (5 mL) was treated with iodine (15.54 mg, 0.061 mmol) and water (50 μL, 2.78 mmol). The reaction mixture was stirred at 80° C. for 8 hours. The reaction mixture was diluted with ethyl acetate, and washed with water. The aqueous layer was extracted with ethyl acetate (4×20 mL). The pooled organic phase was dried over Na2SO4 and concentrated. The residue was triturated with DCM and filtered. The filtrate was concentrated, dissolved in DCM, and purified by flash chromatography, silica column (12 g, gradient elution from hexanes-ethyl acetate in 15 min.). The appropriate fraction was concentrated under reduced pressure and dried in vacuo to yield 253C (57.5 mg, 64.9% yield) as a yellow solid. HPLC: Rt=4.23 min. (PHENOMENEX® Luna C18 4.6×30 mm 3 u, A10-90% aqueous methanol containing 0.1% TFA in 2 min; 4 mL/min flow). MS (ES): m/z=434.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08252795B2
Source datasetuspto-grants-2012_08
ORD IDord-15d262f1fcc740d2aba008a3f14d52fc
Source noteuspto-grants-2012_08