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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2089640Generated: October 26, 2026

Sodium Iodide → HCID 68212832, compound

https://huagongshe.com/reaction/2089640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantCyclohexanecarboxylic acidHCID 7413—
ReactantAmmonium ChlorideHCID 25517—
ReactantPotassium BicarbonateHCID 516893—
Reactant[1-amino-1-[4-({(5-chloromethoxy-1-pyrimidin-2-yl-1H-[1,2,4]triazol-3-yl)-[2-fluoro-3-(2-hydroxyethoxy)-5-methoxyphenyl]methyl}amino)phenyl]methylidene]carbamic acid 2,2-dimethylpropyl esterHCID 67470504—
SolventDimethylformamideHCID 6228—
ProductHCID 68212832HCID 6821283289.9%

Reaction Conditions

Temperature45 °C

Reaction Steps

To a mixture of [1-amino-1-[4-({(5-chloromethoxy-1-pyrimidin-2-yl-1H-[1,2,4]triazol-3-yl)-[2-fluoro-3-(2-hydroxyethoxy)-5-methoxyphenyl]methyl}amino)phenyl]methylidene]carbamic acid 2,2-dimethylpropyl ester (Example 2b, 120 mg), potassium hydrogen carbonate (131 mg), and DMF (16 mL), sodium iodide (140 mg) and cyclohexanecarboxylic acid (163 mg) were added, and the resulting mixture was stirred at 45° C. overnight. After cooling the reaction mixture to room temperature, ice and saturated aqueous ammonium chloride solution were added thereto, and the resulting mixture was extracted three times with a mixture of THF and ethyl acetate. The organic layer was collected, washed with saturated aqueous ammonium chloride solution, and dried over anhydrous magnesium sulfate. The resulting mixture was filtered, and the filtrate obtained was concentrated under reduced pressure. The residue obtained was purified by NAM silica gel column chromatography (mixed solvent of methanol-ethyl acetate) to obtain the captioned compound (123 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436009B2
Source datasetuspto-grants-2013_05
ORD IDord-2cb65d0adad14198a63a76085802c814
Source noteuspto-grants-2013_05