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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640910Generated: October 25, 2026

Trifluoroacetic acid → 6-fluoro-4-iodo-N-(2-methoxyethyl)pyridin-3-amine

https://huagongshe.com/reaction/1640910

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant2-Chloroethyl methyl etherHCID 12316—
ReactantPotassium HydroxideHCID 14797—
ReactantPotassium FluorideHCID 522689—
Reactant6-Fluoro-4-iodopyridin-3-amineHCID 58266641—
CatalystTetrabutylammonium IodideHCID 67553—
Solvent1,4-DioxaneHCID 31275—
Product6-fluoro-4-iodo-N-(2-methoxyethyl)pyridin-3-amineHCID 6673836120%

Reaction Conditions

Temperature100 °C

Reaction Steps

Mix 6-fluoro-4-iodopyridin-3-amine in TFA salt (0.36 g, 1.50 mmol), 2-chloroethyl methyl ether (0.31 g, 3.30 mmol), potassium hydroxide (0.19 g, 3.30 mmol), potassium fluoride (0.19 g, 3.30 mmol), and tetrabutylammonium iodide (0.11 g, 0.30 mmol) in 1,4-dioxane (1.5 mL) in a seal reactor. Heat the reaction mixture at 100° C. overnight. Cool the reaction mixture to RT. Quench with water. Extract with ethyl acetate, wash the organic layer with water and saturated aqueous sodium chloride. Dry over MgSO4. After the filtration, remove the reaction solvent under reduced pressure. Purify by FCC (0.1% to 1% 2 M NH3 methanol solution/CH2Cl2) to give the title compound (0.09 g, 20%) with 80% HPLC purity. MS (ES) m/z 279 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114872B2
Source datasetuspto-grants-2012_02
ORD IDord-62a094c6ad3544529290bd44c05b7c2a
Source noteuspto-grants-2012_02