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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 2-Chloroethyl methyl ether | HCID 12316 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | 6-Fluoro-4-iodopyridin-3-amine | HCID 58266641 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 6-fluoro-4-iodo-N-(2-methoxyethyl)pyridin-3-amine | HCID 66738361 | 20% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08114872B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-62a094c6ad3544529290bd44c05b7c2a |
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| Source note | uspto-grants-2012_02 |
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