HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516578Generated: October 31, 2026
Sodium Iodide → Methyl 4-amino-5-fluoro-6-(4-iodophenyl)-3-vinylpicolinate
https://huagongshe.com/reaction/516578
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | Nitrilooxonium tetrafluoroborate | HCID 11137142 | — |
| Reactant | Methyl 4-amino-6-(4-aminophenyl)-5-fluoro-3-vinylpicolinate | HCID 90409711 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 4-amino-5-fluoro-6-(4-iodophenyl)-3-vinylpicolinate | HCID 90408914 | 23.09% |
Reaction Steps
To a 0° C. suspension of nitrosyl tetrafluoroborate (0.041 g, 0.348 mmol) in CH2Cl2 (1 mL) was added a solution of methyl 4-amino-6-(4-aminophenyl)-5-fluoro-3-vinylpicolinate (0.1 g, 0.348 mmol) in a 1:1 mixture of CH2Cl2 and CH3CN (4 mL). The reaction mixture was stirred at 0° C. for 30 min, then a solution of sodium iodide (0.261 g, 1.740 mmol) dissolved in a minimum of water was added and the reaction was stirred at 20° C. for 30 min. The mixture was then poured into a 10% aqueous solution of sodium sulfite and extracted with EtOAc (3×). The combined organic layers were dried over Na2SO4, filtered and concentrated. The residue was purified by flash column chromatography (SiO2, hexanes/EtOAc gradient) followed by preparative reverse phase HPLC (water/acetonitrile gradient) to afford the title compound as a white solid (32 mg, 0.080 mmol, 23.09%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09113629B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-26343ad24d7149b1a11f8013d2f730df |
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| Source note | uspto-grants-2015_08 |
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