Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantSodium SulfiteHCID 24437—
ReactantNitrilooxonium tetrafluoroborateHCID 11137142—
ReactantMethyl 4-amino-6-(4-aminophenyl)-5-fluoro-3-vinylpicolinateHCID 90409711—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductMethyl 4-amino-5-fluoro-6-(4-iodophenyl)-3-vinylpicolinateHCID 9040891423.09%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09113629B2
Source datasetuspto-grants-2015_08
ORD IDord-26343ad24d7149b1a11f8013d2f730df
Source noteuspto-grants-2015_08