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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516550Generated: October 26, 2026

Potassium Fluoride → Methyl 4-amino-3-chloro-6-(3-fluoro-4-(trifluoromethyl)phenyl)picolinate

https://huagongshe.com/reaction/516550

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium FluorideHCID 522689—
ReactantMethyl 4-amino-3,6-dichloropyridine-2-carboxylateHCID 22677331—
Reactant3-Fluoro-4-(trifluoromethyl)phenylboronic acid pinacol esterHCID 46739054—
CatalystHCID 178418476HCID 178418476—
SolventEthyl AcetateHCID 8857—
SolventAcetonitrile--water (1/1)HCID 18373917—
ProductMethyl 4-amino-3-chloro-6-(3-fluoro-4-(trifluoromethyl)phenyl)picolinateHCID 9040986157.4%

Reaction Steps

Methyl 4-amino-3,6-dichloropicolinate (630 mg, 2.85 mmol), 2-(3-fluoro-4-(trifluoromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (1.06 g, 3.65 mmol, 1.3 equiv), bis(triphenylphosphine)palladium(II) chloride (209 mg, 0.30 mmol, 0.1 equiv), and potassium fluoride (510 mg, 8.8 mmol, 3 equiv) in acetonitrile/water (8 mL, 3:1) was capped in a 25-mL vial on a Biotage Initiator™ microwave reactor for 20 min at 115° C., with external IR-sensor temperature monitoring from the side of the vessel. The reaction mixture was diluted with ethyl acetate and washed with water. The aqueous layer was extracted with ethyl acetate and the combined organic layers were dried over anhydrous sodium sulfate, filtered, and concentrated. The crude compound was loaded onto a Celite™ cartridge and dried in vacuum oven. Purification by reverse-phase flash chromatography (0-60, 60, 60-100% acetonitrile/water) afforded the title compound as a white solid (0.57 g, 57%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09113629B2
Source datasetuspto-grants-2015_08
ORD IDord-0f849c1f5d18405e85e02b41ae6fcc65
Source noteuspto-grants-2015_08