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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516557Generated: October 29, 2026

Acetonitrile → Methyl 4-amino-6-(2,3-difluoro-4-(trifluoromethyl)phenyl)-5-fluoro-3-vinylpicolinate

https://huagongshe.com/reaction/516557

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantSodium CarbonateHCID 10340—
Reactant2-(2,3-Difluoro-4-(trifluoromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 53216808—
ReactantMethyl 4-amino-6-chloro-5-fluoro-3-vinylpicolinateHCID 86668309—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
SolventSodium chloride; waterHCID 57417360—
ProductMethyl 4-amino-6-(2,3-difluoro-4-(trifluoromethyl)phenyl)-5-fluoro-3-vinylpicolinateHCID 9040907124.98%

Reaction Conditions

Temperature120 °C

Reaction Steps

In a microwave vessel, a suspension of 2-(2,3-difluoro-4-(trifluoromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (commercially available) (0.641 g, 2.081 mmol), methyl 4-amino-6-chloro-5-fluoro-3-vinylpicolinate (Head G) (0.4 g, 1.734 mmol), bis(triphenyl phosphine)palladium(II) chloride (0.122 g, 0.173 mmol) and sodium carbonate (0.368 g, 3.47 mmol) in a 3:1 mixture of acetonitrile (3.25 mL) and water (1.084 mL) was stirred under microwave irradiation (120° C., 20 min). The reaction mixture was poured into an half saturated brine solution and was extracted with EtOAc (3×). The combined organic layers were dried over Na2SO4, filtered and concentrated. The residue was purified by preparative reverse phase HPLC (water/acetonitrile gradient) to afford the title compound as a brown solid (0.163 g, 0.433 mmol, 24.98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09113629B2
Source datasetuspto-grants-2015_08
ORD IDord-39738c9841774ed2afee354b69b744e9
Source noteuspto-grants-2015_08