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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516560Generated: October 31, 2026

Acetonitrile → Methyl 4-amino-6-(4-cyanophenyl)-5-fluoro-3-vinylpicolinate

https://huagongshe.com/reaction/516560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantPotassium FluorideHCID 522689—
Reactant4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrileHCID 2734625—
ReactantMethyl 4-amino-6-chloro-5-fluoro-3-vinylpicolinateHCID 86668309—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductMethyl 4-amino-6-(4-cyanophenyl)-5-fluoro-3-vinylpicolinateHCID 90409686—

Reaction Steps

To a 5-mL microwave safe vial was added potassium fluoride (0.227 g, 3.90 mmol), methyl 4-amino-6-chloro-5-fluoro-3-vinylpicolinate (0.3 g, 1.301 mmol), bis(triphenylphosphine)palladium (II) chloride (0.091 g, 0.130 mmol) and 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile (0.313 g, 1.366 mmol. A mixture of water (1 mL) and acetonitrile (2 mL) was added and the reaction was capped and placed in a Biotage Initiator™ microwave reactor for 20 min at 115° C., with external IR-sensor temperature monitoring from the side of the vessel. Upon cooling to room temperature, the reaction mixture was diluted with CH2Cl2 (25 mL) and water (25 mL) and the organic layer was filtered through cotton plug. An additional extraction using EtOAc (25 mL) was combined with the CH2Cl2 and dried over of Na2SO4 (50 g). Following filtration of the combined organics through a cotton plug and concentration on a rotary evaporator, the residue was purified using a Teledyne ISCO purification system with a gradient eluent system of CH2Cl2 and EtOAc to yield the title compound as a tan solid (297 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09113629B2
Source datasetuspto-grants-2015_08
ORD IDord-328c9996709d413e9310efb5a17b0601
Source noteuspto-grants-2015_08