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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile | HCID 2734625 | — |
| Reactant | Methyl 4-amino-6-chloro-5-fluoro-3-vinylpicolinate | HCID 86668309 | — |
| Catalyst | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 4-amino-6-(4-cyanophenyl)-5-fluoro-3-vinylpicolinate | HCID 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
| 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-328c9996709d413e9310efb5a17b0601 |
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| Source note | uspto-grants-2015_08 |
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