HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113413Generated: October 27, 2026
Cesium fluoride → Methyl 4-amino-3-chloro-5-fluoro-6-vinylpyridine-2-carboxylate
https://huagongshe.com/reaction/2113413
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium fluoride | HCID 25953 | — |
| Reactant | Tributylvinyltin | HCID 81998 | — |
| Reactant | Methyl 4-amino-3,6-dichloro-5-fluoropicolinate | HCID 22677265 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 4-amino-3-chloro-5-fluoro-6-vinylpyridine-2-carboxylate | HCID 67026737 | 67.3% |
Reaction Steps
A solution of methyl 4-amino-3,6-dichloro-5-fluoropyridine-2-carboxylate (8.00 g, 33.0 mmol), tributyl(vinyl)tin (13.27 g, 42.0 mmol) and cesium fluoride (11.19 g, 73.6 mmol) in dimethylformamide (250 mL) was sparged with nitrogen for 15 minutes. Dichlorobis(triphenylphosphine)palladium (II) (1.17 g, 1.6 mmol) was then added and the mixture was heated at 90° C. overnight. After cooling, the mixture was concentrated, taken up into ethyl acetate and filtered through a silica gel plug. The solvents were removed and the crude product was purified by column chromatography (50% ethyl acetate in hexane) to give methyl 4-amino-3-chloro-5-fluoro-6-vinylpyridine-2-carboxylate (5.13 g, 22.2 mmol), mp 68-71° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07432227B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-8ecb7cec0a2d499982da6031aa5121ae |
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| Source note | uspto-grants-2008_10 |
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