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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium fluorideHCID 25953—
ReactantTributylvinyltinHCID 81998—
ReactantMethyl 4-amino-3,6-dichloro-5-fluoropicolinateHCID 22677265—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
ProductMethyl 4-amino-3-chloro-5-fluoro-6-vinylpyridine-2-carboxylateHCID 6702673767.3%

Reaction Conditions

Temperature90 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432227B2
Source datasetuspto-grants-2008_10
ORD IDord-8ecb7cec0a2d499982da6031aa5121ae
Source noteuspto-grants-2008_10