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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2185772Generated: October 30, 2026

Tributylvinyltin → 5-Ethenyl-6-fluoropyridin-3-amine

https://huagongshe.com/reaction/2185772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylvinyltinHCID 81998—
Reactant5-Bromo-6-fluoropyridin-3-amineHCID 18379725—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product5-Ethenyl-6-fluoropyridin-3-amineHCID 1845893598%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a stirred solution of 5-amino-3-bromo-2-fluoropyridine (3.25 g, 17.0 mmol) from step 131b above in toluene (20 mL) was added tributyl(vinyl)tin (7.64 g, 20.4 mmol) followed by tetrakis(triphenylphosphine)palladium (Aldrich, 0.63 g, 1.7 mmol). The reaction mixture was heated at 100° C. for 24 h. The solvent was removed in vacuo and the residue was purified by column chromatography (silica gel; EtOAc/hexane, 4:6) to afford the title compound as a beige solid (2.30 g, 98%): 1H NMR (CDCl3, 300 MHz) δ3.61 (br s, 2H), 5.44 (d, J=11.5 Hz, 1H), 5.83 (d, J=17.5 Hz, 1H), 6.66 (m, 1H), 7.18 (dd, J=3.0, 5.0 Hz, 1H), 7.52 (m, 1H); MS (CI/NH3) m/z 139 (M+H)+, 156 (M+NH4)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06403575B1
Source datasetuspto-grants-2002_06
ORD IDord-bd67185bb8e440ffa9a705c0a8b2afad
Source noteuspto-grants-2002_06