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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 367107Generated: October 26, 2026

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

https://huagongshe.com/reaction/367107

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylvinyltinHCID 81998—
Reactant5-Bromo-6-fluoropyridin-3-amineHCID 18379725—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
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) δ 3.61 (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 numberUS06133253
Source datasetuspto-grants-2000_10
ORD IDord-4110db1ecbc14c7db7580a339b34a2af
Source noteuspto-grants-2000_10