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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244323Generated: November 2, 2026

(E)-trimethyl(2-(tributylstannyl)vinyl)silane → HCID 70497566, compound

https://huagongshe.com/reaction/244323

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(E)-trimethyl(2-(tributylstannyl)vinyl)silaneHCID 10949136—
ReactantMethyl 4-amino-6-(4-chloro-3-fluorophenyl)-5-fluoro-3-iodopicolinateHCID 70497132—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 70497566HCID 7049756679.5%

Reaction Conditions

Temperature120 °C

Reaction Steps

Methyl 4-amino-6-(4-chloro-3-fluorophenyl)-5-fluoro-3-iodopicolinate (350 mg, 0.824 mmol), and tetrakis triphenylphosphine palladium(0) (95 mg, 0.082 mmol) were combined in a Biotage microwave reaction vessel that was then sealed and purged with nitrogen. (E)-trimethyl(2-(tributylstannyl)vinyl)silane (417 mg, 1.072 mmol) in dioxane (4122 μl) was added and the reaction mixture was heated in a microwave reactor at 120° C. for 30 min The cooled reaction mixture was diluted with ethyl acetate and washed with saturated sodium chloride. The organic phase was dried over magnesium sulfate, filtered and concentrated on to silica. The product was purified by flash chromatography. (SiO2, 0-20% EtOAc:Hex gradient) to provide the title compound as a tan solid (260 mg, 0.655 mmol, 79% yield); 1H NMR (400 MHz, DMSO-d6) d 0.17 (s, 9H), 3.76 (s, 3H), 6.09 (d, J=19.2 Hz, 1H), 6.60 (s, 2H), 6.91 (d, J=19.2 Hz, 1H), 7.75 (dd, J=3.8, 1.9 Hz, 2H), 7.83 (dd, J=10.8, 1.3 Hz, 1H); 19F NMR (376 MHz, DMSO-d6) d −145.16 , −115.98; ESIMS m/z 398 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658568B2
Source datasetuspto-grants-2014_02
ORD IDord-89294aff165f489099d7c1f0130fd73f
Source noteuspto-grants-2014_02