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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2386139Generated: November 2, 2026

Tributylvinyltin → 4-Amino-6-(4-chlorophenyl)-5-fluoro-3-vinylpyridine-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/2386139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylvinyltinHCID 81998—
ReactantMethyl 4-amino-5-fluoro-3-chloro-6-(4-chlorophenyl)picolinateHCID 22677303—
CatalystHCID 178418476HCID 178418476—
SolventAcetonitrileHCID 6342—
Product4-Amino-6-(4-chlorophenyl)-5-fluoro-3-vinylpyridine-2-carboxylic acid methyl esterHCID 594321009.4%

Reaction Conditions

Temperature110 °C

Reaction Steps

4-Amino-3-chloro-6-(4-chlorophenyl)-5-fluoropyridine-2-carboxylic acid methyl ester (0.5 g, 1.59 mmol), tributyl(vinyl)tin (1.01 g, 3.17 mmol), bis(triphenylphosphine)palladium(II) dichloride (0.111 g, 0.159 mmol), and tetrabutylammonium triphenyldifluorosilicate (1.71 g, 3.17 mmol) were combined in acetonitrile (3 ml) and heated to 110° C. for 15 min in a CEM microwave reactor. The cooled reaction mixture was concentrated onto silica gel and purified by flash chromatography on silica gel (hexane/ethyl acetate gradient) twice to yield the title compound (46 mg, 5% yield) as an off-white solid, mp 81-83° C. 1H NMR (CDCl3) δ 7.9 (m, 1H), 7.43 (m, 1H), 6.89 (dd, 1H), 5.7 (dd, 1H), 5.57 (dd, 1H), 4.72 (br s, 2H), 3.93 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268753B2
Source datasetuspto-grants-2012_09
ORD IDord-df15740585a34df8a3ca557d310956f1
Source noteuspto-grants-2012_09