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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043119Generated: October 26, 2026

Cesium fluoride → Methyl 2-(6-aminopyridin-3-yloxy)-4-fluorobenzoate

https://huagongshe.com/reaction/1043119

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium fluorideHCID 25953—
Reactant5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amineHCID 2756555—
ReactantMethyl 2-bromo-4-fluorobenzoateHCID 7210837—
ReactantDimethoxyethane methanolHCID 86595564—
CatalystHCID 178418476HCID 178418476—
ProductMethyl 2-(6-aminopyridin-3-yloxy)-4-fluorobenzoateHCID 67226188—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine (1.039 g), CsF (1.956 g), bis(triphenylphosphine)palladium(II) dichloride (0.301 g), and methyl 2-bromo-4-fluorobenzoate (1.0 g) in 50 mL dimethoxyethane-methanol (1:1) was heated at 80° C. for 2.5 hours. The reaction mixture was partitioned between water and ethyl acetate. The organic phase was washed with brine, dried over MgSO4, filtered, ad concentrated. The residue was chromatographed on silica gel with 25-80% ethyl acetate in hexanes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557983B2
Source datasetuspto-grants-2013_10
ORD IDord-9d7ca6ba154c4a32a6f31a28f520e6e8
Source noteuspto-grants-2013_10