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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1848866Generated: October 27, 2026

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

https://huagongshe.com/reaction/1848866

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—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
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 numberUS08952157B2
Source datasetuspto-grants-2015_02
ORD IDord-44a72f0d8e2d437393ef32f7b527b284
Source noteuspto-grants-2015_02