HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573100Generated: October 26, 2026
Cesium fluoride → Methyl 2-(6-aminopyridin-3-yloxy)-4-fluorobenzoate
https://huagongshe.com/reaction/573100
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cesium fluoride | HCID 25953 | — |
| Reactant | 5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine | HCID 2756555 | — |
| Reactant | Methyl 2-bromo-4-fluorobenzoate | HCID 7210837 | — |
| Reactant | Dimethoxyethane methanol | HCID 86595564 | — |
| Catalyst | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| Product | Methyl 2-(6-aminopyridin-3-yloxy)-4-fluorobenzoate | HCID 67226188 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09029404B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-c6f441c9564c48fa9a1715097896e559 |
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| Source note | uspto-grants-2015_05 |
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