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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2409368Generated: October 30, 2026

4-Amino-3-fluoropyridine → {1-[2-Bromo-4-(3-fluoro-pyridin-4-ylcarbamoyl)-phenyl]-ethyl}-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/2409368

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-3-fluoropyridineHCID 817122—
Reactant3-Bromo-4-(1-tert-butoxycarbonylamino-ethyl)-benzoic acidHCID 67409093—
SolventTetrahydrofuranHCID 8028—
Product{1-[2-Bromo-4-(3-fluoro-pyridin-4-ylcarbamoyl)-phenyl]-ethyl}-carbamic acid tert-butyl esterHCID 67407943—

Reaction Steps

To a solution of 3-bromo-4-(1-tert-butoxycarbonylamino-ethyl)-benzoic acid (8352 μmol) in dry THF (20 ml) was added Ghosez reagent (2 eq.). The mixture was stirred at RT for 2 hours. The solvent was removed under reduced pressure. The residue was dissolved in dry pyridine (20 ml) and 3-fluoro-pyridin-4-ylamine (1.2 eq) was added. The reaction mixture was stirred at RT for 2.5 hours. The pyridine was removed under reduced pressure. The residue was dissolved in 1N Na2CO3 and extracted with EtOAc. The combined organic layers were washed with 1N NaHCO3, citric acid and water. The organic layer was dried over MgSO4 and the solvent was removed under reduced pressure. The compound was purified by column chromatography (silicagel, DCM/MeOH gradient).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815873B2
Source datasetuspto-grants-2014_08
ORD IDord-5a34995ec1de4ebbb4b62fde4446f434
Source noteuspto-grants-2014_08