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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64176Generated: October 29, 2026

Potassium Fluoride → N-(3-((4-bromo-2-nitrophenyl)amino)-5-(3-fluoropyridin-2-yl)phenyl)acetamide

https://huagongshe.com/reaction/64176

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium FluorideHCID 522689—
Reactant4-Bromo-1-fluoro-2-nitrobenzeneHCID 2736328—
ReactantN-(3-amino-5-(3-fluoropyridin-2-yl)phenyl)acetamideHCID 89500089—
SolventDimethylformamideHCID 6228—
ProductN-(3-((4-bromo-2-nitrophenyl)amino)-5-(3-fluoropyridin-2-yl)phenyl)acetamideHCID 8950027350%

Reaction Steps

Solution of 4-bromo-1-fluoro-2-nitrobenzene (3.0 g, 13.63 mmol), N-(3-amino-5-(3-fluoropyridin-2-yl)phenyl)acetamide (4.0 g, 16.36 mmol), and potassium fluoride (0.95 g, 16.36 mmol) in DMF was heated at 130° C. for 16 h. The mixture was quenched and extracted as in Example 1(d). The solvent was distilled off to afford the crude residue which was purified by column chromatography (60-120 silica gel, 30% ethyl acetate in hexane) to yield the title product in 50% yield (3.4 g). 1H NMR (300 MHz, DMSO-d6): δ 8.55 (brs, 1H), 8.23 (brs, 1H), 7.96 (m, 2H), 7.85 (m, 2H), 7.67 (d, 1H), 7.51 (m, 2H), 7.21 (d, 1H), 2.07 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447091B2
Source datasetuspto-grants-2016_09
ORD IDord-2f04c452ef174e25bf970745daefbe87
Source noteuspto-grants-2016_09