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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364549Generated: October 29, 2026

P-Anisidine → 5-[(4-Fluorophenyl)methyl]-3-{[4-(methyloxy)phenyl]amino}-2-pyridinecarbonitrile

https://huagongshe.com/reaction/2364549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-AnisidineHCID 7732—
ReactantCesium carbonateHCID 10796—
ReactantHCID 59799017HCID 59799017—
Catalystpalladium(II) acetateHCID 167845—
CatalystBinap, (A+-)-HCID 634876—
SolventTolueneHCID 1140—
Product5-[(4-Fluorophenyl)methyl]-3-{[4-(methyloxy)phenyl]amino}-2-pyridinecarbonitrileHCID 6948245183%

Reaction Steps

A dry 50 mL flask was charged with 3-bromo-5-[(4-fluorophenyl)methyl]-2-pyridinecarbonitrile (55.3 mg, 0.190 mmol), cesium carbonate (87 mg, 0.266 mmol), palladium acetate (2.1 mg, 0.0095 mmol), rac-BINAP (8.9 mg, 0.0143 mmol), 4-(methyloxy)aniline (28 mg, 0.228 mmol) and toluene (5 mL). The mixture was refluxed for 5 hours, cooled to ambient temperature, filtered through Celite eluting with dichloromethane, and concentrated under reduced pressure. Purification by silica gel chromatography (0-100% ethyl acetate/hexanes gradient elution) gave 5-[(4-fluorophenyl)methyl]-3-{[4-(methyloxy)phenyl]amino}-2-pyridinecarbonitrile (52.2 mg, 83% yield) as a white solid. 1H NMR (CDCl3) δ 7.88 (s, 1 H), 7.07-7.02 (m, 4 H), 6.98-6.88 (m, 5 H), 6.21 (br s, 1 H), 3.82 (s, 2 H); MS m/z 334 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691991B2
Source datasetuspto-grants-2014_04
ORD IDord-13ddff4dd9cd478a84c707b96cc9cd49
Source noteuspto-grants-2014_04