Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2115753Generated: October 30, 2026

Diisopropylethylamine → n-[6-((6,7-Dimethoxy-4-quinolyl)oxy) (2-naphthyl)](2-fluoro-3-pyridyl)carboxamide

https://huagongshe.com/reaction/2115753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Fluoronicotinic acidHCID 96089—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant6-(6,7-Dimethoxy-4-quinolyloxy)-2-naphthylamineHCID 67520555—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Productn-[6-((6,7-Dimethoxy-4-quinolyl)oxy) (2-naphthyl)](2-fluoro-3-pyridyl)carboxamideHCID 59813676—

Reaction Steps

6-(6,7-Dimethoxy-4-quinolyloxy)-2-naphthylamine (69.2 mg, 0.2 mmol, Example 1c), 2-fluoropyridine-3-carboxylic acid (33.8 mg, 0.24 mmol, Maybridge), DIEA (31 mg, 0.24 mmol, Aldrich) and TBTU (91.2 mg, 0.24 mmol, Advanced ChemTech) were stirred in 6 mL of dry DMF at RT for 24 h. The solution was diluted with 50 mL of EtOAc and washed with saturated aqueous NaHCO3 and brine. The organic layer was dried over MgSO4 and concentrated. The residue was purified by silica gel column chromatography (EtOAc) to give title compound as a white solid. MS (ESI, pos. ion) m/z: 470.0 (M+1). Mass Calc'd for C27H20FN3O4: 469.14.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435823B2
Source datasetuspto-grants-2008_10
ORD IDord-fd5229557a9f469aadb10e3fa4f8c6d7
Source noteuspto-grants-2008_10