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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925242Generated: October 28, 2026

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

https://huagongshe.com/reaction/1925242

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 numberUS08178557B2
Source datasetuspto-grants-2012_05
ORD IDord-c1115df3aa9d481d8594dfea65d9454e
Source noteuspto-grants-2012_05