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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925349Generated: October 28, 2026

2-Chloropyridine → HCID 59813700, compound

https://huagongshe.com/reaction/1925349

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloropyridineHCID 7977—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium t-butoxideHCID 23676156—
Reactant6-(6,7-Dimethoxyquinolin-4-yloxy)naphthalen-1-amineHCID 67520274—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 59813700HCID 59813700—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 6-(6,7-dimethoxyquinolin-4-yloxy)naphthalene-1-amine (150 mg, 0.43 mmol), 2-chloropyridine (45 μl, 0.47 mmol), and NaOtBu (52.0 g, 160 mmol) in dioxane (4 mL) were added Pd2(dba)3 (12 mg, 0.01 mmol) and 2-(dicyclohexylphosphino)-2′-4′-6′-tri-i-propyl-1,1′-biphenyl (25 mg, 0.05 mmol). The resulting mixture was heated at 100° C. for 3 h. After cooling to ambient temperature, the mixture was diluted with EtOAc (25 mL) and poured into sat'd NaHCO3 (50 mL). The phases were separated and the aqueous phase was extracted with EtOAc (2×25 mL). The organic layers were combined, washed with brine, dried over Na2SO4 and concentrated in vacuo. The derived residue was purified by silica gel chromatography (0-10% CH3OH in CH2Cl2) to provide the title compound as a white solid. MS (ESI, pos. ion) m/z: 424.1 (M+1). Mass Calc'd for C26H21N3O3: 423.46.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178557B2
Source datasetuspto-grants-2012_05
ORD IDord-351db496b42c4e3499b0ed9f163149a1
Source noteuspto-grants-2012_05