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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925320Generated: October 28, 2026

1,2-Dichloroethane → 6-((6,7-bis(methoxy)-4-quinolinyl)oxy)-N-(5-methyl-3-isoxazolyl)-1-naphthalenecarboxamide

https://huagongshe.com/reaction/1925320

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantTriethylamineHCID 8471—
Reactant5-Amino-3-methylisoxazoleHCID 84590—
Reactant6-(6,7-Dimethoxyquinolin-4-yloxy)-1-naphthoyl chlorideHCID 24822943—
Product6-((6,7-bis(methoxy)-4-quinolinyl)oxy)-N-(5-methyl-3-isoxazolyl)-1-naphthalenecarboxamideHCID 24824446—

Reaction Conditions

Temperature80 °C

Reaction Steps

A 16×100 mm resealable vial with stir-bar was charged with 1,2-dichloroethane (3.0 mL), 6-(6,7-dimethoxyquinolin-4-yloxy)-1-naphthoyl chloride (0.15 g, 0.38 mmol), and 5-amino-3-methylisoxazole (0.045 g, 0.46 mmol). To the suspension was added triethylamine (0.13 mL, 0.95 mmol) and N,N-dimethylaminopyridine (0.005 g, 0.04 mmol). The mixture stirred at 80° C. for 15 h and was then cooled to RT. The reaction mixture was concentrated and the residue was purified by column chromatography on silica gel (eluting with 2% methanol in dichloromethane) to afford 6-((6,7-bis(methoxy)-4-quinolinyl)oxy)-N-(5-methyl-3-isoxazolyl)-1-naphthalenecarboxamide as an off-white solid. MS (ESI, pos. ion) m/z: 456.1 (M+H). Mass Calc'd for C29H26FN3O5: 455.468

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178557B2
Source datasetuspto-grants-2012_05
ORD IDord-6ca134bde70b49f1bbb8796c5e1e7621
Source noteuspto-grants-2012_05