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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504177Generated: October 26, 2026

Triphenylphosphine → 1-methyl-4-{3-[(2-pyridin-3-ylethyl)pyridin-4-ylmethylamino]propoxy}-1H-quinolin-2-one trihydrochloride

https://huagongshe.com/reaction/1504177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantHydrogen chloride-ethyl acetateHCID 21866389—
Reactant4-Hydroxy-N-methylcarbostyrilHCID 54686436—
Reactant3-[(2-Pyridin-3-ylethyl)pyridin-4-ylmethylamino]propan-1-olHCID 66960937—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product1-methyl-4-{3-[(2-pyridin-3-ylethyl)pyridin-4-ylmethylamino]propoxy}-1H-quinolin-2-one trihydrochlorideHCID 70656663—

Reaction Steps

Triphenyl phosphine(102 mg) and diethyl azodicarboxylate(68 mg) were added to a tetrahydrofuran (THF) solution(5 ml) of 4-hydroxy-1-methyl-1H-quinolin-2-one(63 mg), and 3-[(2-pyridin-3-ylethyl)pyridin-4-ylmethylamino]propane-1-ol(81.4 mg). The mixture was stirred overnight. After the reaction mixture was condensed under reduced pressure, the residue was purified by silica gel column chromatography (dichloromethane: methanol=20:1→10:1). The purified product was condensed under reduced pressure. A 4N-hydrogen chloride ethyl acetate solution(0.29 ml) was added to an ethyl acetate solution of the residue, which was stirred at room temperature for 30 minutes. The generated insoluble matter was separated by filtration, and dried to give the title compound(126.8 mg) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212187B2
Source datasetuspto-grants-2015_12
ORD IDord-1c62243170884866817dae8772968b71
Source noteuspto-grants-2015_12