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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217379Generated: October 25, 2026

Sodium hydride → 1-phenyl-4-(2-phenylbutyryloxy)-1,8-naphthyridin-2(1H)-one

https://huagongshe.com/reaction/217379

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-Phenylbutyryl chlorideHCID 98173—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Hydroxy-1-phenyl-1,8-naphthyridin-2(1H)-oneHCID 54686473—
ReactantHCID 178418361HCID 178418361—
SolventDimethylformamideHCID 6228—
Product1-phenyl-4-(2-phenylbutyryloxy)-1,8-naphthyridin-2(1H)-oneHCID 68948676—

Reaction Steps

In accordance with a process described in JP-61-246183A, 4-hydroxy-1-phenyl-1,8-naphthyridin-2(1H)-one was synthesized. To a suspension of the synthesized compound (1.19 g, 5.0 mmol) in DMF (40 mL) was added sodium hydride (purity of about 60%, 200 mg, 5.0 mmol, 1.0 eq.). The mixture was stirred until no more hydrogen was generated, to obtain a solution. Then, 2-phenylbutyryl chloride (0.92 mL, 5.5 mmol, 1.1 eq.) was added thereto, and the mixture was stirred at a room temperature for 1 hour. To the mixture was added a saturated sodium hydrogencarbonate aqueous solution, and the resulting precipitate was separated by filtration, washed with water, and dried to give 1-phenyl-4-(2-phenylbutyryloxy)-1,8-naphthyridin-2(1H)-one as a form of crystal (1.63 g, yield 85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193356B2
Source datasetuspto-grants-2012_06
ORD IDord-4eabe78405764933b2382d7e4272cf0a
Source noteuspto-grants-2012_06