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HRID 217365생성일: 2026년 10월 23일

Sodium hydride → 4-hydroxy-1-phenyl-3-(4-trifluoromethoxyphenylacetyl)-1,8-naphthyridin-2(1H)-one

https://huagongshe.com/ko/reaction/217365

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참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물Sodium BicarbonateHCID 516892—
반응물4-Hydroxy-1-phenyl-1,8-naphthyridin-2(1H)-oneHCID 54686473—
반응물4-(Trifluoromethoxy)phenylacetyl chlorideHCID 57430096—
반응물HCID 178418361HCID 178418361—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물4-hydroxy-1-phenyl-3-(4-trifluoromethoxyphenylacetyl)-1,8-naphthyridin-2(1H)-oneHCID 6894540723%

반응 단계

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 (893 mg, 3.7 mmol) in DMF (16 mL) was added sodium hydride (purity of about 60%, 360 mg, 9.0 mmol, 2.4 eq.), and the mixture was stirred until no more hydrogen was generated. Then, 4-trifluoromethoxyphenylacetyl chloride (1.2 eq.) was added thereto, and the mixture was stirred at a room temperature for 3 hours. To the mixture was added water and further added a saturated sodium hydrogencarbonate solution, and the resulting mixture was subjected to extraction with dichloromethane. The extract was dried over anhydrous magnesium sulfate, and the solvent was distilled off from the extract. The resulting residue was purified by a flash column chromatography to give 4-hydroxy-1-phenyl-3-(4-trifluoromethoxyphenylacetyl)-1,8-naphthyridin-2(1H)-one (383 mg, yield 23%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08193356B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-232611ede40e4b2daeab917ef1811aab
출처 메모uspto-grants-2012_06