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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 217381생성일: 2026년 10월 23일

Sodium hydride → 1-phenyl-4-(tetrahydro-2H-pyran-4-ylacetoxy)-1,8-naphthyridin-2(1H)-one

https://huagongshe.com/ko/reaction/217381

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물Sodium BicarbonateHCID 516892—
반응물(Tetrahydro-2H-pyran-4-yl)acetyl chlorideHCID 24229747—
반응물4-Hydroxy-1-phenyl-1,8-naphthyridin-2(1H)-oneHCID 54686473—
반응물HCID 178418361HCID 178418361—
용매DimethylformamideHCID 6228—
생성물1-phenyl-4-(tetrahydro-2H-pyran-4-ylacetoxy)-1,8-naphthyridin-2(1H)-oneHCID 68948920—

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 (715 mg, 3.0 mmol) in DMF (20 mL) was added sodium hydride (purity of about 60%, 120 mg, 3.0 mmol, 1.0 eq.). The mixture was stirred until no more hydrogen was generated, to obtain a solution. Then, tetrahydro-2H-pyran-4-ylacetyl chloride (1.2 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-(tetrahydro-2H-pyran-4-ylacetoxy)-1,8-naphthyridin-2(1H)-one as a form of crystal (738 mg, yield 67%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08193356B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-d837dcc9bdcd44b5859129da061ba1ae
출처 메모uspto-grants-2012_06