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HRID 217368생성일: 2026년 10월 25일

Hydrochloric Acid → 4-methoxyacetoxy-1-phenyl-1,8-naphthyridin-2(1H)-one

https://huagongshe.com/reaction/217368

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium hydrideHCID 24758—
반응물Methoxyacetyl chlorideHCID 96623—
반응물4-Hydroxy-1-phenyl-1,8-naphthyridin-2(1H)-oneHCID 54686473—
반응물HCID 178418361HCID 178418361—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물4-methoxyacetoxy-1-phenyl-1,8-naphthyridin-2(1H)-oneHCID 6894806673%

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 (20 mL) was added sodium hydride (purity of about 60%, 192 mg, 4.8 mmol, 1.3 eq.), and the mixture was stirred until no more hydrogen was generated. Then, methoxyacetyl chloride (1.07 g, 9.9 mmol, 2.6 eq.) was added thereto, and the mixture was stirred at a room temperature for 50 minutes. To the mixture was added water. The resulting mixture was acidified with concentrated hydrochloric acid, and then the resulting precipitate was separated by filtration and dried to give 4-methoxyacetoxy-1-phenyl-1,8-naphthyridin-2(1H)-one (847 mg, yield 73%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08193356B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-8cb787f441ec49de8defc03ca7d03e3b
출처 메모uspto-grants-2012_06