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HRID 276862생성일: 2026년 10월 25일

5-Amino-2-methylphenol → 6-Fluoro4-(3-hydroxy-4-methyl-phenylamino)-[1,7]naphthyridine-3-carbonitrile

https://huagongshe.com/reaction/276862

반응식

참여 물질

역할이름HCID투입량
반응물5-Amino-2-methylphenolHCID 17818—
반응물Sodium BicarbonateHCID 516892—
반응물4-Chloro-6-fluoro-1,7-naphthyridine-3-carbonitrileHCID 18548960—
용매EthanolHCID 702—
용매Sodium chloride; waterHCID 57417360—
생성물6-Fluoro4-(3-hydroxy-4-methyl-phenylamino)-[1,7]naphthyridine-3-carbonitrileHCID 1854893790%

반응 단계

To 1.5 g of 4-chloro-6-fluoro-[1.7]naphthyridine-3-carbonitrile in 40 mL of absolute ethanol was added 1.1 g of 3-hydroxy-4-methylaniline. After stirring the reaction under an inert atmosphere for 16 hours, the reaction mixture was poured into a mixture of brine and saturated aqueous sodium bicarbonate and the resultant crystals were filtered and washed with water. The product was then recrystallized from chloroform/ether/hexanes. Drying in vacuo yielded 1.9 g (90%) of 6-fluoro-4-(3-hydroxy-4-methyl-phenylamino)-[1.7]naphthyridine-3-carbonitrile as a yellow powder: melting point 236-239° C. (decomposed); mass spectrum (m/e): M+H 294.9.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06355636B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-77c528527e894238a8e296b6926c0c83
출처 메모uspto-grants-2002_03